def selectSequences(self, inputFname=None, outputFname=None, inputFileFormat='fasta', outputFileFormat='fasta', chromosomeSet=None,\
defaultBasePhredQuality=87):
"""
2012.5.24
"""
sys.stderr.write("Choosing %s chromosome sequences from %s ..." %
(len(chromosomeSet), inputFname))
inf = utils.openGzipFile(inputFname, 'r')
counter = 0
real_counter = 0
outputHandle = utils.openGzipFile(outputFname, 'w')
for seq_record in SeqIO.parse(inf, inputFileFormat):
counter += 1
if seq_record.id in chromosomeSet:
if outputFileFormat == 'fastq' and 'phred_quality' not in seq_record.letter_annotations:
#fake quality for fastq output
seq_record.letter_annotations['phred_quality'] = [
defaultBasePhredQuality
] * len(seq_record.seq)
SeqIO.write([seq_record], outputHandle, outputFileFormat)
real_counter += 1
elif real_counter == len(chromosomeSet): #got enough chromosomes
break
#close the last handle
outputHandle.close()
sys.stderr.write(" %s records chosen into %s.\n" %
(real_counter, outputFname))
def run(self):
"""
2013.2.11
input looks like (inputFileFormat=1)
msHOT-lite 2 1 -t 4781.50413187402 -r 790.4466018 ...
//
segsites: 40567
positions: 0.0002 0.0003
001001101011011001...
101001010100101111...
...
"""
if self.debug:
import pdb
pdb.set_trace()
inf = utils.openGzipFile(self.inputFname, 'r')
outf = utils.openGzipFile(self.outputFname, openMode='w')
self.convertFuncDict[self.inputFileFormat](inf=inf, outf=outf, \
noOfHaplotypesDefault=self.noOfHaplotypesDefault,\
chromosomeLengthToSimulate=self.chromosomeLengthToSimulate)
inf.close()
outf.close()
def countNoOfChromosomesBasesInFastQFile(inputFname=None):
"""
2013.2.16 add the try...except around the parser
2013.2.9 count the #chromosomes, #bases of inputFname
"""
sys.stderr.write("Counting #chromosomes, #bases of %s ..." % (inputFname))
no_of_chromosomes = 0
no_of_bases = 0
inf = utils.openGzipFile(inputFname)
try:
for seq_record in SeqIO.parse(inf, 'fastq'):
no_of_chromosomes += 1
no_of_bases += len(seq_record)
except:
sys.stderr.write("Except after handling %s chromosomes & %s bases.\n" %
(no_of_chromosomes, no_of_bases))
sys.stderr.write('Except type: %s\n' % repr(sys.exc_info()))
import traceback
traceback.print_exc()
raise
inf.close()
sys.stderr.write("%s chromosomes, %s bases\n" %
(no_of_chromosomes, no_of_bases))
return utils.PassingData(no_of_chromosomes=no_of_chromosomes,
no_of_bases=no_of_bases)
def splitFastaFile(self,
inputFname=None,
outputFnamePrefix=None,
noOfSequences=1000,
suffixLength=3,
filenameSuffix=""):
"""
2012.5.24
"""
sys.stderr.write("Splitting fasta file %s ..." % (inputFname))
inf = utils.openGzipFile(inputFname)
counter = 0
real_counter = 0
outputFname = utils.comeUpSplitFilename(outputFnamePrefix=outputFnamePrefix, suffixLength=suffixLength, fileOrder=real_counter,\
filenameSuffix=filenameSuffix)
outputHandle = open(outputFname, 'w')
for seq_record in SeqIO.parse(inf, "fasta"):
counter += 1
SeqIO.write([seq_record], outputHandle, "fasta")
if counter % noOfSequences == 0:
outputHandle.close()
real_counter += 1
outputFname = utils.comeUpSplitFilename(outputFnamePrefix=outputFnamePrefix, suffixLength=suffixLength, fileOrder=real_counter,\
filenameSuffix=filenameSuffix)
outputHandle = open(outputFname, 'w')
#close the last handle
outputHandle.close()
sys.stderr.write(" into %s files.\n" %
(real_counter + 1)) #real_counter starts from 0
def run(self):
"""
"""
if self.debug:
import pdb
pdb.set_trace()
if not os.path.isfile(self.inputFname):
sys.stderr.write("Error: file, %s, is not a file.\n" %
(self.inputFname))
sys.exit(3)
inputFile = utils.openGzipFile(self.inputFname, 'r')
outputPolymorphismFile = PolymorphismTableFile(self.outputFname, openMode='w', isPhased=1, \
ploidy=self.ploidy)
outputChromosomeSequenceFile = open(self.outputChromosomeSequenceFname,
"w")
commandline = inputFile.next().strip()
outputPolymorphismFile.addAttribute('commandline',
value=commandline,
overwrite=True,
tableName='polymorphism')
for line in inputFile:
if self.iterationPattern.search(
line): #one iteration is regarded as one species
self.outputOneIteration(inputFile=inputFile, iterationLine=line, outputPolymorphismFile=outputPolymorphismFile,\
outputChromosomeSequenceFile=outputChromosomeSequenceFile, ploidy=self.ploidy)
inputFile.close()
outputPolymorphismFile.close()
outputChromosomeSequenceFile.close()
def run(self):
"""
input looks like (inputFileFormat=1)
msHOT-lite 2 1 -t 4781.50413187402 -r 790.4466018 ...
