def main():
seqsD = Fasta.load(sys.argv[1])
seqs = seqsD.values()
for w in range(1,7):
allnmers = permute(w)
nmersT = MotifTools.top_nmers(w,seqs,'with counts','purge Ns')
nmersD = {}
total = 0
for nmer in allnmers:
nmersD[nmer] = 1 #Pseudo count
total = total + 1
for nmer,count in nmersT[:]:
try:
rc = MotifTools.revcomplement(nmer)
nmersD[nmer] = nmersD[nmer] + count
nmersD[rc] = nmersD[rc] + count
total = total + 2*count
except KeyError:
pass
_t = nmersD.keys()
_t.sort()
print "# freq in %s (total %d with pseudocounts)"%(sys.argv[1],total)
for nmer in _t:
print "%-7s %20.17f"%(nmer,float(nmersD[nmer]) / total)
sys.stdout.flush()
def info2seeds(N,infofile,probefile,species='YEAST'):
G = ProbeSet(species)
IDs = G.ids_from_file(probefile)
Q = EM.theMarkovBackground.zeroth()
seqs = Fasta.seqs(infofile)
if not N:
nmers = seqs
else:
nmers= MotifTools.top_nmers(N,seqs)
if len(nmers) > 1000: nmers = nmers[0:1000]
print "Scoring enrichment of %d nmers from %s"%len(nmers,infofile)
sys.stdout.flush()
nmers_scoresT = []
for nmer in nmers:
if nmer.isalpha():
p = G.p_value(nmer,IDs,'') #'verbose'
nmers_scoresT.append((nmer,p))
nmers_scoresT.sort(lambda x,y: cmp(x[1],y[1]))
last = min(20,len(nmers_scoresT))
models = []
for i in range(last):
seq = nmers_scoresT[i][0]
m = MotifTools.Motif('',Q)
m.compute_from_text(seq,0.1)
models.append(m)
for tup in nmers_scoresT[0:40]:
print tup
return(models)
def main():
seqsD = Fasta.load(sys.argv[1])
seqs = seqsD.values()
for w in range(1, 7):
allnmers = permute(w)
nmersT = MotifTools.top_nmers(w, seqs, 'with counts', 'purge Ns')
nmersD = {}
total = 0
for nmer in allnmers:
nmersD[nmer] = 1 #Pseudo count
total = total + 1
for nmer, count in nmersT[:]:
try:
rc = MotifTools.revcomplement(nmer)
nmersD[nmer] = nmersD[nmer] + count
nmersD[rc] = nmersD[rc] + count
total = total + 2 * count
except KeyError:
pass
_t = nmersD.keys()
_t.sort()
print "# freq in %s (total %d with pseudocounts)" % (sys.argv[1],
total)
for nmer in _t:
print "%-7s %20.17f" % (nmer, float(nmersD[nmer]) / total)
sys.stdout.flush()
def main(fastafile, outDirectory): # !! 1/2/09 AD added 'fastafile' var and changed 'if __name__' as way to call this from script.
seqsD = Fasta.load(fastafile)
seqs = seqsD.values()
output = []
for w in range(1,7):
allnmers = permute(w)
nmersT = MotifTools.top_nmers(w,seqs,'with counts','purge Ns')
nmersD = {}
total = 0
for nmer in allnmers:
nmersD[nmer] = 1 #Pseudo count
total = total + 1
for nmer,count in nmersT[:]:
try:
rc = MotifTools.revcomplement(nmer)
nmersD[nmer] = nmersD[nmer] + count
nmersD[rc] = nmersD[rc] + count
total = total + 2*count
except KeyError:
pass
_t = nmersD.keys()
_t.sort()
output.append("# freq in %s (total %d with pseudocounts)\n"%(fastafile.split('/')[-1],total)) # AD 02-27-09 added a '\n' to make file look right
for nmer in _t:
output.append( "%-7s %20.17f\n"%(nmer,float(nmersD[nmer]) / total)) # AD 02-27-09 added a '\n' to make file look right
# open output file and write out results
outFile = '%s/%s.freq' % (outDirectory, fastafile.split('/')[-1])
outFile = open(outFile, 'w')
for index in output:
outFile.write(index)
def loadmotif(infile, trimstart=0, trimend=0):
from TAMO import MotifTools
lines = loadlist(infile)
if lines[0] == "A\tC\tG\tT":
ma = []
for l in lines[1:]:
p = l.split("\t")
ma.append({
'A': float(p[0]),
'C': float(p[1]),
'G': float(p[2]),
'T': float(p[3])
})
if trimend == 0: ma = ma[trimstart:]
else: ma = ma[trimstart:-trimend]
return MotifTools.Motif_from_counts(ma)
elif lines[0][0] in 'ACGT':
if trimend == 0: lines = lines[trimstart:]
else: lines = lines[trimstart:-trimend]
return MotifTools.Motif(lines)
else:
na = []
for line in lines:
na.append(list(map(int, line.split())))
ma = []
for i in range(len(na[0])):
ma.append({
'A': na[0][i],
'C': na[1][i],
'G': na[2][i],
'T': na[3][i]
})
return MotifTools.Motif_from_counts(ma)
def tamo2tamo(file, outname):
global probefile, PROBESET, fsafile
motifs = MotifTools.load(file)
if fsafile:
fsaname = fsafile
else:
fsaname = find_fsa(file)
print '# FSA ', fsaname
fsaD = MotifMetrics.fasta2seqs(fsaname, 'want_dict')
probes = fsaD.keys()
if not probefile:
PROBESET = MotifMetrics.ProbeSet('YEAST')
#PROBESET= pick_genome(fsaname)
#for key,seq in fsaD.items():
# PROBESET.probes[key] = seq
print "# %d motifs" % len(motifs)
for motif in motifs:
#motif.pvalue, motif.church = 1,1 #Comment this!
if motif.pvalue == 1:
motif.pvalue = PROBESET.p_value(motif, probes, 'v')
if motif.church == 1:
motif.church = PROBESET.church(motif, probes, 'v')
#if motif.E_site == None: motif.E_site = PROBESET.E_sitef(motif,probes,3,'v')
#if motif.E_chi2 == None: motif.E_chi2 = PROBESET.E_chi2(motif,probes,None,'v')
#if motif.E_seq == None: motif.E_seq = PROBESET.E_seq(motif,probes,'v')
if motif.ROC_auc == None:
motif.ROC_auc = PROBESET.ROC_AUC(motif, probes, 'v')
#if motif.MNCP == None: motif.MNCP = PROBESET.MNCP(motif,probes,'v')
if motif.frac == None:
motif.frac = PROBESET.frac(motif, probes, 'v', 0.7)
if motif.numbound == 0:
matching = PROBESET.matching_ids(motif, [], factor=0.7)
matchbound = [x for x in matching if x in probes]
motif.numbound = len(probes)
motif.nummotif = len(matching)
motif.numboundmotif = len(matchbound)
if 0 and motif.CRA == None:
try:
pass
CRA, Cfrac = PROBESET.cons_ROC_AUC(motif,
probes,
'v',
tuple='YES')
motif.CRA = CRA
motif.Cfrac = Cfrac
except:
pass
MotifTools.save_motifs(motifs, outname)
def memefiles2tamo(files, tamoname):
global probefile, PROBESET, fsafile
motifs = []
for filename in files:
print ">>>SDFSD>F ",filename
if re.search('\.ace$',filename):
mdobject = AlignAce.AlignAce(filename)
if not mdobject.fastafile: mdobject.fastafile=filename.replace('.ace','.fsa')
elif re.search('\.meme.*$',filename):
mdobject = Meme.Meme(filename)
if not mdobject.fastafile:
mdobject.fastafile=re.sub('\..\.meme','.meme',filename).replace('.meme','.fsa')
motifs.extend(mdobject.motifs)
#fsaname = find_fsa(mdobject.fastafile)
print mdobject.fastafile
if fsafile: fsaname = fsafile
else: fsaname = Fasta.find(mdobject.fastafile)
fsaD = Fasta.load(fsaname)
probes = fsaD.keys()
if not probefile:
PROBESET = MotifMetrics.ProbeSet('YEAST')
#PROBESET= pick_genome(fsaname)
for key,seq in fsaD.items():
