def createExpressionDict(annotationFile, projectFolder, projectName, refseqToNameDict, expCutoff,expressionFile=''):
'''
input: an activity table with refseq in first column and expression or promoter
acetylation in second column
output: a dictionary keyed by refseq that points to activity
'''
print 'CREATING EXPRESSION DICTIONARY'
if not expressionFile:
expressionFilename = projectFolder + 'bamliquidator/matrix.txt'
else:
expressionFilename = expressionFile
expressionTable = utils.parseTable(expressionFilename, '\t')
expressionDictNM = {}
expressionDictGene = {}
for line in expressionTable[1:]:
trid = line[0]
geneName = refseqToNameDict[trid]
try:
exp = float(line[2])
except IndexError:
exp = float(line[1])
# Save the expression value of each NMid in a dict, keep higher value if multiple
if trid in expressionDictNM and exp > expressionDictNM[trid]:
expressionDictNM[trid] = exp
elif trid not in expressionDictNM:
expressionDictNM[trid] = exp
# Save the value of the expression if it's the highest for that gene
if geneName in expressionDictGene and exp > expressionDictGene[geneName]:
expressionDictGene[geneName] = exp
elif geneName not in expressionDictGene:
expressionDictGene[geneName] = exp
cutoff = numpy.percentile(expressionDictGene.values(), expCutoff)
print 'Expression cutoff: ' + str(cutoff)
expressedGenes = []
expressedNM = []
for nmid in expressionDictNM:
if float(expressionDictNM[nmid]) > cutoff:
expressedGenes.append(refseqToNameDict[nmid])
expressedNM.append(nmid)
expressedGenes = utils.uniquify(expressedGenes)
Genefilename = projectFolder + projectName + '_EXPRESSED_GENES.txt'
utils.unParseTable(expressedGenes, Genefilename, '')
expressedNM = utils.uniquify(expressedNM)
NMfilename = projectFolder + projectName + '_EXPRESSED_NM.txt'
utils.unParseTable(expressedNM, NMfilename, '')
return expressedNM, expressionDictNM
def getBamChromList(bamFileList):
'''
gets the consensus list of chromosomes mapped by the bams
'''
#start w/ the first bam
cmd = '%s idxstats %s' % (samtoolsPath, bamFileList[0])
idxStats = subprocess.Popen(cmd, stdout=subprocess.PIPE, shell=True)
idxStats = idxStats.communicate()
finalChromList = [
line.split('\t')[0] for line in idxStats[0].split('\n')[0:-2]
]
#now go through each additional bam
for bamFile in bamFileList:
cmd = '%s idxstats %s' % (samtoolsPath, bamFile)
idxStats = subprocess.Popen(cmd, stdout=subprocess.PIPE, shell=True)
idxStats = idxStats.communicate()
chromList = [
line.split('\t')[0] for line in idxStats[0].split('\n')[0:-2]
]
finalChromList = [
chrom for chrom in finalChromList if chromList.count(chrom) != 0
]
return utils.uniquify(finalChromList)
def __init__(self,
poll_id: str,
poll_title: str,
options: List[Any],
is_immortal=False,
updated_since_start=True):
if options is None:
options = []
self.poll_id = poll_id
self.creation_time = time.time()
self.last_update = time.time()
self.poll_title = poll_title
self.options = uniquify(options)
self.reaction_to_option = {
reaction_emojies[k]: options[k]
for k in range(len(options))
}
self.option_to_reaction = {
options[k]: reaction_emojies[k]
for k in range(len(options))
}
self.participants = dict()
self.option_to_participants = {key: [] for key in options}
self.sent_message = None
self.received_message = None
self.is_immortal = is_immortal
self.is_enabled = True
self.updated_since_start = updated_since_start
def mapGFFLineToBed(gffLine, outFolder, nBins, bedCollection, header=''):
'''
for every line produces a file with all of the rectangles to draw
'''
if len(header) == 0:
gffString = '%s_%s_%s_%s' % (gffLine[0], gffLine[6], gffLine[3],
gffLine[4])
else:
gffString = header
diagramTable = [[0, 0, 0, 0]]
nameTable = [['', 0, 0]]
gffLocus = utils.Locus(gffLine[0], int(gffLine[3]), int(gffLine[4]),
gffLine[6], gffLine[1])
scaleFactor = float(nBins) / gffLocus.len()
# plotting buffer for diagrams
# plotBuffer = int(gffLocus.len() / float(nBins) * 20) # UNUSED (?)
overlapLoci = bedCollection.getOverlap(gffLocus, sense='both')
print("IDENTIFIED %s OVERLAPPING BED LOCI FOR REGION %s" %
(len(overlapLoci), gffLine))
# since beds come from multiple sources, we want to figure out how to offset them
offsetDict = {} # this will store each ID name
bedNamesList = utils.uniquify([locus.ID() for locus in overlapLoci])
bedNamesList.sort()
for i in range(len(bedNamesList)):
offsetDict[bedNamesList[
i]] = 2 * i # offsets different categories of bed regions
if gffLine[6] == '-':
refPoint = int(gffLine[4])
else:
refPoint = int(gffLine[3])
# fill out the name table
for name in bedNamesList:
offset = offsetDict[name]
nameTable.append([name, 0, 0.0 - offset])
for bedLocus in overlapLoci:
offset = offsetDict[bedLocus.ID()]
[start,
stop] = [abs(x - refPoint) * scaleFactor for x in bedLocus.coords()]
diagramTable.append([start, -0.5 - offset, stop, 0.5 - offset])
utils.unParseTable(diagramTable,
outFolder + gffString + '_bedDiagramTemp.txt', '\t')
utils.unParseTable(nameTable, outFolder + gffString + '_bedNameTemp.txt',
'\t')
def splitRegions(inputGFF,tssCollection):
#if even a single coordinate is shared with the +/-1kb
splitGFF = []
for line in inputGFF:
chrom = line[0]
regionID = line[1]
lineLocus = utils.Locus(line[0],line[3],line[4],'.')
overlappingLoci = tssCollection.getOverlap(lineLocus)
if len(overlappingLoci) > 0: #case where a tss Overlap
#identify the parts of the line locus that are contained
localTSSCollection = utils.LocusCollection(overlappingLoci,50)
overlappingCoords = lineLocus.coords()
for tssLocus in overlappingLoci:
overlappingCoords += tssLocus.coords()
overlappingCoords = utils.uniquify(overlappingCoords)
overlappingCoords.sort()
#you need to hack and slash add 1 to the last coordinate of the overlappingCoords
overlappingCoords[-1] +=1
i = 0
regionTicker = 1
while i < (len(overlappingCoords)-1):
start = int(overlappingCoords[i])
stop = int(overlappingCoords[(i+1)])-1
if (stop - start) < 50: #this eliminates really tiny regions
i+=1
continue
splitLocus = utils.Locus(chrom,start+1,stop,'.')
if lineLocus.overlaps(splitLocus): #has to be a mycn site
newID = '%s_%s' % (regionID,regionTicker)
tssStatus = 0
if localTSSCollection.getOverlap(splitLocus):
tssStatus = 1
splitGFFLine = [chrom,newID,newID,start,stop,'','.',tssStatus,newID]
splitGFF.append(splitGFFLine)
regionTicker+=1
i+=1
else:
line[7] = 0
splitGFF.append(line)
return splitGFF
def get_all_os_versions():
"""
Collapse the above list of OS versions for usage/display by the CLI/webapp.
"""
results = ['']
for x in VALID_OS_VERSIONS.keys():
for y in VALID_OS_VERSIONS[x]:
results.append(y)
results = utils.uniquify(results)
results.sort()
return results
def findMotifs(subpeakFasta, bg_path, candidate_tf_list, projectFolder,
analysis_name, motifConvertFile, motifDatabaseFile):
'''
takes the refseq to subpeak seq dict
returns the networkx object with all connections
'''
fimoFolder = utils.formatFolder(projectFolder + 'FIMO/', True)
subpeak_name = subpeakFasta.split('/')[-1].split('.')[0]
output = '%s%s_fimo.txt' % (fimoFolder, subpeak_name)
# Create a dictionary to call motif names keyed on gene names
motifDatabase = utils.parseTable(motifConvertFile, '\t')
motifDatabaseDict = {} #create a dict keyed by TF with multiple motifs
for line in motifDatabase:
motifDatabaseDict[line[1]] = []
for line in motifDatabase:
motifDatabaseDict[line[1]].append(line[0])
candidate_tf_list.sort()
print(candidate_tf_list)
#now make a list of all motifs
motif_list = []
for tf in candidate_tf_list:
motif_list += motifDatabaseDict[tf]
motif_list = utils.uniquify(motif_list)
fimo_bash_path = '%s%s_fimo.sh' % (fimoFolder, analysis_name)
fimo_bash = open(fimo_bash_path, 'w')
fimo_bash.write('#!/usr/bin/bash\n\n')
fimoCmd = 'fimo'
for motif in motif_list:
fimoCmd += ' --motif ' + "'%s'" % (str(motif))
#fimoCmd += ' --thresh 1e-5' #if you want to increase stringency
fimoCmd += ' -verbosity 1' # thanks for that ;)!
fimoCmd += ' -text'
fimoCmd += ' -oc ' + projectFolder + 'FIMO'
fimoCmd += ' --bgfile %s' % (bg_path)
fimoCmd += ' ' + motifDatabaseFile + ' '
fimoCmd += subpeakFasta
fimoCmd += ' > ' + output
print fimoCmd
fimo_bash.write(fimoCmd)
fimo_bash.close()
fimoOutput = subprocess.call(
fimoCmd, shell=True) #will wait that fimo is done to go on
return output
def findMotifs(subpeakFasta,bg_path,candidate_tf_list, projectFolder, analysis_name, motifConvertFile, motifDatabaseFile):
'''
takes the refseq to subpeak seq dict
returns the networkx object with all connections
'''
fimoFolder = utils.formatFolder(projectFolder + 'FIMO/', True)
subpeak_name = subpeakFasta.split('/')[-1].split('.')[0]
output = '%s%s_fimo.txt' % (fimoFolder,subpeak_name)
# Create a dictionary to call motif names keyed on gene names
motifDatabase = utils.parseTable(motifConvertFile, '\t')
motifDatabaseDict = {} #create a dict keyed by TF with multiple motifs
for line in motifDatabase:
motifDatabaseDict[line[1]] = []
for line in motifDatabase:
motifDatabaseDict[line[1]].append(line[0])
candidate_tf_list.sort()
print(candidate_tf_list)
#now make a list of all motifs
motif_list = []
for tf in candidate_tf_list:
motif_list += motifDatabaseDict[tf]
motif_list = utils.uniquify(motif_list)
fimo_bash_path = '%s%s_fimo.sh' % (fimoFolder,analysis_name)
fimo_bash = open(fimo_bash_path,'w')
fimo_bash.write('#!/usr/bin/bash\n\n')
fimoCmd = 'fimo'
for motif in motif_list:
fimoCmd += ' --motif ' + "'%s'" % (str(motif))
#fimoCmd += ' --thresh 1e-5' #if you want to increase stringency
fimoCmd += ' -verbosity 1' # thanks for that ;)!
fimoCmd += ' -text'
fimoCmd += ' -oc ' + projectFolder + 'FIMO'
fimoCmd += ' --bgfile %s' % (bg_path)
fimoCmd += ' ' + motifDatabaseFile + ' '
fimoCmd += subpeakFasta
fimoCmd += ' > '+ output
print fimoCmd
fimo_bash.write(fimoCmd)
fimo_bash.close()
fimoOutput = subprocess.call(fimoCmd, shell=True) #will wait that fimo is done to go on
return output
def checkRefCollection(referenceCollection):
'''
makes sure the names of all loci in the reference collection are unique
'''
namesList = [locus.ID() for locus in referenceCollection.getLoci()]
if len(namesList) != len(utils.uniquify(namesList)):
print("ERROR: REGIONS HAVE NON-UNIQUE IDENTIFIERS")
sys.exit()
else:
print("REFERENCE COLLECTION PASSES QC")
return
def checkRefCollection(referenceCollection):
'''
makes sure the names of all loci in the reference collection are unique
'''
namesList = [locus.ID() for locus in referenceCollection.getLoci()]
if len(namesList) != len(utils.uniquify(namesList)):
print("ERROR: REGIONS HAVE NON-UNIQUE IDENTIFIERS")
sys.exit()
else:
print("REFERENCE COLLECTION PASSES QC")
return
def addLengths(gene_table_path, peak_table_path):
'''
add tss and distal lengths to a gene table
using the peak table
'''
output_path = string.replace(gene_table_path, 'GENE_TABLE',
'GENE_TABLE_LENGTH')
print(output_path)
tss_dict = defaultdict(int)
distal_dict = defaultdict(int)
peak_table = utils.parseTable(peak_table_path, '\t')
for line in peak_table[1:]:
#get the genes
gene_list = []
if len(line) == 15:
gene_list += line[-1].split(',')
gene_list += line[-2].split(',')
elif len(line) == 14:
gene_list += line[-1].split(',')
else:
continue
gene_list = utils.uniquify(
[gene for gene in gene_list if len(gene) > 0])
for gene in gene_list:
if int(line[5]) == 1:
tss_dict[gene] += int(line[4])
else:
distal_dict[gene] += int(line[4])
#now fill out the gene table
gene_table = utils.parseTable(gene_table_path, '\t')
output_table = [gene_table[0] + ['TSS_LENGTH', 'DISTAL_LENGTH']]
for line in gene_table[1:]:
gene = line[0]
new_line = line + [tss_dict[gene], distal_dict[gene]]
output_table.append(new_line)
utils.unParseTable(output_table, output_path, '\t')
return output_path
def mapGFFLineToBed(gffLine, outFolder, nBins, bedCollection, header=''):
'''
for every line produces a file with all of the rectangles to draw
'''
if len(header) == 0:
gffString = '%s_%s_%s_%s' % (gffLine[0], gffLine[6], gffLine[3], gffLine[4])
else:
gffString = header
diagramTable = [[0, 0, 0, 0]]
nameTable = [['', 0, 0]]
gffLocus = utils.Locus(gffLine[0], int(gffLine[3]), int(gffLine[4]), gffLine[6], gffLine[1])
scaleFactor = float(nBins) / gffLocus.len()
# plotting buffer for diagrams
# plotBuffer = int(gffLocus.len() / float(nBins) * 20) # UNUSED (?)
overlapLoci = bedCollection.getOverlap(gffLocus, sense='both')
print("IDENTIFIED %s OVERLAPPING BED LOCI FOR REGION %s" % (len(overlapLoci),gffLine))
# since beds come from multiple sources, we want to figure out how to offset them
offsetDict = {} # this will store each ID name
bedNamesList = utils.uniquify([locus.ID() for locus in overlapLoci])
bedNamesList.sort()
for i in range(len(bedNamesList)):
offsetDict[bedNamesList[i]] = 2 * i # offsets different categories of bed regions
if gffLine[6] == '-':
refPoint = int(gffLine[4])
else:
refPoint = int(gffLine[3])
# fill out the name table
for name in bedNamesList:
offset = offsetDict[name]
nameTable.append([name, 0, 0.0 - offset])
for bedLocus in overlapLoci:
offset = offsetDict[bedLocus.ID()]
[start, stop] = [abs(x - refPoint) * scaleFactor for x in bedLocus.coords()]
diagramTable.append([start, -0.5 - offset, stop, 0.5 - offset])
utils.unParseTable(diagramTable, outFolder + gffString + '_bedDiagramTemp.txt', '\t')
utils.unParseTable(nameTable, outFolder + gffString + '_bedNameTemp.txt', '\t')
def filterGFF(gffFile, chromList):
'''
takes in a gff and filters out all lines that don't belong to a chrom in the chromList
'''
gff = utils.parseTable(gffFile, '\t')
filteredGFF = []
excludeList = []
for line in gff:
if chromList.count(line[0]) == 1:
filteredGFF.append(line)
else:
excludeList.append(line[0])
excludeList = utils.uniquify(excludeList)
if len(excludeList) > 0:
print("EXCLUDED GFF REGIONS FROM THE FALLING CHROMS: %s" %
(','.join(excludeList)))
return filteredGFF
def filterGFF(gffFile,chromList):
'''
takes in a gff and filters out all lines that don't belong to a chrom in the chromList
'''
gff = utils.parseTable(gffFile,'\t')
filteredGFF = []
excludeList=[]
for line in gff:
if chromList.count(line[0]) ==1:
filteredGFF.append(line)
else:
excludeList.append(line[0])
excludeList = utils.uniquify(excludeList)
if len(excludeList) > 0:
print("EXCLUDED GFF REGIONS FROM THE FALLING CHROMS: %s" % (','.join(excludeList)))
return filteredGFF
def getBamChromList(bamFileList):
'''
gets the consensus list of chromosomes mapped by the bams
'''
#start w/ the first bam
cmd = '%s idxstats %s' % (samtoolsPath,bamFileList[0])
idxStats = subprocess.Popen(cmd,stdout=subprocess.PIPE,shell=True)
idxStats= idxStats.communicate()
finalChromList = [line.split('\t')[0] for line in idxStats[0].split('\n')[0:-2]]
#now go through each additional bam
for bamFile in bamFileList:
cmd = '%s idxstats %s' % (samtoolsPath,bamFile)
idxStats = subprocess.Popen(cmd,stdout=subprocess.PIPE,shell=True)
idxStats= idxStats.communicate()
chromList = [line.split('\t')[0] for line in idxStats[0].split('\n')[0:-2]]
finalChromList = [chrom for chrom in finalChromList if chromList.count(chrom) != 0]
return utils.uniquify(finalChromList)
def make_probe_to_gene_dict(annotFile, array_1_path, array_2_path):
'''
keyed by probe ID w/ gene as value
'''
#see if it already exists
pickle_path = '%soberthuer_outcome/probe_dict.pkl' % (projectFolder)
if utils.checkOutput(pickle_path, 0, 0):
print('loading previously made probe dict at %s' % (pickle_path))
probe_gene_dict = pickle.load(open(pickle_path, "rb"))
return probe_gene_dict
#we want to intersect refseq common names w/ the array
startDict = utils.makeStartDict(annotFile)
ref_name_list = utils.uniquify(
[startDict[refID]['name'] for refID in startDict.keys()])
probe_gene_dict = {}
array_1 = utils.parseTable(array_1_path, '\t')
array_2 = utils.parseTable(array_2_path, '\t')
ticker = 0
for line in array_1 + array_2:
if len(line) < 5:
continue
ticker += 1
probe_id = line[4]
name = line[-1]
# print(probe_id)
# print(name)
# if ticker== 10:
# sys.exit()
# print(line)
if ref_name_list.count(name) > 0:
probe_gene_dict[probe_id] = name
pickle.dump(probe_gene_dict, open(pickle_path, 'wb'))
return probe_gene_dict
def mapEnhancerToGene(annotFile,enhancerFile,transcribedFile='',uniqueGenes=True,searchWindow =50000,noFormatTable = False):
'''
maps genes to enhancers. if uniqueGenes, reduces to gene name only. Otherwise, gives for each refseq
'''
startDict = utils.makeStartDict(annotFile)
enhancerTable = utils.parseTable(enhancerFile,'\t')
#internal parameter for debugging
byRefseq = False
if len(transcribedFile) > 0:
transcribedTable = utils.parseTable(transcribedFile,'\t')
transcribedGenes = [line[1] for line in transcribedTable]
else:
transcribedGenes = startDict.keys()
print('MAKING TRANSCRIPT COLLECTION')
transcribedCollection = utils.makeTranscriptCollection(annotFile,0,0,500,transcribedGenes)
print('MAKING TSS COLLECTION')
tssLoci = []
for geneID in transcribedGenes:
tssLoci.append(utils.makeTSSLocus(geneID,startDict,0,0))
#this turns the tssLoci list into a LocusCollection
#50 is the internal parameter for LocusCollection and doesn't really matter
tssCollection = utils.LocusCollection(tssLoci,50)
geneDict = {'overlapping':defaultdict(list),'proximal':defaultdict(list)}
#dictionaries to hold ranks and superstatus of gene nearby enhancers
rankDict = defaultdict(list)
superDict= defaultdict(list)
#list of all genes that appear in this analysis
overallGeneList = []
if noFormatTable:
#set up the output tables
#first by enhancer
enhancerToGeneTable = [enhancerTable[0]+['OVERLAP_GENES','PROXIMAL_GENES','CLOSEST_GENE']]
else:
#set up the output tables
#first by enhancer
enhancerToGeneTable = [enhancerTable[0][0:9]+['OVERLAP_GENES','PROXIMAL_GENES','CLOSEST_GENE'] + enhancerTable[5][-2:]]
#next by gene
geneToEnhancerTable = [['GENE_NAME','REFSEQ_ID','PROXIMAL_ENHANCERS']]
#next make the gene to enhancer table
geneToEnhancerTable = [['GENE_NAME','REFSEQ_ID','PROXIMAL_ENHANCERS','ENHANCER_RANKS','IS_SUPER']]
for line in enhancerTable:
if line[0][0] =='#' or line[0][0] == 'R':
continue
enhancerString = '%s:%s-%s' % (line[1],line[2],line[3])
enhancerLocus = utils.Locus(line[1],line[2],line[3],'.',line[0])
#overlapping genes are transcribed genes whose transcript is directly in the stitchedLocus
overlappingLoci = transcribedCollection.getOverlap(enhancerLocus,'both')
overlappingGenes =[]
for overlapLocus in overlappingLoci:
overlappingGenes.append(overlapLocus.ID())
#proximalGenes are transcribed genes where the tss is within 50kb of the boundary of the stitched loci
proximalLoci = tssCollection.getOverlap(utils.makeSearchLocus(enhancerLocus,searchWindow,searchWindow),'both')
proximalGenes =[]
for proxLocus in proximalLoci:
proximalGenes.append(proxLocus.ID())
distalLoci = tssCollection.getOverlap(utils.makeSearchLocus(enhancerLocus,1000000,1000000),'both')
distalGenes =[]
for proxLocus in distalLoci:
distalGenes.append(proxLocus.ID())
overlappingGenes = utils.uniquify(overlappingGenes)
proximalGenes = utils.uniquify(proximalGenes)
distalGenes = utils.uniquify(distalGenes)
allEnhancerGenes = overlappingGenes + proximalGenes + distalGenes
#these checks make sure each gene list is unique.
#technically it is possible for a gene to be overlapping, but not proximal since the
#gene could be longer than the 50kb window, but we'll let that slide here
for refID in overlappingGenes:
if proximalGenes.count(refID) == 1:
proximalGenes.remove(refID)
for refID in proximalGenes:
if distalGenes.count(refID) == 1:
distalGenes.remove(refID)
#Now find the closest gene
if len(allEnhancerGenes) == 0:
closestGene = ''
else:
#get enhancerCenter
enhancerCenter = (int(line[2]) + int(line[3]))/2
#get absolute distance to enhancer center
distList = [abs(enhancerCenter - startDict[geneID]['start'][0]) for geneID in allEnhancerGenes]
#get the ID and convert to name
closestGene = startDict[allEnhancerGenes[distList.index(min(distList))]]['name']
#NOW WRITE THE ROW FOR THE ENHANCER TABLE
if noFormatTable:
newEnhancerLine = list(line)
newEnhancerLine.append(join(utils.uniquify([startDict[x]['name'] for x in overlappingGenes]),','))
newEnhancerLine.append(join(utils.uniquify([startDict[x]['name'] for x in proximalGenes]),','))
newEnhancerLine.append(closestGene)
else:
newEnhancerLine = line[0:9]
newEnhancerLine.append(join(utils.uniquify([startDict[x]['name'] for x in overlappingGenes]),','))
newEnhancerLine.append(join(utils.uniquify([startDict[x]['name'] for x in proximalGenes]),','))
newEnhancerLine.append(closestGene)
newEnhancerLine += line[-2:]
enhancerToGeneTable.append(newEnhancerLine)
#Now grab all overlapping and proximal genes for the gene ordered table
overallGeneList +=overlappingGenes
for refID in overlappingGenes:
geneDict['overlapping'][refID].append(enhancerString)
rankDict[refID].append(int(line[-2]))
superDict[refID].append(int(line[-1]))
overallGeneList+=proximalGenes
for refID in proximalGenes:
geneDict['proximal'][refID].append(enhancerString)
rankDict[refID].append(int(line[-2]))
superDict[refID].append(int(line[-1]))
#End loop through
#Make table by gene
overallGeneList = utils.uniquify(overallGeneList)
#use enhancer rank to order
rankOrder = utils.order([min(rankDict[x]) for x in overallGeneList])
usedNames = []
for i in rankOrder:
refID = overallGeneList[i]
geneName = startDict[refID]['name']
if usedNames.count(geneName) > 0 and uniqueGenes == True:
continue
else:
usedNames.append(geneName)
proxEnhancers = geneDict['overlapping'][refID]+geneDict['proximal'][refID]
superStatus = max(superDict[refID])
enhancerRanks = join([str(x) for x in rankDict[refID]],',')
newLine = [geneName,refID,join(proxEnhancers,','),enhancerRanks,superStatus]
geneToEnhancerTable.append(newLine)
#resort enhancerToGeneTable
if noFormatTable:
return enhancerToGeneTable,geneToEnhancerTable
else:
enhancerOrder = utils.order([int(line[-2]) for line in enhancerToGeneTable[1:]])
sortedTable = [enhancerToGeneTable[0]]
for i in enhancerOrder:
sortedTable.append(enhancerToGeneTable[(i+1)])
return sortedTable,geneToEnhancerTable
def _matrix_entry_maps(self):
"""Set of all mappings used in matrix arguments."""
return list(uniquify(m for arg in self.args if arg._is_mat for m in arg.map))
def _unique_matrix(self):
return list(uniquify(a.data for a in self._matrix_args))
def main():
'''
main run call
'''
debug = False
from optparse import OptionParser
usage = "usage: %prog [options] -g [GENOME] -i [INPUT_REGION_GFF] -r [RANKBY_BAM_FILE] -o [OUTPUT_FOLDER] [OPTIONAL_FLAGS]"
parser = OptionParser(usage=usage)
# required flags
parser.add_option("-i", "--i", dest="input", nargs=1, default=None,
help="Enter a comma separated list of .gff or .bed file of binding sites used to make enhancers")
parser.add_option("-r", "--rankby", dest="rankby", nargs=1, default=None,
help="Enter a comma separated list of bams to rank by")
parser.add_option("-o", "--out", dest="out", nargs=1, default=None,
help="Enter an output folder")
parser.add_option("-g", "--genome", dest="genome", nargs=1, default=None,
help="Enter the genome build (MM9,MM8,HG18,HG19)")
# optional flags
parser.add_option("-n", "--name", dest="name", nargs=1, default=None,
help="Provide a name for the analysis otherwise ROSE will guess")
parser.add_option("-c", "--control", dest="control", nargs=1, default=None,
help="Enter a comma separated list of control bams. Can either provide a single control bam for all rankby bams, or provide a control bam for each individual bam")
parser.add_option("-s", "--stitch", dest="stitch", nargs=1, default='',
help="Enter a max linking distance for stitching. Default will determine optimal stitching parameter")
parser.add_option("-t", "--tss", dest="tss", nargs=1, default=0,
help="Enter a distance from TSS to exclude. 0 = no TSS exclusion")
parser.add_option("--mask", dest="mask", nargs=1, default=None,
help="Mask a set of regions from analysis. Provide a .bed or .gff of masking regions")
# RETRIEVING FLAGS
(options, args) = parser.parse_args()
if not options.input or not options.rankby or not options.out or not options.genome:
print('hi there')
parser.print_help()
exit()
# making the out folder if it doesn't exist
outFolder = utils.formatFolder(options.out, True)
# figuring out folder schema
gffFolder = utils.formatFolder(outFolder + 'gff/', True)
mappedFolder = utils.formatFolder(outFolder + 'mappedGFF/', True)
# GETTING INPUT FILE(s)
inputList = [inputFile for inputFile in options.input.split(',') if len(inputFile) > 1]
#converting all input files into GFFs and moving into the GFF folder
inputGFFList = []
for inputFile in inputList:
if inputFile.split('.')[-1] == 'bed':
# CONVERTING A BED TO GFF
inputGFFName = inputFile.split('/')[-1][0:-4] #strips the last 4 characters i.e. '.bed'
inputGFFFile = '%s%s.gff' % (gffFolder, inputGFFName)
utils.bedToGFF(inputFile, inputGFFFile)
elif options.input.split('.')[-1] == 'gff':
# COPY THE INPUT GFF TO THE GFF FOLDER
os.system('cp %s %s' % (inputFile, gffFolder))
inputGFFFile = '%s%s' % (gffFolder,inputFile.split('/')[-1])
else:
print('WARNING: INPUT FILE DOES NOT END IN .gff or .bed. ASSUMING .gff FILE FORMAT')
# COPY THE INPUT GFF TO THE GFF FOLDER
os.system('cp %s %s' % (inputFile, gffFolder))
inputGFFFile = '%s%s' % (gffFolder,inputFile.split('/')[-1])
inputGFFList.append(inputGFFFile)
# GETTING THE LIST OF BAMFILES TO PROCESS
#either same number of bams for rankby and control
#or only 1 control #or none!