//
segsites: 40567
positions: 0.0002 0.0003
001001101011011001...
101001010100101111...
...
./msHOT-lite 2 1 -t 84989.8346003745 -r 34490.1412746802 30000000 -l -en 0.0013 1 0.0670 -en 0.0022 1 0.3866 -en 0.0032 1 0.3446 -en 0.0044 1 0.21
79 -en 0.0059 1 0.1513 -en 0.0076 1 0.1144 -en 0.0096 1 0.0910 -en 0.0121 1 0.0757 -en 0.0150 1 0.0662 -en 0.0184 1 0.0609 -en 0.0226 1 0.0583 -en
0.0275 1 0.0572 -en 0.0333 1 0.0571 -en 0.0402 1 0.0577 -en 0.0485 1 0.0589 -en 0.0583 1 0.0603 -en 0.0700 1 0.0615 -en 0.0839 1 0.0624 -en 0.100
5 1 0.0632 -en 0.1202 1 0.0641 -en 0.1437 1 0.0651 -en 0.1716 1 0.0663 -en 0.2048 1 0.0678 -en 0.2444 1 0.0696 -en 0.2914 1 0.0719 -en 0.3475 1 0.
0752 -en 0.4935 1 0.0794
//
@begin 6422
30000000
1100 01
6074 10
29966899 10
29971027 01
29973740 01
29982767 01
29985696 10
@end
"""
if self.debug:
import pdb
pdb.set_trace()
if not os.path.isfile(self.inputFname):
sys.stderr.write("Error: file, %s, is not a file.\n" %
(self.inputFname))
sys.exit(3)
inputFile = utils.openGzipFile(self.inputFname, 'r')
outputPolymorphismFile = PolymorphismTableFile(self.outputFname, openMode='w', isPhased=1, \
ploidy=self.ploidy)
commandline = inputFile.next().strip()
outputPolymorphismFile.addAttribute('commandline',
value=commandline,
overwrite=True,
tableName='polymorphism')
self._convert(inputFile=inputFile,
outputPolymorphismFile=outputPolymorphismFile,
ploidy=self.ploidy)
inputFile.close()
outputPolymorphismFile.close()
def run(self): """ """ if self.debug: import pdb pdb.set_trace() inf = utils.openGzipFile(self.inputFname, openMode='r') reader = csv.reader(inf, delimiter=figureOutDelimiter(inf)) header = None for i in xrange(self.noOfLinesInHeader): if i==0: header = reader.next() #first line is taken as header else: reader.next() if header is not None: colName2Index = getColName2IndexFromHeader(header) newHeader = ['alignmentID', 'total_base_count', 'sampled_base_count', 'meanDepth', 'medianDepth', 'modeDepth'] inputStatLs = [] writer = csv.writer(utils.openGzipFile(self.outputFname, openMode='w'), delimiter='\t') writer.writerow(newHeader) counter = 0 real_counter = 0 for row in reader: counter += 1 if real_counter <= self.maxNumberOfSamplings: r = random.random() if r<=self.fractionToSample and real_counter<=self.maxNumberOfSamplings: inputStatLs.append(float(row[self.whichColumn])) real_counter += 1 meanDepth = numpy.mean(inputStatLs) medianDepth = numpy.median(inputStatLs) modeDepth = scipy.stats.mode(inputStatLs)[0][0] outputRow = [self.alignmentID, counter, real_counter, meanDepth, medianDepth, modeDepth] writer.writerow(outputRow) del writer
def run(self):
if self.debug:
import pdb
pdb.set_trace()
header = None
outf = utils.openGzipFile(self.outputFname, 'w')
for inputFname in self.inputFnameLs:
sys.stderr.write("File %s ... " % (inputFname))
if not os.path.isfile(inputFname):
if self.exitNonZeroIfAnyInputFileInexistent:
sys.stderr.write(" doesn't exist. Exit 3.\n")
sys.exit(3)
else:
continue
suffix = os.path.splitext(inputFname)[1]
if suffix == '.gz':
import gzip
inf = gzip.open(inputFname, 'r')
else:
inf = open(inputFname, 'r')
if self.noHeader == 0: #in the case that every input has a common header
if not header: #2012.7.26 bugfix: empty file will return an empty string, which "is not None".