PROBESET.probes[key] = seq
for motif in motifs:
if motif.pvalue == 1: motif.pvalue = PROBESET.p_value(motif,probes,'v')
if motif.church == 1: motif.church = PROBESET.church(motif,probes,'v')
#if motif.E_site == None: motif.E_site = PROBESET.E_sitef(motif,probes,3,'v')
#if motif.E_chi2 == None: motif.E_chi2 = PROBESET.E_chi2(motif,probes,None,'v')
#if motif.E_seq == None: motif.E_seq = PROBESET.E_seq(motif,probes,'v')
if motif.ROC_auc== None: motif.ROC_auc= PROBESET.ROC_AUC(motif,probes,'v')
#if motif.MNCP == None: motif.MNCP = PROBESET.MNCP(motif,probes,'v')
if motif.frac == None: motif.frac = PROBESET.frac(motif,probes,'v',0.7)
if re.search('\.meme$',filename):
motif.MAP = -math.log(motif.evalue)/math.log(10)
if 0 and (motif.CRA == None):
try:
pass
CRA, Cfrac = PROBESET.cons_ROC_AUC(motif,probes,'v',tuple='YES')
motif.CRA = CRA
motif.Cfrac = Cfrac
except: pass
if re.search('\.meme$',filename):
mdobject.motifs.sort(lambda x,y: cmp(x.pvalue, y.pvalue))
else:
mdobject.motifs.sort(lambda x,y: cmp(x.church, y.church))
MotifTools.save_motifs(motifs,tamoname)
def tamo2tf(TAMO_file):
'''Converts TAMO files to the TRANSFAC format
'''
ml = MotifTools.txt2motifs(TAMO_file)
TAMO_file_name = TAMO_file.split("/")[-1]
ACGT = ["A", "C", "G", "T"]
n = 1
oup = open("%s.tf" % (TAMO_file), "w")
for m in ml:
if m.source == "":
oup.write("DE\t%s_%s\t%s_%s\n" %
(TAMO_file_name, n, TAMO_file_name, n))
else:
oup.write("DE\t%s\t%s\n" % (m.source, m.source))
count = 0
#print m.source
for i in range(m.width):
oup.write("%s\t" % count)
for letter in ACGT:
if m.logP:
Pij = pow(2.0, m.logP[i][letter])
oup.write("%s\t" % int(Pij * 100))
oup.write("\n")
count += 1
oup.write("XX\n")
n += 1
oup.close()
def averagemotifs(motifs,ovlp=2,template=None,DFUNC=negcommonbitsrange,VERBOSE=1,prop=''):
if not template:
Dmat = computeDmat(motifs)
idx = centroididx(Dmat)
template = motifs[idx]
for m in motifs:
off, rc = minshortestoverhangdiff(template,m,OVLP(template,m),'want_offset',DFUNC=DFUNC)
m.offset = off
m.rc = rc
#Find most negative offset
offsets = [m.offset for m in motifs] ; offsets.sort()
maxposs = [(m.offset + m.width) for m in motifs] ; maxposs.sort()
minpos = -offsets[0]
maxpos = maxposs[-1] + minpos
pmotifs = []
for m in motifs:
if m.rc: _m = m.revcomp()
else : _m = m
leftpad = minpos + m.offset
rightpad = maxpos - (leftpad + m.width)
padded = _m[-leftpad,_m.width+rightpad]
#print '%s%s%s\t%s'%('*'*leftpad,_m.oneletter,'*'*rightpad,padded)
pmotifs.append(padded)
AVE = MotifTools.sum(pmotifs,[])
if VERBOSE:
for m in pmotifs:
d = minshortestoverhangdiff(AVE,m,OVLP(AVE,m),DFUNC=DFUNC)
print '%s %5.3f'%(m.oneletter,d),
if m.__dict__.has_key('key'): print m.key,
if prop and m.__dict__.has_key(prop): print m.__dict__[prop],
print
print '-'*m.width
return AVE
def __init__(self,seed_seqs, all_seqs, width = 6, verbose = ''):
self.seed_seqs = seed_seqs #Sequences to be scanned for seeds
self.seqs = all_seqs
self.candidates = []
self.models = [] #Set directly or computed from seed_seqs
self.width = width
self.verbose = verbose
if width:
self.goodwmersT = MotifTools.top_nmers(self.width,self.seed_seqs,1,"")
else:
self.goodwmersT = zip(self.seed_seqs,range(len(self.seed_seqs)))
self.bgprob = {'A': 0.31, 'C': .19, 'G': .19, 'T': .31}
self.beta = 0.001
self.deltamin = 1e-3
self.probes = []
self.method = "ZOOPS" # OOPS or ZOOPS )
self.param = {}
self.gapflank = 0
self.gapweight = 0.2
self.seedbeta = 0.02
self.joint = 1
global theMarkovBackground
if theMarkovBackground:
self.bgprob = theMarkovBackground.zeroth()
'''DELETE
def parse_opts():
global GLOBALS
global DFUNC, DMAX
short_opts = 'm:'
long_opts = ['dfunc:']
try: opts, args = getopt.getopt(sys.argv[1:], short_opts, long_opts)
except getopt.GetoptError:
print getopt.GetoptError.__dict__
usage()
if not opts: usage()
GLOBALS['args'] = args
GLOBALS['motifs'] = []
DFUNCtxt = None
for opt,value in opts:
if opt == '-m': GLOBALS['motifs'] = MotifTools.txt2motifs(value)
if opt == '--dfunc': DFUNCtxt = value
if opt == '-d': DMAX = float(value)
# Deal with DFUNC and DMAX
if DFUNCtxt == 'NCB':
_DFUNC = MotifCompare.negcommonbits
elif DFUNCtxt:
try:
exec ("_DFUNC = MotifCompare.%s"%DFUNCtxt)
except:
usage("No such distance metric: %s"%DFUNCtxt)
if _DFUNC: set_dfunc(_DFUNC,DMAX)
def tamo2tamo(file, outname):
global probefile, PROBESET, fsafile
motifs = MotifTools.load(file)
if fsafile:
fsaname = fsafile
else:
fsaname = find_fsa(file)
print '# FSA ',fsaname
fsaD = MotifMetrics.fasta2seqs(fsaname,'want_dict')
probes = fsaD.keys()
if not probefile:
PROBESET = MotifMetrics.ProbeSet('YEAST')
#PROBESET= pick_genome(fsaname)
#for key,seq in fsaD.items():
# PROBESET.probes[key] = seq
print "# %d motifs"%len(motifs)
for motif in motifs:
#motif.pvalue, motif.church = 1,1 #Comment this!
if motif.pvalue == 1: motif.pvalue = PROBESET.p_value(motif,probes,'v')
if motif.church == 1: motif.church = PROBESET.church(motif,probes,'v')
#if motif.E_site == None: motif.E_site = PROBESET.E_sitef(motif,probes,3,'v')
#if motif.E_chi2 == None: motif.E_chi2 = PROBESET.E_chi2(motif,probes,None,'v')
#if motif.E_seq == None: motif.E_seq = PROBESET.E_seq(motif,probes,'v')
if motif.ROC_auc== None: motif.ROC_auc= PROBESET.ROC_AUC(motif,probes,'v')
#if motif.MNCP == None: motif.MNCP = PROBESET.MNCP(motif,probes,'v')
if motif.frac == None: motif.frac = PROBESET.frac(motif,probes,'v',0.7)
if motif.numbound == 0:
matching = PROBESET.matching_ids(motif,[],factor=0.7)
matchbound = [x for x in matching if x in probes]
motif.numbound = len(probes)
motif.nummotif = len(matching)
motif.numboundmotif = len(matchbound)
if 0 and motif.CRA == None:
try:
pass
CRA, Cfrac = PROBESET.cons_ROC_AUC(motif,probes,'v',tuple='YES')
motif.CRA = CRA
motif.Cfrac = Cfrac
except: pass
MotifTools.save_motifs(motifs,outname)
def pick_chunk_score(wdir, TAMO_file, target, genome):
'''Trims and returns the top motif in a cluster.
This script takes in the TAMO file from the motifs in a single cluster. It
trims the low-information ends from each motifs. It then indentifies the
motif that is most significantly represented in the target genes in your
genome. If no motif is significantly represented, then a blank top motif
file is created.