#bamlist should be all rankby bams followed by control bams
bamFileList = []
if options.control:
controlBamList = [bam for bam in options.control.split(',') if len(bam) >0]
rankbyBamList = [bam for bam in options.rankby.split(',') if len(bam) >0]
if len(controlBamList) == len(rankbyBamList):
#case where an equal number of backgrounds are given
bamFileList = rankbyBamList + controlBamList
elif len(controlBamList) == 1:
#case where a universal background is applied
bamFileList = rankbyBamList + controlBamList*len(rankbyBamList)
else:
print('ERROR: EITHER PROVIDE A SINGLE CONTROL BAM FOR ALL SAMPLES, OR ONE CONTROL BAM FOR EACH SAMPLE')
sys.exit()
else:
bamFileList = [bam for bam in options.rankby.split(',') if len(bam) > 0]
# Stitch parameter
if options.stitch == '':
stitchWindow = ''
else:
stitchWindow = int(options.stitch)
# tss options
tssWindow = int(options.tss)
if tssWindow != 0:
removeTSS = True
else:
removeTSS = False
# GETTING THE GENOME
genome = string.upper(options.genome)
print('USING %s AS THE GENOME' % (genome))
# GETTING THE CORRECT ANNOT FILE
genomeDict = {
'HG18': '%s/annotation/hg18_refseq.ucsc' % (pipeline_dir),
'MM9': '%s/annotation/mm9_refseq.ucsc' % (pipeline_dir),
'HG19': '%s/annotation/hg19_refseq.ucsc' % (pipeline_dir),
'MM8': '%s/annotation/mm8_refseq.ucsc' % (pipeline_dir),
'MM10': '%s/annotation/mm10_refseq.ucsc' % (pipeline_dir),
'RN4': '%s/annotation/rn4_refseq.ucsc' % (pipeline_dir),
}
try:
annotFile = genomeDict[genome.upper()]
except KeyError:
print('ERROR: UNSUPPORTED GENOMES TYPE %s' % (genome))
sys.exit()
#FINDING THE ANALYSIS NAME
if options.name:
inputName = options.name
else:
inputName = inputGFFList[0].split('/')[-1].split('.')[0]
print('USING %s AS THE ANALYSIS NAME' % (inputName))
print('FORMATTING INPUT REGIONS')
# MAKING THE RAW INPUT FILE FROM THE INPUT GFFs
#use a simpler unique region naming system
if len(inputGFFList) == 1:
inputGFF = utils.parseTable(inputGFFList[0],'\t')
else:
inputLoci = []
for gffFile in inputGFFList:
print('\tprocessing %s' % (gffFile))
gff = utils.parseTable(gffFile,'\t')
gffCollection = utils.gffToLocusCollection(gff,50)
inputLoci += gffCollection.getLoci()
inputCollection = utils.LocusCollection(inputLoci,50)
inputCollection = inputCollection.stitchCollection() # stitches to produce unique regions
inputGFF = utils.locusCollectionToGFF(inputCollection)
formattedGFF = []
#now number things appropriately
for i,line in enumerate(inputGFF):
#use the coordinates to make a new id inputname_chr_sense_start_stop
chrom = line[0]
coords = [int(line[3]) ,int(line[4])]
sense = line[6]
lineID = '%s_%s' % (inputName,str(i+1)) #1 indexing
newLine = [chrom,lineID,lineID,min(coords),max(coords),'',sense,'',lineID]
formattedGFF.append(newLine)
#name of the master input gff file
masterGFFFile = '%s%s_%s_ALL_-0_+0.gff' % (gffFolder,string.upper(genome),inputName)
utils.unParseTable(formattedGFF,masterGFFFile,'\t')
print('USING %s AS THE INPUT GFF' % (masterGFFFile))
# MAKING THE START DICT
print('MAKING START DICT')
startDict = utils.makeStartDict(annotFile)
#GET CHROMS FOUND IN THE BAMS
print('GETTING CHROMS IN BAMFILES')
bamChromList = getBamChromList(bamFileList)
print("USING THE FOLLOWING CHROMS")
print(bamChromList)
#LOADING IN THE GFF AND FILTERING BY CHROM
print('LOADING AND FILTERING THE GFF')
inputGFF = filterGFF(masterGFFFile,bamChromList)
# LOADING IN THE BOUND REGION REFERENCE COLLECTION
print('LOADING IN GFF REGIONS')
referenceCollection = utils.gffToLocusCollection(inputGFF)
print('CHECKING REFERENCE COLLECTION:')
checkRefCollection(referenceCollection)
# MASKING REFERENCE COLLECTION
# see if there's a mask
if options.mask:
maskFile = options.mask
# if it's a bed file
if maskFile.split('.')[-1].upper() == 'BED':
maskGFF = utils.bedToGFF(maskFile)
elif maskFile.split('.')[-1].upper() == 'GFF':
maskGFF = utils.parseTable(maskFile, '\t')
else:
print("MASK MUST BE A .gff or .bed FILE")
sys.exit()
maskCollection = utils.gffToLocusCollection(maskGFF)
# now mask the reference loci
referenceLoci = referenceCollection.getLoci()
filteredLoci = [locus for locus in referenceLoci if len(maskCollection.getOverlap(locus, 'both')) == 0]
print("FILTERED OUT %s LOCI THAT WERE MASKED IN %s" % (len(referenceLoci) - len(filteredLoci), maskFile))
referenceCollection = utils.LocusCollection(filteredLoci, 50)
# NOW STITCH REGIONS
print('STITCHING REGIONS TOGETHER')
stitchedCollection, debugOutput, stitchWindow = regionStitching(referenceCollection, inputName, outFolder, stitchWindow, tssWindow, annotFile, removeTSS)
# NOW MAKE A STITCHED COLLECTION GFF
print('MAKING GFF FROM STITCHED COLLECTION')
stitchedGFF = utils.locusCollectionToGFF(stitchedCollection)
print(stitchWindow)
print(type(stitchWindow))
if not removeTSS:
stitchedGFFFile = '%s%s_%sKB_STITCHED.gff' % (gffFolder, inputName, str(stitchWindow / 1000))
stitchedGFFName = '%s_%sKB_STITCHED' % (inputName, str(stitchWindow / 1000))
debugOutFile = '%s%s_%sKB_STITCHED.debug' % (gffFolder, inputName, str(stitchWindow / 1000))
else:
stitchedGFFFile = '%s%s_%sKB_STITCHED_TSS_DISTAL.gff' % (gffFolder, inputName, str(stitchWindow / 1000))
stitchedGFFName = '%s_%sKB_STITCHED_TSS_DISTAL' % (inputName, str(stitchWindow / 1000))
debugOutFile = '%s%s_%sKB_STITCHED_TSS_DISTAL.debug' % (gffFolder, inputName, str(stitchWindow / 1000))
# WRITING DEBUG OUTPUT TO DISK
if debug:
print('WRITING DEBUG OUTPUT TO DISK AS %s' % (debugOutFile))
utils.unParseTable(debugOutput, debugOutFile, '\t')
# WRITE THE GFF TO DISK
print('WRITING STITCHED GFF TO DISK AS %s' % (stitchedGFFFile))
utils.unParseTable(stitchedGFF, stitchedGFFFile, '\t')
# SETTING UP THE OVERALL OUTPUT FILE
outputFile1 = outFolder + stitchedGFFName + '_ENHANCER_REGION_MAP.txt'
print('OUTPUT WILL BE WRITTEN TO %s' % (outputFile1))
# MAPPING TO THE NON STITCHED (ORIGINAL GFF)
# MAPPING TO THE STITCHED GFF
# Try to use the bamliquidatior_path.py script on cluster, otherwise, failover to local (in path), otherwise fail.
bamFileListUnique = list(bamFileList)
bamFileListUnique = utils.uniquify(bamFileListUnique)
#prevent redundant mapping
print("MAPPING TO THE FOLLOWING BAMS:")
print(bamFileListUnique)
for bamFile in bamFileListUnique:
bamFileName = bamFile.split('/')[-1]
# MAPPING TO THE STITCHED GFF
mappedOut1Folder = '%s%s_%s_MAPPED' % (mappedFolder, stitchedGFFName, bamFileName)
mappedOut1File = '%s%s_%s_MAPPED/matrix.txt' % (mappedFolder, stitchedGFFName, bamFileName)
if utils.checkOutput(mappedOut1File, 0.2, 0.2):
print("FOUND %s MAPPING DATA FOR BAM: %s" % (stitchedGFFFile, mappedOut1File))
else:
cmd1 = bamliquidator_path + " --sense . -e 200 --match_bamToGFF -r %s -o %s %s" % (stitchedGFFFile, mappedOut1Folder, bamFile)
print(cmd1)
os.system(cmd1)
if utils.checkOutput(mappedOut1File,0.2,5):
print("SUCCESSFULLY MAPPED TO %s FROM BAM: %s" % (stitchedGFFFile, bamFileName))
else:
print("ERROR: FAILED TO MAP %s FROM BAM: %s" % (stitchedGFFFile, bamFileName))
sys.exit()
print('BAM MAPPING COMPLETED NOW MAPPING DATA TO REGIONS')
# CALCULATE DENSITY BY REGION
# NEED TO FIX THIS FUNCTION TO ACCOUNT FOR DIFFERENT OUTPUTS OF LIQUIDATOR
mapCollection(stitchedCollection, referenceCollection, bamFileList, mappedFolder, outputFile1, refName=stitchedGFFName)
print('FINDING AVERAGE SIGNAL AMONGST BAMS')
metaOutputFile = collapseRegionMap(outputFile1,inputName + '_MERGED_SIGNAL',controlBams=options.control)
#now try the merging
print('CALLING AND PLOTTING SUPER-ENHANCERS')
rankbyName = inputName + '_MERGED_SIGNAL'
controlName = 'NONE'
cmd = 'Rscript %sROSE2_callSuper.R %s %s %s %s' % (pipeline_dir,outFolder, metaOutputFile, inputName, controlName)
print(cmd)
os.system(cmd)
# calling the gene mapper
print('CALLING GENE MAPPING')
superTableFile = "%s_SuperEnhancers.table.txt" % (inputName)
#for now don't use ranking bam to call top genes
cmd = "python %sROSE2_geneMapper.py -g %s -i %s%s -f" % (pipeline_dir,genome, outFolder, superTableFile)
print(cmd)
os.system(cmd)
stretchTableFile = "%s_StretchEnhancers.table.txt" % (inputName)
cmd = "python %sROSE2_geneMapper.py -g %s -i %s%s -f" % (pipeline_dir,genome, outFolder, stretchTableFile)
print(cmd)
os.system(cmd)
superStretchTableFile = "%s_SuperStretchEnhancers.table.txt" % (inputName)
cmd = "python %sROSE2_geneMapper.py -g %s -i %s%s -f" % (pipeline_dir,genome, outFolder, superStretchTableFile)
os.system(cmd)
def model_prediction():
model_path = 'networks/resnet-18_trained.t7'
test_dir = 'Result/'
cuda = True
log_file = 'evalss_data'
eval_rot = True
eval_no_crop = True
n_tries = 10
seed = 42
output_dir = 'Result'
running = True
print("loading model", model_path)
torch.cuda.manual_seed_all(seed)
torch.manual_seed(seed)
np.random.seed(seed)
log_file = utils.uniquify(os.path.join(output_dir, log_file), sep='-')
eval_data = test_dir
net = utils.load_model(model_path, cuda)
image_array = cv2.imread(os.path.join(test_dir, 'data', 'image.png'))
mean_of_image = np.mean(image_array, axis=(0, 1))/1000
std_of_image = np.std(image_array, axis=(0, 1))/100
### Load the data into PyTorch using dataloader
dataloader = utils.get_dataloader(test_dir,
[0.6000, 0.3946, 0.6041],
[0.2124, 0.2335, 0.2360],
eval_no_crop, eval_rot, batch_size=1)
#dataloader = utils.get_dataloader(test_dir, mean_of_image, std_of_image, eval_no_crop, eval_rot, batch_size=1)
print(type(dataloader))
'''
# A function to get probabililties using only one iteration
net = net.eval()
for img, label in dataloader:
print(type(img))
print(type(label))
img = img.cuda()
print('IMAGE TYPE:',img)
pred = net(img).data.cpu().numpy()
print('checking', pred)
probs = nn.functional.softmax(pred)
print('PROBABILITIES:', probs)
'''
if not running:
net.eval()
utils.set_strategy(net, 'sample')
have_do = utils.set_do_to_train(net)
res = utils.predict_proba(dataloader, net, n_classes=5, return_logits=True, ensembles=n_tries, cuda=cuda)
print('Result', res)
'''
eval_data['test'] = {
'ensemble/proba': res[0],
'ensemble/logits': res[2],
'eval/labels': res[1],
'ensemble/filenames': res[3]
} '''
else:
net.eval()
utils.set_strategy(net, 'running')
have_do = utils.set_do_to_train(net)
res = utils.predict_proba(dataloader, net, n_classes=5, return_logits=True, ensembles=n_tries if have_do else 3)
print('type(eval_data):', type(eval_data))
'''
eval_data['test'].update({
'eval/proba': res[0],
'eval/logits': res[2],
'eval/labels': res[1],
'ensemble/filenames': res[3]
}) '''
# Get the mean of predictions for n_tries iterations for each class
prob_means_en = np.mean(res[0], axis=0)
output_file_name = 'res_norotate'
torch.save(res, output_dir + '/' + output_file_name)
#print(res[2].shape)
print('Created output file \'', output_file_name, ' \' ')
torch.cuda.empty_cache()
return (prob_means_en)
def finishRankOutput(dataFile,
rankOutput,
genome,
mergeFolder,
mergeName,
name1,
name2,
cutOff=1.5,
window=100000,
superOnly=True,
plotBam=True):
'''
cleans up the rank output table
makes a gff of all of the gained/lost supers beyond
a certain cutoff w/ a window
makes a list of gained genes and lost genes
makes a bed of gained loss
'''
dataDict = pipeline_dfci.loadDataTable(dataFile)
#making sure window and cutoff are int/float
cutOff = float(cutOff)
window = int(window)
genome = string.upper(genome)
#make the output folder
outputFolder = pipeline_dfci.formatFolder(mergeFolder + 'output/', True)
#bring in the old rank table
rankEnhancerTable = utils.parseTable(rankOutput, '\t')
#make a new formatted table
header = rankEnhancerTable[0]
header[-4] = 'DELTA RANK'
header[-3] = 'IS_SUPER'
formattedRankTable = [header]
#the gffs
gainedGFF = []
lostGFF = []
gainedWindowGFF = []
lostWindowGFF = []
if superOnly:
enhancerType = 'SUPERS'
else:
enhancerType = 'ENHANCERS'
#the beds
if superOnly:
gainedTrackHeader = 'track name="%s %s only SEs" description="%s super enhancers that are found only in %s vs %s" itemRGB=On color=255,0,0' % (
genome, name2, genome, name2, name1)
gainedBed = [[gainedTrackHeader]]
conservedTrackHeader = 'track name="%s %s and %s SEs" description="%s super enhancers that are found in both %s vs %s" itemRGB=On color=0,0,0' % (
genome, name1, name2, genome, name1, name2)
conservedBed = [[conservedTrackHeader]]
lostTrackHeader = 'track name="%s %s only SEs" description="%s super enhancers that are found only in %s vs %s" itemRGB=On color=0,255,0' % (
genome, name1, genome, name1, name2)
lostBed = [[lostTrackHeader]]
else:
gainedTrackHeader = 'track name="%s %s only enhancers" description="%s enhancers that are found only in %s vs %s" itemRGB=On color=255,0,0' % (
genome, name2, genome, name2, name1)
gainedBed = [[gainedTrackHeader]]
conservedTrackHeader = 'track name="%s %s and %s enhancers" description="%s enhancers that are found in both %s vs %s" itemRGB=On color=0,0,0' % (
genome, name1, name2, genome, name1, name2)
conservedBed = [[conservedTrackHeader]]
lostTrackHeader = 'track name="%s %s only enhancers" description="%s enhancers that are found only in %s vs %s" itemRGB=On color=0,255,0' % (
genome, name1, genome, name1, name2)
lostBed = [[lostTrackHeader]]
#the genes
geneTable = [[
'GENE', 'ENHANCER_ID', 'ENHANCER_CHROM', 'ENHANCER_START',
'ENHANCER_STOP', header[6], header[7], header[8], 'STATUS'
]]
for line in rankEnhancerTable[1:]:
#fixing the enhancer ID
line[0] = line[0].replace('_lociStitched', '')
formattedRankTable.append(line)
#getting the genes
geneList = []
geneList += line[9].split(',')
geneList += line[10].split(',')
geneList += line[11].split(',')
geneList = [x for x in geneList if len(x) > 0]
geneList = utils.uniquify(geneList)
geneString = string.join(geneList, ',')
bedLine = [line[1], line[2], line[3], line[0], line[-4]]
#for gained
if float(line[6]) > cutOff:
gffLine = [
line[1], line[0], '', line[2], line[3], '', '.', '', geneString
]
gffWindowLine = [
line[1], line[0], '',
int(line[2]) - window,
int(line[3]) + window, '', '.', '', geneString
]
gainedGFF.append(gffLine)
gainedWindowGFF.append(gffWindowLine)
geneStatus = name2
gainedBed.append(bedLine)
#for lost
elif float(line[6]) < (-1 * cutOff):
gffLine = [
line[1], line[0], '', line[2], line[3], '', '.', '', geneString
]
gffWindowLine = [
line[1], line[0], '',
int(line[2]) - window,
int(line[3]) + window, '', '.', '', geneString
]
lostGFF.append(gffLine)
lostWindowGFF.append(gffWindowLine)
geneStatus = name1
lostBed.append(bedLine)
#for conserved
else:
geneStatus = 'CONSERVED'
conservedBed.append(bedLine)
#now fill in the gene Table
for gene in geneList:
geneTableLine = [
gene, line[0], line[1], line[2], line[3], line[6], line[7],
line[8], geneStatus
]
geneTable.append(geneTableLine)
#concat the bed
fullBed = gainedBed + conservedBed + lostBed
#start writing the output
#there's the two gffs, the bed,the formatted table, the gene table
#formatted table
formattedFilename = "%s%s_%s_MERGED_%s_RANK_TABLE.txt" % (
outputFolder, genome, mergeName, enhancerType)
utils.unParseTable(formattedRankTable, formattedFilename, '\t')
#gffs
gffFolder = pipeline_dfci.formatFolder(outputFolder + 'gff/', True)
gffFilename_gained = "%s%s_%s_%s_ONLY_%s_-0_+0.gff" % (
gffFolder, genome, mergeName, string.upper(name2), enhancerType)
gffFilenameWindow_gained = "%s%s_%s_%s_ONLY_%s_-%sKB_+%sKB.gff" % (
gffFolder, genome, mergeName, string.upper(name2), enhancerType,
window / 1000, window / 1000)
gffFilename_lost = "%s%s_%s_%s_ONLY_%s_-0_+0.gff" % (
gffFolder, genome, mergeName, string.upper(name1), enhancerType)
gffFilenameWindow_lost = "%s%s_%s_%s_ONLY_%s_-%sKB_+%sKB.gff" % (
gffFolder, genome, mergeName, string.upper(name1), enhancerType,
window / 1000, window / 1000)
utils.unParseTable(gainedGFF, gffFilename_gained, '\t')
utils.unParseTable(gainedWindowGFF, gffFilenameWindow_gained, '\t')
utils.unParseTable(lostGFF, gffFilename_lost, '\t')
utils.unParseTable(lostWindowGFF, gffFilenameWindow_lost, '\t')
#bed
bedFilename = "%s%s_%s_MERGED_%s.bed" % (outputFolder, genome, mergeName,
enhancerType)
utils.unParseTable(fullBed, bedFilename, '\t')
#geneTable
geneFilename = "%s%s_%s_MERGED_%s_GENE_TABLE.txt" % (
outputFolder, genome, mergeName, enhancerType)
utils.unParseTable(geneTable, geneFilename, '\t')
#finally, move all of the plots to the output folder
cmd = "cp %s%s_ROSE/*.pdf %s%s_%s_MERGED_%s_DELTA.pdf" % (
mergeFolder, name1, outputFolder, genome, mergeName, enhancerType)
os.system(cmd)
cmd = "cp %s%s_ROSE/*RANK_PLOT.png %s%s_%s_MERGED_%s_RANK_PLOT.png" % (
mergeFolder, name1, outputFolder, genome, mergeName, enhancerType)
os.system(cmd)
#now execute the bamPlot_turbo.py commands
if plotBam:
bam1 = dataDict[name1]['bam']
bam2 = dataDict[name2]['bam']
bamString = "%s,%s" % (bam1, bam2)
nameString = "%s,%s" % (name1, name2)
colorString = "0,0,0:100,100,100"
#change dir
os.chdir(pipelineDir)
if len(gainedGFF) > 0:
#gained command
plotTitle = "%s_ONLY_SE" % (name2)
cmd = 'python bamPlot_turbo.py -g %s -b %s -i %s -o %s -n %s -c %s -t %s -r -y UNIFORM -p MULTIPLE' % (
genome, bamString, gffFilename_gained, outputFolder,
nameString, colorString, plotTitle)
os.system(cmd)
#gained window command
plotTitle = "%s_ONLY_SE_%sKB_WINDOW" % (name2, window / 1000)
cmd = 'python bamPlot_turbo.py -g %s -b %s -i %s -o %s -n %s -c %s -t %s -r -y UNIFORM -p MULTIPLE' % (
genome, bamString, gffFilenameWindow_gained, outputFolder,
nameString, colorString, plotTitle)
os.system(cmd)
if len(lostGFF) > 0:
#lost command
plotTitle = "%s_ONLY_SE" % (name1)
cmd = 'python bamPlot_turbo.py -g %s -b %s -i %s -o %s -n %s -c %s -t %s -r -y UNIFORM -p MULTIPLE' % (
genome, bamString, gffFilename_lost, outputFolder, nameString,
colorString, plotTitle)
os.system(cmd)
#lost command
plotTitle = "%s_ONLY_SE_%sKB_WINDOW" % (name1, window / 1000)
cmd = 'python bamPlot_turbo.py -g %s -b %s -i %s -o %s -n %s -c %s -t %s -r -y UNIFORM -p MULTIPLE' % (
genome, bamString, gffFilenameWindow_lost, outputFolder,
nameString, colorString, plotTitle)
os.system(cmd)
return
def createExpressionDict(annotationFile, projectFolder, projectName, refseqToNameDict,expressionTable):
'''
takes as input an activity table with refseq NMID in first column and expression or promoter
acetylation level in a second column
output a dictionary keyed by refseq containing activity
'''
print 'CREATING EXPRESSION DICTIONARY'
annotTable = utils.parseTable(annotationFile, '\t')
for line in annotTable:
gid = line[1]
genename = upper(line[12])
refseqToNameDict[gid] = genename
expresionFilename = projectFolder + 'matrix.gff'
expressionTable = utils.parseTable(expresionFilename, '\t')
expressionDictNM = {}
expressionDictGene = {}
for line in expressionTable[1:]:
trid = line[0]
geneName = refseqToNameDict[trid]
if len(expressionTable[1]) == 3: #when expressionTable is an output from bamToGFF.py
exp = float(line[2])
else: #when expressionTable is passed as an option (2 columns)
exp = float(line[1])
# Store the expression value for each NMid in a dict, keep higher value if multiple identical NMIDs
if trid in expressionDictNM and exp > expressionDictNM[trid]:
expressionDictNM[trid] = exp
elif trid not in expressionDictNM:
expressionDictNM[trid] = exp
# Store the highest value of transcript expression for each gene
if geneName in expressionDictGene and exp > expressionDictGene[geneName]:
expressionDictGene[geneName] = exp
elif geneName not in expressionDictGene:
expressionDictGene[geneName] = exp
# Calculate the cutoff H3K27ac signal value to consider top 2/3 of genes expressed
# or the percentile of genes considered expressed passed in option
cutoff = numpy.percentile(expressionDictGene.values(), 33)
print 'Expression cutoff: ' + str(cutoff)
# Select all NMids that are above the computed cutoff
expressedGenes = []
expressedNM = []
for trid in expressionDictNM:
if float(expressionDictNM[trid]) >= cutoff:
expressedGenes.append(refseqToNameDict[trid])
expressedNM.append(trid)
expressedGenes = utils.uniquify(expressedGenes)
# Output the list of transcripts considered expressed
NMfilename = projectFolder + projectName + '_EXPRESSED_TRANSCRIPTS.txt'
# Output the list of genes considered expressed
Genefilename = projectFolder + projectName + '_EXPRESSED_GENES.txt'
utils.unParseTable(expressedNM, NMfilename, '')
utils.unParseTable(expressedGenes, Genefilename, '')
return expressedNM
def mapBamToGFF(bamFile,gff,sense = '.',extension = 200,rpm = False,clusterGram = None,matrix = None):
'''maps reads from a bam to a gff'''
#creating a new gff to output
newGFF = []
#reading in the bam
bam = utils.Bam(bamFile)
#getting RPM normalization
if rpm:
MMR= round(float(bam.getTotalReads('mapped'))/1000000,4)
else:
MMR = 1
print('using a MMR value of %s' % (MMR))
#creating a sense trans
senseTrans = string.maketrans('-+.','+-+')
#reading in the gff
if type(gff) == str:
gff = utils.parseTable(gff,'\t')
#setting up a clustergram table
if clusterGram:
binSize = int(clusterGram)
binSizeList = []
#now go through each line of the gff and make sure they're all the same length
for i in range(0,len(gff),1):
line = gff[i]
gffLocus = utils.Locus(line[0],int(line[3]),int(line[4]),line[6],line[1])
binSizeList.append(gffLocus.len()/binSize)
binSizeList = utils.uniquify(binSizeList)
if len(binSizeList) > 1:
print('WARNING: lines in gff are of different length. Output clustergram will have variable row length')
newGFF.append(['GENE_ID','locusLine'] + [str(x*binSize)+'_'+bamFile.split('/')[-1] for x in range(1,max(binSizeList)+1,1)])
#setting up a maxtrix table
if matrix:
newGFF.append(['GENE_ID','locusLine'] + ['bin_'+str(n)+'_'+bamFile.split('/')[-1] for n in range(1,int(matrix)+1,1)])
nBin = int(matrix)
# Try to use the bamliquidatior script on cluster, otherwise, failover to local (in path), otherwise fail.
bamliquidatorString = '/opt/bamliquidator/pipeline/bamliquidator_internal/bamliquidator'
if not os.path.isfile(bamliquidatorString):
bamliquidatorString = './bamliquidator'
if not os.path.isfile(bamliquidatorString):
raise ValueError('bamliquidator not found in path')
#getting and processing reads for gff lines
ticker = 0
print('Number lines processed')
for line in gff:
line = line[0:9]
if ticker%100 == 0:
print(ticker)
ticker+=1
gffLocus = utils.Locus(line[0],int(line[3]),int(line[4]),line[6],line[1])
#get the nBin and binSize
if clusterGram:
nBin =gffLocus.len()/int(clusterGram)
binSize = int(clusterGram)
if matrix:
nBin = int(matrix)
binSize = gffLocus.len()/nBin
#some regions will be too short to get info on
if binSize == 0:
clusterLine = [gffLocus.ID(),gffLocus.__str__()] + ['NA']*nBin
newGFF.append(clusterLine)
continue
#flippy flip if sense is negative
if sense == '-':
bamSense = string.translate(gffLocus.sense(),senseTrans)
elif sense == '+':
bamSense = gffLocus.sense()
else:
bamSense = '.'