try:
header = inf.readline()
outf.write(header)
except: #in case something wrong (i.e. file is empty)
sys.stderr.write('Except type: %s\n' %
repr(sys.exc_info()))
import traceback
traceback.print_exc()
print sys.exc_info()
else:
#skip the header for other input files
try:
inf.readline()
except: #in case something wrong (i.e. file is empty)
sys.stderr.write('Except type: %s\n' %
repr(sys.exc_info()))
import traceback
traceback.print_exc()
print sys.exc_info()
for line in inf:
isEmpty = self.isInputLineEmpty(
line.strip(),
inputFile=inf,
inputEmptyType=self.inputEmptyType)
if not isEmpty: #only write when it's not empty
outf.write(line)
sys.stderr.write(".\n")
def getNoOfSequencesFromFasta(self, inputFastaFname=None):
"""
2012.5.24
"""
sys.stderr.write("Getting number of sequences from %s ..." %
(inputFastaFname))
inf = utils.openGzipFile(inputFastaFname)
no_of_sequences = 0
for line in inf:
if line[0] == '>':
no_of_sequences += 1
del inf
sys.stderr.write("%s sequences.\n" % (no_of_sequences))
return no_of_sequences
def _initializeInput(self, inputFname=None): """ 2012.5.10 split out of __init__() """ if inputFname and self.openMode[0]=='r': self.inf = utils.openGzipFile(inputFname, openMode='r') """ if inputFname[-3:]=='.gz': import gzip self.inf = gzip.open(inputFname, 'rb') else: self.inf = open(inputFname) """ self.reader =csv.reader(self.inf, delimiter='\t') self._parseHeader()
def getReadBaseCount(cls, inputFname, ignore_set = set(['>', '+', '@']), onlyForEmptyCheck=False): """ 2012.3.19 inputFname could be fastq or fasta """ inf = utils.openGzipFile(inputFname, openMode='r') read_count = 0 base_count = 0 for line in inf: if line[0] in ignore_set: if line[0]=='+': #skip the quality-score line right after this "+" line inf.next() continue read_count += 1 base_count += len(line.strip()) if onlyForEmptyCheck: #2012.3.19 one read is enough. break del inf return PassingData(read_count=read_count, base_count=base_count)
def run(self):
"""
"""
if self.debug:
import pdb
pdb.set_trace()
inf = utils.openGzipFile(self.inputFname)
outf = open(self.outputFname, 'w')
lineNumber = 0
real_counter = 0
for line in inf:
lineNumber += 1
if lineNumber >= self.startLineNumber and lineNumber <= self.stopLineNumber:
outf.write(line)
real_counter += 1
elif lineNumber > self.stopLineNumber: #stop here
break
inf.close()
outf.close()
sys.stderr.write("%s lines chosen.\n" % (real_counter))
def run(self):
"""
"""
if self.debug:
import pdb
pdb.set_trace()
if not os.path.isfile(self.inputFname):
sys.stderr.write("Error: file, %s, is not a file.\n" %
(self.inputFname))
sys.exit(3)
inf = utils.openGzipFile(self.inputFname, 'r')
outf = open(self.outputFname, 'w')
for line in inf:
newLine = re.sub(r'%s' % (self.oldMSPath), r'%s' % (self.msPath),
line)
if self.replaceTheHengLiOutputFlagAsWell:
newLine = newLine.replace(
" -l", ""
) #it's global and exhaustive, any " -l " will be replaced.
outf.write(newLine)
inf.close()
outf.close()
def __init__(self, inputFname=None, **keywords): self.ad = ProcessOptions.process_function_arguments(keywords, self.option_default_dict, error_doc=self.__doc__, \ class_to_have_attr=self) if not self.inputFname: self.inputFname = inputFname if self.inputFname and self.inputFile is None: self.inputFile = utils.openGzipFile(self.inputFname, openMode=self.openMode) self.filename = self.inputFname #2013.05.03 for easy access self.csvFile = None self.isRealCSV = False if self.openMode=='r': #reading mode if self.delimiter is None: self.delimiter = figureOutDelimiter(self.inputFile) if self.delimiter=='\t' or self.delimiter==',': self.csvFile = csv.reader(self.inputFile, delimiter=self.delimiter) self.isRealCSV = True else: self.csvFile = self.inputFile self.isRealCSV = False else: #writing mode if not self.delimiter: self.delimiter = '\t' self.csvFile = csv.writer(self.inputFile, delimiter=self.delimiter) self.isRealCSV = True #else: # self.csvFile = self.inputFile # self.isRealCSV = False self.col_name2index = None self._row = None #2013.08.30 to store the current row being read self.headerPattern = re.compile(r'^[a-zA-Z]') #default header pattern, line beginned with letter self.commentPattern = re.compile(r'^#') #default, beginned with # self.comment_row_list = []
def run(self):
if self.debug:
import pdb
pdb.set_trace()
try:
inf = utils.openGzipFile(self.inputFname)
delimiter = figureOutDelimiter(inf)
if not delimiter:
delimiter='\t'
reader = csv.reader(inf, delimiter=delimiter)
writer = csv.writer(open(self.outputFname, 'w'), delimiter=delimiter)
extendHeader = []
if self.addChrName:
extendHeader.append(self.chrHeader)
extendHeader.append(self.chrLengthHeader)
except:
sys.stderr.write('Except type: %s\n'%repr(sys.exc_info()))
import traceback
traceback.print_exc()
print sys.exc_info()
sys.exit(0)
try:
header = self.processHeader(reader=reader, extendHeader=extendHeader, chrLengthHeader = self.chrLengthHeader)
writer.writerow(header)
for row in reader:
new_data_row = self.processRow(row)
writer.writerow(new_data_row)
del reader
del writer
except: #in case something wrong (i.e. file is empty)
sys.stderr.write('Except type: %s\n'%repr(sys.exc_info()))
import traceback
traceback.print_exc()
print sys.exc_info()
sys.exit(0)
def outputSNPDataInNewCoordinate(self, querySNPDataFname=None, querySNPID2NewReferenceCoordinateLs=None,\