'''
os.system("cd %s" % wdir)
os.chdir(wdir)
script_dir = '/'.join(os.path.abspath(__file__).split('/')
[:-1]) # path to pcc_merge_CC.py script
##
# step 1 trim tamo to eliminate low information flanking sequence
trim_motif(TAMO_file, 0.1)
##
# step 2 Group Specificity Score" from the Church lab
# python MotifMetrics.py [Genes of interest] -genome [FASTA of promoter sequence] -t [Trimmed TAMO of cluster motifs]
# MotifMetrics.py checks if the motifs appear disproportionatly to the
# targets compared to the rest of the genes.
os.system(
"python %s/MotifMetrics.py %s -genome %s -t %s_0.1.trim -spec > %s_0.1.trim_Cout"
% (script_dir, target, genome, TAMO_file, TAMO_file))
##
# Gets the motif that is most significantly represented in your target genes
# Returns "None" if none of the motifs has a p-value above 0.001.
topm = parse_out_pcs("%s_0.1.trim_Cout" % TAMO_file)
print "topm", topm
##
# Writes the top motif to its own directory.
if topm != "None":
newdic = {}
ml = MotifTools.txt2motifs("%s_0.1.trim" % TAMO_file)
for m in ml:
if m.oneletter == topm:
newdic[m.oneletter] = m
save_motifs(newdic.values(), "%s.TOP" % TAMO_file)
os.system("rm %s_0.1.trim" % TAMO_file)
os.system("rm %s_0.1.trim_Cout" % TAMO_file)
##
# Writes a blank document if there was no top motif.
else:
oup = open("%s.TOP" % TAMO_file, "w")
oup.close()
def ace2tamo(filename, tamoname):
global probefile, PROBESET
if re.search('\.ace$',filename):
mdobject = AlignAce.AlignAce(filename)
elif re.search('\.meme$',filename):
mdobject = Meme.Meme(filename)
fsaname = find_fsa(mdobject.fastafile)
fsaD = MotifMetrics.fasta2seqs(fsaname,'want_dict')
probes = fsaD.keys()
if not probefile:
PROBESET = MotifMetrics.ProbeSet('HUMAN_250')
#PROBESET= pick_genome(fsaname)
for key,seq in fsaD.items():
PROBESET.probes[key] = seq
for motif in mdobject.motifs:
if motif.pvalue == 1: motif.pvalue = PROBESET.p_value(motif,probes,'v')
if motif.church == 1: motif.church = PROBESET.church(motif,probes,'v')
if motif.E_site == None: motif.E_site = PROBESET.E_sitef(motif,probes,3,'v')
#if motif.E_chi2 == None: motif.E_chi2 = PROBESET.E_chi2(motif,probes,None,'v')
if motif.E_seq == None: motif.E_seq = PROBESET.E_seq(motif,probes,'v')
if motif.ROC_auc== None: motif.ROC_auc= PROBESET.ROC_AUC(motif,probes,'v')
if motif.MNCP == None: motif.MNCP = PROBESET.MNCP(motif,probes,'v')
if re.search('\.meme$',filename):
motif.MAP = -math.log(motif.evalue)/math.log(10)
sys.stdout.flush()
i = 0
for motif in mdobject.motifs:
motif.seednum = i ; i=i+1
kmers = motif.bogus_kmers(100)
motif.maxscore = -100
scores = [motif.scan(kmer)[2][0] for kmer in kmers]
print Arith.avestd(scores)
if re.search('\.meme$',filename):
mdobject.motifs.sort(lambda x,y: cmp(x.pvalue, y.pvalue))
else:
mdobject.motifs.sort(lambda x,y: cmp(x.church, y.church))
MotifTools.save_motifs(mdobject.motifs,tamoname)
def ace2tamo(filename, tamoname):
global probefile, PROBESET
if re.search('\.ace$',filename):
mdobject = AlignAce.AlignAce(filename)
elif re.search('\.meme$',filename):
mdobject = Meme.Meme(filename)
fsaname = find_fsa(mdobject.fastafile)
fsaD = MotifMetrics.fasta2seqs(fsaname,'want_dict')
probes = fsaD.keys()
if not probefile:
PROBESET = MotifMetrics.ProbeSet('HUMAN_250')
#PROBESET= pick_genome(fsaname)
for key,seq in fsaD.items():
PROBESET.probes[key] = seq
for motif in mdobject.motifs:
if motif.pvalue == 1: motif.pvalue = PROBESET.p_value(motif,probes,'v')
if motif.church == 1: motif.church = PROBESET.church(motif,probes,'v')
if motif.E_site == None: motif.E_site = PROBESET.E_sitef(motif,probes,3,'v')
#if motif.E_chi2 == None: motif.E_chi2 = PROBESET.E_chi2(motif,probes,None,'v')
if motif.E_seq == None: motif.E_seq = PROBESET.E_seq(motif,probes,'v')
if motif.ROC_auc== None: motif.ROC_auc= PROBESET.ROC_AUC(motif,probes,'v')
if motif.MNCP == None: motif.MNCP = PROBESET.MNCP(motif,probes,'v')
if re.search('\.meme$',filename):
motif.MAP = -math.log(motif.evalue)/math.log(10)
sys.stdout.flush()
i = 0
for motif in mdobject.motifs:
motif.seednum = i ; i=i+1
kmers = motif.bogus_kmers(100)
motif.maxscore = -100
scores = [motif.scan(kmer)[2][0] for kmer in kmers]
print Arith.avestd(scores)
if re.search('\.meme$',filename):
mdobject.motifs.sort(lambda x,y: cmp(x.pvalue, y.pvalue))
else:
mdobject.motifs.sort(lambda x,y: cmp(x.church, y.church))
MotifTools.save_motifs(mdobject.motifs,tamoname)
def trim_motif(TAMO_file, cut=0.4):
'''Trims the motifs in TAMO_file, eliminating low-information flanks.'''
testmotifs = MotifTools.load(TAMO_file)
file = TAMO_file + "_" + str(cut) + ".trim"
new_mlist = []
for motif in testmotifs:
m = motif.trimmed(cut)
new_mlist.append(m)
save_motifs(new_mlist, file)
def TAMO_split(TAMO_file, motifs_per_file=190):
'''This function splits a TAMO into smaller files for create_cc'''
ml = MotifTools.txt2motifs(TAMO_file)
total = len(ml) / int(motifs_per_file) # Total number of TAMOs to generate
by = motifs_per_file
for i in range(total):
print i
print i * by + by, TAMO_file + '_n%s' % i
save_motifs(ml[i * by:i * by + by], TAMO_file + '_n%s' % i)
print total * by, len(ml), TAMO_file + '_n%s' % (total)
save_motifs(ml[total * by:len(ml)], TAMO_file + '_n%s' % (total))
return (total)
def opentamo(fileloc):
'''
Opens a tamo file with MotifTools.load and returns the list of motifs,
except when the input file doesn't exist, in which case it returns an empty list.
Has 1 argument:
- fileloc: a string with the location of the file
'''
try:
return MotifTools.load(fileloc)
except IOError:
return []
def Reduce_Nmers(Info):
print 'COMPUTING Nmers ....'