#using the bamLiquidator to get the readstring
#print('using nBin of %s' % nBin)
bamCommand = "%s %s %s %s %s %s %s %s" % (bamliquidatorString,bamFile,line[0],gffLocus.start(),gffLocus.end(),bamSense,nBin,extension)
#print(bamCommand)
getReads = subprocess.Popen(bamCommand,stdin = subprocess.PIPE,stderr = subprocess.PIPE,stdout = subprocess.PIPE,shell = True)
readString, stderr = getReads.communicate()
if stderr:
print("STDERR out: %s" % (stderr))
denList = readString.split('\n')[:-1]
#print("denlist is: %s" % denList)
#flip the denList if the actual gff region is -
if gffLocus.sense() == '-':
denList = denList[::-1]
#converting from units of total bp of read sequence per bin to rpm/bp
denList = [round(float(x)/binSize/MMR,4) for x in denList]
#if the gff region is - strand, flip the
clusterLine = [gffLocus.ID(),gffLocus.__str__()] + denList
newGFF.append(clusterLine)
return newGFF
def main():
'''
main run call
'''
debug = False
from optparse import OptionParser
usage = "usage: %prog [options] -g [GENOME] -i [INPUT_REGION_GFF] -r [RANKBY_BAM_FILE] -o [OUTPUT_FOLDER] [OPTIONAL_FLAGS]"
parser = OptionParser(usage=usage)
# required flags
parser.add_option("-i", "--i", dest="input", nargs=1, default=None,
help="Enter a .gff or .bed file of binding sites used to make enhancers")
parser.add_option("-r", "--rankby", dest="rankby", nargs=1, default=None,
help="bamfile to rank enhancer by")
parser.add_option("-o", "--out", dest="out", nargs=1, default=None,
help="Enter an output folder")
parser.add_option("-g", "--genome", dest="genome", nargs=1, default=None,
help="Enter the genome build (MM9,MM8,HG18,HG19)")
# optional flags
parser.add_option("-b", "--bams", dest="bams", nargs=1, default=None,
help="Enter a comma separated list of additional bam files to map to")
parser.add_option("-c", "--control", dest="control", nargs=1, default=None,
help="bamfile to rank enhancer by")
parser.add_option("-s", "--stitch", dest="stitch", nargs=1, default='',
help="Enter a max linking distance for stitching. Default will determine optimal stitching parameter")
parser.add_option("-t", "--tss", dest="tss", nargs=1, default=0,
help="Enter a distance from TSS to exclude. 0 = no TSS exclusion")
parser.add_option("--mask", dest="mask", nargs=1, default=None,
help="Mask a set of regions from analysis. Provide a .bed or .gff of masking regions")
# RETRIEVING FLAGS
(options, args) = parser.parse_args()
if not options.input or not options.rankby or not options.out or not options.genome:
print('hi there')
parser.print_help()
exit()
# making the out folder if it doesn't exist
outFolder = utils.formatFolder(options.out, True)
# figuring out folder schema
gffFolder = utils.formatFolder(outFolder + 'gff/', True)
mappedFolder = utils.formatFolder(outFolder + 'mappedGFF/', True)
# GETTING INPUT FILE
if options.input.split('.')[-1] == 'bed':
# CONVERTING A BED TO GFF
inputGFFName = options.input.split('/')[-1][0:-4]
inputGFFFile = '%s%s.gff' % (gffFolder, inputGFFName)
utils.bedToGFF(options.input, inputGFFFile)
elif options.input.split('.')[-1] == 'gff':
# COPY THE INPUT GFF TO THE GFF FOLDER
inputGFFFile = options.input
os.system('cp %s %s' % (inputGFFFile, gffFolder))
else:
print('WARNING: INPUT FILE DOES NOT END IN .gff or .bed. ASSUMING .gff FILE FORMAT')
# COPY THE INPUT GFF TO THE GFF FOLDER
inputGFFFile = options.input
os.system('cp %s %s' % (inputGFFFile, gffFolder))
# GETTING THE LIST OF BAMFILES TO PROCESS
if options.control:
bamFileList = [options.rankby, options.control]
else:
bamFileList = [options.rankby]
if options.bams:
bamFileList += options.bams.split(',')
bamFileList = utils.uniquify(bamFileList)
# optional args
# Stitch parameter
if options.stitch == '':
stitchWindow = ''
else:
stitchWindow = int(options.stitch)
# tss options
tssWindow = int(options.tss)
if tssWindow != 0:
removeTSS = True
else:
removeTSS = False
# GETTING THE BOUND REGION FILE USED TO DEFINE ENHANCERS
print('USING %s AS THE INPUT GFF' % (inputGFFFile))
inputName = inputGFFFile.split('/')[-1].split('.')[0]
# GETTING THE GENOME
genome = options.genome
print('USING %s AS THE GENOME' % genome)
# GETTING THE CORRECT ANNOT FILE
cwd = os.getcwd()
genomeDict = {
'HG18': '%s/annotation/hg18_refseq.ucsc' % (cwd),
'MM9': '%s/annotation/mm9_refseq.ucsc' % (cwd),
'HG19': '%s/annotation/hg19_refseq.ucsc' % (cwd),
'MM8': '%s/annotation/mm8_refseq.ucsc' % (cwd),
'MM10': '%s/annotation/mm10_refseq.ucsc' % (cwd),
}
annotFile = genomeDict[genome.upper()]
# MAKING THE START DICT
print('MAKING START DICT')
startDict = utils.makeStartDict(annotFile)
# LOADING IN THE BOUND REGION REFERENCE COLLECTION
print('LOADING IN GFF REGIONS')
referenceCollection = utils.gffToLocusCollection(inputGFFFile)
# MASKING REFERENCE COLLECTION
# see if there's a mask
if options.mask:
maskFile = options.mask
# if it's a bed file
if maskFile.split('.')[-1].upper() == 'BED':
maskGFF = utils.bedToGFF(maskFile)
elif maskFile.split('.')[-1].upper() == 'GFF':
maskGFF = utils.parseTable(maskFile, '\t')
else:
print("MASK MUST BE A .gff or .bed FILE")
sys.exit()
maskCollection = utils.gffToLocusCollection(maskGFF)
# now mask the reference loci
referenceLoci = referenceCollection.getLoci()
filteredLoci = [locus for locus in referenceLoci if len(maskCollection.getOverlap(locus, 'both')) == 0]
print("FILTERED OUT %s LOCI THAT WERE MASKED IN %s" % (len(referenceLoci) - len(filteredLoci), maskFile))
referenceCollection = utils.LocusCollection(filteredLoci, 50)
# NOW STITCH REGIONS
print('STITCHING REGIONS TOGETHER')
stitchedCollection, debugOutput, stitchWindow = regionStitching(inputGFFFile, inputName, outFolder, stitchWindow, tssWindow, annotFile, removeTSS)
# NOW MAKE A STITCHED COLLECTION GFF
print('MAKING GFF FROM STITCHED COLLECTION')
stitchedGFF = utils.locusCollectionToGFF(stitchedCollection)
# making sure start/stop ordering are correct
for i in range(len(stitchedGFF)):
line = stitchedGFF[i]
start = int(line[3])
stop = int(line[4])
if start > stop:
line[3] = stop
line[4] = start
print(stitchWindow)
print(type(stitchWindow))
if not removeTSS:
stitchedGFFFile = '%s%s_%sKB_STITCHED.gff' % (gffFolder, inputName, str(stitchWindow / 1000))
stitchedGFFName = '%s_%sKB_STITCHED' % (inputName, str(stitchWindow / 1000))
debugOutFile = '%s%s_%sKB_STITCHED.debug' % (gffFolder, inputName, str(stitchWindow / 1000))
else:
stitchedGFFFile = '%s%s_%sKB_STITCHED_TSS_DISTAL.gff' % (gffFolder, inputName, str(stitchWindow / 1000))
stitchedGFFName = '%s_%sKB_STITCHED_TSS_DISTAL' % (inputName, str(stitchWindow / 1000))
debugOutFile = '%s%s_%sKB_STITCHED_TSS_DISTAL.debug' % (gffFolder, inputName, str(stitchWindow / 1000))
# WRITING DEBUG OUTPUT TO DISK
if debug:
print('WRITING DEBUG OUTPUT TO DISK AS %s' % (debugOutFile))
utils.unParseTable(debugOutput, debugOutFile, '\t')
# WRITE THE GFF TO DISK
print('WRITING STITCHED GFF TO DISK AS %s' % (stitchedGFFFile))
utils.unParseTable(stitchedGFF, stitchedGFFFile, '\t')
# SETTING UP THE OVERALL OUTPUT FILE
outputFile1 = outFolder + stitchedGFFName + '_ENHANCER_REGION_MAP.txt'
print('OUTPUT WILL BE WRITTEN TO %s' % (outputFile1))
# MAPPING TO THE NON STITCHED (ORIGINAL GFF)
# MAPPING TO THE STITCHED GFF
# Try to use the bamliquidatior_path.py script on cluster, otherwise, failover to local (in path), otherwise fail.
bamliquidator_path = '/ark/home/jdm/pipeline/bamliquidator_batch.py'
if not os.path.isfile(bamliquidator_path):
bamliquidator_path = 'bamliquidator_batch.py'
if not os.path.isfile(bamliquidator_path):
raise ValueError('bamliquidator_batch.py not found in path')
for bamFile in bamFileList:
bamFileName = bamFile.split('/')[-1]
# MAPPING TO THE STITCHED GFF
mappedOut1Folder = '%s%s_%s_MAPPED' % (mappedFolder, stitchedGFFName, bamFileName)
mappedOut1File = '%s%s_%s_MAPPED/matrix.gff' % (mappedFolder, stitchedGFFName, bamFileName)
if utils.checkOutput(mappedOut1File, 0.2, 0.2):
print("FOUND %s MAPPING DATA FOR BAM: %s" % (stitchedGFFFile, mappedOut1File))
else:
cmd1 = "python " + bamliquidator_path + " --sense . -e 200 --match_bamToGFF -r %s -o %s %s" % (stitchedGFFFile, mappedOut1Folder, bamFile)
print(cmd1)
output1 = subprocess.Popen(cmd1, stdout=subprocess.PIPE, shell=True)
output1 = output1.communicate()
if len(output1[0]) > 0: # test if mapping worked correctly
print("SUCCESSFULLY MAPPED TO %s FROM BAM: %s" % (stitchedGFFFile, bamFileName))
else:
print("ERROR: FAILED TO MAP %s FROM BAM: %s" % (stitchedGFFFile, bamFileName))
sys.exit()
# MAPPING TO THE ORIGINAL GFF
mappedOut2Folder = '%s%s_%s_MAPPED' % (mappedFolder, inputName, bamFileName)
mappedOut2File = '%s%s_%s_MAPPED/matrix.gff' % (mappedFolder, inputName, bamFileName)
if utils.checkOutput(mappedOut2File, 0.2, 0.2):
print("FOUND %s MAPPING DATA FOR BAM: %s" % (stitchedGFFFile, mappedOut2File))
else:
cmd2 = "python " + bamliquidator_path + " --sense . -e 200 --match_bamToGFF -r %s -o %s %s" % (inputGFFFile, mappedOut2Folder, bamFile)
print(cmd2)
output2 = subprocess.Popen(cmd2, stdout=subprocess.PIPE, shell=True)
output2 = output2.communicate()
if len(output2[0]) > 0: # test if mapping worked correctly
print("SUCCESSFULLY MAPPED TO %s FROM BAM: %s" % (inputGFFFile, bamFileName))
else:
print("ERROR: FAILED TO MAP %s FROM BAM: %s" % (inputGFFFile, bamFileName))
sys.exit()
print('BAM MAPPING COMPLETED NOW MAPPING DATA TO REGIONS')
# CALCULATE DENSITY BY REGION
# NEED TO FIX THIS FUNCTION TO ACCOUNT FOR DIFFERENT OUTPUTS OF LIQUIDATOR
mapCollection(stitchedCollection, referenceCollection, bamFileList, mappedFolder, outputFile1, refName=stitchedGFFName)
print('CALLING AND PLOTTING SUPER-ENHANCERS')
if options.control:
rankbyName = options.rankby.split('/')[-1]
controlName = options.control.split('/')[-1]
cmd = 'R --no-save %s %s %s %s < ROSE2_callSuper.R' % (outFolder, outputFile1, inputName, controlName)
else:
rankbyName = options.rankby.split('/')[-1]
controlName = 'NONE'
cmd = 'R --no-save %s %s %s %s < ROSE2_callSuper.R' % (outFolder, outputFile1, inputName, controlName)
print(cmd)
os.system(cmd)
# calling the gene mapper
time.sleep(20)
superTableFile = "%s_SuperEnhancers.table.txt" % (inputName)
if options.control:
cmd = "python ROSE2_geneMapper.py -g %s -r %s -c %s -i %s%s" % (genome, options.rankby, options.control, outFolder, superTableFile)
else:
cmd = "python ROSE2_geneMapper.py -g %s -r %s -i %s%s" % (genome, options.rankby, outFolder, superTableFile)
os.system(cmd)
stretchTableFile = "%s_StretchEnhancers.table.txt" % (inputName)
if options.control:
cmd = "python ROSE2_geneMapper.py -g %s -r %s -c %s -i %s%s" % (genome, options.rankby, options.control, outFolder, stretchTableFile)
else:
cmd = "python ROSE2_geneMapper.py -g %s -r %s -i %s%s" % (genome, options.rankby, outFolder, stretchTableFile)
os.system(cmd)
superStretchTableFile = "%s_SuperStretchEnhancers.table.txt" % (inputName)
if options.control:
cmd = "python ROSE2_geneMapper.py -g %s -r %s -c %s -i %s%s" % (genome, options.rankby, options.control, outFolder, superStretchTableFile)
else:
cmd = "python ROSE2_geneMapper.py -g %s -r %s -i %s%s" % (genome, options.rankby, outFolder, superStretchTableFile)
os.system(cmd)
def _matrix_entry_maps(self):
"""Set of all mappings used in matrix arguments."""
return list(uniquify(m for arg in self.args if arg._is_mat for m in arg.map))
def _unique_matrix(self):
return list(uniquify(a.data for a in self._matrix_args))
def make_mycn_stats_table(nb_all_chip_dataFile,outFile):
'''
making a table of conserved mycn peaks w/ some additional stats
mycn and h3k27ac signal is avg. background normalized across 4 samples
active tss defined as the union of all H3K27ac occupied promoters in NB
active enhancers defined as the union of all H3K27ac sites outside of promoters
'''
dataDict = pipeline_dfci.loadDataTable(nb_all_chip_dataFile)
print('SETTING UP OUTPUT TABLE')
outTable = [['PEAK_ID','CHROM','START','STOP','LENGTH','ACTIVE_TSS_OVERLAP','ENHANCER_OVERLAP','CPG_ISLAND_OVERLAP','CPG_ISLAND_FRACTION','GC_FREQ','MYCN_RANK','AVG_MYCN_SIGNAL','AVG_H3K27AC_SIGNAL','CANON_EBOX_COUNT','NONCANON_EBOX_COUNT','TOTAL_EBOX_COUNT','CANON_EXP','NON_CANON_EXP','GABPA_COUNT','GABPA_EXP','GATA_COUNT','GATA_EXP']]
dinuc = nmers(2,['A','T','G','C'])
#input files
mycnSignalFile = '%sHG19_NB_MYCN_CONSERVED_-0_+0_NB_ALL_SIGNAL.txt' % (signalFolder)
h3k27acSignalFile = '%sHG19_NB_MYCN_CONSERVED_-500_+500_NB_ALL_SIGNAL.txt' % (signalFolder)
mycnRankFile = '%smeta_rose/NB_MYCN/NB_MYCN_0KB_STITCHED_ENHANCER_REGION_RANK_CONSERVED.txt' % (projectFolder)
activeGeneFile = '%sHG19_NB_H3K27AC_ACTIVE_UNION.txt' % (geneListFolder)
#note, this is the ucsc hg19 cpg islands extended file
#to download and format run ./beds/download_cpg.sh
cpgFile = '%sbeds/hg19_cpg_islands.bed' % (projectFolder)
enhancerFile = '%smeta_rose/NB_H3K27AC/NB_H3K27AC_AllEnhancers.table.txt' % (projectFolder)
print('LOADING MYCN BINDING DATA')
mycnSignalTable = utils.parseTable(mycnSignalFile,'\t')
#making a signal dictionary for MYCN binding
names_list = ['BE2C_MYCN','KELLY_MYCN','NGP_MYCN','SHEP21_0HR_MYCN_NOSPIKE']
background_list = [dataDict[name]['background'] for name in names_list]
header = mycnSignalTable[0]
chip_columns = [header.index(name) for name in names_list]
background_columns = [header.index(background_name) for background_name in background_list]
mycn_sig_dict = {}
#this only works if the first column are unique identifiers
if len(mycnSignalTable) != len(utils.uniquify([line[0] for line in mycnSignalTable])):
print('Error: Column 1 of must contain unique identifiers.' % (mycnSignalFile))
sys.exit()
for line in mycnSignalTable[1:]:
line_sig = []
for i in range(len(names_list)):
line_sig.append(float(line[chip_columns[i]]) - float(line[background_columns[i]]))
mycn_sig_dict[line[0]] = numpy.mean(line_sig)
print('LOADING MYCN RANK DATA')
mycnRankTable = utils.parseTable(mycnRankFile,'\t')
print('LOADING H3K27AC BINDING DATA')
h3k27acSignalTable = utils.parseTable(h3k27acSignalFile,'\t')
#making a signal dictionary for background subtracted H3K27ac binding
names_list = ['BE2C_H3K27AC','KELLY_H3K27AC','NGP_H3K27AC','SHEP21_0HR_H3K27AC_NOSPIKE']
background_list = [dataDict[name]['background'] for name in names_list]
header = h3k27acSignalTable[0]
chip_columns = [header.index(name) for name in names_list]
background_columns = [header.index(background_name) for background_name in background_list]
h3k27ac_sig_dict = {}
#this only works if the first column are unique identifiers
if len(h3k27acSignalTable) != len(utils.uniquify([line[0] for line in h3k27acSignalTable])):
print('Error: Column 1 of must contain unique identifiers.' % (h3k27acSignalFile))
sys.exit()
for line in h3k27acSignalTable[1:]:
line_sig = []
for i in range(len(names_list)):
line_sig.append(float(line[chip_columns[i]]) - float(line[background_columns[i]]))
h3k27ac_sig_dict[line[0]] = numpy.mean(line_sig)
#making the cpg collection
print('LOADING CPGS ISLANDS')
cpgBed = utils.parseTable(cpgFile,'\t')
cpgLoci = []
for line in cpgBed:
cpgLoci.append(utils.Locus(line[0],line[1],line[2],'.',line[-1]))
cpgCollection = utils.LocusCollection(cpgLoci,50)
#next make the tss collection of active promoters
print('LOADING ACTIVE PROMOTERS')
startDict = utils.makeStartDict(annotFile)
activeTable = utils.parseTable(activeGeneFile,'\t')
tss_1kb_loci = []
for line in activeTable:
tss_1kb_loci.append(utils.makeTSSLocus(line[1],startDict,1000,1000))
tss_1kb_collection = utils.LocusCollection(tss_1kb_loci,50)
#enhancer file
print("LOADING ACTIVE ENHANCERS")
enhancerTable = utils.parseTable(enhancerFile,'\t')
print('STARTING WITH THE FOLLOWING NUMBER OF ENHANCERS IN NB')
print(len(enhancerTable) - 6)
enhancerLoci = []
for line in enhancerTable:
if line[0][0] != '#' and line[0][0] != 'R':
try:
lineLocus = utils.Locus(line[1],int(line[2]),int(line[3]),'.',line[0])
enhancerLoci.append(lineLocus)
except IndexError:
print(line)
sys.exit()
enhancerCollection = utils.LocusCollection(enhancerLoci,50)
print('CLASSIFYING MYCN PEAKS')
ticker = 0
for i in range(1,len(mycnSignalTable)):
if ticker%100 == 0:
print(ticker)
ticker +=1
line = mycnSignalTable[i]
mycn_signal = round(mycn_sig_dict[line[0]],4)
h3k27ac_signal = round(h3k27ac_sig_dict[line[0]],4)
peakID = line[0]
locusString = line[1]
chrom = locusString.split('(')[0]
[start,stop] = [int(x) for x in line[1].split(':')[-1].split('-')]
lineLocus = utils.Locus(chrom,start,stop,'.',peakID)
tssOverlap = 0
if tss_1kb_collection.getOverlap(lineLocus,'both'):
tssOverlap = 1
enhancerOverlap = 0
if enhancerCollection.getOverlap(lineLocus,'both') and tssOverlap == 0:
enhancerOverlap = 1
cpgIslandOverlap = 0
if cpgCollection.getOverlap(lineLocus,'both'):
cpgIslandOverlap = 1
#now do fractional cpgOverlap
overlappingCpGLoci = cpgCollection.getOverlap(lineLocus,'both')
overlappingBases = 0
for locus in overlappingCpGLoci:
cpgStart = max(locus.start(),lineLocus.start())
cpgEnd = min(locus.end(),lineLocus.end())
overlappingBases += (cpgEnd-cpgStart)
overlapFraction = round(float(overlappingBases)/lineLocus.len(),2)
#now get the seq
lineSeq = string.upper(utils.fetchSeq(genomeDirectory,chrom,start,stop,True))
gcFreq = round(float(lineSeq.count('GC') + lineSeq.count('CG'))/len(lineSeq),2)
dinuc_dict = {}
for nmer in dinuc:
dinuc_dict[nmer] = float(lineSeq.count('GC'))/len(lineSeq)
mycnRankLine = mycnRankTable[i]
mycnRank = numpy.mean([float(x) for x in mycnRankLine[6:]])
canonMatchList = re.findall('CACGTG',lineSeq)
canon_count = len(canonMatchList)
eboxMatchList = re.findall('CA..TG',lineSeq)
ebox_count = len(eboxMatchList)
non_canon_count = ebox_count-canon_count
#get the expected values
canon_exp = dinuc_dict['CA']*dinuc_dict['CG']*dinuc_dict['TG']*(len(lineSeq) - 5)
canon_exp = round(canon_exp,2)
notCG = 1- dinuc_dict['CG']
non_exp = dinuc_dict['CA']*notCG*dinuc_dict['TG']*(len(lineSeq) - 5)
non_exp = round(non_exp,2)
#for gata and GABPA
gabpaMatchList = re.findall('CGGAAG',lineSeq) + re.findall('CTTCCG',lineSeq)
gabpa_count = len(gabpaMatchList)
gabpa_exp_f = dinuc_dict['CG'] * dinuc_dict['GA'] * dinuc_dict['AG']*(len(lineSeq) - 5)
gabpa_exp_r = dinuc_dict['CT'] * dinuc_dict['TC'] * dinuc_dict['CG']*(len(lineSeq) - 5)
gabpa_exp = round(gabpa_exp_f,2) + round(gabpa_exp_r,2)
gataMatchList = re.findall('GATAA',lineSeq) + re.findall('TTATC',lineSeq)
gata_count = len(gataMatchList)
an_freq = 1 - dinuc_dict['AA'] - dinuc_dict['AT'] - dinuc_dict['AG'] -dinuc_dict['AC']
cn_freq = 1 - dinuc_dict['CA'] - dinuc_dict['CT'] - dinuc_dict['CG'] -dinuc_dict['CC']
gata_exp_f = dinuc_dict['GA'] * dinuc_dict['TA'] * an_freq*(len(lineSeq) - 5)
gata_exp_r = dinuc_dict['TT'] * dinuc_dict['AT'] * cn_freq*(len(lineSeq) - 5)
gata_exp = round(gata_exp_f,2) + round(gata_exp_r,2)
newLine = [peakID,chrom,start,stop,lineLocus.len(),tssOverlap,enhancerOverlap,cpgIslandOverlap,overlapFraction,gcFreq,mycnRank,mycn_signal,h3k27ac_signal,canon_count,non_canon_count,ebox_count,canon_exp,non_exp,gabpa_count,gabpa_exp,gata_count,gata_exp]
outTable.append(newLine)
utils.unParseTable(outTable,outFile,'\t')
return outFile
def make_exp_table(probe_gene_dict, exp_1_path, exp_2_path, ob_s1_path,
exp_table_path, patient_table_path):
'''
making gene expression table
first use an intermediary dictionary
exp_dict[gene][patient] = list <- in case multiple exp values present at probe or patient level
'''
#check if this has already been done
if utils.checkOutput(exp_table_path, 0, 0) and utils.checkOutput(
patient_table_path, 0, 0):
print(
'loading premade expression table at %s and formatted patient table at %s'
% (exp_table_path, patient_table_path))
return exp_table_path, patient_table_path
#first get a master list of patients
print('formatting patient data')
table_s1 = utils.parseTable(ob_s1_path, '\t')
patient_list = utils.uniquify([line[0] for line in table_s1[1:]])
#make a dict w/ relevant patient info
patient_dict = {}
for line in table_s1[1:]:
patient_line = [line[3]] + line[8:12]
if line[12] == 'Amp':
patient_line.append(1)
else:
patient_line.append(0)
patient_dict[line[0]] = patient_line
gene_list = utils.uniquify(
[probe_gene_dict[probe_id] for probe_id in probe_gene_dict.keys()])
gene_list.sort()
exp_dict = {}
for gene in gene_list:
exp_dict[gene] = {}
for patient in patient_list:
exp_dict[gene][patient] = []
#next load up both expression tables
exp_1 = utils.parseTable(exp_1_path, '\t')
exp_2 = utils.parseTable(exp_2_path, '\t')
exp_1_header = exp_1[0]
exp_1_cols = [
i for i in range(1, len(exp_1_header))
if patient_list.count(exp_1_header[i].split('_')[1]) > 0
]
exp_1_patients = [
exp_1_header[i].split('_')[1] for i in range(1, len(exp_1_header))
if patient_list.count(exp_1_header[i].split('_')[1]) > 0
]
exp_2_header = exp_2[0]
exp_2_cols = [
i for i in range(1, len(exp_2_header))
if patient_list.count(exp_2_header[i].split('_')[1]) > 0
]
exp_2_patients = [
exp_2_header[i].split('_')[1] for i in range(1, len(exp_2_header))
if patient_list.count(exp_2_header[i].split('_')[1]) > 0
]
print('loading expression dataset %s' % exp_1_path)
for line in exp_1:
if probe_gene_dict.has_key(line[0]):
for i in range(len(exp_1_cols)):
patient_name = exp_1_patients[i]
col = exp_1_cols[i]
expression = float(line[col])
gene_name = probe_gene_dict[line[0]]
exp_dict[gene_name][patient_name].append(expression)
print('loading expression dataset %s' % exp_2_path)
for line in exp_2:
if probe_gene_dict.has_key(line[0]):
for i in range(len(exp_2_cols)):
patient_name = exp_2_patients[i]
col = exp_2_cols[i]
expression = float(line[col])
gene_name = probe_gene_dict[line[0]]
exp_dict[gene_name][patient_name].append(expression)
print('making gene expression table')
exp_table = [['GENE_NAME'] + exp_1_patients + exp_2_patients]
for gene in gene_list:
if min([
len(exp_dict[gene][patient])
for patient in exp_1_patients + exp_2_patients
]) == 0:
print(gene)
continue
exp_line = [gene] + [
numpy.mean(exp_dict[gene][patient])
for patient in exp_1_patients + exp_2_patients
]
exp_table.append(exp_line)
patient_table = [[
'PATIENT', 'STAGE', 'EFS_D', 'EFS_STATUS', 'OS_D', 'OS_STATUS',
'MYCN_STATUS'
]]
for patient in exp_1_patients + exp_2_patients:
patient_line = [patient] + patient_dict[patient]
patient_table.append(patient_line)
utils.unParseTable(exp_table, exp_table_path, '\t')
utils.unParseTable(patient_table, patient_table_path, '\t')
return exp_table_path, patient_table_path
def geneToEnhancerDict(genome, enhancer_file, activity_path):
'''
Assign each Super-Enhancer to the closest active TSS to its center
Return a dictionary keyed by TF that points to a list of loci
'''
print('Identifying enhancers and target genes from %s' % (enhancer_file))
#should this do gene assignment????