newSNPDataOutputFname=None, newSNPDataOutputFormat=1):
"""
2013.07.03 added argument newSNPDataOutputFormat
2012.10.14
split out of findSNPPositionOnNewRef()
"""
sys.stderr.write("Converting querySNPDataFname %s into individual X SNP format, format=%s ... "%\
(querySNPDataFname, newSNPDataOutputFormat))
"""
Sample Geno SNP
1999010 CC cs_primer1082_247
1999068 CC cs_primer1082_247
2000022 CT cs_primer1082_247
2000064 CT cs_primer1082_247
2000117 CC cs_primer1082_247
"""
inf = utils.openGzipFile(querySNPDataFname)
reader = csv.reader(inf, delimiter=figureOutDelimiter(inf))
col_name2index = getColName2IndexFromHeader(reader.next())
sampleIndex = col_name2index.get("Sample")
genotypeIndex = col_name2index.get("Geno")
SNPIDIndex = col_name2index.get("SNP")
row_id2index = {}
row_id_ls = []
col_id_ls = []
col_id2index = {}
row_col_index2genotype = {}
for row in reader:
sampleID = row[sampleIndex]
genotype = row[genotypeIndex]
querySNPID = row[SNPIDIndex]
if querySNPID in querySNPID2NewReferenceCoordinateLs:
newRefCoordinateLs = querySNPID2NewReferenceCoordinateLs.get(querySNPID)
if len(newRefCoordinateLs)==1:
newRefCoordinate = newRefCoordinateLs[0]
if newSNPDataOutputFormat==2:
col_id = '%s_%s'%(newRefCoordinate.newChr, newRefCoordinate.newRefStart)
else:
col_id = '%s_%s_%s'%(newRefCoordinate.newChr, newRefCoordinate.newRefStart, newRefCoordinate.newRefStop)
queryStrand = newRefCoordinate.queryStrand
if col_id not in col_id2index:
col_id2index[col_id] = len(col_id2index)
col_id_ls.append(col_id)
if sampleID not in row_id2index:
row_id2index[sampleID] = len(row_id2index)
row_id_ls.append(sampleID)
if queryStrand == "-":
genotype = SNP.reverseComplement(genotype)
row_index = row_id2index[sampleID]
col_index = col_id2index[col_id]
row_col_index2genotype[(row_index, col_index)] = genotype
else:
continue
data_matrix = numpy.zeros([len(row_id_ls), len(col_id2index)], dtype=numpy.int8)
for row_col_index, genotype in row_col_index2genotype.iteritems():
row_index, col_index = row_col_index[:2]
data_matrix[row_index, col_index] = SNP.nt2number[genotype]
sys.stderr.write("\n")
snpData = SNP.SNPData(row_id_ls=row_id_ls, col_id_ls=col_id_ls, data_matrix=data_matrix)
snpData.tofile(newSNPDataOutputFname)
def vcftoolsOutputStatFileWalker(self, inputFname, processFunc=None, run_type=1, \
chrColumnHeader='CHR', minChrLength=1000000, chrLengthColumnHeader='chrLength',\
xColumnHeader="BIN_START", valueForNonPositiveYValue=-1):
"""
2012.10.26 skip sites if chr_cumu_start is not available
2012.10.25 only skip except during file opening, not file reading
2012.9.18 chrLengthColumnHeader could be nothing
2012.8.31 add argument valueForNonPositiveYValue
2012.8.13 bugfix. pass inf to figureOutDelimiter
2012.8.1
2011-11-2
remove the maxDepth filter. apply afterwards through filterDataByDepth().
2011-9-30
"""
sys.stderr.write("walking through %s ..."%(inputFname))
counter =0
chr2xy_ls = self.chr2xy_ls
try:
inf = utils.openGzipFile(inputFname)
delimiter=figureOutDelimiter(inf) #2012.8.13 bugfix. pass inf to figureOutDelimiter
sys.stderr.write(" delimiter is '%s' "%(delimiter))
reader = csv.reader(inf, delimiter=delimiter)
header = reader.next()
col_name2index = getColName2IndexFromHeader(header, skipEmptyColumn=True)
except: #in case something wrong (i.e. file is empty)
sys.stderr.write('Except type: %s\n'%repr(sys.exc_info()))
import traceback
traceback.print_exc()
print sys.exc_info()
return
chr_id_index = col_name2index.get(chrColumnHeader, None)
if chr_id_index is None:
chr_id_index = col_name2index.get("CHROM", None)
if chr_id_index is None:
chr_id_index = col_name2index.get("CHR", None)
if chr_id_index is None:
sys.stderr.write("Error chr_id_index is None.\n")
sys.exit(3)
bin_start_index = col_name2index.get(xColumnHeader, None)
if chrLengthColumnHeader: #could be nothing
chrLength_index = col_name2index.get(chrLengthColumnHeader, None)
else:
chrLength_index = None
if self.whichColumnHeader:
whichColumn = col_name2index.get(self.whichColumnHeader, None)
else:
whichColumn = self.whichColumn
for row in reader:
if self.samplingRate<1 and self.samplingRate>=0:
r = random.random()
if r>self.samplingRate:
continue
if chrLength_index:
chrLength = int(row[chrLength_index])
if chrLength<minChrLength:
continue
chr_id = row[chr_id_index]
bin_start = int(float(row[bin_start_index]))
yValue = row[whichColumn]
yValue = self.handleYValue(yValue)
if chr_id not in chr2xy_ls:
chr2xy_ls[chr_id] = [[],[]]
chr_cumu_start = self.chr_id2cumu_start.get(chr_id)
if chr_cumu_start is None: #2012.10.26 skip sites
sys.stderr.write("Chromosome %s does not have chr_cumu_start.\n"%(chr_id))
continue
chr2xy_ls[chr_id][0].append(chr_cumu_start + bin_start + 1)
chr2xy_ls[chr_id][1].append(yValue)
counter += 1
del reader
inf.close()
sys.stderr.write("%s data.\n"%(counter))
def parse_chromosome_fasta_file(self, db=None, filename=None, tax_id=None, version=None, chunk_size=10000, \
sequence_type_name=None, sequence_type_id=None, run_type=1,
maxNoOfFastaRecords=500):
"""
2011-7-10
add argument maxNoOfFastaRecords: the max number of fasta records before quitting
2011-7-6
add argument run_type
1: chromosome sequences from NCBI genbank
2: vervet scaffolds from WUSTL
3: full vervet BACs from McGill
2010-12-15
fix a bug that _tax_id shall be used in query AnnotAssembly.