mseqs = ReduceInfo2seqs(Info,70, lambda L: MotifTools.top_nmers(6,L)[0:3])
print "Combining representative sequences...: "
for i in range(len(mseqs)):
i = i + 1
print '\t%s'%mseqs[i-1],
if (i%5 == 0): print
print
top_seq_pairs = MotifTools.top_nmers(5,mseqs,1)
total_nmers = 0
for (mner,count) in top_seq_pairs:
total_nmers = total_nmers + count
for (nmer,count) in top_seq_pairs[0:8]:
print "RESULT: %s\t%2d (%5.2f%%) occurences: "%(nmer,count,
100*float(count)/total_nmers),
for bsite in Info.query['bsites']:
seq = bsite.cleantxt()
(max,s1,s2) = MotifTools.compare_seqs(nmer,seq)
print ' %s vs %s %4.2f correct'%(s1,s2,max)
def tamofile2motifs(filename):
FID = open(filename,'r')
lines = FID.readlines()
FID.close()
motifs = []
seedD = {}
seedfile = ''
for i in range(len(lines)):
if lines[i][0:10] == 'Log-odds matrix'[0:10]:
w = len(lines[i+1].split())-1
ll = []
for pos in range(w):
ll.append({})
for j in range(0,4):
toks = lines[i+j+2].split()
L = toks[0][1]
for pos in range(w):
ll[pos][L] = float(toks[pos+1])
m = MotifTools.Motif_from_ll(ll)
motifs.append(m)
if lines[i][0:6] == 'Motif '[0:6]:
toks = lines[i].split()
motifs[-1].nseqs = float(re.sub('[\(\)]','',toks[3]))
motifs[-1].totalbits= float(toks[5])
motifs[-1].MAP = float(toks[7])
motifs[-1].seeddist = float(toks[9])
motifs[-1].seednum = int(toks[10][0:-1])
motifs[-1].pvalue = math.pow(10,-float(toks[12]))
if 'ch:' in toks:
motifs[-1].church = math.pow(10,-float(toks[14]))
if lines[i][0:10] == 'Threshold: '[0:10]:
toks = lines[i].split()
motifs[-1].threshold= float(toks[1])
if lines[i][0:5] == 'Seed '[0:5]:
toks = lines[i].split()
id = int(toks[1][0:-1]) #'10:' -> '10'
seedD[id] = toks[2]
if lines[i][0:7] == 'Source: '[0:7]:
motifs[-1].source = lines[i][7:].strip()
if lines[i][0:6] == 'Gamma: '[0:6]:
motifs[-1].gamma = float(lines[i][6:])
if lines[i][0:6] == 'Evalue: '[0:6]:
motifs[-1].evalue = float(lines[i][7:].strip())
if lines[i].find('Using')>=0 and lines[i].find('as seeds')>=0:
'''#Using all (132) motifs in SLT_081503.seeds as seeds:'''
seedfile = lines[i].split()[-3]
for i in range(len(motifs)):
if seedfile: motifs[i].seedfile = seedfile
seednum = motifs[i].seednum
if seedD.has_key(seednum):
motifs[i].seedtxt = seedD[seednum]
return(motifs)
def motifs2tamo(motifs, outname):
global probefile, PROBESET
fsaname = find_fsa(outname)
fsaD = MotifMetrics.fasta2seqs(fsaname,'want_dict')
probes = fsaD.keys()
if not probefile:
PROBESET = MotifMetrics.ProbeSet('YEAST')
#PROBESET= pick_genome(fsaname)
#for key,seq in fsaD.items():
# PROBESET.probes[key] = seq
print "# %d motifs"%len(motifs)
for motif in motifs:
if motif.pvalue == 1: motif.pvalue = PROBESET.p_value(motif,probes,'v')
if motif.church == 1: motif.church = PROBESET.church(motif,probes,'v')
if motif.E_site == None: motif.E_site = PROBESET.E_sitef(motif,probes,3,'v')
#if motif.E_chi2 == None: motif.E_chi2 = PROBESET.E_chi2(motif,probes,None,'v')
if motif.E_seq == None: motif.E_seq = PROBESET.E_seq(motif,probes,'v')
if motif.ROC_auc== None: motif.ROC_auc= PROBESET.ROC_AUC(motif,probes,'v')
if motif.MNCP == None: motif.MNCP = PROBESET.MNCP(motif,probes,'v')
MotifTools.save_motifs(motifs,outname)
def parse_block(name, block):
mat = []
ACGT = {"A": 1, "C": 2, "G": 3, "T": 4}
for i in block:
L = i.strip().split()
D = {'A': 0, 'C': 0, 'T': 0, 'G': 0}
for j in ACGT.keys():
D[j] = float(L[ACGT[j]])
mat.append(D)
m = MotifTools.Motif_from_counts(mat)
m.source = name
#print m._print_p()
return m
def test():
motifs = []
betalist = [0.001, 0.005, 0.01, 0.05, 0.1, 0.5, 1.0, 2.0, 4.0]
for beta in [1.0]:
m = MotifTools.Motif()
m.compute_from_text('GGTTTCAT', beta) #STE12 binding site
print m
m._print_ll()
print "Against Ste12:"
match = validate(m, "STE12", 'V', 'T')
print "Against Fkh2:"
fmatch = validate(m, "FKH2", 'V', 'T')
print beta, match, fmatch
def freq_from_seqs_old(self,seqs):
self.highestorder = 4
for depth in range(1,6):
nmersT = MotifTools.top_nmers(depth, seqs, "TUPLES")
self.nmers_by_size[depth] = map(lambda x:x[0],nmersT)
total = 0
for nmer,count in nmersT:
total = total + count
for nmer,count in nmersT:
rc = MotifTools.revcomplement(nmer)
if nmer == rc: #correct top_nmers
f = float(count)/total #palindrome count
else:
f = float(count)/total/2
self.F[nmer] = f
self.F[rc] = f
for depth in range(0): #For debugging
total = 0
for k in self.F.keys():
if len(k) == depth:
total = total + self.F[k]
print k, self.F[k]
print depth,total
def alignAndCombineMotifs(motifs, weights):
# zip motifs and weights
simMotifs = zip(motifs, weights)
# sort by weights
simMotifs.sort(key=lambda x: abs(x[1]))
simMotifs.reverse()
aligned = alignSimilarMotifs([x[0] for x in simMotifs], minoverlap=4)
#print '--'
#for each in aligned: print each.oneletter
#print '\n'
comboMotif = MotifTools.sum(aligned,[-x[1] for x in simMotifs])
return comboMotif
def combine_distance_matrix_for_2(wdir, TAMO_file_1, TAMO_file_2):
'''Combines matricies made from two TAMO files.
This script is used to create the final matrix after all jobs from
create_cc_for_2 are complete.
'''
ml_1 = MotifTools.txt2motifs(TAMO_file_1)
ml_2 = MotifTools.txt2motifs(TAMO_file_2)
n_split_1 = len(ml_1) / 100
n_split_2 = len(ml_2) / 100
print n_split_1, len(ml_1)