#for now assume gene assignment has been done
#can later toggle to do gene assignment
#first load the TF lists
tf_table = utils.parseTable(genome.returnFeature('tf_file'), '\t')
motif_table = utils.parseTable(genome.returnFeature('motif_convert'), '\t')
#this gives all tfs that have a motif
motif_tfs = utils.uniquify([line[1] for line in motif_table])
#intersect w/ the activity table
if len(activity_path) > 0:
activity_table = utils.parseTable(activity_path, '\t')
#figure out the right column for actual gene names (basically not NM or NR and not a numeral)
for i in range(len(activity_table[0])):
# try:
# foo = int(activity_table[0][i])
# except ValueError: # case where it is not an integer
if activity_table[0][i][0:2] != 'NM' and activity_table[0][i][
0:2] != 'NR': #assumes refseq
gene_col = i
break
print('using column %s of %s gene activity table for common names' %
(gene_col + 1, activity_path))
active_gene_list = [
string.upper(line[gene_col]) for line in activity_table
]
tf_list_refseq = [
line[0] for line in tf_table if active_gene_list.count(line[1]) > 0
and motif_tfs.count(line[1]) > 0
]
tf_list_name = utils.uniquify([
line[1] for line in tf_table if active_gene_list.count(line[1]) > 0
and motif_tfs.count(line[1]) > 0
])
else:
tf_list_refseq = [
line[0] for line in tf_table if motif_tfs.count(line[1]) > 0
]
tf_list_name = [
line[1] for line in tf_table if motif_tfs.count(line[1]) > 0
]
print('Identified %s TFs from %s that have motifs' %
(len(tf_list_name), genome.returnFeature('tf_file')))
#keyed by gene with loci objects in the list
gene_to_enhancer_dict = defaultdict(list)
enhancer_to_gene_dict = defaultdict(list)
#assuming id,chrom,start,stop w/ gene names in the last 3 columns per standard ROSE output
enhancer_table = utils.parseTable(enhancer_file, '\t')
print('Analyzing %s cis-regulatory regions' % (len(enhancer_table)))
#now let's make the enhancer table by region and then by gene
enhancerTable = [['ENHANCER_ID', 'CHROM', 'START', 'STOP', 'GENE_LIST']]
enhancerTFTable = [['ENHANCER_ID', 'CHROM', 'START', 'STOP', 'GENE_LIST']]
geneTable = [['GENE', 'TF', 'CHROM', 'START', 'STOP', 'ENHANCER_ID']]
geneTFTable = [['GENE', 'CHROM', 'START', 'STOP', 'ENHANCER_ID']]
geneSummaryTable = [['GENE', 'TF', 'ENHANCER_LIST']]
#will need to track which ones are TFs
candidate_tf_list = []
#find the columns for gene assignment
header = enhancer_table[0]
header_length = len(enhancer_table[0])
closest_index = header.index('CLOSEST_GENE')
proximal_index = header.index('PROXIMAL_GENES')
overlap_index = header.index('OVERLAP_GENES')
for line in enhancer_table[1:]:
if len(
line
) != header_length: #don't bother trying to figure out lines w/o target genes
continue
enhancer_locus = utils.Locus(line[1], line[2], line[3], '.', line[0])
closest_gene_list = line[closest_index].split(',')
proximal_gene_list = line[proximal_index].split(',')
overlap_gene_list = line[overlap_index].split(',')
all_gene_list = closest_gene_list + proximal_gene_list + overlap_gene_list
all_gene_list = [string.upper(gene) for gene in all_gene_list]
#print(all_gene_list)
#print(activity_path)
#print(active_gene_list)
#gets a unique list of all tfs
if len(activity_path) > 0:
all_gene_list = utils.uniquify([
gene for gene in all_gene_list
if active_gene_list.count(gene) > 0
])
else:
all_gene_list = utils.uniquify(all_gene_list)
candidate_gene_list = utils.uniquify(
[gene for gene in all_gene_list if tf_list_name.count(gene) > 0])
if len(all_gene_list) > 0:
for gene in all_gene_list:
gene_to_enhancer_dict[gene].append(enhancer_locus)
enhancer_to_gene_dict[enhancer_locus].append(gene)
newLine = line[0:4] + [','.join(all_gene_list)]
else:
newLine = line[0:4] + ['']
enhancerTable.append(newLine)
if len(candidate_gene_list) > 0:
tfLine = line[0:4] + [','.join(candidate_gene_list)]
enhancerTFTable.append(tfLine)
#now iterate through each gene and list the enhancers
gene_list = gene_to_enhancer_dict.keys()
print(gene_list)
gene_list.sort()
for gene in gene_list:
if tf_list_name.count(gene) > 0:
tf_status = 1
candidate_tf_list.append(gene)
else:
tf_status = 0
enhancer_loci = gene_to_enhancer_dict[gene]
enhancerString = ','.join(
[enhancer.ID() for enhancer in enhancer_loci])
geneSummaryTable.append([gene, tf_status, enhancerString])
for enhancer in enhancer_loci:
newLine = [
gene, tf_status,
enhancer.chr(),
enhancer.start(),
enhancer.end(),
enhancer.ID()
]
geneTable.append(newLine)
if tf_status == 1:
newLine = [
gene,
enhancer.chr(),
enhancer.start(),
enhancer.end(),
enhancer.ID()
]
geneTFTable.append(newLine)
return geneTable, geneTFTable, enhancerTable, enhancerTFTable, geneSummaryTable, candidate_tf_list, gene_to_enhancer_dict
def main():
from optparse import OptionParser
usage = "usage: %prog [options] -e [ENHANCER_FILE] -b [BAM_FILE] -g [GENOME] -o [OUTPUTFOLDER] -n [NAME] -s [SUBPEAKS] -x [EXP_CUTOFF] -l [EXTENSION_LENGTH]"
parser = OptionParser(usage = usage)
# Required flags
parser.add_option("-e","--enhancer_file", dest="enhancers",nargs = 1, default=None,
help = "Provide a ROSE generated enhancer table (_AllEnhancers.table.txt)")
parser.add_option("-b","--bam_file",dest="bam",nargs =1, default = None,
help = "Provide a sorted indexed bam file for H3K27ac sequencing reads")
parser.add_option("-g","--genome",dest="genome",nargs =1, default = None,
help = "Provide the build of the genome to be used for the analysis. Currently supports HG19, HG18 and MM9")
parser.add_option("-f","--fasta",dest="fasta",nargs =1, default = None,
help = "Enter location of the fasta files for the genome version used")
parser.add_option("-s","--subpeaks", dest="subpeaks",nargs=1,default=None,
help = "Enter a bedfile of peaks output from MACS used to identify SE constituents")
parser.add_option("-x","--exp_Cutoff", dest="expCutoff",nargs=1,default=33,
help = "Enter the percentage of transcripts that are not considered expressed, default=33")
parser.add_option("-l","--extension_length", dest="extension",nargs = 1, default = 500,
help = "Enter the length (in bp) to extend constituents for motif search, default=500")
parser.add_option("-n","--name",dest="name",nargs =1, default = None,
help = "Enter the sample name")
parser.add_option("-o","--output",dest="output",nargs =1, default = None,
help = "Enter directory to be used for storing output")
# Options
parser.add_option("-a","--activity", dest="activity",nargs = 1, default=None,
help = "Enter a two column table with refseq in the first column and the associated activity (expression or promoter acetylation level) in the second column")
parser.add_option("-E","--enhancer_number", dest="Enumber",nargs = 1, default='supers',
help = "Enter the number of top ranked enhancers to include in the anlaysis, default = supers")
(options,args) = parser.parse_args()
print(options)
if options.enhancers and options.bam and options.genome and options.fasta and options.subpeaks and options.expCutoff and options.extension and options.name and options.output:
# Set parameters
genomeDirectory = options.fasta
genome = options.genome
genome = upper(genome)
if genome == 'HG19':
annotationFile = './annotation/hg19_refseq.ucsc'
TFfile = './TFlist_NMid_hg.txt'
if genome == 'HG18':
annotationFile = './annotation/hg18_refseq.ucsc'
TFfile = './TFlist_NMid_hg.txt'
if genome == 'MM9':
annotationFile = './annotation/mm9_refseq.ucsc'
TFfile = './TFlist_NMid_ms.txt'
motifConvertFile = './MotifDictionary.txt'
motifDatabaseFile = './VertebratePWMs.txt'
TFtable = utils.parseTable(TFfile, '\t')
TFlist = [line[0] for line in TFtable]
TFlistGene = [line[1] for line in TFtable]
superFile = options.enhancers
superTable = utils.parseTable(superFile, '\t')
bamFile = options.bam
bam = utils.Bam(bamFile)
subpeaks = options.subpeaks
expCutoff = int(options.expCutoff)
motifExtension = int(options.extension)
projectName = options.name
projectFolder = options.output
refseqToNameDict = {}
expressionFile = options.activity
if expressionFile:
expressionTable = utils.parseTable(expressionFile, '\t')
else:
calculatePromoterActivity(annotationFile, bamFile, projectName, projectFolder, refseqToNameDict)
expresionFilename = projectFolder + 'matrix.gff'
expressionTable = utils.parseTable(expresionFilename, '\t')
if options.Enumber != 'super':
enhancerNumber = options.Enumber
else:
enhancerNumber = 'super'
# Run the program
superLoci = createSuperLoci(superTable)
expressedNM = createExpressionDict(annotationFile, projectFolder, projectName, refseqToNameDict, expressionTable)
TFandSuperDict = findCanidateTFs(annotationFile, superLoci, expressedNM, TFlist, refseqToNameDict, projectFolder, projectName)
formatOutput(TFandSuperDict, refseqToNameDict, projectName, projectFolder)
candidateGenes = [upper(refseqToNameDict[x]) for x in TFandSuperDict.keys()]
candidateGenes = utils.uniquify(candidateGenes)
generateSubpeakFASTA(TFandSuperDict, subpeaks, genomeDirectory, projectName, projectFolder, motifExtension)
findMotifs(candidateGenes, projectFolder, projectName, motifConvertFile, motifDatabaseFile)
graph = buildNetwork(projectFolder, projectName, candidateGenes, refseqToNameDict, motifConvertFile)
formatNetworkOutput(graph, projectFolder, projectName, candidateGenes)
# Return help
else:
parser.print_help()
sys.exit()
def tf_edge_delta_out(crc_folder,
chip_dataFile,
analysis_name,
group1_list,
group2_list,
output=''):
'''
calculates changes in brd4 out degree at each predicted motif occurrence this is by subpeaks
'''
crc_folder = utils.formatFolder(crc_folder, False)
edge_path = '%s%s_EDGE_TABLE.txt' % (crc_folder, analysis_name)
#make a gff of the edge table
edge_table = utils.parseTable(edge_path, '\t')
edge_gff = []
for line in edge_table[1:]:
gff_line = [
line[2],
'%s_%s' % (line[0], line[1]), '', line[3], line[4], '', '.', '',
'%s_%s' % (line[0], line[1])
]
edge_gff.append(gff_line)
edge_gff_path = '%s%s_EDGE_TABLE.gff' % (crc_folder, analysis_name)
utils.unParseTable(edge_gff, edge_gff_path, '\t')
#direct the output to the crc folder
signal_path = '%s%s_EDGE_TABLE_signal.txt' % (crc_folder, analysis_name)
#get a list of all chip datasets
all_chip_list = group1_list + group2_list
if utils.checkOutput(signal_path, 0, 0) == False:
signal_table_list = pipeline_dfci.map_regions(chip_dataFile,
[edge_gff_path],
mappedFolder,
signalFolder,
all_chip_list,
True,
signal_path,
extendReadsTo=100)
print(signal_table_list)
else:
print('Found previous signal table at %s' % (signal_path))
#now bring in the signal table as a dictionary using the locus line as the id
print('making log2 group1 over group2 signal table at edges')
signal_table = utils.parseTable(signal_path, '\t')
signal_dict = defaultdict(float)
#figure out columns for group1 and group2
group2_columns = [signal_table[0].index(name) for name in group2_list]
group1_columns = [signal_table[0].index(name) for name in group1_list]
group2_signal_vector = []
group1_signal_vector = []
for line in signal_table[1:]:
group2_signal = numpy.mean(
[float(line[col]) for col in group2_columns])
group1_signal = numpy.mean(
[float(line[col]) for col in group1_columns])
group2_signal_vector.append(group2_signal)
group1_signal_vector.append(group1_signal)
group2_median = numpy.median(group2_signal_vector)
group1_median = numpy.median(group1_signal_vector)
print('group2 median signal (rpm/bp)')
print(group2_median)
print('group1 median signal (rpm/bp)')
print(group1_median)
#now that we have the median, we can take edges where at least 1 edge is above the median
#and both are above zero and generate a new table w/ the fold change
signal_filtered_path = string.replace(signal_path, '.txt', '_filtered.txt')
if utils.checkOutput(signal_filtered_path, 0, 0):
print('Found filtered signal table for edges at %s' %
(signal_filtered_path))
signal_table_filtered = utils.parseTable(signal_filtered_path, '\t')
else:
signal_table_filtered = [
signal_table[0] +
['GROUP2_MEAN', 'GROUP1_MEAN', 'LOG2_GROUP1_OVER_GROUP2']
]
for line in signal_table[1:]:
group2_signal = numpy.mean(
[float(line[col]) for col in group2_columns])
group1_signal = numpy.mean(
[float(line[col]) for col in group1_columns])
if (group2_signal > group2_median or group1_signal > group1_median
) and min(group2_signal, group1_signal) > 0:
delta = numpy.log2(group1_signal / group2_signal)
new_line = line + [group2_signal, group1_signal, delta]
signal_table_filtered.append(new_line)
utils.unParseTable(signal_table_filtered, signal_filtered_path, '\t')
#now get a list of all TFs in the system
tf_list = utils.uniquify(
[line[0].split('_')[0] for line in signal_table_filtered[1:]])
tf_list.sort()
print(tf_list)
out_degree_table = [[
'TF_NAME', 'EDGE_COUNT', 'DELTA_MEAN', 'DELTA_MEDIAN', 'DELTA_STD',
'DELTA_SEM'
]]
for tf_name in tf_list:
print(tf_name)
edge_vector = [
float(line[-1]) for line in signal_table_filtered[1:]
if line[0].split('_')[0] == tf_name
]
edge_count = len(edge_vector)
delta_mean = round(numpy.mean(edge_vector), 4)
delta_median = round(numpy.median(edge_vector), 4)
delta_std = round(numpy.std(edge_vector), 4)
delta_sem = round(stats.sem(edge_vector), 4)
tf_out_line = [
tf_name, edge_count, delta_mean, delta_median, delta_std, delta_sem
]
out_degree_table.append(tf_out_line)
if output == '':
#set final output
output_path = '%s%s_EDGE_DELTA_OUT.txt' % (crc_folder, analysis_name)
else:
output_path = output
utils.unParseTable(out_degree_table, output_path, '\t')
print(output_path)
return (output_path)
def regionStitching(referenceCollection, name, outFolder, stitchWindow, tssWindow, annotFile, removeTSS=True):
print('PERFORMING REGION STITCHING')
# first have to turn bound region file into a locus collection
# need to make sure this names correctly... each region should have a unique name
#referenceCollection
debugOutput = []
# filter out all bound regions that overlap the TSS of an ACTIVE GENE
if removeTSS:
print('REMOVING TSS FROM REGIONS USING AN EXCLUSION WINDOW OF %sBP' % (tssWindow))
# first make a locus collection of TSS
startDict = utils.makeStartDict(annotFile)
# now makeTSS loci for active genes
removeTicker = 0
# this loop makes a locus centered around +/- tssWindow of transcribed genes
# then adds it to the list tssLoci
tssLoci = []
for geneID in startDict.keys():
tssLoci.append(utils.makeTSSLocus(geneID, startDict, tssWindow, tssWindow))
# this turns the tssLoci list into a LocusCollection
# 50 is the internal parameter for LocusCollection and doesn't really matter
tssCollection = utils.LocusCollection(tssLoci, 50)
# gives all the loci in referenceCollection
boundLoci = referenceCollection.getLoci()
# this loop will check if each bound region is contained by the TSS exclusion zone
# this will drop out a lot of the promoter only regions that are tiny
# typical exclusion window is around 2kb
for locus in boundLoci:
if len(tssCollection.getContainers(locus, 'both')) > 0:
# if true, the bound locus overlaps an active gene
referenceCollection.remove(locus)
debugOutput.append([locus.__str__(), locus.ID(), 'CONTAINED'])
removeTicker += 1
print('REMOVED %s LOCI BECAUSE THEY WERE CONTAINED BY A TSS' % (removeTicker))
# referenceCollection is now all enriched region loci that don't overlap an active TSS
if stitchWindow == '':
print('DETERMINING OPTIMUM STITCHING PARAMTER')
optCollection = copy.deepcopy(referenceCollection)
stitchWindow = optimizeStitching(optCollection, name, outFolder, stepSize=500)
print('USING A STITCHING PARAMETER OF %s' % stitchWindow)
stitchedCollection = referenceCollection.stitchCollection(stitchWindow, 'both')
if removeTSS:
# now replace any stitched region that overlap 2 distinct genes
# with the original loci that were there
fixedLoci = []
tssLoci = []
for geneID in startDict.keys():
tssLoci.append(utils.makeTSSLocus(geneID, startDict, 50, 50))
# this turns the tssLoci list into a LocusCollection
# 50 is the internal parameter for LocusCollection and doesn't really matter
tssCollection = utils.LocusCollection(tssLoci, 50)
removeTicker = 0
originalTicker = 0
for stitchedLocus in stitchedCollection.getLoci():
overlappingTSSLoci = tssCollection.getOverlap(stitchedLocus, 'both')
tssNames = [startDict[tssLocus.ID()]['name'] for tssLocus in overlappingTSSLoci]
tssNames = utils.uniquify(tssNames)
if len(tssNames) > 2:
# stitchedCollection.remove(stitchedLocus)
originalLoci = referenceCollection.getOverlap(stitchedLocus, 'both')
originalTicker += len(originalLoci)
fixedLoci += originalLoci
debugOutput.append([stitchedLocus.__str__(), stitchedLocus.ID(), 'MULTIPLE_TSS'])
removeTicker += 1
else:
fixedLoci.append(stitchedLocus)
print('REMOVED %s STITCHED LOCI BECAUSE THEY OVERLAPPED MULTIPLE TSSs' % (removeTicker))
print('ADDED BACK %s ORIGINAL LOCI' % (originalTicker))
fixedCollection = utils.LocusCollection(fixedLoci, 50)
return fixedCollection, debugOutput, stitchWindow
else:
return stitchedCollection, debugOutput, stitchWindow
def regionStitching(referenceCollection,
name,
outFolder,
stitchWindow,
tssWindow,
annotFile,
removeTSS=True):
print('PERFORMING REGION STITCHING')
# first have to turn bound region file into a locus collection
# need to make sure this names correctly... each region should have a unique name
#referenceCollection
debugOutput = []
# filter out all bound regions that overlap the TSS of an ACTIVE GENE
if removeTSS:
print('REMOVING TSS FROM REGIONS USING AN EXCLUSION WINDOW OF %sBP' %
(tssWindow))
# first make a locus collection of TSS
startDict = utils.makeStartDict(annotFile)
# now makeTSS loci for active genes
removeTicker = 0
# this loop makes a locus centered around +/- tssWindow of transcribed genes
# then adds it to the list tssLoci
tssLoci = []
for geneID in startDict.keys():
tssLoci.append(
utils.makeTSSLocus(geneID, startDict, tssWindow, tssWindow))
# this turns the tssLoci list into a LocusCollection
# 50 is the internal parameter for LocusCollection and doesn't really matter
tssCollection = utils.LocusCollection(tssLoci, 50)
# gives all the loci in referenceCollection
boundLoci = referenceCollection.getLoci()
# this loop will check if each bound region is contained by the TSS exclusion zone
# this will drop out a lot of the promoter only regions that are tiny
# typical exclusion window is around 2kb
for locus in boundLoci:
if len(tssCollection.getContainers(locus, 'both')) > 0:
# if true, the bound locus overlaps an active gene
referenceCollection.remove(locus)
debugOutput.append([locus.__str__(), locus.ID(), 'CONTAINED'])
removeTicker += 1
print('REMOVED %s LOCI BECAUSE THEY WERE CONTAINED BY A TSS' %
(removeTicker))
# referenceCollection is now all enriched region loci that don't overlap an active TSS
if stitchWindow == '':
print('DETERMINING OPTIMUM STITCHING PARAMTER')
optCollection = copy.deepcopy(referenceCollection)
stitchWindow = optimizeStitching(optCollection,
name,
outFolder,
stepSize=500)
print('USING A STITCHING PARAMETER OF %s' % stitchWindow)
stitchedCollection = referenceCollection.stitchCollection(
stitchWindow, 'both')
if removeTSS:
# now replace any stitched region that overlap 2 distinct genes
# with the original loci that were there
fixedLoci = []
tssLoci = []
for geneID in startDict.keys():
tssLoci.append(utils.makeTSSLocus(geneID, startDict, 50, 50))
# this turns the tssLoci list into a LocusCollection
# 50 is the internal parameter for LocusCollection and doesn't really matter
tssCollection = utils.LocusCollection(tssLoci, 50)
removeTicker = 0
originalTicker = 0
for stitchedLocus in stitchedCollection.getLoci():
overlappingTSSLoci = tssCollection.getOverlap(
stitchedLocus, 'both')
tssNames = [
startDict[tssLocus.ID()]['name']
for tssLocus in overlappingTSSLoci
]
tssNames = utils.uniquify(tssNames)
if len(tssNames) > 2:
# stitchedCollection.remove(stitchedLocus)
originalLoci = referenceCollection.getOverlap(
stitchedLocus, 'both')
originalTicker += len(originalLoci)
fixedLoci += originalLoci
debugOutput.append([
stitchedLocus.__str__(),
stitchedLocus.ID(), 'MULTIPLE_TSS'
])
removeTicker += 1
else:
fixedLoci.append(stitchedLocus)
print(
'REMOVED %s STITCHED LOCI BECAUSE THEY OVERLAPPED MULTIPLE TSSs' %
(removeTicker))
print('ADDED BACK %s ORIGINAL LOCI' % (originalTicker))
fixedCollection = utils.LocusCollection(fixedLoci, 50)
return fixedCollection, debugOutput, stitchWindow
else:
return stitchedCollection, debugOutput, stitchWindow
def makePeakTable(paramDict,
splitGFFPath,
averageTablePath,
startDict,
geneList,
genomeDirectory,
tads_path=''):
'''
makes the final peak table with ebox info
'''
peakTable = [[
'REGION_ID', 'CHROM', 'START', 'STOP', 'LENGTH', 'TSS', 'CPG',
'CPG_FRACTION', 'GC_FREQ', 'SIGNAL', 'CANON_EBOX_COUNT',
'NON_CANON_EBOX_COUNT', 'TOTAL_EBOX_COUNT', 'OVERLAPPING_GENES',
'PROXIMAL_GENES'
]]
print('LOADING PEAK REGIONS')
peakGFF = utils.parseTable(splitGFFPath, '\t')
print('LOADING BINDING DATA')
signalTable = utils.parseTable(averageTablePath, '\t')
print('LOADING CPGS ISLANDS')
cpgBed = utils.parseTable(paramDict['cpgPath'], '\t')
cpgLoci = []
for line in cpgBed:
cpgLoci.append(utils.Locus(line[0], line[1], line[2], '.', line[-1]))
cpgCollection = utils.LocusCollection(cpgLoci, 50)
print("MAKING TSS COLLECTIONS")
if len(geneList) == 0:
geneList = startDict.keys()
tss_1kb_loci = []
tss_50kb_loci = []
for refID in geneList:
tss_1kb_loci.append(utils.makeTSSLocus(refID, startDict, 1000, 1000))
tss_50kb_loci.append(utils.makeTSSLocus(refID, startDict, 50000,
50000))
#make a 1kb flanking and 50kb flanking collection
tss_1kb_collection = utils.LocusCollection(tss_1kb_loci, 50)
tss_50kb_collection = utils.LocusCollection(tss_50kb_loci, 50)
if len(tads_path) > 0:
print('LOADING TADS FROM %s' % (tads_path))
tad_collection = utils.importBoundRegion(tads_path, 'tad')
use_tads = True
#building a tad dict keyed by tad ID w/ genes in that tad provided
tad_dict = defaultdict(list)
for tss_locus in tss_1kb_loci:
overlapping_tads = tad_collection.getOverlap(tss_locus, 'both')
for tad_locus in overlapping_tads:
tad_dict[tad_locus.ID()].append(tss_locus.ID())
else:
use_tads = False
print('CLASSIFYING PEAKS')
ticker = 0
no_tad_count = 0
for i in range(len(peakGFF)):
if ticker % 1000 == 0:
print(ticker)
ticker += 1
#getting the particulars of the region
gffLine = peakGFF[i]
peakID = gffLine[1]
chrom = gffLine[0]
start = int(gffLine[3])
stop = int(gffLine[4])
lineLocus = utils.Locus(chrom, start, stop, '.', peakID)
#getting the mapped signal
signalLine = signalTable[(i + 1)]
signalVector = [float(x) for x in signalLine[2:]]
#setting up the new line
newLine = [peakID, chrom, start, stop, lineLocus.len()]
#get the tss status from the gff itself (we are able to do this nicely from the split gff code earlier
newLine.append(gffLine[7])
#check cpg status
if cpgCollection.getOverlap(lineLocus, 'both'):
newLine.append(1)
else:
newLine.append(0)
#now do fractional cpgOverlap
overlappingCpGLoci = cpgCollection.getOverlap(lineLocus, 'both')
overlappingBases = 0
for locus in overlappingCpGLoci:
cpgStart = max(locus.start(), lineLocus.start())
cpgEnd = min(locus.end(), lineLocus.end())
overlappingBases += (cpgEnd - cpgStart)
overlapFraction = float(overlappingBases) / lineLocus.len()
newLine.append(round(overlapFraction, 2))
#now get the seq
lineSeq = string.upper(
utils.fetchSeq(genomeDirectory, chrom, start, stop, True))
if len(lineSeq) == 0:
print('UH OH')
print(lineSeq)
print(gffLine)
print(i)
print(chrom)
print(start)
print(stop)
sys.exit()
gcFreq = float(lineSeq.count('GC') +
lineSeq.count('CG')) / len(lineSeq)
newLine.append(gcFreq)
#this is where we add the ChIP-Seq signal
newLine += signalVector
eboxMatchList = re.findall('CA..TG', lineSeq)
if len(eboxMatchList) == 0:
newLine += [0] * 3
else:
totalCount = len(eboxMatchList)
canonCount = eboxMatchList.count('CACGTG')
otherCount = totalCount - canonCount
newLine += [canonCount, otherCount, totalCount]
#now find the overlapping and proximal genes
#here each overlapping gene the tss 1kb locus overlaps the peak
if use_tads:
tad_loci = tad_collection.getOverlap(lineLocus, 'both')
tad_id_list = [tad_locus.ID() for tad_locus in tad_loci]
tad_genes = []
for tad_id in tad_id_list:
tad_genes += tad_dict[tad_id]
if len(tad_genes) == 0:
#print('no tad for this region')
#print(gffLine)
no_tad_count += 1
else:
tad_genes = []
if len(tad_genes) > 0:
overlappingGenes = [
startDict[locus.ID()]['name']
for locus in tss_1kb_collection.getOverlap(lineLocus, 'both')
if tad_genes.count(locus.ID()) > 0
]
proximalGenes = [
startDict[locus.ID()]['name']
for locus in tss_50kb_collection.getOverlap(lineLocus, 'both')
if tad_genes.count(locus.ID()) > 0
]
# print('linked peak to tad genes')
# print([startDict[x]['name'] for x in tad_genes])
# print(tad_id_list)
# print(gffLine)
# print(overlappingGenes)
# print(proximalGenes)
else:
overlappingGenes = [
startDict[locus.ID()]['name']
for locus in tss_1kb_collection.getOverlap(lineLocus, 'both')
]
proximalGenes = [
startDict[locus.ID()]['name']
for locus in tss_50kb_collection.getOverlap(lineLocus, 'both')
]
overlappingGenes = utils.uniquify(overlappingGenes)
#here the tss 50kb locus overlaps the peak
#overlap takes priority over proximal
proximalGenes = [
gene for gene in proximalGenes if overlappingGenes.count(gene) == 0
]
proximalGenes = utils.uniquify(proximalGenes)
overlappingString = string.join(overlappingGenes, ',')
proximalString = string.join(proximalGenes, ',')
newLine += [overlappingString, proximalString]
peakTable.append(newLine)
print('Out of %s regions, %s were assigned to at least 1 tad' %
(len(peakTable), no_tad_count))
return peakTable
def mapBamToGFF(bamFile,
gff,
sense='.',
extension=200,
rpm=False,
clusterGram=None,
matrix=None):
'''maps reads from a bam to a gff'''
#creating a new gff to output
newGFF = []
#reading in the bam
bam = utils.Bam(bamFile)
#getting RPM normalization
if rpm:
MMR = round(float(bam.getTotalReads('mapped')) / 1000000, 4)
else:
MMR = 1
print('using a MMR value of %s' % (MMR))
#creating a sense trans
senseTrans = string.maketrans('-+.', '+-+')
#reading in the gff
if type(gff) == str:
gff = utils.parseTable(gff, '\t')
#setting up a clustergram table
if clusterGram:
binSize = int(clusterGram)
binSizeList = []
#now go through each line of the gff and make sure they're all the same length
for i in range(0, len(gff), 1):
line = gff[i]
gffLocus = utils.Locus(line[0], int(line[3]), int(line[4]),
line[6], line[1])
binSizeList.append(gffLocus.len() / binSize)
binSizeList = utils.uniquify(binSizeList)
if len(binSizeList) > 1:
print(
'WARNING: lines in gff are of different length. Output clustergram will have variable row length'
)
newGFF.append(['GENE_ID', 'locusLine'] + [
str(x * binSize) + '_' + bamFile.split('/')[-1]
for x in range(1,
max(binSizeList) + 1, 1)
])
#setting up a maxtrix table
if matrix:
newGFF.append(['GENE_ID', 'locusLine'] + [
'bin_' + str(n) + '_' + bamFile.split('/')[-1]
for n in range(1,
int(matrix) + 1, 1)
])
nBin = int(matrix)
# Try to use the bamliquidatior script on cluster, otherwise, failover to local (in path), otherwise fail.
bamliquidatorString = '/usr/bin/bamliquidator'
if not os.path.isfile(bamliquidatorString):
bamliquidatorString = './bamliquidator'
if not os.path.isfile(bamliquidatorString):
raise ValueError('bamliquidator not found in path')
#getting and processing reads for gff lines
ticker = 0
print('Number lines processed')
for line in gff:
line = line[0:9]
if ticker % 100 == 0:
print(ticker)
ticker += 1
gffLocus = utils.Locus(line[0], int(line[3]), int(line[4]), line[6],
line[1])
#get the nBin and binSize
if clusterGram:
nBin = gffLocus.len() / int(clusterGram)
binSize = int(clusterGram)
if matrix:
nBin = int(matrix)
binSize = gffLocus.len() / nBin
#some regions will be too short to get info on
if binSize == 0:
clusterLine = [gffLocus.ID(),
gffLocus.__str__()] + ['NA'] * nBin
newGFF.append(clusterLine)
continue
#flippy flip if sense is negative
if sense == '-':
bamSense = string.translate(gffLocus.sense(), senseTrans)
elif sense == '+':
bamSense = gffLocus.sense()
else:
bamSense = '.'