This bug caused the db redundancy check to fail.
2010-12-15
if entry already exists in AnnotAssembly, skip it.
2008-07-29
figure out tax_id via FigureOutTaxID
filename could contain multiple fasta blocks
2008-07-27
change to use data structures from GenomeDB.py
2008-07-06
use the firstline (header) of the fasta file to extract which chromosome. using filename is unreliable.
"""
inf = utils.openGzipFile(filename, openMode='r')
line = inf.readline()
new_fasta_block = 1 #'line' is not enough to stop the 'while' loop. after the file reading is exhausted by "for line in inf:", 'line' still contains the stuff from the last line.
no_of_fasta_blocks = 0
while line and new_fasta_block:
new_fasta_block = 0 #set it to 0, assuming only one fasta block, change upon new fasta block
if line[0]!='>': #not fasta block header
for line in inf: #exhaust this fasta block as it's not what's wanted.
if line[0]=='>':
new_fasta_block = 1
break #start from while again
continue
headerData = self.parseFastaDescriptionDict[run_type](line, self.FigureOutTaxID_ins)
if not headerData.chromosome:
sys.stderr.write("Error chromosome for header %s is empty %s.\n"%(line, headerData.chromosome))
import pdb
pdb.set_trace()
if tax_id is not None and headerData.tax_id and tax_id!=headerData.tax_id:
sys.stderr.write("tax_id (%s) not matching the one given (%s). Ignore.\n"%(headerData.tax_id, tax_id))
line = inf.readline()
new_fasta_block = 1
continue
chromosome = headerData.chromosome
sequence_type = db.getSequenceType(short_name=sequence_type_name, id=sequence_type_id)
start = 1
aa_attr_instance = db.checkAnnotAssembly(version=version, tax_id=tax_id, \
chromosome=chromosome, start=start, stop=None, \
sequence_type_id=sequence_type.id)
if aa_attr_instance and aa_attr_instance.raw_sequence_start_id is not None:
# if raw sequences have been associated with this AnnotAssembly and
sys.stderr.write("raw sequences have been associated with this AnnotAssembly (tax_id %s, chr=%s, start=%s). Ignore.\n"%\
(tax_id, chromosome, start))
line = inf.readline()
new_fasta_block = 1
continue
if aa_attr_instance is None:
aa_attr_instance = db.getAnnotAssembly(gi=headerData.gi, acc_ver=headerData.acc_ver, accession =None, \
version =None, tax_id=tax_id, chromosome =chromosome, \
start =start, stop =None, orientation=None, sequence = None,\
raw_sequence_start_id=None, original_path=os.path.abspath(filename),\
sequence_type_id=sequence_type.id, \
chromosome_type_id=None, chromosome_type_name=None, comment=headerData.comment)
if aa_attr_instance.acc_ver and self.p_acc_ver.search(aa_attr_instance.acc_ver):
aa_attr_instance.accession, aa_attr_instance.version = self.p_acc_ver.search(aa_attr_instance.acc_ver).groups()
aa_attr_instance.version = int(aa_attr_instance.version)
else:
aa_attr_instance.accession = None
aa_attr_instance.version = version
if self.debug:
sys.stderr.write("tax_id=%s for %s.\n"%(aa_attr_instance.tax_id, line))
#aa_attr_instance.raw_sequence_start_id = self.get_current_max_raw_sequence_id(curs, raw_sequence_table)+1
passingdata = PassingData()
passingdata.current_start = 1
passingdata.raw_sequence_initiated = False
seq = ''
for line in inf:
if line[0]=='>':
if seq: #last segment from the previous fasta block
self.saveRawSequence(db.session, seq, passingdata, aa_attr_instance)
seq = '' #set to nothing to avoid saving one more RawSequence
new_fasta_block = 1
break #start from while again
seq += line.strip()
if len(seq)>=chunk_size:
seq_to_db = seq[:chunk_size]
self.saveRawSequence(db.session, seq_to_db, passingdata, aa_attr_instance)
seq = seq[chunk_size:] #remove the one already in db
if self.report:
sys.stderr.write("%s\t%s\t%s"%('\x08'*20, no_of_fasta_blocks, passingdata.current_start/chunk_size+1))
if seq: # last segment from last line
self.saveRawSequence(db.session, seq, passingdata, aa_attr_instance)
aa_attr_instance.stop = passingdata.current_stop
db.session.add(aa_attr_instance)
db.session.flush()
no_of_fasta_blocks += 1
if no_of_fasta_blocks>=maxNoOfFastaRecords:
break
sys.stderr.write(" Number of fasta blocks/chromosomes: %s.\n"%(no_of_fasta_blocks))
del inf
def run(self):
"""
"""
if self.debug:
import pdb
pdb.set_trace()
"""
2012.4.3
the output of samtools flagstat looks like:
2725130 + 0 in total (QC-passed reads + QC-failed reads)
0 + 0 duplicates
2725130 + 0 mapped (100.00%:-nan%)
2725130 + 0 paired in sequencing
1360823 + 0 read1
1364307 + 0 read2
576948 + 0 properly paired (21.17%:-nan%)
609252 + 0 with itself and mate mapped
2115878 + 0 singletons (77.64%:-nan%)
0 + 0 with mate mapped to a different chr
0 + 0 with mate mapped to a different chr (mapQ>=5)
"""
inf = utils.openGzipFile(self.inputFname, openMode="r")
writer = csv.writer(utils.openGzipFile(self.outputFname, openMode="w"), delimiter="\t")