print n_split_2
# Change to the working directory.
os.system("cd %s" % wdir)
os.chdir(wdir)
# This loop will paste together matricies
for i in range(n_split_1 + 1):
com = "paste "
for j in range(n_split_2 + 1):
com += "%s_n%s-%s_n%s.dm " % (TAMO_file_1, i, TAMO_file_2, j)
com += "> distance_%s" % i
print com
os.system(com)
#
com = "cat "
for i in range(n_split_1 + 1):
com += "distance_%s " % i
com += "> %s-%s.dm" % (TAMO_file_1, TAMO_file_2)
print com
os.system(com)
def parse_opts():
global GLOBALS
short_opts = 'm:g:'
long_opts = ['genome=','top=']
try: opts, args = getopt.getopt(sys.argv[1:], short_opts, long_opts)
except getopt.GetoptError:
print getopt.GetoptError.__dict__
usage()
if not opts: usage()
GLOBALS['args'] = args
for opt,value in opts:
if opt == '-m': GLOBALS['motifs'] = MotifTools.txt2motifs(value)
if opt in ['-g', '--genome']: GLOBALS['genomefile'] = value
if opt == '--top': GLOBALS['top'] = int(value)
def Read_Dreme_PSSM(lines):
pwm = []
name = "Dreme Motif";
vals = []
for line in lines.split('\n'):
for item in line.split():
vals.append(float(item))
pwm.append(vals)
vals = [];
#print pwm
m = MotifTools.toDict(pwm)
motif = MotifTools.Motif_from_counts(m)
return motif;
def study_seqs(self,seqs):
for depth in range(1,6):
nmersT = MotifTools.top_nmers(depth, seqs, "TUPLES")
total = 0
for nmer,count in nmersT:
total = total + count
rc = MotifTools.revcomplement(nmer)
for nmer,count in nmersT:
f = math.log(float(count)/total)/math.log(2)
f_2 = math.log(0.5 * float(count)/total)/math.log(2)
rc = MotifTools.revcomplement(nmer)
if rc != nmer:
self.D[nmer] = f_2
self.D[rc] = f_2
else:
self.D[nmer] = f
for depth in range(0):
total = 0
for k in self.D.keys():
if len(k) == depth:
total = total + pow(2,self.D[k])
print k, pow(2,self.D[k])
print depth,total
self.highestorder = 5
def freq_from_seqs(self,seqs):
self.highestorder = 6
for w in range(1,7):
allnmers = permute(w)
nmersT = MotifTools.top_nmers(w,seqs,'with counts','purge Ns')
self.nmers_by_size[w] = allnmers[:]
nmersD = {}
total = 0.0
for nmer in allnmers: #Pseudo count
nmersD[nmer] = 1
total = total + 1
for nmer,count in nmersT:
try:
rc = MotifTools.revcomplement(nmer)
nmersD[nmer] = nmersD[nmer] + count
nmersD[rc] = nmersD[rc] + count
total = total + 2*count
except KeyError:
pass
for nmer in nmersD.keys():
rc = MotifTools.revcomplement(nmer)
f = nmersD[nmer]/total
self.F[nmer] = f
self.F[rc] = f
def Make_PWM_Motif(filename, motifBackGround=""): #print "# Reading PWM from: [%s]"%filename name, pwm = Read_PWM(filename) m = MotifTools.toDict(pwm) #print m motif = MotifTools.Motif_from_ll(m); motif.source = name #print "Motif:", motif.source #print "Max Motif Score:", motif.maxscore #print "Motif Summary:", motif.summary() #motif.printlogo(2.3,10) return motif
def averagemotifs(motifs,
ovlp=2,
template=None,
DFUNC=negcommonbitsrange,
VERBOSE=1,
prop=''):
if not template:
Dmat = computeDmat(motifs)
idx = centroididx(Dmat)
template = motifs[idx]
for m in motifs:
off, rc = minshortestoverhangdiff(template,
m,
OVLP(template, m),
'want_offset',
DFUNC=DFUNC)
m.offset = off
m.rc = rc
#Find most negative offset
offsets = [m.offset for m in motifs]
offsets.sort()
maxposs = [(m.offset + m.width) for m in motifs]
maxposs.sort()
minpos = -offsets[0]
maxpos = maxposs[-1] + minpos
pmotifs = []
for m in motifs:
if m.rc: _m = m.revcomp()
else: _m = m
leftpad = minpos + m.offset
rightpad = maxpos - (leftpad + m.width)
padded = _m[-leftpad, _m.width + rightpad]
#print '%s%s%s\t%s'%('*'*leftpad,_m.oneletter,'*'*rightpad,padded)
pmotifs.append(padded)
AVE = MotifTools.sum(pmotifs, [])
if VERBOSE:
for m in pmotifs:
d = minshortestoverhangdiff(AVE, m, OVLP(AVE, m), DFUNC=DFUNC)
print '%s %5.3f' % (m.oneletter, d),
if m.__dict__.has_key('key'): print m.key,
if prop and m.__dict__.has_key(prop): print m.__dict__[prop],
print
print '-' * m.width
return AVE
def showdiffXvert(motif, seq, OVLP_FCN=None, DIFF_FCN=None):
'''
The funtion converts the sequence to a Motif, computes the D
of the best alignment, and prints the alignment that generated
that D.
'''
MSOdiff = minshortestoverhangdiff
if not OVLP_FCN: OVLP_FCN = lambda A, B: min(min(A.width, B.width) - 1, 7)
bg = motif.background
other = MotifTools.Motif_from_text(seq, bg=bg)
ovlp = OVLP_FCN(motif, other)
diff = MSOdiff(motif, other, ovlp, DFUNC=DIFF_FCN)
offset, rcflag = MSOdiff(motif, other, ovlp, 'want_offset', DFUNC=DIFF_FCN)
if rcflag: m = other.revcomp()
else: m = other
print 'MSOdiff: %8.4f %s%s%s' % (diff, ' ' * 15, motif.oneletter, ' ' *
(30 - motif.width))
print ' %8s %s%s%s' % (' ', ' ' *
(15 + offset), m.oneletter, ' ' *
(30 - offset - other.width))
return diff
def main():
fsa_fcn = up_and_no_N
parse()
FID = open(sys.argv[1])
tokss = [x.strip().split(',') for x in FID.readlines()]
FID.close()
D = {}
for expt,motif,score,source in tokss:
print expt,motif
if expt == 'Category': continue
if motif == 'x': continue
motif = MotifTools.Motif_from_text(motif)
motif.kellis = float(score)
motif.source = source
try: D[expt].append(motif)
except: D[expt] = [motif]
for expt,motifs in D.items():
root = expt
ext = 'cons'
if root[0:3] == 'Rnd':
num = re.sub('.*_','',root)
if len(num) == 1:
root = re.sub('_','_00',root)
else:
root = re.sub('_','_0',root)
root = re.sub('Rnd','random_',root)
outname = '%s.t%s'%(root,ext)
print '%-18s --> %s'%(root,outname)
sys.stdout.flush()
motifs2tamo(motifs,outname)
try:
pass
#tamo2tamo(filename,outname)
except:
print "Error: Could not convert %s [[ %s ]]"%(
filename, outname)
def memefiles2tamo(files, tamoname):
global probefile, PROBESET
motifs = []
for filename in files:
print ">>>SDFSD>F ", filename
if re.search('\.ace$', filename):
mdobject = AlignAce.AlignAce(filename)
if not mdobject.fastafile:
mdobject.fastafile = filename.replace('.ace', '.fsa')
elif re.search('\.meme.*$', filename):
mdobject = Meme.Meme(filename)
if not mdobject.fastafile:
mdobject.fastafile = re.sub('\..\.meme', '.meme',
filename).replace('.meme', '.fsa')
motifs.extend(mdobject.motifs)
#fsaname = find_fsa(mdobject.fastafile)
print mdobject.fastafile
fsaname = Fasta.find(mdobject.fastafile)
fsaD = Fasta.load(fsaname)
probes = fsaD.keys()
if not probefile:
PROBESET = MotifMetrics.ProbeSet('YEAST')
#PROBESET= pick_genome(fsaname)
for key, seq in fsaD.items():
PROBESET.probes[key] = seq
for motif in motifs:
if motif.pvalue == 1:
motif.pvalue = PROBESET.p_value(motif, probes, 'v')
if motif.church == 1:
motif.church = PROBESET.church(motif, probes, 'v')
if motif.E_site == None:
motif.E_site = PROBESET.E_sitef(motif, probes, 3, 'v')
#if motif.E_chi2 == None: motif.E_chi2 = PROBESET.E_chi2(motif,probes,None,'v')
#if motif.E_seq == None: motif.E_seq = PROBESET.E_seq(motif,probes,'v')
if motif.ROC_auc == None:
motif.ROC_auc = PROBESET.ROC_AUC(motif, probes, 'v')
if motif.MNCP == None: motif.MNCP = PROBESET.MNCP(motif, probes, 'v')
if motif.frac == None:
motif.frac = PROBESET.frac(motif, probes, 'v', 0.7)
if re.search('\.meme$', filename):
motif.MAP = -math.log(motif.evalue) / math.log(10)
if 1 and (motif.CRA == None):
try:
pass
CRA, Cfrac = PROBESET.cons_ROC_AUC(motif,
probes,
'v',
tuple='YES')
motif.CRA = CRA
motif.Cfrac = Cfrac
except:
pass
if re.search('\.meme$', filename):
mdobject.motifs.sort(lambda x, y: cmp(x.pvalue, y.pvalue))
else:
mdobject.motifs.sort(lambda x, y: cmp(x.church, y.church))
MotifTools.save_motifs(motifs, tamoname)
def all_Wmers(self,N,seq):
forw = []
rev = []
seqrc = MotifTools.revcomplement(seq)
Mlh = theMarkovBackground.highestorder
Mlb = theMarkovBackground.logbackground
MCP = theMarkovBackground.CP
Fbg = Mlb(seq)
Rbg = Mlb(seqrc)
nmask = map(lambda x:1-x, self.mask)
'''
?? QUESTION: Is it sensible to compute the background probabilities
this way?
1) BG of complementary strand is taken as equal to primary strand.
2) Letters inside the motif window are not used for conditional probabilities.
As a result, the calculation essentially breaks down to the log probability the
background emits the sequence to the left of the window plus the log probability
the background emits the sequence to the right.