#using the bamLiquidator to get the readstring
#print('using nBin of %s' % nBin)
bamCommand = "%s %s %s %s %s %s %s %s" % (
bamliquidatorString, bamFile, line[0], gffLocus.start(),
gffLocus.end(), bamSense, nBin, extension)
#print(bamCommand)
getReads = subprocess.Popen(bamCommand,
stdin=subprocess.PIPE,
stderr=subprocess.PIPE,
stdout=subprocess.PIPE,
shell=True)
readString, stderr = getReads.communicate()
if stderr:
print("STDERR out: %s" % (stderr))
denList = readString.split('\n')[:-1]
#print("denlist is: %s" % denList)
#flip the denList if the actual gff region is -
if gffLocus.sense() == '-':
denList = denList[::-1]
#converting from units of total bp of read sequence per bin to rpm/bp
denList = [round(float(x) / binSize / MMR, 4) for x in denList]
#if the gff region is - strand, flip the
clusterLine = [gffLocus.ID(), gffLocus.__str__()] + denList
newGFF.append(clusterLine)
return newGFF
def loadAnnotFile(genome, window, geneList=[], skip_cache=False):
"""
load in the annotation and create a startDict and tss collection for a set of refseq IDs a given genome
"""
genomeDict = {
'HG18': 'annotation/hg18_refseq.ucsc',
'MM9': 'annotation/mm9_refseq.ucsc',
'MM10': 'annotation/mm10_refseq.ucsc',
'HG19': 'annotation/hg19_refseq.ucsc',
'HG19_RIBO': 'annotation/hg19_refseq.ucsc',
'RN4': 'annotation/rn4_refseq.ucsc',
'RN6': 'annotation/rn6_refseq.ucsc',
'HG38': 'annotation/hg38_refseq.ucsc',
}
genomeDirectoryDict = {
'HG19':
'/storage/cylin/grail/genomes/Homo_sapiens/UCSC/hg19/Sequence/Chromosomes/',
'RN6':
'/storage/cylin/grail/genomes/Rattus_norvegicus/UCSC/rn6/Sequence/Chromosomes/',
'MM9':
'/storage/cylin/grail/genomes/Mus_musculus/UCSC/mm9/Sequence/Chromosomes/',
'MM10':
'/storage/cylin/grail/genomes/Mus_musculus/UCSC/mm10/Sequence/Chromosomes/',
'HG38':
'/storage/cylin/grail/genomes/Homo_sapiens/UCSC/hg38/Sequence/Chromosomes/',
}
mouse_convert_file = '%s/annotation/HMD_HumanPhenotype.rpt' % (whereAmI)
#making a dictionary for mouse to human conversion
mouse_convert_dict = defaultdict(str)
mouse_convert_table = utils.parseTable(mouse_convert_file, '\t')
for line in mouse_convert_table:
mouse_convert_dict[line[4]] = line[0]
genomeDirectory = genomeDirectoryDict[string.upper(genome)]
#making a chrom_dict that is a list of all chroms with sequence
chrom_list = utils.uniquify([
name.split('.')[0] for name in os.listdir(genomeDirectory)
if len(name) > 0
])
annotFile = whereAmI + '/' + genomeDict[string.upper(genome)]
if not skip_cache:
# Try loading from a cache, if the crc32 matches
annotPathHash = zlib.crc32(
annotFile) & 0xFFFFFFFF # hash the entire location of this script
annotFileHash = zlib.crc32(open(annotFile, "rb").read()) & 0xFFFFFFFF
cache_file_name = "%s.%s.%s.cache" % (genome, annotPathHash,
annotFileHash)
cache_file_path = '%s/%s' % (tempfile.gettempdir(), cache_file_name)
if os.path.isfile(cache_file_path):
# Cache exists! Load it!
try:
print('\tLoading genome data from cache.')
with open(cache_file_path, 'rb') as cache_fh:
cached_data = cPickle.load(cache_fh)
print('\tCache loaded.')
return cached_data
except (IOError, cPickle.UnpicklingError):
# Pickle corrupt? Let's get rid of it.
print('\tWARNING: Cache corrupt or unreadable. Ignoring.')
else:
print('\tNo cache exists: Loading annotation (slow).')
# We're still here, so either caching was disabled, or the cache doesn't exist
startDict = utils.makeStartDict(annotFile, geneList)
tssLoci = []
if geneList == []:
geneList = startDict.keys()
for gene in geneList:
tssLoci.append(utils.makeTSSLocus(gene, startDict, window, window))
tssCollection = utils.LocusCollection(tssLoci, 50)
if not skip_cache:
print('Writing cache for the first time.')
with open(cache_file_path, 'wb') as cache_fh:
cPickle.dump((startDict, tssCollection), cache_fh,
cPickle.HIGHEST_PROTOCOL)
return startDict, tssCollection, genomeDirectory, chrom_list, mouse_convert_dict
def main():
'''
using argparse
'''
parser = argparse.ArgumentParser(usage='%(prog)s -i DATAFILE -1 GROUP1_NAMES -2 GROUP2_NAMES')
# required flags
parser.add_argument("-d", "--data_table", dest="data_table", type=str,
help="input a data table with all datasets to be analyzed", required=True)
parser.add_argument("-1", "--group1", dest="group1", type=str,
help="input a comma separated list of all datasets in group1", required=True)
parser.add_argument("-2", "--group2", dest="group2", type=str,
help="input a comma separated list of all datasets in group2", required=True)
#optional input override
parser.add_argument("-i", "--input", dest="input", type=str,
help="input a gff of regions to analyze", required=False)
#optional arguments
parser.add_argument("-n", "--name", dest="name", type=str,
help="specify a name for the analysis. Default is drawn from the data table name", required=False)
parser.add_argument("--group1-name", dest="group1_name", default='GROUP1',type=str,
help="Enter a name for group1. Default is 'GROUP1'", required=False)
parser.add_argument("--group2-name", dest="group2_name", default='GROUP2',type=str,
help="Enter a name for group2. Default is 'GROUP2'", required=False)
parser.add_argument("-a", "--activity", dest="activity", type=str,default='',
help="a table with active gene names in the first column", required=False)
parser.add_argument("-t", "--tss", dest="tss", type=int,default=2500,
help="Specify a TSS exclusion distance. Default is 2500", required=False)
parser.add_argument("-s", "--stitch", dest="stitch", type=int,default=None,
help="Specify a stitching distance. Default is auto stitching", required=False)
parser.add_argument("-o", "--output", dest="output", default='./',type=str,
help="Enter the output folder. Default is the current working directory", required=False)
parser.add_argument("--log", dest="log", default='',type=str,
help="Enter a path to log output", required=False)
# # DEBUG OPTION TO SAVE TEMP FILES
# parser.add_argument("--scale", dest="scale", default='',
# help="Enter a comma separated list of scaling factors for your bams. Default is none")
# parser.add_argument("--save-temp", dest="save", action='store_true', default=False,
# help="If flagged will save temporary files made by bamPlot")
# parser.add_argument("--bed", dest="bed",
# help="Add a space-delimited list of bed files to plot")
# parser.add_argument("--multi-page", dest="multi", action='store_true', default=False,
# help="If flagged will create a new pdf for each region")
args = parser.parse_args()
#now we can begin to parse the arguments
#=====================================================================================
#===============================I. PARSING ARGUMENTS==================================
#=====================================================================================
#pulling in the data table
data_file = os.path.abspath(args.data_table)
dataDict = pipeline_dfci.loadDataTable(data_file)
#setting naming conventions
if not args.name:
analysis_name = data_file.split('/')[-1].split('.')[0]
else:
analysis_name = args.name
#getting the optional input gff
if args.input:
inputGFF = args.input
else:
inputGFF = ''
#getting group names
group1_name = args.group1_name
group2_name = args.group2_name
#getting group1
group1_string = args.group1
group1_list = [name for name in string.split(group1_string,',') if len(name) > 0]
#getting group2
group2_string = args.group2
group2_list = [name for name in string.split(group2_string,',') if len(name) > 0]
#checking that all datasets are in the data table
for name in group1_list + group2_list:
if name not in dataDict:
print('ERROR: DATASET %s NOT FOUND IN DATA TABLE %s. EXITING NOW' % (name,data_file))
sys.exit()
#loading in the genome object from the data table
genome_list = utils.uniquify([dataDict[name]['genome'] for name in group1_list + group2_list])
if len(genome_list) > 1:
print('ERROR: ATTEMPTING TO ANALYZE DATASETS FROM MULTIPLE GENOME BUILDS. EXITING NOW.')
sys.exit()
#the load genome function has an assertion test to make sure the genome is supported
genome = loadGenome(genome_list[0])
parent_folder = utils.formatFolder(args.output,True)
output_folder = utils.formatFolder(parent_folder + analysis_name,True)
#these are the user defined optional arguments
tss = int(args.tss)
stitch = args.stitch
print('stitch')
print(stitch)
#list of active genes to constrain analysis
if len(args.activity) == 0:
#assumes all genes are active unless told otherwise
#activity_path,activity_table = getActivity() # fix this function
print('using all active genes')
else:
activity_path = args.activity
activity_table = utils.parseTable(activity_path,'\t')
print('\n\n#======================================\n#===========I. DATA SUMMARY============\n#======================================\n')
print('Analyzing datasets described in %s\n' % (data_file))
print('Name for the analysis: %s\n' % (analysis_name))
print('Using genome: %s\n' % (genome.name()))
print('%s datasets: %s\n' % (group1_name,group1_string))
print('%s datasets: %s\n' % (group2_name,group2_string))
if len(activity_path) > 0:
print('Identified %s active genes in the analysis using %s as a list of active genes' % (len(activity_table),activity_path))
else:
print('Identified %s active genes in the analysis using aggregate data from %s and %s' % (len(activity_table),group1_name,group2_name))
print('Writing output to: %s\n' % (output_folder))
#=====================================================================================
#======================II. DEFINING CIS-REGULATORY ELEMENTS===========================
#=====================================================================================
print('\n\n#======================================\n#=II. MAPPING CIS-REGULATORY ELEMENTS==\n#======================================\n')
#crc_wrapper will act at the group level and not consider individual datasets
#since a data table is used as the input, the code will rely heavily on pipeline_dfci
#embedded tools
#1. first we need to run meta rose using default parameters and check the output
#exists for each group
meta_rose_folder = utils.formatFolder(output_folder + 'meta_rose/',True)
group1_output = '%s%s/%s_AllEnhancers.table.txt' % (meta_rose_folder,group1_name,group1_name)
group2_output = '%s%s/%s_AllEnhancers.table.txt' % (meta_rose_folder,group2_name,group2_name)
#print(group1_output)
#print(group2_output)
#for each output check to see if they exist
#if not launch
try:
foo = open(group1_output,'r')
except IOError:
print('No META_ROSE output found for %s. Running META_ROSE now' % (group1_name))
launchMetaRose(group1_name,group1_list,meta_rose_folder,genome,data_file,stitch,tss)
try:
foo = open(group2_output,'r')
except IOError:
print('No META_ROSE output found for %s. Running META_ROSE now' % (group2_name))
launchMetaRose(group2_name,group2_list,meta_rose_folder,genome,data_file,stitch,tss)
#now check for completion
if utils.checkOutput(group1_output,1,10):
print('META_ROSE finished for %s' % (group1_name))
else:
print('META_ROSE timed out for %s. EXITING NOW.' % (group1_name))
sys.exit()
if utils.checkOutput(group2_output,1,10):
print('META_ROSE finished for %s' % (group2_name))
else:
print('META_ROSE timed out for %s. EXITING NOW.' % (group2_name))
sys.exit()
#Meta rose does not give all regions that are SE in at least one sample
#and can be blown out by amplicons etc...
#sooo we need to run clustering to generate a good input gff
#ideally we just rewrite dynamic meta to run off of clustering output
#until we do that let's just overwrite w/ an input gff
print('Comparing cis-regulatory landscapes of %s and %s' % (group1_name,group2_name))
dynamic_rose_folder = utils.formatFolder(output_folder + 'dynamic_meta_rose/',True)
#here we will use the rank table as the primary output
dynamic_rose_output = '%soutput/%s_%s_%s_merged_MERGED_SUPERS_RANK_TABLE.txt' % (dynamic_rose_folder,genome.name(),group1_name,group2_name)
try:
foo = open(dynamic_rose_output,'r')
except IOError:
print('No DYNAMIC_ROSE output found for %s. Running DYNAMIC_ROSE now' % (analysis_name))
launchDynamicRose(analysis_name,group1_name,group2_name,group1_list,group2_list,meta_rose_folder,dynamic_rose_folder,genome,data_file,activity_path,inputGFF)
if utils.checkOutput(dynamic_rose_output,1,10):
print('DYNAMIC_ROSE finsihed for %s' % (analysis_name))
else:
print('DYNAMIC_ROSE analysis timed out for %s. EXITING NOW.' % (analysis_name))
sys.exit()
#=====================================================================================
#======================III. IDENTIFYING TF NODES IN NETWORK===========================
#=====================================================================================
print('\n\n#======================================\n#===III. RUNNING CIRCUITRY ANALYSIS====\n#======================================\n')
#now we want to call circuitry on each group... ok to have different subpeaks and motif calls
#if as a first approximation we weight by the overall enhancer
crc_folder = utils.formatFolder('%scrc/' % (output_folder),True)
#for all
all_crc_folder = utils.formatFolder('%s%s' % (crc_folder,analysis_name),True)
launchCRC(data_file,genome,dynamic_rose_output,analysis_name,group1_list+group2_list,all_crc_folder,activity_path)
#for group1
group1_crc_folder = utils.formatFolder('%s%s' % (crc_folder,group1_name),True)
launchCRC(data_file,genome,dynamic_rose_output,group1_name,group1_list,group1_crc_folder,activity_path)
#for group2
group2_crc_folder = utils.formatFolder('%s%s' % (crc_folder,group2_name),True)
launchCRC(data_file,genome,dynamic_rose_output,group2_name,group2_list,group2_crc_folder,activity_path)
def main():
'''
main run call
'''
debug = False
from optparse import OptionParser
usage = "usage: %prog [options] -g [GENOME] -i [INPUT_REGION_GFF] -r [RANKBY_BAM_FILE] -o [OUTPUT_FOLDER] [OPTIONAL_FLAGS]"
parser = OptionParser(usage=usage)
# required flags
parser.add_option(
"-i",
"--i",
dest="input",
nargs=1,
default=None,
help="Enter a .gff or .bed file of binding sites used to make enhancers"
)
parser.add_option("-r",
"--rankby",
dest="rankby",
nargs=1,
default=None,
help="bamfile to rank enhancer by")
parser.add_option("-o",
"--out",
dest="out",
nargs=1,
default=None,
help="Enter an output folder")
parser.add_option("-g",
"--genome",
dest="genome",
nargs=1,
default=None,
help="Enter the genome build (MM9,MM8,HG18,HG19)")
# optional flags
parser.add_option(
"-b",
"--bams",
dest="bams",
nargs=1,
default=None,
help="Enter a comma separated list of additional bam files to map to")
parser.add_option("-c",
"--control",
dest="control",
nargs=1,
default=None,
help="bamfile to rank enhancer by")
parser.add_option(
"-s",
"--stitch",
dest="stitch",
nargs=1,
default='',
help=
"Enter a max linking distance for stitching. Default will determine optimal stitching parameter"
)
parser.add_option(
"-t",
"--tss",
dest="tss",
nargs=1,
default=0,
help="Enter a distance from TSS to exclude. 0 = no TSS exclusion")
parser.add_option(
"--mask",
dest="mask",
nargs=1,
default=None,
help=
"Mask a set of regions from analysis. Provide a .bed or .gff of masking regions"
)
# RETRIEVING FLAGS
(options, args) = parser.parse_args()
if not options.input or not options.rankby or not options.out or not options.genome:
print('hi there')
parser.print_help()
exit()
# making the out folder if it doesn't exist
outFolder = utils.formatFolder(options.out, True)
# figuring out folder schema
gffFolder = utils.formatFolder(outFolder + 'gff/', True)
mappedFolder = utils.formatFolder(outFolder + 'mappedGFF/', True)
# GETTING INPUT FILE
if options.input.split('.')[-1] == 'bed':
# CONVERTING A BED TO GFF
inputGFFName = options.input.split('/')[-1][0:-4]
inputGFFFile = '%s%s.gff' % (gffFolder, inputGFFName)
utils.bedToGFF(options.input, inputGFFFile)
elif options.input.split('.')[-1] == 'gff':
# COPY THE INPUT GFF TO THE GFF FOLDER
inputGFFFile = options.input
os.system('cp %s %s' % (inputGFFFile, gffFolder))
else:
print(
'WARNING: INPUT FILE DOES NOT END IN .gff or .bed. ASSUMING .gff FILE FORMAT'
)
# COPY THE INPUT GFF TO THE GFF FOLDER
inputGFFFile = options.input
os.system('cp %s %s' % (inputGFFFile, gffFolder))
# GETTING THE LIST OF BAMFILES TO PROCESS
if options.control:
bamFileList = [options.rankby, options.control]
else:
bamFileList = [options.rankby]
if options.bams:
bamFileList += options.bams.split(',')
#bamFileList = utils.uniquify(bamFileList) # makes sad when you have the same control bam over and over again
# optional args
# Stitch parameter
if options.stitch == '':
stitchWindow = ''
else:
stitchWindow = int(options.stitch)
# tss options
tssWindow = int(options.tss)
if tssWindow != 0:
removeTSS = True
else:
removeTSS = False
# GETTING THE BOUND REGION FILE USED TO DEFINE ENHANCERS
print('USING %s AS THE INPUT GFF' % (inputGFFFile))
inputName = inputGFFFile.split('/')[-1].split('.')[0]
# GETTING THE GENOME
genome = options.genome
print('USING %s AS THE GENOME' % genome)
# GETTING THE CORRECT ANNOT FILE
cwd = os.getcwd()
genomeDict = {
'HG18': '%s/annotation/hg18_refseq.ucsc' % (cwd),
'MM9': '%s/annotation/mm9_refseq.ucsc' % (cwd),
'HG19': '%s/annotation/hg19_refseq.ucsc' % (cwd),
'MM8': '%s/annotation/mm8_refseq.ucsc' % (cwd),
'MM10': '%s/annotation/mm10_refseq.ucsc' % (cwd),
'RN4': '%s/annotation/rn4_refseq.ucsc' % (cwd),
'RN6': '%s/annotation/rn6_refseq.ucsc' % (cwd),
}
annotFile = genomeDict[genome.upper()]
# MAKING THE START DICT
print('MAKING START DICT')
startDict = utils.makeStartDict(annotFile)
#GET CHROMS FOUND IN THE BAMS
print('GETTING CHROMS IN BAMFILES')
bamChromList = getBamChromList(bamFileList)
print("USING THE FOLLOWING CHROMS")
print(bamChromList)
#LOADING IN THE GFF AND FILTERING BY CHROM
print('LOADING AND FILTERING THE GFF')
inputGFF = filterGFF(inputGFFFile, bamChromList)
# LOADING IN THE BOUND REGION REFERENCE COLLECTION
print('LOADING IN GFF REGIONS')
referenceCollection = utils.gffToLocusCollection(inputGFF)
print('CHECKING REFERENCE COLLECTION:')
checkRefCollection(referenceCollection)
# MASKING REFERENCE COLLECTION
# see if there's a mask
if options.mask:
maskFile = options.mask
# if it's a bed file
if maskFile.split('.')[-1].upper() == 'BED':
maskGFF = utils.bedToGFF(maskFile)
elif maskFile.split('.')[-1].upper() == 'GFF':
maskGFF = utils.parseTable(maskFile, '\t')
else:
print("MASK MUST BE A .gff or .bed FILE")
sys.exit()
maskCollection = utils.gffToLocusCollection(maskGFF)
# now mask the reference loci
referenceLoci = referenceCollection.getLoci()
filteredLoci = [
locus for locus in referenceLoci
if len(maskCollection.getOverlap(locus, 'both')) == 0
]
print("FILTERED OUT %s LOCI THAT WERE MASKED IN %s" %
(len(referenceLoci) - len(filteredLoci), maskFile))
referenceCollection = utils.LocusCollection(filteredLoci, 50)
# NOW STITCH REGIONS
print('STITCHING REGIONS TOGETHER')
stitchedCollection, debugOutput, stitchWindow = regionStitching(
referenceCollection, inputName, outFolder, stitchWindow, tssWindow,
annotFile, removeTSS)
# NOW MAKE A STITCHED COLLECTION GFF
print('MAKING GFF FROM STITCHED COLLECTION')
stitchedGFF = utils.locusCollectionToGFF(stitchedCollection)
# making sure start/stop ordering are correct
for i in range(len(stitchedGFF)):
line = stitchedGFF[i]
start = int(line[3])
stop = int(line[4])
if start > stop:
line[3] = stop
line[4] = start
print(stitchWindow)
print(type(stitchWindow))
if not removeTSS:
stitchedGFFFile = '%s%s_%sKB_STITCHED.gff' % (gffFolder, inputName,
str(stitchWindow / 1000))
stitchedGFFName = '%s_%sKB_STITCHED' % (inputName,
str(stitchWindow / 1000))
debugOutFile = '%s%s_%sKB_STITCHED.debug' % (gffFolder, inputName,
str(stitchWindow / 1000))
else:
stitchedGFFFile = '%s%s_%sKB_STITCHED_TSS_DISTAL.gff' % (
gffFolder, inputName, str(stitchWindow / 1000))
stitchedGFFName = '%s_%sKB_STITCHED_TSS_DISTAL' % (
inputName, str(stitchWindow / 1000))
debugOutFile = '%s%s_%sKB_STITCHED_TSS_DISTAL.debug' % (
gffFolder, inputName, str(stitchWindow / 1000))
# WRITING DEBUG OUTPUT TO DISK
if debug:
print('WRITING DEBUG OUTPUT TO DISK AS %s' % (debugOutFile))
utils.unParseTable(debugOutput, debugOutFile, '\t')
# WRITE THE GFF TO DISK
print('WRITING STITCHED GFF TO DISK AS %s' % (stitchedGFFFile))
utils.unParseTable(stitchedGFF, stitchedGFFFile, '\t')
# SETTING UP THE OVERALL OUTPUT FILE
outputFile1 = outFolder + stitchedGFFName + '_ENHANCER_REGION_MAP.txt'
print('OUTPUT WILL BE WRITTEN TO %s' % (outputFile1))