header = [
"alignmentID",
"total_no_of_reads",
"perc_reads_mapped",
"perc_duplicates",
"perc_paired",
"perc_properly_paired",
"perc_both_mates_mapped",
"perc_singletons",
"perc_mapped_to_diff_chrs",
"perc_mapq5_mapped_to_diff_chrs",
]
writer.writerow(header)
total_no_of_reads = float(
self.getNumberOutOfFlagStatLine(inf.next())
) # float it now so that no "float" upon division
no_of_duplicates = self.getNumberOutOfFlagStatLine(inf.next())
no_of_mapped = self.getNumberOutOfFlagStatLine(inf.next())
no_of_paired = self.getNumberOutOfFlagStatLine(inf.next())
no_of_read1 = self.getNumberOutOfFlagStatLine(inf.next())
no_of_read2 = self.getNumberOutOfFlagStatLine(inf.next())
no_of_properly_paired = self.getNumberOutOfFlagStatLine(inf.next())
no_of_both_mates_mapped = self.getNumberOutOfFlagStatLine(inf.next())
no_of_singletons = self.getNumberOutOfFlagStatLine(inf.next())
no_of_mates_mapped_to_diff_chrs = self.getNumberOutOfFlagStatLine(inf.next())
no_of_mates_mapped_to_diff_chrs_mapQAbove5 = self.getNumberOutOfFlagStatLine(inf.next())
#
del inf
data_row = [
self.alignmentID,
total_no_of_reads,
no_of_mapped / total_no_of_reads * 100,
no_of_duplicates / total_no_of_reads * 100,
no_of_paired / total_no_of_reads * 100,
no_of_properly_paired / total_no_of_reads * 100,
no_of_both_mates_mapped / total_no_of_reads * 100,
no_of_singletons / total_no_of_reads * 100,
no_of_mates_mapped_to_diff_chrs / total_no_of_reads * 100,
no_of_mates_mapped_to_diff_chrs_mapQAbove5 / total_no_of_reads * 100,
]
writer.writerow(data_row)
del writer
def traverse(self):
"""
2012.1.9
"""
newHeader = []
key2dataLs = {
} #key is the keyColumn, dataLs corresponds to the sum of each column from valueColumnLs
delimiter = None
for inputFname in self.inputFnameLs:
if not os.path.isfile(inputFname):
if self.exitNonZeroIfAnyInputFileInexistent:
sys.exit(3)
else:
continue
reader = None
try:
inputFile = utils.openGzipFile(inputFname)
delimiter = figureOutDelimiter(inputFile)
reader = MatrixFile(inputFile=inputFile, delimiter=delimiter)
except:
sys.stderr.write('Except type: %s\n' % repr(sys.exc_info()))
import traceback
traceback.print_exc()
try:
#if isCSVReader:
header = reader.next()
#else:
# header = inputFile.readline().strip().split() #whatever splits them
self.handleNewHeader(header,
newHeader,
self.keyColumnLs,
self.valueColumnLs,
keyColumnSet=self.keyColumnSet)
if self.noHeader: #2012.8.10
inputFile.seek(0)
reader = MatrixFile(inputFile=inputFile,
delimiter=delimiter)
except: #in case something wrong (i.e. file is empty)
sys.stderr.write('Except type: %s\n' % repr(sys.exc_info()))
import traceback
traceback.print_exc()
if reader is not None:
for row in reader:
#if not isCSVReader:
# row = row.strip().split()
try:
self.handleValueColumns(
row,
key2dataLs=key2dataLs,
keyColumnLs=self.keyColumnLs,
valueColumnLs=self.valueColumnLs)
except: #in case something wrong (i.e. file is empty)
sys.stderr.write('Ignore this row: %s.\n' % repr(row))
sys.stderr.write('Except type: %s\n' %
repr(sys.exc_info()))
import traceback
traceback.print_exc()
del reader
if self.noHeader: #2012.8.10
newHeader = None
returnData = PassingData(key2dataLs=key2dataLs,
delimiter=delimiter,
header=newHeader)
return returnData
def run(self):
if self.debug:
import pdb
pdb.set_trace()
#['trio_set', 'chromosome', 'pos', 'depthOfFather','depthOfMother', 'depthOfChild', 'isInconsistent']
chr_pos2inconsistentData = {} #key is (chr,pos),
#value is (noOfInconsistencyInTrio, noOfTotalInTrio, noOfInconsistencyInDuo, noOfTotalInDuo)
sys.stderr.write("Reading from %s files ...\n"%(len(self.inputFnameLs)))
for inputFname in self.inputFnameLs:
if not os.path.isfile(inputFname):
continue
reader = None
trioSetStrIndex = None
chromosomeIndex = None
posIndex = None
isInconsistentIndex = None
try:
inputFile = utils.openGzipFile(inputFname)
delimiter = figureOutDelimiter(inputFile)
reader = csv.reader(inputFile, delimiter=delimiter)
header = reader.next()
col_name2index = getColName2IndexFromHeader(header)
trioSetStrIndex = col_name2index.get("#trio_set")
chromosomeIndex = col_name2index.get("chromosome")
posIndex = col_name2index.get("pos")
isInconsistentIndex = col_name2index.get("isInconsistent")
except:
sys.stderr.write('Except type: %s\n'%repr(sys.exc_info()))
import traceback
traceback.print_exc()
if reader is not None and isInconsistentIndex is not None:
for row in reader:
trio_set_str = row[trioSetStrIndex]
chromosome = row[chromosomeIndex]
pos = int(row[posIndex])
isInconsistent = int(row[isInconsistentIndex])
chr_pos = (chromosome, pos)
if chr_pos not in chr_pos2inconsistentData:
chr_pos2inconsistentData[chr_pos] = [0, 0, 0, 0]
#trio_set_ls = trio_set_str.split(',')
if trio_set_str.find("0")==0 or trio_set_str.find(",0")!=-1: #it's a duo. one parent is missing.