3) I\'ve worked out an efficient way to compute this by
a) Compute the background probability for the entire probe/sequence
b) (Quick) Compute logQdiff below
c) Subtract
'''
for i in range(len(seq)-N+1):
subseq = seq[i:i+N]
'''Build Wmer information'''
#Wtmp = Wmer(subseq)
left = seq[0:i]
right = seq[i+N:]
#Wtmp.lflank = left
#Wtmp.rflank = right
#if i==0: Wtmp.src = seq
#Wtmp.srcQ = Fbg
#Wtmp.i = i
'''This is the fast way'''
logQdiff = Mlb(left[-Mlh:] + subseq + right[0:Mlh]) - Mlb(left[-Mlh:]) - Mlb(right[0:Mlh])
logQtot = Fbg - logQdiff
'''Add a bit back for intervening bases in the "gap" '''
gapbg = 0
for p in range(N):
gapbg = gapbg + MCP[subseq[p]] * nmask[p]
logQtot = logQtot + gapbg
'''Build Wmer-reverse complement information'''
#Wtmprc = Wmer(Wtmp.rc)
#Wtmprc.lflank = seqrc[0:-(i+N)] #Check this in case it is ever necessary
#if i!=0:
# Wtmprc.rflank = seqrc[-i:] #Necessary [11-12-02]
#else:
# Wtmprc.rflank = ''
#Wtmprc.logQtot = Wtmp.logQtot
#Wtmprc.srcQ = Wtmp.srcQ
#Wtmprc.i = i
forw.append(logQtot)
rev.append(logQtot)
W = []
W.extend(forw)
W.extend(rev)
#seq.c_wmerbgs = MDsupport.list2double(map(lambda x: x.logQtot, W))
#MDsupport.printdouble(seq.c_wmerbgs,len(W))
return(W)
def merge_runs(TAMO_file, wdir, height, distance, ancestor, target, genome):
'''This script is used to merge motifs with the PCC matrix of all motifs.
The script was originally written by Cheng Zou, and then converted to a
function by Alex Seddon.
'''
print "Here are the parameters you specified in this run "
print "-tamo %s" % TAMO_file
print "-wdir %s" % wdir
print "-h height to cut the tree, %s" % height
print "-distance %s" % distance
print "-ancestor %s" % ancestor
print "-target %s" % target
print "-genome %s" % genome
if TAMO_file == '' or wdir == '':
help()
os.system("cd %s" % wdir)
os.chdir(wdir)
# This code was in the original clustering script. It has been taken out
# because the processes involved take too long and have been replaced by
# the matrix creation scripts and the run_UPGMA script.
#if distance==0:
# os.system("python /mnt/home/seddonal/scripts/5_motif_merging/3.calculate_distance_matrix.py -i %s --dfunc pccrange" % TAMO_file)
#os.system("R --vanilla --slave --args %s.dm %s< /mnt/home/seddonal/scripts/5_motif_merging/UPGMA_final.R> %s.Rout" % (TAMO_file,height,TAMO_file))
cl_dic = {}
n = 0
# The file, TAMO_file.dm_UPGMA_Cl_0.05, is inorder of the motifs that appear
# in the TAMO_file. If two motifs have the same number, they are considered
# a part of the same cluster.
# This loop pulls the clustering information out of this file and creats
# the dictionary cl_dic = {cluster_index:{motif_index:'1'}}
for line in open("%s.dm_UPGMA_Cl_%s" % (TAMO_file, height), "r"):
# Gets the clusterindex of this motif
cl = line.strip()
# Adds the cluster index if it has not been
if not cl_dic.has_key(cl):
cl_dic[cl] = {}
cl_dic[cl][n] = "1" # Adds the motif to that cluster
n += 1 # Increases the motif index for the next motif
#print cl_dic
ml = MotifTools.txt2motifs(TAMO_file)
old = [] # List of motifs that are the sole members of a cluster.
# I think I can divide up this portion of the code to create a series
print ancestor, ancestor == 0
if ancestor == 0:
# This loop Looks at each cluster and attempts to merge the motifs
# in the cluster if there are multiple motifs.
for i in cl_dic.keys():
print i, cl_dic[i]
# If there are multiple motifs in the cluster, it merges the motifs
if len(cl_dic[i]) > 1:
# Adds all of the motifs in the cluster to an object called
# mlist.
mlist = []
for j in cl_dic[i]:
mlist.append(ml[j])
# Saves these motifs to there own TAMO file.
save_motifs(mlist, "%s_sub_%s.tm" % (TAMO_file, i))
# I am fairly certain that this process of converting to TF and
# then returning it to TAMO format is only for keeping the names
# consistent. I need to verify this suspicion
tamo2tf("%s_sub_%s.tm" % (TAMO_file, i))
os.system("cat %s_sub_%s.tm.tf > %s_sub_%s_sum.tm.tf" %
(TAMO_file, i, TAMO_file, i))
tf2tamo("%s_sub_%s_sum.tm.tf" % (TAMO_file, i))
# Gets the top motif in the cluster.
pick_chunk_score(wdir,
'%s_sub_%s_sum.tm.tf.tm' % (TAMO_file, i),
target, genome)
# Removes the files that were created.
os.system("rm %s_sub_%s_sum.tm.tf.tm" % (TAMO_file, i))
os.system("rm %s_sub_%s_sum.tm.tf" % (TAMO_file, i))
os.system("rm -R %s_sub_%s.tm.tf_ST*" % (TAMO_file, i))
# If there is only one motif in the cluster, it leaves it alone,
# And adds it to old
else:
key = cl_dic[i].keys()[0]
old.append(ml[key])
if ancestor == 1:
# This loop Looks at each cluster and attempts to merge the motifs
# in the cluster if there are multiple motifs.
for i in cl_dic.keys():
print i, cl_dic[i]
# If there are multiple motifs in the cluster, it merges the motifs
if len(cl_dic[i]) > 1:
# Adds all of the motifs in the cluster to an object called
# mlist.
mlist = []
for j in cl_dic[i]:
mlist.append(ml[j])
# Saves these motifs to there own TAMO file.
save_motifs(mlist, "%s_sub_%s.tm" % (TAMO_file, i))
# Merges the motifs in the same cluster using STAMP
tamo2tf("%s_sub_%s.tm" % (TAMO_file, i))
# Gets the JASPER motifs that best match the motifs from within
# the cluster.
os.system(
"STAMP -tf %s_sub_%s.tm.tf -sd /home/chengzou/bin/STAMP/ScoreDists/JaspRand_PCC_SWU.scores \
-go 1000 -ge 1000 -cc PCC -align SWU -out %s_sub_%s.tm.tf_STout -chp > %s_sub_%s.tm.tf_STout.log"
% (TAMO_file, i, TAMO_file, i, TAMO_file, i))
parse_out_STAMP(TAMO_file, i)
# combines the JASPER motifs with the cluster motif and then
# converts them all to one TAMO file
os.system(
"cat %s_sub_%s.tm.tf %s_sub_%s.tm.tf_SToutFBP.txt.mod %s_sub_%s.tm.tf_STout_tree_clusters.txt > %s_sub_%s_sum.tm.tf"
% (TAMO_file, i, TAMO_file, i, TAMO_file, i, TAMO_file, i))
tf2tamo("%s_sub_%s_sum.tm.tf" % (TAMO_file, i))
# Gets the top motif within the TAMO file.
pick_chunk_score(wdir,
'%s_sub_%s_sum.tm.tf.tm' % (TAMO_file, i),
target, genome)
# Removes any files created in the processing.
os.system("rm %s_sub_%s_sum.tm.tf.tm" % (TAMO_file, i))
os.system("rm %s_sub_%s_sum.tm.tf" % (TAMO_file, i))
os.system("rm -R %s_sub_%s.tm.tf_ST*" % (TAMO_file, i))
else:
key = cl_dic[i].keys()[0]
old.append(ml[key])
# Combine together the top motifs from every
os.system("cat %s_sub_*_sum.tm.tf.tm.TOP > %s_sub_new.tm" %
(TAMO_file, TAMO_file))
save_motifs(old, "%s_sub_old.tm" % (TAMO_file))
os.system("cat %s_sub_old.tm %s_sub_new.tm > %s_P1.tm" %
(TAMO_file, TAMO_file, TAMO_file))
genelist = argv[1].split('/')[-1]
allclusters = argv[1] + '/' + genelist + '_allclusters.tamo'
#print genelist
oneletters = argv[1] + '/other/' + genelist + '_oneletter.tmp'
symbols = argv[1] + '/other/' + genelist + '_symbols.tmp'
# Open output files for writing
oneletters = open(oneletters, 'w')
symbols = open(symbols, 'w')
# Define output variables
oneletterlist = []
symbolstring = '1234567890ABCDEFGHIJKLMNOPQRSTUVWXYZ*+.,:;!'