# MAPPING TO THE NON STITCHED (ORIGINAL GFF)
# MAPPING TO THE STITCHED GFF
# Try to use the bamliquidatior_path.py script on cluster, otherwise, failover to local (in path), otherwise fail.
bamliquidator_path = 'bamliquidator_batch.py'
bamFileListUnique = list(bamFileList)
bamFileListUnique = utils.uniquify(bamFileListUnique)
#prevent redundant mapping
print("MAPPING TO THE FOLLOWING BAMS:")
print(bamFileListUnique)
for bamFile in bamFileListUnique:
bamFileName = bamFile.split('/')[-1]
# MAPPING TO THE STITCHED GFF
mappedOut1Folder = '%s%s_%s_MAPPED' % (mappedFolder, stitchedGFFName,
bamFileName)
mappedOut1File = '%s%s_%s_MAPPED/matrix.txt' % (
mappedFolder, stitchedGFFName, bamFileName)
if utils.checkOutput(mappedOut1File, 0.2, 0.2):
print("FOUND %s MAPPING DATA FOR BAM: %s" %
(stitchedGFFFile, mappedOut1File))
else:
cmd1 = bamliquidator_path + " --sense . -e 200 --match_bamToGFF -r %s -o %s %s" % (
stitchedGFFFile, mappedOut1Folder, bamFile)
print(cmd1)
os.system(cmd1)
if utils.checkOutput(mappedOut1File, 0.2, 5):
print("SUCCESSFULLY MAPPED TO %s FROM BAM: %s" %
(stitchedGFFFile, bamFileName))
else:
print("ERROR: FAILED TO MAP %s FROM BAM: %s" %
(stitchedGFFFile, bamFileName))
sys.exit()
print('BAM MAPPING COMPLETED NOW MAPPING DATA TO REGIONS')
# CALCULATE DENSITY BY REGION
# NEED TO FIX THIS FUNCTION TO ACCOUNT FOR DIFFERENT OUTPUTS OF LIQUIDATOR
mapCollection(stitchedCollection,
referenceCollection,
bamFileList,
mappedFolder,
outputFile1,
refName=stitchedGFFName)
print('CALLING AND PLOTTING SUPER-ENHANCERS')
if options.control:
rankbyName = options.rankby.split('/')[-1]
controlName = options.control.split('/')[-1]
cmd = 'R --no-save %s %s %s %s < ROSE2_callSuper.R' % (
outFolder, outputFile1, inputName, controlName)
else:
rankbyName = options.rankby.split('/')[-1]
controlName = 'NONE'
cmd = 'R --no-save %s %s %s %s < ROSE2_callSuper.R' % (
outFolder, outputFile1, inputName, controlName)
print(cmd)
os.system(cmd)
# calling the gene mapper
time.sleep(20)
superTableFile = "%s_SuperEnhancers.table.txt" % (inputName)
if options.control:
cmd = "python ROSE2_geneMapper.py -g %s -r %s -c %s -i %s%s &" % (
genome, options.rankby, options.control, outFolder, superTableFile)
else:
cmd = "python ROSE2_geneMapper.py -g %s -r %s -i %s%s &" % (
genome, options.rankby, outFolder, superTableFile)
os.system(cmd)
stretchTableFile = "%s_StretchEnhancers.table.txt" % (inputName)
if options.control:
cmd = "python ROSE2_geneMapper.py -g %s -r %s -c %s -i %s%s &" % (
genome, options.rankby, options.control, outFolder,
stretchTableFile)
else:
cmd = "python ROSE2_geneMapper.py -g %s -r %s -i %s%s &" % (
genome, options.rankby, outFolder, stretchTableFile)
os.system(cmd)
superStretchTableFile = "%s_SuperStretchEnhancers.table.txt" % (inputName)
if options.control:
cmd = "python ROSE2_geneMapper.py -g %s -r %s -c %s -i %s%s &" % (
genome, options.rankby, options.control, outFolder,
superStretchTableFile)
else:
cmd = "python ROSE2_geneMapper.py -g %s -r %s -i %s%s &" % (
genome, options.rankby, outFolder, superStretchTableFile)
os.system(cmd)
def findCanidateTFs(annotationFile, enhancerLoci, expressedNM, expressionDictNM,
bamFile, TFlist, refseqToNameDict, projectFolder, projectName, promoter):
'''
Assign each Super-Enhancer to the closest active TSS to its center
Return a dictionary keyed by TF that points to a list of loci
'''
print 'FINDING CANIDATE TFs'
enhancerAssignment = []
TFtoEnhancerDict = defaultdict(list)
startDict = utils.makeStartDict(annotationFile)
tssLoci = []
for gene in expressedNM:
tssLoci.append(utils.makeTSSLocus(gene,startDict,1000,1000))
tssCollection = utils.LocusCollection(tssLoci,50)
# Loop through enhancers
for enhancer in enhancerLoci:
# If the enhancer overlaps a TSS, save it
overlappingLoci = tssCollection.getOverlap(enhancer, 'both')
overlappingGenes =[]
for overlapLocus in overlappingLoci:
overlappingGenes.append(overlapLocus.ID())
# Find all gene TSS within 100 kb
proximalLoci = tssCollection.getOverlap(utils.makeSearchLocus(enhancer,100000,100000),'both')
proximalGenes =[]
for proxLocus in proximalLoci:
proximalGenes.append(proxLocus.ID())
# If no genes are within 100 kb, find the closest active gene
closestGene = ''
if len(overlappingGenes) == 0 and len(proximalGenes) == 0:
distalLoci = tssCollection.getOverlap(utils.makeSearchLocus(enhancer,1000000,1000000),'both')
distalGenes =[]
for distalLocus in distalLoci:
distalGenes.append(distalLocus.ID())
enhancerCenter = (int(enhancer.start()) + int(enhancer.end())) / 2
distList = [abs(enhancerCenter - startDict[geneID]['start'][0])
for geneID in distalGenes]
if distList:
closestGene = distalGenes[distList.index(min(distList))]
overlappingGenes = utils.uniquify(overlappingGenes)
proximalGenes = utils.uniquify(proximalGenes)
for refID in overlappingGenes:
if proximalGenes.count(refID) == 1:
proximalGenes.remove(refID)
# If a TSS overlaps an enhancer, assign them together
if overlappingGenes:
for gene in overlappingGenes:
if gene in TFlist:
TFtoEnhancerDict[gene].append(enhancer)
enhancerAssignment.append([gene, enhancer.chr(), enhancer.start(), enhancer.end(), enhancer.ID()])
# Otherwise, assign the enhancer to the most active gene in 100 kb
elif not overlappingGenes and proximalGenes:
highestGene = ''
highestActivity = 0
for gene in proximalGenes:
if expressionDictNM[gene] > highestActivity:
highestActivity = expressionDictNM[gene]
highestGene = gene
if highestGene in TFlist:
TFtoEnhancerDict[gene].append(enhancer)
enhancerAssignment.append([gene, enhancer.chr(), enhancer.start(), enhancer.end(), enhancer.ID()])
elif not overlappingGenes and not proximalGenes and closestGene:
if closestGene in TFlist:
gene = closestGene
TFtoEnhancerDict[gene].append(enhancer)
enhancerAssignment.append([gene, enhancer.chr(), enhancer.start(), enhancer.end(), enhancer.ID()])
# Add promoter is it's not contained in the super
if promoter:
for gene in TFtoEnhancerDict.keys():
promoter = utils.Locus(startDict[gene]['chr'], int(startDict[gene]['start'][0]) - 2000,
int(startDict[gene]['start'][0]) + 2000, startDict[gene]['sense'])
overlapBool = False
for enhancer in TFtoEnhancerDict[gene]:
if promoter.overlaps(enhancer):
overlapBool = True
if not overlapBool:
TFtoEnhancerDict[gene].append(promoter)
seAssignmentFile = projectFolder + projectName + '_ENHANCER_ASSIGNMENT.txt'
utils.unParseTable(enhancerAssignment, seAssignmentFile, '\t')
return TFtoEnhancerDict
def main():
'''
main run call
'''
debug = False
from optparse import OptionParser
usage = "usage: %prog [options] -g [GENOME] -i [INPUT_REGION_GFF] -r [RANKBY_BAM_FILE] -o [OUTPUT_FOLDER] [OPTIONAL_FLAGS]"
parser = OptionParser(usage=usage)
# required flags
parser.add_option(
"-i",
"--i",
dest="input",
nargs=1,
default=None,
help=
"Enter a comma separated list of .gff or .bed file of binding sites used to make enhancers"
)
parser.add_option("-r",
"--rankby",
dest="rankby",
nargs=1,
default=None,
help="Enter a comma separated list of bams to rank by")
parser.add_option("-o",
"--out",
dest="out",
nargs=1,
default=None,
help="Enter an output folder")
parser.add_option("-g",
"--genome",
dest="genome",
nargs=1,
default=None,
help="Enter the genome build (MM9,MM8,HG18,HG19)")
# optional flags
parser.add_option(
"-n",
"--name",
dest="name",
nargs=1,
default=None,
help="Provide a name for the analysis otherwise ROSE will guess")
parser.add_option(
"-c",
"--control",
dest="control",
nargs=1,
default=None,
help=
"Enter a comma separated list of control bams. Can either provide a single control bam for all rankby bams, or provide a control bam for each individual bam"
)
parser.add_option(
"-s",
"--stitch",
dest="stitch",
nargs=1,
default='',
help=
"Enter a max linking distance for stitching. Default will determine optimal stitching parameter"
)
parser.add_option(
"-t",
"--tss",
dest="tss",
nargs=1,
default=0,
help="Enter a distance from TSS to exclude. 0 = no TSS exclusion")
parser.add_option(
"--mask",
dest="mask",
nargs=1,
default=None,
help=
"Mask a set of regions from analysis. Provide a .bed or .gff of masking regions"
)
# RETRIEVING FLAGS
(options, args) = parser.parse_args()
if not options.input or not options.rankby or not options.out or not options.genome:
print('hi there')
parser.print_help()
exit()
# making the out folder if it doesn't exist
outFolder = utils.formatFolder(options.out, True)
# figuring out folder schema
gffFolder = utils.formatFolder(outFolder + 'gff/', True)
mappedFolder = utils.formatFolder(outFolder + 'mappedGFF/', True)
# GETTING INPUT FILE(s)
inputList = [
inputFile for inputFile in options.input.split(',')
if len(inputFile) > 1
]
#converting all input files into GFFs and moving into the GFF folder
inputGFFList = []
for inputFile in inputList:
if inputFile.split('.')[-1] == 'bed':
# CONVERTING A BED TO GFF
inputGFFName = inputFile.split('/')[-1][
0:-4] #strips the last 4 characters i.e. '.bed'
inputGFFFile = '%s%s.gff' % (gffFolder, inputGFFName)
utils.bedToGFF(inputFile, inputGFFFile)
elif options.input.split('.')[-1] == 'gff':
# COPY THE INPUT GFF TO THE GFF FOLDER
os.system('cp %s %s' % (inputFile, gffFolder))
inputGFFFile = '%s%s' % (gffFolder, inputFile.split('/')[-1])
else:
print(
'WARNING: INPUT FILE DOES NOT END IN .gff or .bed. ASSUMING .gff FILE FORMAT'
)
# COPY THE INPUT GFF TO THE GFF FOLDER
os.system('cp %s %s' % (inputFile, gffFolder))
inputGFFFile = '%s%s' % (gffFolder, inputFile.split('/')[-1])
inputGFFList.append(inputGFFFile)
# GETTING THE LIST OF BAMFILES TO PROCESS
#either same number of bams for rankby and control
#or only 1 control #or none!
#bamlist should be all rankby bams followed by control bams
bamFileList = []
if options.control:
controlBamList = [
bam for bam in options.control.split(',') if len(bam) > 0
]
rankbyBamList = [
bam for bam in options.rankby.split(',') if len(bam) > 0
]
if len(controlBamList) == len(rankbyBamList):
#case where an equal number of backgrounds are given
bamFileList = rankbyBamList + controlBamList
elif len(controlBamList) == 1:
#case where a universal background is applied
bamFileList = rankbyBamList + controlBamList * len(rankbyBamList)
else:
print(
'ERROR: EITHER PROVIDE A SINGLE CONTROL BAM FOR ALL SAMPLES, OR ONE CONTROL BAM FOR EACH SAMPLE'
)
sys.exit()
else:
bamFileList = [
bam for bam in options.rankby.split(',') if len(bam) > 0
]
# Stitch parameter
if options.stitch == '':
stitchWindow = ''
else:
stitchWindow = int(options.stitch)
# tss options
tssWindow = int(options.tss)
if tssWindow != 0:
removeTSS = True
else:
removeTSS = False
# GETTING THE GENOME
genome = string.upper(options.genome)
print('USING %s AS THE GENOME' % (genome))
# GETTING THE CORRECT ANNOT FILE
genomeDict = {
'HG18': '%s/annotation/hg18_refseq.ucsc' % (pipeline_dir),
'MM9': '%s/annotation/mm9_refseq.ucsc' % (pipeline_dir),
'HG19': '%s/annotation/hg19_refseq.ucsc' % (pipeline_dir),
'MM8': '%s/annotation/mm8_refseq.ucsc' % (pipeline_dir),
'MM10': '%s/annotation/mm10_refseq.ucsc' % (pipeline_dir),
'RN4': '%s/annotation/rn4_refseq.ucsc' % (pipeline_dir),
}
try:
annotFile = genomeDict[genome.upper()]
except KeyError:
print('ERROR: UNSUPPORTED GENOMES TYPE %s' % (genome))
sys.exit()
#FINDING THE ANALYSIS NAME
if options.name:
inputName = options.name
else:
inputName = inputGFFList[0].split('/')[-1].split('.')[0]
print('USING %s AS THE ANALYSIS NAME' % (inputName))
print('FORMATTING INPUT REGIONS')
# MAKING THE RAW INPUT FILE FROM THE INPUT GFFs
#use a simpler unique region naming system
if len(inputGFFList) == 1:
inputGFF = utils.parseTable(inputGFFList[0], '\t')
else:
inputLoci = []
for gffFile in inputGFFList:
print('\tprocessing %s' % (gffFile))
gff = utils.parseTable(gffFile, '\t')
gffCollection = utils.gffToLocusCollection(gff, 50)
inputLoci += gffCollection.getLoci()
inputCollection = utils.LocusCollection(inputLoci, 50)
inputCollection = inputCollection.stitchCollection(
) # stitches to produce unique regions
inputGFF = utils.locusCollectionToGFF(inputCollection)
formattedGFF = []
#now number things appropriately
for i, line in enumerate(inputGFF):
#use the coordinates to make a new id inputname_chr_sense_start_stop
chrom = line[0]
coords = [int(line[3]), int(line[4])]
sense = line[6]
lineID = '%s_%s' % (inputName, str(i + 1)) #1 indexing
newLine = [
chrom, lineID, lineID,
min(coords),
max(coords), '', sense, '', lineID
]
formattedGFF.append(newLine)
#name of the master input gff file
masterGFFFile = '%s%s_%s_ALL_-0_+0.gff' % (gffFolder, string.upper(genome),
inputName)
utils.unParseTable(formattedGFF, masterGFFFile, '\t')
print('USING %s AS THE INPUT GFF' % (masterGFFFile))
# MAKING THE START DICT
print('MAKING START DICT')
startDict = utils.makeStartDict(annotFile)
#GET CHROMS FOUND IN THE BAMS
print('GETTING CHROMS IN BAMFILES')
bamChromList = getBamChromList(bamFileList)
print("USING THE FOLLOWING CHROMS")
print(bamChromList)
#LOADING IN THE GFF AND FILTERING BY CHROM
print('LOADING AND FILTERING THE GFF')
inputGFF = filterGFF(masterGFFFile, bamChromList)
# LOADING IN THE BOUND REGION REFERENCE COLLECTION
print('LOADING IN GFF REGIONS')
referenceCollection = utils.gffToLocusCollection(inputGFF)
print('CHECKING REFERENCE COLLECTION:')
checkRefCollection(referenceCollection)
# MASKING REFERENCE COLLECTION
# see if there's a mask
if options.mask:
maskFile = options.mask
# if it's a bed file
if maskFile.split('.')[-1].upper() == 'BED':
maskGFF = utils.bedToGFF(maskFile)
elif maskFile.split('.')[-1].upper() == 'GFF':
maskGFF = utils.parseTable(maskFile, '\t')
else:
print("MASK MUST BE A .gff or .bed FILE")
sys.exit()
maskCollection = utils.gffToLocusCollection(maskGFF)
# now mask the reference loci
referenceLoci = referenceCollection.getLoci()
filteredLoci = [
locus for locus in referenceLoci
if len(maskCollection.getOverlap(locus, 'both')) == 0
]
print("FILTERED OUT %s LOCI THAT WERE MASKED IN %s" %
(len(referenceLoci) - len(filteredLoci), maskFile))
referenceCollection = utils.LocusCollection(filteredLoci, 50)
# NOW STITCH REGIONS
print('STITCHING REGIONS TOGETHER')
stitchedCollection, debugOutput, stitchWindow = regionStitching(
referenceCollection, inputName, outFolder, stitchWindow, tssWindow,
annotFile, removeTSS)
# NOW MAKE A STITCHED COLLECTION GFF
print('MAKING GFF FROM STITCHED COLLECTION')
stitchedGFF = utils.locusCollectionToGFF(stitchedCollection)
print(stitchWindow)
print(type(stitchWindow))
if not removeTSS:
stitchedGFFFile = '%s%s_%sKB_STITCHED.gff' % (gffFolder, inputName,
str(stitchWindow / 1000))
stitchedGFFName = '%s_%sKB_STITCHED' % (inputName,
str(stitchWindow / 1000))
debugOutFile = '%s%s_%sKB_STITCHED.debug' % (gffFolder, inputName,
str(stitchWindow / 1000))
else:
stitchedGFFFile = '%s%s_%sKB_STITCHED_TSS_DISTAL.gff' % (
gffFolder, inputName, str(stitchWindow / 1000))
stitchedGFFName = '%s_%sKB_STITCHED_TSS_DISTAL' % (
inputName, str(stitchWindow / 1000))
debugOutFile = '%s%s_%sKB_STITCHED_TSS_DISTAL.debug' % (
gffFolder, inputName, str(stitchWindow / 1000))
# WRITING DEBUG OUTPUT TO DISK
if debug:
print('WRITING DEBUG OUTPUT TO DISK AS %s' % (debugOutFile))
utils.unParseTable(debugOutput, debugOutFile, '\t')
# WRITE THE GFF TO DISK
print('WRITING STITCHED GFF TO DISK AS %s' % (stitchedGFFFile))
utils.unParseTable(stitchedGFF, stitchedGFFFile, '\t')
# SETTING UP THE OVERALL OUTPUT FILE
outputFile1 = outFolder + stitchedGFFName + '_ENHANCER_REGION_MAP.txt'
print('OUTPUT WILL BE WRITTEN TO %s' % (outputFile1))
# MAPPING TO THE NON STITCHED (ORIGINAL GFF)
# MAPPING TO THE STITCHED GFF
# Try to use the bamliquidatior_path.py script on cluster, otherwise, failover to local (in path), otherwise fail.
bamFileListUnique = list(bamFileList)
bamFileListUnique = utils.uniquify(bamFileListUnique)
#prevent redundant mapping
print("MAPPING TO THE FOLLOWING BAMS:")
print(bamFileListUnique)
for bamFile in bamFileListUnique:
bamFileName = bamFile.split('/')[-1]
# MAPPING TO THE STITCHED GFF
mappedOut1Folder = '%s%s_%s_MAPPED' % (mappedFolder, stitchedGFFName,
bamFileName)
mappedOut1File = '%s%s_%s_MAPPED/matrix.txt' % (
mappedFolder, stitchedGFFName, bamFileName)
if utils.checkOutput(mappedOut1File, 0.2, 0.2):
print("FOUND %s MAPPING DATA FOR BAM: %s" %
(stitchedGFFFile, mappedOut1File))
else:
cmd1 = bamliquidator_path + " --sense . -e 200 --match_bamToGFF -r %s -o %s %s" % (
stitchedGFFFile, mappedOut1Folder, bamFile)
print(cmd1)
os.system(cmd1)
if utils.checkOutput(mappedOut1File, 0.2, 5):
print("SUCCESSFULLY MAPPED TO %s FROM BAM: %s" %
(stitchedGFFFile, bamFileName))
else:
print("ERROR: FAILED TO MAP %s FROM BAM: %s" %
(stitchedGFFFile, bamFileName))
sys.exit()
print('BAM MAPPING COMPLETED NOW MAPPING DATA TO REGIONS')
# CALCULATE DENSITY BY REGION
# NEED TO FIX THIS FUNCTION TO ACCOUNT FOR DIFFERENT OUTPUTS OF LIQUIDATOR
mapCollection(stitchedCollection,
referenceCollection,
bamFileList,
mappedFolder,
outputFile1,
refName=stitchedGFFName)
print('FINDING AVERAGE SIGNAL AMONGST BAMS')
metaOutputFile = collapseRegionMap(outputFile1,
inputName + '_MERGED_SIGNAL',
controlBams=options.control)
#now try the merging
print('CALLING AND PLOTTING SUPER-ENHANCERS')
rankbyName = inputName + '_MERGED_SIGNAL'
controlName = 'NONE'
cmd = 'Rscript %sROSE2_callSuper.R %s %s %s %s' % (
pipeline_dir, outFolder, metaOutputFile, inputName, controlName)
print(cmd)
os.system(cmd)
# calling the gene mapper
print('CALLING GENE MAPPING')
superTableFile = "%s_SuperEnhancers.table.txt" % (inputName)
#for now don't use ranking bam to call top genes
cmd = "python %sROSE2_geneMapper.py -g %s -i %s%s -f" % (
pipeline_dir, genome, outFolder, superTableFile)
print(cmd)
os.system(cmd)
stretchTableFile = "%s_StretchEnhancers.table.txt" % (inputName)
cmd = "python %sROSE2_geneMapper.py -g %s -i %s%s -f" % (
pipeline_dir, genome, outFolder, stretchTableFile)
print(cmd)
os.system(cmd)
superStretchTableFile = "%s_SuperStretchEnhancers.table.txt" % (inputName)
cmd = "python %sROSE2_geneMapper.py -g %s -i %s%s -f" % (
pipeline_dir, genome, outFolder, superStretchTableFile)
os.system(cmd)
def main():
from optparse import OptionParser
usage = "usage: %prog [options] -e [ENHANCER_FILE] -b [BAM_FILE] -g [GENOME] -o [OUTPUTFOLDER] -n [NAME]"
parser = OptionParser(usage = usage)
#required flags
parser.add_option("-e","--enhancer_file", dest="enhancers",nargs = 1, default=None,
help = "Provide a ROSE generated enhancer table (_AllEnhancers.table.txt)")
parser.add_option("-b","--bam",dest="bam",nargs =1, default = None,
help = "Provide a bam that corresponds to the super enhancer table")
parser.add_option("-g","--genome",dest="genome",nargs =1, default = None,
help = "Provide the build of the genome to be used for the analysis. Currently supports HG19, HG18 and MM9")
parser.add_option("-o","--output",dest="output",nargs =1, default = None,
help = "Enter an output folder")
parser.add_option("-n","--name",dest="name",nargs =1, default = None,
help = "Provide a name for the job")
#additional options
parser.add_option("-s","--subpeaks", dest="subpeaks",nargs=1,default=None,
help = "Enter a BED file of regions to search for motifs")
parser.add_option("-x","--expCutoff", dest="expCutoff",nargs=1,default=33,
help = "Enter the expression cutoff to be used to define canidate TFs")
parser.add_option("-l","--extension-length", dest="extension",nargs = 1, default=100,
help = "Enter the length to extend subpeak regions for motif finding")
parser.add_option("-B","--background", dest="background",nargs = 1, default=None,
help = "Provide a background BAM file")
parser.add_option("-a","--activity", dest="activity",nargs = 1, default=None,
help = "A table with refseq in the first column and activity (expression or promoter acetylation) in second")
parser.add_option("-E","--enhancer_number", dest="Enumber",nargs = 1, default='super',
help = "Enter the number of top ranked enhancers to include in the anlaysis. Default is all super-enhancers")
parser.add_option("-N", "--number", dest="number",nargs = 1, default=2,
help = "Enter the number of motifs required to assign a binding event") #I have modified the destination of -N option so that it is different from the destination of -E option
parser.add_option("--promoter", dest="promoter",nargs = 1, default=False,
help = "Enter True if the promoters should be included in the analysis")
parser.add_option("--motifs", dest="motifs",nargs = 1, default=False,
help = "Enter an alternative PWM file for the analysis")
parser.add_option("-t","--tfs", dest="tfs",nargs=1,default=None,
help = "Enter additional TFs (comma separated) to be used in the bindinf analysis")
parser.add_option("-u","--ucsc", dest="is_ucsc", action='store_true', default=False,
help = "If set, use the ucsc folders or files with chromosome names as chr1, chr2, etc.")
(options,args) = parser.parse_args()
print(options)
if options.enhancers and options.genome and options.output and options.name:
###
# Define all global file names
###
if options.motifs:
motifDatabaseFile = options.motifs
else:
motifConvertFile = '/home/rad/users/gaurav/projects/ctrc/scripts/CLL_TFnetworks_2018/annotations/MotifDictionary.txt'
motifDatabaseFile = '/home/rad/users/gaurav/projects/ctrc/scripts/CLL_TFnetworks_2018/annotations/VertebratePWMs.txt'
# User input files
enhancerFile = options.enhancers
enhancerTable = utils.parseTable(enhancerFile, '\t')
if options.bam:
bamFile = options.bam
bam = utils.Bam(bamFile)
if options.background:
background = options.background
else:
background = None
genome = options.genome
genome = upper(genome)
if genome == 'HG19':
genomeDirectory = '/home/rad/packages/data/fasta/human/hg19/chromosomes/'
annotationFile = '/home/rad/users/gaurav/projects/ctrc/scripts/pipeline/annotation/hg19_refseq.ucsc'
TFfile = '/home/rad/users/gaurav/projects/ctrc/scripts/CLL_TFnetworks_2018/annotations/TFlist_NMid_hg19.txt'
if genome == 'HG18':
genomeDirectory = '/grail/genomes/Homo_sapiens/human_gp_mar_06_no_random/fasta/'
annotationFile = '/ark/home/cl512/src/pipeline/annotation/hg18_refseq.ucsc'
TFfile = '/home/rad/users/gaurav/projects/ctrc/scripts/CLL_TFnetworks_2018/annotations/TFlist_NMid_hg19.txt'
if genome == 'MM9':
genomeDirectory = '/grail/genomes/Mus_musculus/UCSC/mm9/Sequence/Chromosomes/'
annotationFile = '/home/rad/users/gaurav/projects/ctrc/scripts/pipeline/annotation/mm9_refseq.ucsc'
TFfile = '/home/rad/users/gaurav/projects/ctrc/scripts/CLL_TFnetworks_2018/annotations/TFlist_NMid_mm9.txt'
if genome == 'MM10':
TFfile = '/home/rad/users/gaurav/projects/ctrc/scripts/CLL_TFnetworks_2018/annotations/TFlist_NMid_mm10.txt'
if options.is_ucsc:
genomeDirectory = '/home/rad/packages/data/fasta/mouse/mm10/ucsc_chromosomes/'
annotationFile = '/home/rad/users/gaurav/projects/ctrc/scripts/pipeline/annotation/ucsc/mm10_refseq.ucsc'
else:
genomeDirectory = '/home/rad/packages/data/fasta/mouse/mm10/chromosomes/'
annotationFile = '/home/rad/users/gaurav/projects/ctrc/scripts/pipeline/annotation/mm10_refseq.ucsc'
TFtable = utils.parseTable(TFfile, '\t')
TFlist = [line[0] for line in TFtable]
TFlistGene = [line[1] for line in TFtable]
projectFolder = options.output
projectName = options.name
if options.subpeaks:
subpeakFile = options.subpeaks
else: subpeakFile = None
refseqToNameDict = {}
expressionFile = options.activity
if expressionFile:
expressionTable = utils.parseTable(expressionFile, '\t')
else:
expressionTable = calculatePromoterActivity(annotationFile, bamFile, projectName, projectFolder, refseqToNameDict, background)
expCutoff = int(options.expCutoff)
constExtension = int(options.extension)
enhancerNumber = options.Enumber
if options.Enumber != 'super':
enhancerNumber = options.Enumber
else:
enhancerNumber = 'super'
promoter = options.promoter
additionalTFs = options.tfs
number = options.number
annotTable = utils.parseTable(annotationFile, '\t')
for line in annotTable:
gid = line[1]
genename = upper(line[12])
refseqToNameDict[gid] = genename
###
# Now run all the functions
###
enhancerLoci = createEnhancerLoci(enhancerTable, enhancerNumber)
expressedNM, expressionDictNM = createExpressionDict(annotationFile, projectFolder, projectName, refseqToNameDict, expCutoff,expressionFile)
TFtoEnhancerDict = findCanidateTFs(annotationFile, enhancerLoci, expressedNM, expressionDictNM, bamFile, TFlist, refseqToNameDict, projectFolder, projectName, promoter)
# print TFtoEnhancerDict
# sys.exit()
formatOutput(TFtoEnhancerDict, refseqToNameDict, projectName, projectFolder)
canidateGenes = [upper(refseqToNameDict[x]) for x in TFtoEnhancerDict.keys()]
if additionalTFs:
for tf in additionalTFs.split(','):
canidateGenes.append(tf)
canidateGenes = utils.uniquify(canidateGenes)
print canidateGenes
if subpeakFile == None:
subpeakFile = findValleys(TFtoEnhancerDict, bamFile, projectName, projectFolder, cutoff = 0.2)
generateSubpeakFASTA(TFtoEnhancerDict, subpeakFile, genomeDirectory, projectName, projectFolder, constExtension)
subpeakFile = projectFolder + projectName + '_SUBPEAKS.fa'
findMotifs(canidateGenes, projectFolder, projectName, motifConvertFile, motifDatabaseFile)
graph = buildGraph(projectFolder, projectName, motifConvertFile, refseqToNameDict, canidateGenes)
formatNetworkOutput(graph, projectFolder, projectName, canidateGenes)
else:
parser.print_help()
sys.exit()
def geneToEnhancerDict(genome, enhancer_file, activity_path):
'''
Assign each Super-Enhancer to the closest active TSS to its center
Return a dictionary keyed by TF that points to a list of loci
'''
print('Identifying enhancers and target genes from %s' %(enhancer_file))
#should this do gene assignment????