chr_pos2inconsistentData[chr_pos][2] += isInconsistent
chr_pos2inconsistentData[chr_pos][3] += 1
else: #it's a trio
chr_pos2inconsistentData[chr_pos][0] += isInconsistent
chr_pos2inconsistentData[chr_pos][1] += 1
sys.stderr.write("Done.\n")
sys.stderr.write("Outputting ...")
writer = csv.writer(open(self.outputFname, 'w'), delimiter='\t')
writer.writerow(['#chromosome', 'pos', 'noOfInconsistencyInTrio', 'noOfTotalInTrio', 'inconsistencyRateInTrio',\
'noOfInconsistencyInDuo', 'noOfTotalInDuo', 'inconsistencyRateInDuo'])
chr_pos_ls = chr_pos2inconsistentData.keys()
chr_pos_ls.sort()
for chr_pos in chr_pos_ls:
chromosome, pos = chr_pos
noOfInconsistencyInTrio, noOfTotalInTrio, noOfInconsistencyInDuo, noOfTotalInDuo = chr_pos2inconsistentData.get(chr_pos)
if noOfTotalInTrio>0:
inconsistencyRateInTrio = noOfInconsistencyInTrio/float(noOfTotalInTrio)
else:
inconsistencyRateInTrio = -1
if noOfTotalInDuo>0:
inconsistencyRateInDuo = noOfInconsistencyInDuo/float(noOfTotalInDuo)
else:
inconsistencyRateInDuo = -1
writer.writerow([chromosome, pos, noOfInconsistencyInTrio, noOfTotalInTrio, inconsistencyRateInTrio,\
noOfInconsistencyInDuo, noOfTotalInDuo, inconsistencyRateInDuo])
del writer
sys.stderr.write("Done.\n")
def traverse(self):
"""
self.noHeader: #2012.8.10
2012.1.9
"""
newHeader = []
key2dataLs = {} #key is the keyColumn, dataLs corresponds to the sum of each column from valueColumnLs
delimiter = None
noOfDataColumnsFromPriorFiles = 0
for inputFname in self.inputFnameLs:
if not os.path.isfile(inputFname):
if self.exitNonZeroIfAnyInputFileInexistent:
sys.exit(3)
else:
continue
reader = None
try:
inputFile = utils.openGzipFile(inputFname)
delimiter = figureOutDelimiter(inputFile)
reader = MatrixFile(inputFile=inputFile, delimiter=delimiter)
except:
sys.stderr.write('Except type: %s\n'%repr(sys.exc_info()))
import traceback
traceback.print_exc()
valueColumnLs = []
try:
header = reader.next()
self.handleNewHeader(header, newHeader, self.keyColumnLs, valueColumnLs, keyColumnSet=self.keyColumnSet)
if self.noHeader: #2012.8.10
inputFile.seek(0)
reader = MatrixFile(inputFile=inputFile, delimiter=delimiter)
except: #in case something wrong (i.e. file is empty)
sys.stderr.write('Except type: %s\n'%repr(sys.exc_info()))
import traceback
traceback.print_exc()
if reader is not None and valueColumnLs:
visitedKeySet = set()
for row in reader:
try:
self.handleValueColumns(row, key2dataLs=key2dataLs, keyColumnLs=self.keyColumnLs, \
valueColumnLs=valueColumnLs, noOfDataColumnsFromPriorFiles=noOfDataColumnsFromPriorFiles, \
visitedKeySet=visitedKeySet)
except: #in case something wrong (i.e. file is empty)
sys.stderr.write('Ignore this row: %s.\n'%repr(row))
sys.stderr.write('Except type: %s\n'%repr(sys.exc_info()))
import traceback
traceback.print_exc()
del reader
#append empty data to keys who are not present in this current "reader" file
totalKeySet = set(key2dataLs.keys())
unvisitedKeySet = totalKeySet - visitedKeySet
for key in unvisitedKeySet:
for i in valueColumnLs:
key2dataLs[key].append('')
noOfDataColumnsFromPriorFiles += len(valueColumnLs)
if self.noHeader: #2012.8.10
newHeader = None
returnData = PassingData(key2dataLs=key2dataLs, delimiter=delimiter, header=newHeader)
return returnData
def parse_chromosome_fasta_file(self, db=None, filename=None, tax_id=None, version=None, chunk_size=10000, \
sequence_type_name=None, sequence_type_id=None, run_type=1,
maxNoOfFastaRecords=500):
"""
2011-7-10
add argument maxNoOfFastaRecords: the max number of fasta records before quitting
2011-7-6
add argument run_type
1: chromosome sequences from NCBI genbank
2: vervet scaffolds from WUSTL
3: full vervet BACs from McGill
2010-12-15
fix a bug that _tax_id shall be used in query AnnotAssembly.