# Open list
motiflist = MotifTools.load(allclusters)
# Try to verify the initial list is not too long
if len(motiflist) > len(symbolstring):
# If the list is too long, raise an exception so that the program quits
raise ValueError("The cluster list is too long for sitemap.py")
# If the list is not too long, adjust the symbols string to the appropriate length
else:
symbolstring = symbolstring[:len(motiflist)]
# Save symbol string in the symbols file and close that file
symbols.write(symbolstring)
symbols.close()
# Add oneletter summaries to the list
for num in range(len(motiflist)):
def EM_Cstart(self):
verbose = self.verbose
if verbose:
print "Seeding models..."
sys.stdout.flush()
self.seed_models()
#Initialize parameters
if not self.param.has_key('gamma'): self.param['gamma'] = 0.2
timings = {'Probes':0, 'Background':0, 'C EM':0, 'Post':0}
_time = time.time()
for seq in self.seqs:
P = Probe(seq)
self.probes.append(P)
_time2 = time.time(); timings['Probes'] = _time2-_time; _time = _time2
if verbose: print "Optimizing candidates by EM."
if verbose: sys.stdout.flush()
c_logZ_sets = {}
for Model,i in zip(self.models,range(len(self.models))):
width = Model.width
self.calcmask(width)
if not c_logZ_sets.has_key(width):
c_logZs_set = []
if verbose: print "#%s |%s|"%(' '*28,'-'*len(self.seqs))
if verbose: sys.stdout.flush()
if verbose: print "Computing background (width %2d) "%width,
for P in self.probes:
if verbose: sys.stdout.write('.')
if verbose: sys.stdout.flush()
logZs = self.all_Wmers(width,P)
c_logZs = MDsupport.list2double(logZs)
c_logZs_set.append(c_logZs)
#P.c_wmerbgs = MDsupport.list2double(map(lambda x: x.logQtot, Wlist))
c_logZ_sets[width] = c_logZs_set
if verbose: print
c_logZ_set = c_logZ_sets[width]
for P,c_logZs in zip(self.probes,c_logZ_set):
P.c_wmerbgs = c_logZs
_time2 = time.time()
timings['Background'] = timings['Background'] +_time2-_time
_time = _time2
'''Perform EM'''
_time = time.time()
newModel = self.EM_C(Model, self.probes)
_time2 = time.time(); timings['C EM'] = timings['C EM'] + _time2-_time; _time = _time2
#print "cLL: ",newModel.joint
#print "pLL: ",self.compute_joint(newModel,Wmers_by_seq)
'''Was there a problem?'''
if newModel == None:
continue
'''Set various things in PSSM'''
#Distance(s)
seeddist = MotifTools.infomaskdiff(newModel,Model)
print '%s ----> %s'%(Model,newModel)
print "Seed %2d: %s --> %s mask:%9.5f infoMask:%9.5f d:%9.5f"%(
i, Model, newModel,
MotifTools.maskdiff(newModel,Model),
MotifTools.infomaskdiff(newModel,Model), #order is important
Model-newModel)
#Seed
if Model.seedtxt: newModel.seedtxt = Model.seedtxt
if Model.source: newModel.source = Model.source
#newModel.denoise()
newModel.seeddist = seeddist
newModel.seednum = i
print newModel
newModel._print_p()
newModel._print_ll()
'''Set various things in Candidate (like a wrapper for PSSM)'''
C = MotifCandidate()
C.pssm = newModel.copy()
#C.wmers = self.best_by_Z(Wmers_by_seq)
C.wmers = [newModel.emit() for junk in range(20)]
#C._update() #MAJOR REMOVAL????????? DBG 10-14-03
#C.MAPpurge()
C.pssm = newModel.copy()
self.candidates.append(C)
_time2 = time.time(); timings['Post'] = timings['Post']+_time2-_time;_time = _time2
'''Print Timing Information'''
if verbose:
print "# Timing Information"
_t = 0
for timing in timings.keys():
_t = _t + timings[timing]
for timing in timings.keys():
print "# %12s %f %f%%"%(timing,timings[timing],timings[timing]*100/_t)
# TAMOify kmers and logify pVals
for i in range(len(testMotifs)):
testMotifs[i] = (Motif(testMotifs[i][0]),numpy.log10(float(testMotifs[i][1])))
# Sort on log'd pVals
testMotifs.sort(key=lambda x: x[1])
comboMotifs = []
for i in range(0,int(len(testMotifs)*0.2)):
simMotifs = getKmersWithOneMisMtch(testMotifs[i][0],testMotifs)
alndMotifs = alignSimilarMotifs([x[0] for x in simMotifs])
#for m in simMotifs:
#print m[0].oneletter
comboMotifs.append(MotifTools.sum(alndMotifs,[-x[1] for x in simMotifs])) # -x[1] to convert neg logs to pos weights
print len(comboMotifs)
t2 = time.time()
oFile = '/Users/biggus/Documents/James/Collaborations/Campbell/data/Results_HyperGeoScreen/masked/Results_gGEMS/CCupAt4Days.gte2x.5-16mers.shfSeq.3.gGEMS.tmo'
pFile = '/Users/biggus/Documents/James/Collaborations/Campbell/data/Results_HyperGeoScreen/masked/Results_gGEMS/CCupAt4Days.gte2x.5-16mers.shfSeq.3.gGEMS.pkl'
MotifTools.save_motifs(comboMotifs,oFile,kmer_count=60)
pFile = open(pFile, 'w')
cPickle.dump(comboMotifs,pFile)
t3 = time.time()
print 'Calculations took %.3f min.\nWriting/Pickling took %.3f min.' % ((float(t2)-t1)/60, (float(t3)-t2)/60)
def has_wmer(self,wmer):
rc = MotifTools.revcomplement(wmer)
if (wmer in self.wmers) or (rc in self.wmers):
return(1)
else:
return(0)
def main():
try:
opts, args = getopt.getopt(sys.argv[1:], "f:m:n:L:t:a:S:i:", ["help", "output="]) # AD added 'i'
except getopt.GetoptError:
usage()
sys.exit(1)
if not opts:
usage()
sys.exit(1)
print "#" + ' '.join(sys.argv)
fastafile, motiffile, motifnums, labels, thresh = (None, None, [], None, 0.75) # AD changed thresh val to 0.75 from 0.7
ambigs = []
scale = 50.0 / 1000.0
motifs = []
for opt, value in opts:
#print opt, value
if opt == '-f': fastafile = value
elif opt == '-m': motifs.extend(MotifTools.txt2motifs(value))
elif opt == '-n': motifnums = [int(x) for x in value.split(',')]
elif opt == '-L': labels = list(value)
elif opt == '-t': thresh = float(value)
elif opt == '-a': ambigs.extend(value.split(','))
elif opt == '-S': scale = float(value)
elif opt == '-i': motiffile = value # AD added this option to ACTUALLY supply the tamo motif file at the command-line. The code to deal with motiffiles already existed. There was just no code for User to supply one.