#for now assume gene assignment has been done
#can later toggle to do gene assignment
#first load the TF lists
tf_table = utils.parseTable(genome.returnFeature('tf_file'), '\t')
motif_table = utils.parseTable(genome.returnFeature('motif_convert'),'\t')
#this gives all tfs that have a motif
motif_tfs = utils.uniquify([line[1] for line in motif_table])
#intersect w/ the activity table
if len(activity_path) > 0:
activity_table = utils.parseTable(activity_path,'\t')
#figure out the right column for actual gene names (basically not NM or NR and not a numeral)
for i in range(len(activity_table[0])):
# try:
# foo = int(activity_table[0][i])
# except ValueError: # case where it is not an integer
if activity_table[0][i][0:2] != 'NM' and activity_table[0][i][0:2] != 'NR': #assumes refseq
gene_col = i
break
print('using column %s of %s gene activity table for common names' % (gene_col + 1, activity_path))
active_gene_list = [string.upper(line[gene_col]) for line in activity_table]
tf_list_refseq = [line[0] for line in tf_table if active_gene_list.count(line[1]) > 0 and motif_tfs.count(line[1]) > 0]
tf_list_name = utils.uniquify([line[1] for line in tf_table if active_gene_list.count(line[1]) > 0 and motif_tfs.count(line[1]) > 0])
else:
tf_list_refseq = [line[0] for line in tf_table if motif_tfs.count(line[1]) >0]
tf_list_name = [line[1] for line in tf_table if motif_tfs.count(line[1]) >0]
print('Identified %s TFs from %s that have motifs' % (len(tf_list_name),genome.returnFeature('tf_file')))
#keyed by gene with loci objects in the list
gene_to_enhancer_dict = defaultdict(list)
enhancer_to_gene_dict = defaultdict(list)
#assuming id,chrom,start,stop w/ gene names in the last 3 columns per standard ROSE output
enhancer_table = utils.parseTable(enhancer_file,'\t')
print('Analyzing %s cis-regulatory regions' % (len(enhancer_table)))
#now let's make the enhancer table by region and then by gene
enhancerTable = [['ENHANCER_ID','CHROM','START','STOP','GENE_LIST']]
enhancerTFTable = [['ENHANCER_ID','CHROM','START','STOP','GENE_LIST']]
geneTable = [['GENE','TF','CHROM','START','STOP','ENHANCER_ID']]
geneTFTable = [['GENE','CHROM','START','STOP','ENHANCER_ID']]
geneSummaryTable = [['GENE','TF','ENHANCER_LIST']]
#will need to track which ones are TFs
candidate_tf_list = []
#find the columns for gene assignment
header = enhancer_table[0]
header_length = len(enhancer_table[0])
closest_index = header.index('CLOSEST_GENE')
proximal_index = header.index('PROXIMAL_GENES')
overlap_index = header.index('OVERLAP_GENES')
for line in enhancer_table[1:]:
if len(line) != header_length: #don't bother trying to figure out lines w/o target genes
continue
enhancer_locus = utils.Locus(line[1],line[2],line[3],'.',line[0])
closest_gene_list = line[closest_index].split(',')
proximal_gene_list = line[proximal_index].split(',')
overlap_gene_list = line[overlap_index].split(',')
all_gene_list = closest_gene_list + proximal_gene_list + overlap_gene_list
all_gene_list = [string.upper(gene) for gene in all_gene_list]
#print(all_gene_list)
#print(activity_path)
#print(active_gene_list)
#gets a unique list of all tfs
if len(activity_path) > 0:
all_gene_list = utils.uniquify([gene for gene in all_gene_list if active_gene_list.count(gene) > 0])
else:
all_gene_list = utils.uniquify(all_gene_list)
candidate_gene_list = utils.uniquify([gene for gene in all_gene_list if tf_list_name.count(gene) > 0])
if len(all_gene_list) > 0:
for gene in all_gene_list:
gene_to_enhancer_dict[gene].append(enhancer_locus)
enhancer_to_gene_dict[enhancer_locus].append(gene)
newLine = line[0:4] + [','.join(all_gene_list)]
else:
newLine = line[0:4] + ['']
enhancerTable.append(newLine)
if len(candidate_gene_list) > 0:
tfLine = line[0:4] + [','.join(candidate_gene_list)]
enhancerTFTable.append(tfLine)
#now iterate through each gene and list the enhancers
gene_list = gene_to_enhancer_dict.keys()
print(gene_list)
gene_list.sort()
for gene in gene_list:
if tf_list_name.count(gene) > 0:
tf_status = 1
candidate_tf_list.append(gene)
else:
tf_status = 0
enhancer_loci = gene_to_enhancer_dict[gene]
enhancerString =','.join([enhancer.ID() for enhancer in enhancer_loci])
geneSummaryTable.append([gene,tf_status,enhancerString])
for enhancer in enhancer_loci:
newLine = [gene,tf_status,enhancer.chr(),enhancer.start(),enhancer.end(),enhancer.ID()]
geneTable.append(newLine)
if tf_status == 1:
newLine = [gene,enhancer.chr(),enhancer.start(),enhancer.end(),enhancer.ID()]
geneTFTable.append(newLine)
return geneTable,geneTFTable,enhancerTable,enhancerTFTable,geneSummaryTable,candidate_tf_list,gene_to_enhancer_dict
def finishRankOutput(dataFile, rankOutput, genome, mergeFolder, mergeName, name1, name2, cutOff=1.5, window=100000):
"""
cleans up the rank output table
makes a gff of all of the gained/lost supers beyond
a certain cutoff w/ a window
makes a list of gained genes and lost genes
makes a bed of gained loss
"""
dataDict = pipeline_dfci.loadDataTable(dataFile)
# making sure window and cutoff are int/float
cutOff = float(cutOff)
window = int(window)
genome = string.upper(genome)
# make the output folder
outputFolder = pipeline_dfci.formatFolder(mergeFolder + "output/", True)
# bring in the old rank table
rankEnhancerTable = utils.parseTable(rankOutput, "\t")
# make a new formatted table
header = rankEnhancerTable[0]
header[-4] = "DELTA RANK"
header[-3] = "IS_SUPER"
formattedRankTable = [header]
# the gffs
gainedGFF = []
lostGFF = []
gainedWindowGFF = []
lostWindowGFF = []
# the beds
gainedTrackHeader = (
'track name="%s %s only SEs" description="%s super enhancers that are found only in %s vs %s" itemRGB=On color=255,0,0'
% (genome, name2, genome, name2, name1)
)
gainedBed = [[gainedTrackHeader]]
conservedTrackHeader = (
'track name="%s %s and %s SEs" description="%s super enhancers that are found in both %s vs %s" itemRGB=On color=0,0,0'
% (genome, name1, name2, genome, name1, name2)
)
conservedBed = [[conservedTrackHeader]]
lostTrackHeader = (
'track name="%s %s only SEs" description="%s super enhancers that are found only in %s vs %s" itemRGB=On color=0,255,0'
% (genome, name1, genome, name1, name2)
)
lostBed = [[lostTrackHeader]]
# the genes
geneTable = [
[
"GENE",
"ENHANCER_ID",
"ENHANCER_CHROM",
"ENHANCER_START",
"ENHANCER_STOP",
header[6],
header[7],
header[8],
"STATUS",
]
]
for line in rankEnhancerTable[1:]:
# fixing the enhancer ID
line[0] = line[0].replace("_lociStitched", "")
formattedRankTable.append(line)
# getting the genes
geneList = []
geneList += line[9].split(",")
geneList += line[10].split(",")
geneList += line[11].split(",")
geneList = [x for x in geneList if len(x) > 0]
geneList = utils.uniquify(geneList)
geneString = string.join(geneList, ",")
bedLine = [line[1], line[2], line[3], line[0], line[-4]]
# for gained
if float(line[6]) > cutOff:
gffLine = [line[1], line[0], "", line[2], line[3], "", ".", "", geneString]
gffWindowLine = [
line[1],
line[0],
"",
int(line[2]) - window,
int(line[3]) + window,
"",
".",
"",
geneString,
]
gainedGFF.append(gffLine)
gainedWindowGFF.append(gffWindowLine)
geneStatus = name2
gainedBed.append(bedLine)
# for lost
elif float(line[6]) < (-1 * cutOff):
gffLine = [line[1], line[0], "", line[2], line[3], "", ".", "", geneString]
gffWindowLine = [
line[1],
line[0],
"",
int(line[2]) - window,
int(line[3]) + window,
"",
".",
"",
geneString,
]
lostGFF.append(gffLine)
lostWindowGFF.append(gffWindowLine)
geneStatus = name1
lostBed.append(bedLine)
# for conserved
else:
geneStatus = "CONSERVED"
conservedBed.append(bedLine)
# now fill in the gene Table
for gene in geneList:
geneTableLine = [gene, line[0], line[1], line[2], line[3], line[6], line[7], line[8], geneStatus]
geneTable.append(geneTableLine)
# concat the bed
fullBed = gainedBed + conservedBed + lostBed
# start writing the output
# there's the two gffs, the bed,the formatted table, the gene table
# formatted table
formattedFilename = "%s%s_%s_MERGED_SUPERS_RANK_TABLE.txt" % (outputFolder, genome, mergeName)
utils.unParseTable(formattedRankTable, formattedFilename, "\t")
# gffs
gffFolder = pipeline_dfci.formatFolder(outputFolder + "gff/", True)
gffFilename_gained = "%s%s_%s_%s_ONLY_SUPERS_-0_+0.gff" % (gffFolder, genome, mergeName, string.upper(name2))
gffFilenameWindow_gained = "%s%s_%s_%s_ONLY_SUPERS_-%sKB_+%sKB.gff" % (
gffFolder,
genome,
mergeName,
string.upper(name2),
window / 1000,
window / 1000,
)
gffFilename_lost = "%s%s_%s_%s_ONLY_SUPERS_-0_+0.gff" % (gffFolder, genome, mergeName, string.upper(name1))
gffFilenameWindow_lost = "%s%s_%s_%s_ONLY_SUPERS_-%sKB_+%sKB.gff" % (
gffFolder,
genome,
mergeName,
string.upper(name1),
window / 1000,
window / 1000,
)
utils.unParseTable(gainedGFF, gffFilename_gained, "\t")
utils.unParseTable(gainedWindowGFF, gffFilenameWindow_gained, "\t")
utils.unParseTable(lostGFF, gffFilename_lost, "\t")
utils.unParseTable(lostWindowGFF, gffFilenameWindow_lost, "\t")
# bed
bedFilename = "%s%s_%s_MERGED_SUPERS.bed" % (outputFolder, genome, mergeName)
utils.unParseTable(fullBed, bedFilename, "\t")
# geneTable
geneFilename = "%s%s_%s_MERGED_SUPERS_GENE_TABLE.txt" % (outputFolder, genome, mergeName)
utils.unParseTable(geneTable, geneFilename, "\t")
# finally, move all of the plots to the output folder
cmd = "cp %s%s_ROSE/*.pdf %s%s_%s_MERGED_SUPERS_DELTA.pdf" % (mergeFolder, name1, outputFolder, genome, mergeName)
os.system(cmd)
cmd = "cp %s%s_ROSE/*RANK_PLOT.png %s%s_%s_MERGED_SUPERS_RANK_PLOT.png" % (
mergeFolder,
name1,
outputFolder,
genome,
mergeName,
)
os.system(cmd)
# now execute the bamPlot_turbo.py commands
bam1 = dataDict[name1]["bam"]
bam2 = dataDict[name2]["bam"]
bamString = "%s,%s" % (bam1, bam2)
nameString = "%s,%s" % (name1, name2)
colorString = "0,0,0:100,100,100"
# change dir
os.chdir("/ark/home/cl512/pipeline/")
if len(gainedGFF) > 0:
# gained command
plotTitle = "%s_ONLY_SE" % (name2)
cmd = "python bamPlot_turbo.py -g %s -b %s -i %s -o %s -n %s -c %s -t %s -r -y UNIFORM -p MULTIPLE" % (
genome,
bamString,
gffFilename_gained,
outputFolder,
nameString,
colorString,
plotTitle,
)
os.system(cmd)
# gained window command
plotTitle = "%s_ONLY_SE_%sKB_WINDOW" % (name2, window / 1000)
cmd = "python bamPlot_turbo.py -g %s -b %s -i %s -o %s -n %s -c %s -t %s -r -y UNIFORM -p MULTIPLE" % (
genome,
bamString,
gffFilenameWindow_gained,
outputFolder,
nameString,
colorString,
plotTitle,
)
os.system(cmd)
if len(lostGFF) > 0:
# lost command
plotTitle = "%s_ONLY_SE" % (name1)
cmd = "python bamPlot_turbo.py -g %s -b %s -i %s -o %s -n %s -c %s -t %s -r -y UNIFORM -p MULTIPLE" % (
genome,
bamString,
gffFilename_lost,
outputFolder,
nameString,
colorString,
plotTitle,
)
os.system(cmd)
# lost command
plotTitle = "%s_ONLY_SE_%sKB_WINDOW" % (name1, window / 1000)
cmd = "python bamPlot_turbo.py -g %s -b %s -i %s -o %s -n %s -c %s -t %s -r -y UNIFORM -p MULTIPLE" % (
genome,
bamString,
gffFilenameWindow_lost,
outputFolder,
nameString,
colorString,
plotTitle,
)
os.system(cmd)
return
def findCanidateTFs(genome, enhancer_gff, expressedNM, expressionDictNM,
bamFile, TFlist, refseqToNameDict, projectFolder, projectName, promoter):
'''
Assign each Super-Enhancer to the closest active TSS to its center
Return a dictionary keyed by TF that points to a list of loci
'''
#loading in the enhancer gff regions
enhancer_collection = utils.gffToLocusCollection(enhancer_gff)
enhancer_loci = enhancer_collection.getLoci()
#loading in the genome and TF info
annot_file = genome.returnFeature('annot_file')
startDict = utils.makeStartDict(annot_file)
tf_table = utils.parseTable(genome.returnFeature('tf_file'),'\t')
refID_list = [line[0] for line in tf_table] #creates a list of all NM IDs for TFs
#make a collection of all TF TSSs
tssLoci = []
for refID in refID_list:
tssLoci.append(utils.makeTSSLocus(refID,startDict,0,0)) #this is a precise 1 coordinate TSS locus
tssCollection = utils.LocusCollection(tssLoci,50)
enhancerTable = [['ENHANCER_ID','CHROM','START','STOP','GENE_LIST']]
gene_to_enhancer_dict = defaultdict(list)
# Loop through enhancers
#all gene nnames stored by refID
for enhancer in enhancer_loci:
# If the enhancer overlaps a TSS, save it
overlapping_loci = tssCollection.getOverlap(enhancer, 'both')
overlapping_refIDs =[locus.ID() for locus in overlapping_loci]
# Find all gene TSS within 100 kb
proximal_loci = tssCollection.getOverlap(utils.makeSearchLocus(enhancer,100000,100000),'both')
proximal_refIDs =[locus.ID() for locus in proximal_loci]
# If no genes are within 100 kb, find the closest active gene within 1 million bp
closest_refID = []
if len(overlapping_refIDs) == 0 and len(proximal_refIDs) == 0:
distal_loci = tssCollection.getOverlap(utils.makeSearchLocus(enhancer,1000000,1000000),'both')
distal_refIDs =[locus.ID() for locus in distal_loci]
enhancerCenter = (int(enhancer.start()) + int(enhancer.end())) / 2
distance_list = [abs(enhancerCenter - startDict[geneID]['start'][0])
for geneID in distal_refIDs]
if len(distance_list) > 0:
closest_refID = [distalGenes[distance_list.index(min(distance_list))]]
#now we have all potential gene cases
all_refIDs = overlappingGenes + proximalGenes + closest_refID
#now we get all names and refIDs
all_refIDs = utils.uniquify([refID for refID in all_refIDs if len(refID) > 0 ])
all_names = utils.uniquify([startDict[refID]['name'] for refID in all_refIDs])
#first do enhancer level assignment
names_string = ','.join(all_names)
enhancer_table.append([enhancer.ID(),enhancer.chr(),enhancer.start(),enhancer.end(),names_string])
#now do gene level assignment
for refID in all_refIDs:
gene_to_enhancer_dict[refID].append(enhancer.ID())
#an enhancer can be assigned to multiple genes
#a promoter can only be assigned to 1 gene
#promoters don't have enhancerIDs so don't add them yet
#this should just be an enhancer level table
#followed by a gene level table
overlappingGenes = utils.uniquify(overlappingGenes)
proximalGenes = utils.uniquify(proximalGenes)
for refID in overlappingGenes:
if proximalGenes.count(refID) == 1:
proximalGenes.remove(refID)
# If a TSS overlaps an enhancer, assign them together
if overlappingGenes:
for gene in overlappingGenes:
if gene in tf_list:
TFtoEnhancerDict[gene].append(enhancer)
enhancerAssignment.append([gene, enhancer.chr(), enhancer.start(), enhancer.end(), enhancer.ID()])
# Otherwise, assign the enhancer to the most active gene in 100 kb
elif not overlappingGenes and proximalGenes:
highestGene = ''
highestActivity = 0
for gene in proximalGenes:
if expressionDictNM[gene] > highestActivity:
highestActivity = expressionDictNM[gene]
highestGene = gene
if highestGene in TFlist:
TFtoEnhancerDict[gene].append(enhancer)
enhancerAssignment.append([gene, enhancer.chr(), enhancer.start(), enhancer.end(), enhancer.ID()])
elif not overlappingGenes and not proximalGenes and closestGene:
if closestGene in TFlist:
gene = closestGene
TFtoEnhancerDict[gene].append(enhancer)
enhancerAssignment.append([gene, enhancer.chr(), enhancer.start(), enhancer.end(), enhancer.ID()])
# Add promoter is it's not contained in the super
if promoter:
for gene in TFtoEnhancerDict.keys():
promoter = utils.Locus(startDict[gene]['chr'], int(startDict[gene]['start'][0]) - 2000,
int(startDict[gene]['start'][0]) + 2000, startDict[gene]['sense'])
overlapBool = False
for enhancer in TFtoEnhancerDict[gene]:
if promoter.overlaps(enhancer):
overlapBool = True
if not overlapBool:
TFtoEnhancerDict[gene].append(promoter)
seAssignmentFile = projectFolder + projectName + '_ENHANCER_ASSIGNMENT.txt'
utils.unParseTable(enhancerAssignment, seAssignmentFile, '\t')
return TFtoEnhancerDict
def mapEnhancerToGeneTop(rankByBamFile, controlBamFile, genome, annotFile, enhancerFile, transcribedFile='', uniqueGenes=True, searchWindow=50000, noFormatTable=False):
'''
maps genes to enhancers. if uniqueGenes, reduces to gene name only. Otherwise, gives for each refseq
'''
startDict = utils.makeStartDict(annotFile)
enhancerName = enhancerFile.split('/')[-1].split('.')[0]
enhancerTable = utils.parseTable(enhancerFile, '\t')
# internal parameter for debugging
byRefseq = False
if len(transcribedFile) > 0:
transcribedTable = utils.parseTable(transcribedFile, '\t')
transcribedGenes = [line[1] for line in transcribedTable]
else:
transcribedGenes = startDict.keys()
print('MAKING TRANSCRIPT COLLECTION')
transcribedCollection = utils.makeTranscriptCollection(
annotFile, 0, 0, 500, transcribedGenes)
print('MAKING TSS COLLECTION')
tssLoci = []
for geneID in transcribedGenes:
tssLoci.append(utils.makeTSSLocus(geneID, startDict, 0, 0))
# this turns the tssLoci list into a LocusCollection
# 50 is the internal parameter for LocusCollection and doesn't really
# matter
tssCollection = utils.LocusCollection(tssLoci, 50)
geneDict = {'overlapping': defaultdict(
list), 'proximal': defaultdict(list)}
# dictionaries to hold ranks and superstatus of gene nearby enhancers
rankDict = defaultdict(list)
superDict = defaultdict(list)
# list of all genes that appear in this analysis
overallGeneList = []
# find the damn header
for line in enhancerTable:
if line[0][0] == '#':
continue
else:
header = line
break
if noFormatTable:
# set up the output tables
# first by enhancer
enhancerToGeneTable = [
header + ['OVERLAP_GENES', 'PROXIMAL_GENES', 'CLOSEST_GENE']]
else:
# set up the output tables
# first by enhancer
enhancerToGeneTable = [
header[0:9] + ['OVERLAP_GENES', 'PROXIMAL_GENES', 'CLOSEST_GENE'] + header[-2:]]
# next by gene
geneToEnhancerTable = [
['GENE_NAME', 'REFSEQ_ID', 'PROXIMAL_ENHANCERS']]
# next make the gene to enhancer table
geneToEnhancerTable = [
['GENE_NAME', 'REFSEQ_ID', 'PROXIMAL_ENHANCERS', 'ENHANCER_RANKS', 'IS_SUPER', 'ENHANCER_SIGNAL']]
for line in enhancerTable:
if line[0][0] == '#' or line[0][0] == 'R':
continue
enhancerString = '%s:%s-%s' % (line[1], line[2], line[3])
enhancerLocus = utils.Locus(line[1], line[2], line[3], '.', line[0])
# overlapping genes are transcribed genes whose transcript is directly
# in the stitchedLocus
overlappingLoci = transcribedCollection.getOverlap(
enhancerLocus, 'both')
overlappingGenes = []
for overlapLocus in overlappingLoci:
overlappingGenes.append(overlapLocus.ID())
# proximalGenes are transcribed genes where the tss is within 50kb of
# the boundary of the stitched loci
proximalLoci = tssCollection.getOverlap(
utils.makeSearchLocus(enhancerLocus, searchWindow, searchWindow), 'both')
proximalGenes = []
for proxLocus in proximalLoci:
proximalGenes.append(proxLocus.ID())
distalLoci = tssCollection.getOverlap(
utils.makeSearchLocus(enhancerLocus, 1000000, 1000000), 'both')
distalGenes = []
for proxLocus in distalLoci:
distalGenes.append(proxLocus.ID())
overlappingGenes = utils.uniquify(overlappingGenes)
proximalGenes = utils.uniquify(proximalGenes)
distalGenes = utils.uniquify(distalGenes)
allEnhancerGenes = overlappingGenes + proximalGenes + distalGenes
# these checks make sure each gene list is unique.
# technically it is possible for a gene to be overlapping, but not proximal since the
# gene could be longer than the 50kb window, but we'll let that slide
# here
for refID in overlappingGenes:
if proximalGenes.count(refID) == 1:
proximalGenes.remove(refID)
for refID in proximalGenes:
if distalGenes.count(refID) == 1:
distalGenes.remove(refID)
# Now find the closest gene
if len(allEnhancerGenes) == 0:
closestGene = ''
else:
# get enhancerCenter
enhancerCenter = (int(line[2]) + int(line[3])) / 2
# get absolute distance to enhancer center
distList = [abs(enhancerCenter - startDict[geneID]['start'][0])
for geneID in allEnhancerGenes]
# get the ID and convert to name
closestGene = startDict[
allEnhancerGenes[distList.index(min(distList))]]['name']
# NOW WRITE THE ROW FOR THE ENHANCER TABLE
if noFormatTable:
newEnhancerLine = list(line)
newEnhancerLine.append(
join(utils.uniquify([startDict[x]['name'] for x in overlappingGenes]), ','))
newEnhancerLine.append(
join(utils.uniquify([startDict[x]['name'] for x in proximalGenes]), ','))
newEnhancerLine.append(closestGene)
else:
newEnhancerLine = line[0:9]
newEnhancerLine.append(
join(utils.uniquify([startDict[x]['name'] for x in overlappingGenes]), ','))
newEnhancerLine.append(
join(utils.uniquify([startDict[x]['name'] for x in proximalGenes]), ','))
newEnhancerLine.append(closestGene)
newEnhancerLine += line[-2:]
enhancerToGeneTable.append(newEnhancerLine)
# Now grab all overlapping and proximal genes for the gene ordered
# table
overallGeneList += overlappingGenes
for refID in overlappingGenes:
geneDict['overlapping'][refID].append(enhancerString)
rankDict[refID].append(int(line[-2]))
superDict[refID].append(int(line[-1]))
overallGeneList += proximalGenes
for refID in proximalGenes:
geneDict['proximal'][refID].append(enhancerString)
rankDict[refID].append(int(line[-2]))
superDict[refID].append(int(line[-1]))
# End loop through
# Make table by gene
print('MAKING ENHANCER ASSOCIATED GENE TSS COLLECTION')
overallGeneList = utils.uniquify(overallGeneList)
enhancerGeneCollection = utils.makeTranscriptCollection(
annotFile, 5000, 5000, 500, overallGeneList)
enhancerGeneGFF = utils.locusCollectionToGFF(enhancerGeneCollection)
# dump the gff to file
enhancerFolder = utils.getParentFolder(enhancerFile)
gffRootName = "%s_TSS_ENHANCER_GENES_-5000_+5000" % (genome)
enhancerGeneGFFFile = "%s%s_%s.gff" % (enhancerFolder, enhancerName,gffRootName)
utils.unParseTable(enhancerGeneGFF, enhancerGeneGFFFile, '\t')