This bug caused the db redundancy check to fail.
2010-12-15
if entry already exists in AnnotAssembly, skip it.
2008-07-29
figure out tax_id via FigureOutTaxID
filename could contain multiple fasta blocks
2008-07-27
change to use data structures from GenomeDB.py
2008-07-06
use the firstline (header) of the fasta file to extract which chromosome. using filename is unreliable.
"""
inf = utils.openGzipFile(filename, openMode='r')
line = inf.readline()
new_fasta_block = 1 #'line' is not enough to stop the 'while' loop. after the file reading is exhausted by "for line in inf:", 'line' still contains the stuff from the last line.
no_of_fasta_blocks = 0
while line and new_fasta_block:
new_fasta_block = 0 #set it to 0, assuming only one fasta block, change upon new fasta block
if line[0]!='>': #not fasta block header
for line in inf: #exhaust this fasta block as it's not what's wanted.
if line[0]=='>':
new_fasta_block = 1
break #start from while again
continue
headerData = self.parseFastaDescriptionDict[run_type](line, self.FigureOutTaxID_ins)
if not headerData.chromosome:
sys.stderr.write("Error chromosome for header %s is empty %s.\n"%(line, headerData.chromosome))
import pdb
pdb.set_trace()
if tax_id is not None and headerData.tax_id and tax_id!=headerData.tax_id:
sys.stderr.write("tax_id (%s) not matching the one given (%s). Ignore.\n"%(headerData.tax_id, tax_id))
line = inf.readline()
new_fasta_block = 1
continue
chromosome = headerData.chromosome
sequence_type = db.getSequenceType(short_name=sequence_type_name, id=sequence_type_id)
start = 1
aa_attr_instance = db.checkAnnotAssembly(version=version, tax_id=tax_id, \
chromosome=chromosome, start=start, stop=None, \
sequence_type_id=sequence_type.id)
if aa_attr_instance and aa_attr_instance.raw_sequence_start_id is not None:
# if raw sequences have been associated with this AnnotAssembly and
sys.stderr.write("raw sequences have been associated with this AnnotAssembly (tax_id %s, chr=%s, start=%s). Ignore.\n"%\
(tax_id, chromosome, start))
line = inf.readline()
new_fasta_block = 1
continue
if aa_attr_instance is None:
aa_attr_instance = db.getAnnotAssembly(gi=headerData.gi, acc_ver=headerData.acc_ver, accession =None, \
version =version, tax_id=tax_id, chromosome =chromosome, \
start =start, stop =None, orientation=None, sequence = None,\
raw_sequence_start_id=None, original_path=os.path.abspath(filename),\
sequence_type_id=sequence_type.id, \
chromosome_type_id=None, chromosome_type_name=None, comment=headerData.comment)
if aa_attr_instance.acc_ver and self.p_acc_ver.search(aa_attr_instance.acc_ver):
aa_attr_instance.accession, aa_attr_instance.version = self.p_acc_ver.search(aa_attr_instance.acc_ver).groups()
aa_attr_instance.version = int(aa_attr_instance.version)
else:
aa_attr_instance.accession = None
aa_attr_instance.version = version
if self.debug:
sys.stderr.write("tax_id=%s for %s.\n"%(aa_attr_instance.tax_id, line))
#aa_attr_instance.raw_sequence_start_id = self.get_current_max_raw_sequence_id(curs, raw_sequence_table)+1
passingdata = PassingData()
passingdata.current_start = 1
passingdata.raw_sequence_initiated = False
seq = ''
for line in inf:
if line[0]=='>':
if seq: #last segment from the previous fasta block
self.saveRawSequence(db.session, seq, passingdata, aa_attr_instance)
seq = '' #set to nothing to avoid saving one more RawSequence
new_fasta_block = 1
break #start from while again
seq += line.strip()
if len(seq)>=chunk_size:
seq_to_db = seq[:chunk_size]
self.saveRawSequence(db.session, seq_to_db, passingdata, aa_attr_instance)
seq = seq[chunk_size:] #remove the one already in db
if self.report:
sys.stderr.write("%s\t%s\t%s"%('\x08'*20, no_of_fasta_blocks, passingdata.current_start/chunk_size+1))
if seq: # last segment from last line
self.saveRawSequence(db.session, seq, passingdata, aa_attr_instance)
aa_attr_instance.stop = passingdata.current_stop
db.session.add(aa_attr_instance)
db.session.flush()
no_of_fasta_blocks += 1
if no_of_fasta_blocks>=maxNoOfFastaRecords:
break
sys.stderr.write(" Number of fasta records/chromosomes: %s.\n"%(no_of_fasta_blocks))
del inf