# now we need to run bamToGFF
# Try to use the bamliquidatior_path.py script on cluster, otherwise, failover to local (in path), otherwise fail.
bamliquidator_path = '/ark/home/jdm/pipeline/bamliquidator_batch.py'
if not os.path.isfile(bamliquidator_path):
bamliquidator_path = 'bamliquidator_batch.py'
if not os.path.isfile(bamliquidator_path):
raise ValueError('bamliquidator_batch.py not found in path')
print('MAPPING SIGNAL AT ENHANCER ASSOCIATED GENE TSS')
# map density at genes in the +/- 5kb tss region
# first on the rankBy bam
bamName = rankByBamFile.split('/')[-1]
mappedRankByFolder = "%s%s_%s_%s/" % (enhancerFolder, enhancerName,gffRootName, bamName)
mappedRankByFile = "%s%s_%s_%s/matrix.gff" % (enhancerFolder,enhancerName, gffRootName, bamName)
cmd = 'python ' + bamliquidator_path + ' --sense . -e 200 --match_bamToGFF -r %s -o %s %s' % (enhancerGeneGFFFile, mappedRankByFolder,rankByBamFile)
print("Mapping rankby bam %s" % (rankByBamFile))
print(cmd)
outputRank = subprocess.Popen(cmd, stdout=subprocess.PIPE, shell=True)
outputRank = outputRank.communicate()
if len(outputRank[0]) > 0: # test if mapping worked correctly
print("SUCCESSFULLY MAPPED TO %s FROM BAM: %s" % (enhancerGeneGFFFile, rankByBamFile))
else:
print("ERROR: FAILED TO MAP %s FROM BAM: %s" % (enhancerGeneGFFFile, rankByBamFile))
sys.exit()
# next on the control bam if it exists
if len(controlBamFile) > 0:
controlName = controlBamFile.split('/')[-1]
mappedControlFolder = "%s%s_%s_%s/" % (
enhancerFolder, enhancerName,gffRootName, controlName)
mappedControlFile = "%s%s_%s_%s/matrix.gff" % (
enhancerFolder, enhancerName,gffRootName, controlName)
cmd = 'python ' + bamliquidator_path + ' --sense . -e 200 --match_bamToGFF -r %s -o %s %s' % (enhancerGeneGFFFile, mappedControlFolder,controlBamFile)
print("Mapping control bam %s" % (controlBamFile))
print(cmd)
outputControl = subprocess.Popen(cmd, stdout=subprocess.PIPE, shell=True)
outputControl = outputControl.communicate()
if len(outputControl[0]) > 0: # test if mapping worked correctly
print("SUCCESSFULLY MAPPED TO %s FROM BAM: %s" % (enhancerGeneGFFFile, controlBamFile))
else:
print("ERROR: FAILED TO MAP %s FROM BAM: %s" % (enhancerGeneGFFFile, controlBamFile))
sys.exit()
# now get the appropriate output files
if len(controlBamFile) > 0:
print("CHECKING FOR MAPPED OUTPUT AT %s AND %s" %
(mappedRankByFile, mappedControlFile))
if utils.checkOutput(mappedRankByFile, 1, 1) and utils.checkOutput(mappedControlFile, 1, 1):
print('MAKING ENHANCER ASSOCIATED GENE TSS SIGNAL DICTIONARIES')
signalDict = makeSignalDict(mappedRankByFile, mappedControlFile)
else:
print("NO MAPPING OUTPUT DETECTED")
sys.exit()
else:
print("CHECKING FOR MAPPED OUTPUT AT %s" % (mappedRankByFile))
if utils.checkOutput(mappedRankByFile, 1, 30):
print('MAKING ENHANCER ASSOCIATED GENE TSS SIGNAL DICTIONARIES')
signalDict = makeSignalDict(mappedRankByFile)
else:
print("NO MAPPING OUTPUT DETECTED")
sys.exit()
# use enhancer rank to order
rankOrder = utils.order([min(rankDict[x]) for x in overallGeneList])
usedNames = []
# make a new dict to hold TSS signal by max per geneName
geneNameSigDict = defaultdict(list)
print('MAKING GENE TABLE')
for i in rankOrder:
refID = overallGeneList[i]
geneName = startDict[refID]['name']
if usedNames.count(geneName) > 0 and uniqueGenes == True:
continue
else:
usedNames.append(geneName)
proxEnhancers = geneDict['overlapping'][
refID] + geneDict['proximal'][refID]
superStatus = max(superDict[refID])
enhancerRanks = join([str(x) for x in rankDict[refID]], ',')
enhancerSignal = signalDict[refID]
geneNameSigDict[geneName].append(enhancerSignal)
newLine = [geneName, refID, join(
proxEnhancers, ','), enhancerRanks, superStatus, enhancerSignal]
geneToEnhancerTable.append(newLine)
#utils.unParseTable(geneToEnhancerTable,'/grail/projects/newRose/geneMapper/foo.txt','\t')
print('MAKING ENHANCER TO TOP GENE TABLE')
if noFormatTable:
enhancerToTopGeneTable = [
enhancerToGeneTable[0] + ['TOP_GENE', 'TSS_SIGNAL']]
else:
enhancerToTopGeneTable = [enhancerToGeneTable[0][0:12] + [
'TOP_GENE', 'TSS_SIGNAL'] + enhancerToGeneTable[0][-2:]]
for line in enhancerToGeneTable[1:]:
geneList = []
if noFormatTable:
geneList += line[-3].split(',')
geneList += line[-2].split(',')
else:
geneList += line[10].split(',')
geneList += line[11].split(',')
geneList = utils.uniquify([x for x in geneList if len(x) > 0])
if len(geneList) > 0:
try:
sigVector = [max(geneNameSigDict[x]) for x in geneList]
maxIndex = sigVector.index(max(sigVector))
maxGene = geneList[maxIndex]
maxSig = sigVector[maxIndex]
if maxSig == 0.0:
maxGene = 'NONE'
maxSig = 'NONE'
except ValueError:
if len(geneList) == 1:
maxGene = geneList[0]
maxSig = 'NONE'
else:
maxGene = 'NONE'
maxSig = 'NONE'
else:
maxGene = 'NONE'
maxSig = 'NONE'
if noFormatTable:
newLine = line + [maxGene, maxSig]
else:
newLine = line[0:12] + [maxGene, maxSig] + line[-2:]
enhancerToTopGeneTable.append(newLine)
# resort enhancerToGeneTable
if noFormatTable:
return enhancerToGeneTable, enhancerToTopGeneTable, geneToEnhancerTable
else:
enhancerOrder = utils.order([int(line[-2])
for line in enhancerToGeneTable[1:]])
sortedTable = [enhancerToGeneTable[0]]
sortedTopGeneTable = [enhancerToTopGeneTable[0]]
for i in enhancerOrder:
sortedTable.append(enhancerToGeneTable[(i + 1)])
sortedTopGeneTable.append(enhancerToTopGeneTable[(i + 1)])
return sortedTable, sortedTopGeneTable, geneToEnhancerTable
def makeGeneTable(peakTable, analysisName):
'''
takes the peak table and makes a gene centric table
'''
geneDict = {}
geneTable = [[
'GENE',
'%s_TSS_SIGNAL' % (analysisName),
'%s_DISTAL_SIGNAL' % (analysisName)
]]
#now iterate through the table
for line in peakTable[1:]:
regionLength = int(line[4])
signal = float(line[9]) * regionLength
#genes where this particular peak overlaps the tss 1kb window
#where there are both overlap and proximal meet
if len(line) == 15:
overlapGeneList = [
gene for gene in line[-2].split(',') if len(gene) > 0
]
if overlapGeneList.count('107'):
print(line)
sys.exit()
for overlapGene in overlapGeneList:
if geneDict.has_key(overlapGene) == False:
geneDict[overlapGene] = {'tss': 0.0, 'distal': 0.0}
#there can be a nasty 1 overlap case where the region might overlap by the overlapping gene list, but not be real
if int(line[5]) == 1:
geneDict[overlapGene]['tss'] += signal
else: #this is the case where the mycn site is just outside of the promoter or overlapping the gene locus/body these are rar
geneDict[overlapGene]['distal'] += signal
proximalGeneList = [
gene for gene in line[-1].split(',') if len(gene) > 0
]
for proximalGene in proximalGeneList:
if geneDict.has_key(proximalGene) == False:
geneDict[proximalGene] = {'tss': 0.0, 'distal': 0.0}
if int(line[5]) == 0:
geneDict[proximalGene]['distal'] += signal
#where there's just overlap
if len(line) == 14:
overlapGeneList = [
gene for gene in line[-1].split(',') if len(gene) > 0
]
if overlapGeneList.count('107'):
print(line)
sys.exit()
for overlapGene in overlapGeneList:
if geneDict.has_key(overlapGene) == False:
geneDict[overlapGene] = {'tss': 0.0, 'distal': 0.0}
#there can be a nasty 1 overlap case where the region might overlap by the overlapping gene list, but not be real
if int(line[5]) == 1:
geneDict[overlapGene]['tss'] += signal
else: #this is the case where the mycn site is just outside of the promoter or overlapping the gene locus/body these are rar
geneDict[overlapGene]['distal'] += signal
geneList = geneDict.keys()
geneList = utils.uniquify(geneList)
geneList.sort()
for gene in geneList:
newLine = [gene]
newLine.append(geneDict[gene]['tss'])
newLine.append(geneDict[gene]['distal'])
geneTable.append(newLine)
return geneTable
def makeNESTable(nes_path_list,names_list,output =''):
'''
combines the GSEA NES output from the enhancerPromoter analysis
creates a table of all represented gene sets
'''
if len(nes_path_list) != len(names_list):
print('please provide the same number of nes table paths and sample names')
sys.exit()
#nested dictionaries gsea['pathway']['name][nes,fdr]
gsea_dict = defaultdict(dict)
pathway_list = []
#iterate once to just get all potential pathways
for i in range(len(nes_path_list)):
nes_path = nes_path_list[i]
nes = utils.parseTable(nes_path,'\t')
for line in nes[1:]:
pathway_list.append(line[0])
pathway_list = utils.uniquify(pathway_list)
pathway_list.sort()
#now blank the dictionary w defaul NES of 0 and FDR of 1
for pathway in pathway_list:
for name in names_list:
gsea_dict[pathway][name] = [0.0,1.0]
#now loop again to fill out properly
for i in range(len(nes_path_list)):
nes_path = nes_path_list[i]
name = names_list[i]
nes = utils.parseTable(nes_path,'\t')
for line in nes[1:]:
if line[2] == 'NA':
continue
try:
nes_vector = [float(line[2]),float(line[3])]
except ValueError:
print(line)
print(nes_path)
print(name)
sys.exit()
pathway = line[0]
gsea_dict[pathway][name] = nes_vector
#set up the output table
header = ['PATHWAY']
for name in names_list:
header += ['%s_NES' % (name),'%s_FDR' % (name)]
nes_table = [header]
for pathway in pathway_list:
nes_line = [pathway]
for name in names_list:
nes_line += gsea_dict[pathway][name]
nes_table.append(nes_line)
if len(output) != 0:
utils.unParseTable(nes_table,output,'\t')
else:
return nes_table
def finishRankOutput(dataFile,rankOutput,genome,mergeFolder,mergeName,name1,name2,cutOff=1.5,window = 100000,superOnly=True,plotBam=True):
'''
cleans up the rank output table
makes a gff of all of the gained/lost supers beyond
a certain cutoff w/ a window
makes a list of gained genes and lost genes
makes a bed of gained loss
'''
dataDict = pipeline_dfci.loadDataTable(dataFile)
#making sure window and cutoff are int/float
cutOff = float(cutOff)
window = int(window)
genome = string.upper(genome)
#make the output folder
outputFolder =pipeline_dfci.formatFolder(mergeFolder+'output/',True)
#bring in the old rank table
rankEnhancerTable = utils.parseTable(rankOutput,'\t')
#make a new formatted table
header = rankEnhancerTable[0]
header[-4] = 'DELTA RANK'
header[-3] = 'IS_SUPER'
formattedRankTable =[header]
#the gffs
gainedGFF = []
lostGFF = []
gainedWindowGFF = []
lostWindowGFF = []
if superOnly:
enhancerType = 'SUPERS'
else:
enhancerType = 'ENHANCERS'
#the beds
if superOnly:
gainedTrackHeader = 'track name="%s %s only SEs" description="%s super enhancers that are found only in %s vs %s" itemRGB=On color=255,0,0' % (genome,name2,genome,name2,name1)
gainedBed = [[gainedTrackHeader]]
conservedTrackHeader = 'track name="%s %s and %s SEs" description="%s super enhancers that are found in both %s vs %s" itemRGB=On color=0,0,0' % (genome,name1,name2,genome,name1,name2)
conservedBed = [[conservedTrackHeader]]
lostTrackHeader = 'track name="%s %s only SEs" description="%s super enhancers that are found only in %s vs %s" itemRGB=On color=0,255,0' % (genome,name1,genome,name1,name2)
lostBed = [[lostTrackHeader]]
else:
gainedTrackHeader = 'track name="%s %s only enhancers" description="%s enhancers that are found only in %s vs %s" itemRGB=On color=255,0,0' % (genome,name2,genome,name2,name1)
gainedBed = [[gainedTrackHeader]]
conservedTrackHeader = 'track name="%s %s and %s enhancers" description="%s enhancers that are found in both %s vs %s" itemRGB=On color=0,0,0' % (genome,name1,name2,genome,name1,name2)
conservedBed = [[conservedTrackHeader]]
lostTrackHeader = 'track name="%s %s only enhancers" description="%s enhancers that are found only in %s vs %s" itemRGB=On color=0,255,0' % (genome,name1,genome,name1,name2)
lostBed = [[lostTrackHeader]]
#the genes
geneTable =[['GENE','ENHANCER_ID','ENHANCER_CHROM','ENHANCER_START','ENHANCER_STOP',header[6],header[7],header[8],'STATUS']]
for line in rankEnhancerTable[1:]:
#fixing the enhancer ID
line[0] = line[0].replace('_lociStitched','')
formattedRankTable.append(line)
#getting the genes
geneList = []
geneList += line[9].split(',')
geneList += line[10].split(',')
geneList += line[11].split(',')
geneList = [x for x in geneList if len(x) >0]
geneList = utils.uniquify(geneList)
geneString = string.join(geneList,',')
bedLine = [line[1],line[2],line[3],line[0],line[-4]]
#for gained
if float(line[6]) > cutOff:
gffLine = [line[1],line[0],'',line[2],line[3],'','.','',geneString]
gffWindowLine = [line[1],line[0],'',int(line[2])-window,int(line[3])+window,'','.','',geneString]
gainedGFF.append(gffLine)
gainedWindowGFF.append(gffWindowLine)
geneStatus = name2
gainedBed.append(bedLine)
#for lost
elif float(line[6]) < (-1 * cutOff):
gffLine = [line[1],line[0],'',line[2],line[3],'','.','',geneString]
gffWindowLine = [line[1],line[0],'',int(line[2])-window,int(line[3])+window,'','.','',geneString]
lostGFF.append(gffLine)
lostWindowGFF.append(gffWindowLine)
geneStatus = name1
lostBed.append(bedLine)
#for conserved
else:
geneStatus = 'CONSERVED'
conservedBed.append(bedLine)
#now fill in the gene Table
for gene in geneList:
geneTableLine = [gene,line[0],line[1],line[2],line[3],line[6],line[7],line[8],geneStatus]
geneTable.append(geneTableLine)
#concat the bed
fullBed = gainedBed + conservedBed + lostBed
#start writing the output
#there's the two gffs, the bed,the formatted table, the gene table
#formatted table
formattedFilename = "%s%s_%s_MERGED_%s_RANK_TABLE.txt" % (outputFolder,genome,mergeName,enhancerType)
utils.unParseTable(formattedRankTable,formattedFilename,'\t')
#gffs
gffFolder = pipeline_dfci.formatFolder(outputFolder+'gff/',True)
gffFilename_gained = "%s%s_%s_%s_ONLY_%s_-0_+0.gff" % (gffFolder,genome,mergeName,string.upper(name2),enhancerType)
gffFilenameWindow_gained = "%s%s_%s_%s_ONLY_%s_-%sKB_+%sKB.gff" % (gffFolder,genome,mergeName,string.upper(name2),enhancerType,window/1000,window/1000)
gffFilename_lost = "%s%s_%s_%s_ONLY_%s_-0_+0.gff" % (gffFolder,genome,mergeName,string.upper(name1),enhancerType)
gffFilenameWindow_lost = "%s%s_%s_%s_ONLY_%s_-%sKB_+%sKB.gff" % (gffFolder,genome,mergeName,string.upper(name1),enhancerType,window/1000,window/1000)
utils.unParseTable(gainedGFF,gffFilename_gained,'\t')
utils.unParseTable(gainedWindowGFF,gffFilenameWindow_gained,'\t')
utils.unParseTable(lostGFF,gffFilename_lost,'\t')
utils.unParseTable(lostWindowGFF,gffFilenameWindow_lost,'\t')
#bed
bedFilename = "%s%s_%s_MERGED_%s.bed" % (outputFolder,genome,mergeName,enhancerType)
utils.unParseTable(fullBed,bedFilename,'\t')
#geneTable
geneFilename = "%s%s_%s_MERGED_%s_GENE_TABLE.txt" % (outputFolder,genome,mergeName,enhancerType)
utils.unParseTable(geneTable,geneFilename,'\t')
#finally, move all of the plots to the output folder
cmd = "cp %s%s_ROSE/*.pdf %s%s_%s_MERGED_%s_DELTA.pdf" % (mergeFolder,name1,outputFolder,genome,mergeName,enhancerType)
os.system(cmd)
cmd = "cp %s%s_ROSE/*RANK_PLOT.png %s%s_%s_MERGED_%s_RANK_PLOT.png" % (mergeFolder,name1,outputFolder,genome,mergeName,enhancerType)
os.system(cmd)
#now execute the bamPlot_turbo.py commands
if plotBam:
bam1 = dataDict[name1]['bam']
bam2 = dataDict[name2]['bam']
bamString = "%s,%s" % (bam1,bam2)
nameString = "%s,%s" % (name1,name2)
colorString = "0,0,0:100,100,100"
#change dir
os.chdir(pipelineDir)
if len(gainedGFF) > 0:
#gained command
plotTitle = "%s_ONLY_SE" % (name2)
cmd = 'python bamPlot_turbo.py -g %s -b %s -i %s -o %s -n %s -c %s -t %s -r -y UNIFORM -p MULTIPLE' % (genome,bamString,gffFilename_gained,outputFolder,nameString,colorString,plotTitle)
os.system(cmd)
#gained window command
plotTitle = "%s_ONLY_SE_%sKB_WINDOW" % (name2,window/1000)
cmd = 'python bamPlot_turbo.py -g %s -b %s -i %s -o %s -n %s -c %s -t %s -r -y UNIFORM -p MULTIPLE' % (genome,bamString,gffFilenameWindow_gained,outputFolder,nameString,colorString,plotTitle)
os.system(cmd)
if len(lostGFF) > 0:
#lost command
plotTitle = "%s_ONLY_SE" % (name1)
cmd = 'python bamPlot_turbo.py -g %s -b %s -i %s -o %s -n %s -c %s -t %s -r -y UNIFORM -p MULTIPLE' % (genome,bamString,gffFilename_lost,outputFolder,nameString,colorString,plotTitle)
os.system(cmd)
#lost command
plotTitle = "%s_ONLY_SE_%sKB_WINDOW" % (name1,window/1000)
cmd = 'python bamPlot_turbo.py -g %s -b %s -i %s -o %s -n %s -c %s -t %s -r -y UNIFORM -p MULTIPLE' % (genome,bamString,gffFilenameWindow_lost,outputFolder,nameString,colorString,plotTitle)
os.system(cmd)
return
def finishRankOutput(dataFile,statOutput,diffOutput,genome,mergeFolder,mergeName,name1,name2,namesList1,namesList2,cutOff=1.0,window = 100000,superOnly=True,plotBam=True):
'''
cleans up the rank output table
makes a gff of all of the gained/lost supers beyond
a certain cutoff w/ a window
makes a list of gained genes and lost genes
makes a bed of gained loss
'''
dataDict = pipeline_dfci.loadDataTable(dataFile)
#making sure window and cutoff are int/float
cutOff = float(cutOff)
window = int(window)
genome = string.upper(genome)
#make the output folder
outputFolder =pipeline_dfci.formatFolder(mergeFolder+'output/',True)
#bring in the old rank table
rankEnhancerTable = utils.parseTable(statOutput,'\t')
#make a new formatted table
header = rankEnhancerTable[0]
formattedRankTable =[header]
#the gffs
gainedGFF = []
lostGFF = []
gainedWindowGFF = []
lostWindowGFF = []
if superOnly:
enhancerType = 'SUPERS'
else:
enhancerType = 'ENHANCERS'
#the beds
if superOnly:
gainedTrackHeader = 'track name="%s %s only SEs" description="%s super enhancers that are found only in %s vs %s" itemRGB=On color=255,0,0' % (genome,name2,genome,name2,name1)
gainedBed = [[gainedTrackHeader]]
conservedTrackHeader = 'track name="%s %s and %s SEs" description="%s super enhancers that are found in both %s vs %s" itemRGB=On color=0,0,0' % (genome,name1,name2,genome,name1,name2)
conservedBed = [[conservedTrackHeader]]
lostTrackHeader = 'track name="%s %s only SEs" description="%s super enhancers that are found only in %s vs %s" itemRGB=On color=0,255,0' % (genome,name1,genome,name1,name2)
lostBed = [[lostTrackHeader]]
else:
gainedTrackHeader = 'track name="%s %s only enhancers" description="%s enhancers that are found only in %s vs %s" itemRGB=On color=255,0,0' % (genome,name2,genome,name2,name1)
gainedBed = [[gainedTrackHeader]]
conservedTrackHeader = 'track name="%s %s and %s enhancers" description="%s enhancers that are found in both %s vs %s" itemRGB=On color=0,0,0' % (genome,name1,name2,genome,name1,name2)
conservedBed = [[conservedTrackHeader]]
lostTrackHeader = 'track name="%s %s only enhancers" description="%s enhancers that are found only in %s vs %s" itemRGB=On color=0,255,0' % (genome,name1,genome,name1,name2)
lostBed = [[lostTrackHeader]]
#the genes
geneTable =[['GENE','ENHANCER_ID','ENHANCER_CHROM','ENHANCER_START','ENHANCER_STOP',header[6],header[7],header[8],'STATUS']]
headerLength = len(rankEnhancerTable[0])
for line in rankEnhancerTable[1:]:
#fix line lengths
if len(line) != headerLength:
line += ['']*(headerLength-len(line))
#fixing the enhancer ID
line[0] = line[0].replace('_lociStitched','')
formattedRankTable.append(line)
#getting the genes
geneList = []
geneList += line[-1].split(',')
geneList += line[-2].split(',')
geneList += line[-3].split(',')
geneList = [x for x in geneList if len(x) >0]
geneList = utils.uniquify(geneList)
geneString = string.join(geneList,',')
bedLine = [line[1],line[2],line[3],line[0],line[-4]]
#for gained
#this applies both the statistical test chosen (default fdr <= 0.05) and the cutoff
#the cutoff is hard wired, but we can add an option to change the test
#stats are done in the R script. FDR norm can kinda suck if no genes are considered diff
#print(line)
if float(line[-8]) > cutOff and int(line[-4]) == 1:
gffLine = [line[1],line[0],'',line[2],line[3],'','.','',geneString]
gffWindowLine = [line[1],line[0],'',int(line[2])-window,int(line[3])+window,'','.','',geneString]
gainedGFF.append(gffLine)
gainedWindowGFF.append(gffWindowLine)
geneStatus = name2
gainedBed.append(bedLine)
#for lost
elif float(line[-8]) < (-1 * cutOff) and int(line[-4]) == 1:
gffLine = [line[1],line[0],'',line[2],line[3],'','.','',geneString]
gffWindowLine = [line[1],line[0],'',int(line[2])-window,int(line[3])+window,'','.','',geneString]
lostGFF.append(gffLine)
lostWindowGFF.append(gffWindowLine)
geneStatus = name1
lostBed.append(bedLine)
#for conserved
else:
geneStatus = 'UNCHANGED'
conservedBed.append(bedLine)
#now fill in the gene Table
for gene in geneList:
geneTableLine = [gene,line[0],line[1],line[2],line[3],line[6],line[7],line[8],geneStatus]
geneTable.append(geneTableLine)
#concat the bed
fullBed = gainedBed + conservedBed + lostBed
#start writing the output
#there's the two gffs, the bed,the formatted table, the gene table
#formatted table
formattedFilename = "%s%s_%s_MERGED_%s_RANK_TABLE.txt" % (outputFolder,genome,mergeName,enhancerType)
utils.unParseTable(formattedRankTable,formattedFilename,'\t')
#formatted diff table
#possible that no genes are differential
rankEnhancerDiffTable = utils.parseTable(diffOutput,'\t')
#make a new formatted table
header = rankEnhancerDiffTable[0]
formattedRankDiffTable =[header]
for line in rankEnhancerDiffTable[1:]:
#fixing the enhancer ID
line[0] = line[0].replace('_lociStitched','')
formattedRankDiffTable.append(line)
formattedDiffFilename = "%s%s_%s_MERGED_%s_RANK_DIFF_TABLE.txt" % (outputFolder,genome,mergeName,enhancerType)
utils.unParseTable(formattedRankDiffTable,formattedDiffFilename,'\t')
#gffs
gffFolder = pipeline_dfci.formatFolder(outputFolder+'gff/',True)
gffFilename_gained = "%s%s_%s_%s_ONLY_%s_-0_+0.gff" % (gffFolder,genome,mergeName,string.upper(name2),enhancerType)
gffFilenameWindow_gained = "%s%s_%s_%s_ONLY_%s_-%sKB_+%sKB.gff" % (gffFolder,genome,mergeName,string.upper(name2),enhancerType,window/1000,window/1000)
gffFilename_lost = "%s%s_%s_%s_ONLY_%s_-0_+0.gff" % (gffFolder,genome,mergeName,string.upper(name1),enhancerType)
gffFilenameWindow_lost = "%s%s_%s_%s_ONLY_%s_-%sKB_+%sKB.gff" % (gffFolder,genome,mergeName,string.upper(name1),enhancerType,window/1000,window/1000)
utils.unParseTable(gainedGFF,gffFilename_gained,'\t')
utils.unParseTable(gainedWindowGFF,gffFilenameWindow_gained,'\t')
utils.unParseTable(lostGFF,gffFilename_lost,'\t')
utils.unParseTable(lostWindowGFF,gffFilenameWindow_lost,'\t')
#bed
bedFilename = "%s%s_%s_MERGED_%s.bed" % (outputFolder,genome,mergeName,enhancerType)
utils.unParseTable(fullBed,bedFilename,'\t')
#geneTable
geneFilename = "%s%s_%s_MERGED_%s_GENE_TABLE.txt" % (outputFolder,genome,mergeName,enhancerType)
utils.unParseTable(geneTable,geneFilename,'\t')
#finally, move all of the plots to the output folder
cmd = "cp %s%s_ROSE/*DELTA*.pdf %s%s_%s_MERGED_%s_DELTA.pdf" % (mergeFolder,namesList1[0],outputFolder,genome,mergeName,enhancerType)
os.system(cmd)
cmd = "cp %s%s_ROSE/*REGION_GAINED*.pdf %s%s_%s_MERGED_%s_REGION_GAINED.pdf" % (mergeFolder,namesList1[0],outputFolder,genome,mergeName,enhancerType)
os.system(cmd)
cmd = "cp %s%s_ROSE/*REGION_LOST*.pdf %s%s_%s_MERGED_%s_REGION_LOST.pdf" % (mergeFolder,namesList1[0],outputFolder,genome,mergeName,enhancerType)
os.system(cmd)
cmd = "cp %s%s_ROSE/*REGION_LOST*.pdf %s%s_%s_MERGED_%s_REGION_UNCHANGED.pdf" % (mergeFolder,namesList1[0],outputFolder,genome,mergeName,enhancerType)
os.system(cmd)
cmd = "cp %s%s_ROSE/*RANK_PLOT.png %s%s_%s_MERGED_%s_RANK_PLOT.png" % (mergeFolder,namesList1[0],outputFolder,genome,mergeName,enhancerType)
os.system(cmd)
#now execute the bamPlot_turbo.py commands
if plotBam:
bamList1 = [dataDict[name]['bam'] for name in namesList1]
bamList2 = [dataDict[name]['bam'] for name in namesList2]
bamList = bamList1 + bamList2
bamString = string.join(bamList,',')
nameList = [name1]*len(namesList1) + [name2]*len(namesList2)
nameString = string.join(nameList,',')
print(namesList1[0])
print(namesList2[0])
print(namesList1)
print(namesList2)
print(dataDict[namesList1[0]]['color'])
if dataDict[namesList1[0]]['color'] != dataDict[namesList2[0]]['color']:
colorList = [dataDict[namesList1[0]]['color']]*len(namesList1) + [dataDict[namesList2[0]]['color']]*len(namesList2)
else:
colorList = ['0,0,0']*len(namesList1) + ['100,100,100']*len(namesList2)
colorString = string.join(colorList,':')
#change dir
if len(gainedGFF) > 0:
#gained command
plotTitle = "%s_ONLY_SE" % (name2)
cmd = 'python %sbamPlot_turbo.py -g %s -b %s -i %s -o %s -n %s -c %s -t %s -r -y UNIFORM -p MERGE' % (pipelineDir,genome,bamString,gffFilename_gained,outputFolder,nameString,colorString,plotTitle)
os.system(cmd)
#gained window command
plotTitle = "%s_ONLY_SE_%sKB_WINDOW" % (name2,window/1000)
cmd = 'python %sbamPlot_turbo.py -g %s -b %s -i %s -o %s -n %s -c %s -t %s -r -y UNIFORM -p MERGE' % (pipelineDir,genome,bamString,gffFilenameWindow_gained,outputFolder,nameString,colorString,plotTitle)
os.system(cmd)
if len(lostGFF) > 0:
#lost command
plotTitle = "%s_ONLY_SE" % (name1)
cmd = 'python %sbamPlot_turbo.py -g %s -b %s -i %s -o %s -n %s -c %s -t %s -r -y UNIFORM -p MERGE' % (pipelineDir,genome,bamString,gffFilename_lost,outputFolder,nameString,colorString,plotTitle)
os.system(cmd)
#lost command
plotTitle = "%s_ONLY_SE_%sKB_WINDOW" % (name1,window/1000)
cmd = 'python %sbamPlot_turbo.py -g %s -b %s -i %s -o %s -n %s -c %s -t %s -r -y UNIFORM -p MERGE' % (pipelineDir,genome,bamString,gffFilenameWindow_lost,outputFolder,nameString,colorString,plotTitle)
os.system(cmd)
return