probes = Fasta.load(fastafile)
if motiffile:
for f in motiffile.split(','): # AD added this to allow supplying multiple tamo files at the prompt like you can supply multiple motifs
motifs.extend(MotifTools.load(f))
if ambigs:
for ambig in ambigs:
motifs.append( MotifTools.Motif_from_text(ambig,0.1) )
if not motifnums: motifnums = range(len(motifs))
print '# %d: %s'%(len(motifs),motifnums)
for i in range(len(motifnums)):
motif = motifs[motifnums[i]]
if labels and i < len(labels):
txt = labels[i]
else:
txt = '%d'%i
print '%-3s : %s %5.2f (%4.2f)'%(txt,motif,thresh*motif.maxscore,thresh)
probehits = {}
for key in probes.keys():
hits_by_motif = []
save_flag = 0
if re.search('[BDHU]',probes[key]): continue
for num in motifnums:
result = motifs[num].scan(probes[key],thresh*motif.maxscore)
if result[0]:
hits_by_motif.append(result)
save_flag = 1
else:
hits_by_motif.append(None)
if save_flag:
probehits[key]=hits_by_motif
#scale = .1
maxw = 40
for key in probehits.keys():
l = len(probes[key])
a = list('-'* int(scale*l) )
a.extend( list(' '*10 ) )
desc = []
matches = probehits[key]
for i in range(len(matches)):
if matches[i]:
subseqs,endpoints,scores = matches[i]
for idx in range(len(subseqs)):
start,stop = endpoints[idx]
subseq = subseqs[idx]
score = scores[idx]
if labels and (i<len(labels)): ID = labels[i]
else : ID = '%d'%i
desc.append('%s %s %d-%d %4.2f '%(ID,subseq,start,stop,score))
start = int(start*scale)
for offset in range(10):
if a[start+offset] == '-':
if labels and (i < len(labels)):
a[start+offset] = labels[i]
else:
a[start+offset] = '%d'%i
break
print '%-14s %s'%(key,''.join(a)),
print ' '*max(0,maxw-len(a)), '| '.join(['%-27s'%x for x in desc])
print
print "Found matches in %d of %d input probes"%(len(probehits),len(probes))
def main():
if len(sys.argv) < 2:
print "Usage: %s <fasta_file> [width = None ] [options]"%(re.sub('^.*/','',sys.argv[0]))
print "Options include:"
print ""
print " EM Parameters:"
print " -beta [0.01] Beta for pseudocounts"
print " -seedbeta[0.02] Beta for pseudocounts for seeds from text"
print " -gamma [0.2] Gamma (fraction of sequences)"
print " -delta [0.001] Convergence criteria"
print " "
print " Seeds (not actually proper priors)"
print " -prior Seqences or motifs for seeds (may be repeated)"
print " -top N [0] Include w-mers in top N probes"
print " -gap string sample gapped motifs"
# print " -TF Seed with (all) TRANSFAC PSSMs (buggy)"
print " -kmerseeds Use kmers with best enrichment score as seeds for EM"
print " -pad add NN..NN to seed"
print " "
print " Genome / Background model "
print " -human (250,1000) Use Human Background model"
print " -g genome.fsa Use specicied Fasta file as background (searches first for matching frequency file)"
# print " -Y2K, -Y5C Use Yeast Upstream Intergenic regions (2000, 500)"
# print " -B Use Bacterial Orfs"
print " "
print "Examples:"
print " %s t.fsa 5 -prior GGGTA -prior AAAAAC "%(sys.argv[0].split('/')[-1])
print " will start an EM with 3 seeds: GGGTA, AAAAA, and AAAAC"
print
print " %s t.fsa 5 -info CUP9.info -gamma 0.5 "%(sys.argv[0].split('/')[-1])
print " will start an EM with Enriched seeds in CUP9.info, with"
print " Gamma expectation of 50% of all probes"
print
print " %s t.fsa -prior MCM1_5.tamo:0 "%(sys.argv[0].split('/')[-1])
print " will start an EM with 0th motif of the file MCM1_5.tamo"
print " as a seed"
print
sys.exit(1)
fastafile = sys.argv[1]
#Echo the command line
print "#" + ' '.join(map(lambda x: re.sub(' ','\ ',x), sys.argv))
if sys.argv[2].isdigit():
width = sys.argv[2]
else: width = None
algorithm = ''
beta = ''
seedbeta = ''
deltamin = ''
gamma = 0.2
infofile = ''
seedmodels= []
species = 'YEAST'
valid_tfs = [] #NOT USED
gapped_syl= None
gapflank = 0
gapweight = 0.2
enrichfact= 0.7
pmax = 0 #False
TFSEEDS = 0
TFMids = []
pad = None
bgfile = None
seed_count = 0 #Default: Take the top 0
seed_s = [] #Initialize seq array
'''Parse command-line arguments'''
for tok,i in zip(sys.argv,xrange(len(sys.argv))):
if tok == '-top' : seed_count = int(sys.argv[i+1])
elif tok == '-greedy': algorithm = "GREEDY"
elif tok == '-prior' : seed_s.append(sys.argv[i+1])
elif tok == '-beta' : beta = float(sys.argv[i+1])
elif tok == '-seedbeta': seedbeta = float(sys.argv[i+1])
elif tok == '-gamma' : gamma = float(sys.argv[i+1])
elif tok == '-delta' : deltamin = float(sys.argv[i+1])
elif tok == '-kmerseeds' : infofile = 1
elif tok == '-valid' : valid_tfs.append(sys.argv[i+1]) #NOT USED
elif tok == '-w' : width = sys.argv[i+1]
elif tok == '-width' : width = sys.argv[i+1]
elif tok == '-gap' : gapped_syl = sys.argv[i+1]
elif tok == '-gapflank' :gapflank = int(sys.argv[i+1])
elif tok == '-gapweight':gapweight = float(sys.argv[i+1])
elif tok == '-enrichfact':enrichfact= float(sys.argv[i+1])
elif tok == '-pmax' : pmax = 1
elif tok == '-Y2K' : species = "YEAST_2000_UP"
elif tok == '-Y5C' : species = "YEAST_500_UP"
elif tok == '-B' : species = "BAC_ORF"
elif tok == '-Ch22' : species = "Ch22"
elif tok == '-genome': species = sys.argv[i+1]
elif tok == '-pad' : pad = "TRUE"
elif tok == '-bgfile': bgfile = sys.argv[i+1]
elif tok == '-TF' : #NOT USED (TRANSFAC NOT SUPPLIED WITH DISTRIBUTION)
TFSEEDS = 1
for j in range(i+1,len(sys.argv)):
if re.match('M0',sys.argv[j]):
TFMids.append(sys.argv[j])
else:
break
elif tok == '-human' :
_s = ''
if sys.argv[i+1].isdigit(): _s = '_'+sys.argv[i+1]
else: _s = ''
species = 'HUMAN'+_s
if infofile: infofile = fastafile
if bgfile:
EM.loadMarkovBackground(bgfile)
elif not ('-random_background' in sys.argv or '-nomarkov' in sys.argv):
EM.loadMarkovBackground(species)
else:
EM.theMarkovBackground = EM.Zeroth()
fsaD = Fasta.load(fastafile)
Fasta.delN(fsaD)
seqs = fsaD.values()
probes = fsaD.keys()
all_seqs = seqs
seed_s.extend(seqs[0:min(seed_count,len(seqs))])
if infofile and width=='info':
width = info2width(infofile)
elif width != None:
width = int(width)
#Alternate source of seeds
if infofile:
if 1 or width:
seedmodels.extend(info2seeds(width,infofile,fastafile,species))
else:
print 'Error: need to specify motif width w/ .info file'
#Any -prior pointers to motifs in other files?
(seed_s, motifs) = parse_priors(seed_s)
seedmodels.extend(motifs)
#Should we get seeds from TRANSFAC?
if TFSEEDS: #NOT USED
tf = []
D = tfmats()
if not TFMids:
keys = D.keys()
else:
keys = []
for TFMid in TFMids:
for key in D.keys():
if key[0:6] == TFMid:
keys.append(key)
break
for key in keys:
m = D[key]
m.seednum = int(re.sub('M0*','',key.split()[0]))
m.seedtxt = '%-24s %s'%(m,key)
tf.append(m)
tf.sort(lambda x,y: cmp(x.seednum,y.seednum))
seedmodels.extend(tf)
#seedmodels.append(tf[33])
if gapped_syl:
gapped_priors = gapped_motifs(gapped_syl)
gapped_priors = map(lambda x:'N'+x+'N', gapped_priors)
seed_s.extend(gapped_priors)
if pad:
print '# Padding models with NN-m-NN'
newmodels = []
left = MotifTools.Motif_from_text('@')
right = MotifTools.Motif_from_text('N')
for m in seedmodels:
newmodels.append(left + m + right)
print left + m + right
seedmodels = newmodels
'''
Set everything up and GO!!
'''
global theEM
theEM = EM.EM(seed_s,[],width,"VERBOSE")
if beta: theEM.beta = beta
if deltamin: theEM.deltamin = deltamin
if seedbeta: theEM.seedbeta = seedbeta
theEM.param['gamma'] = gamma
theEM.seqs.extend(all_seqs)
theEM.models = seedmodels
theEM.gapflank = gapflank
theEM.gapweight = gapweight
theEM.report()
theEM.EM_Cstart() #GO!!
#print "#Sorting candidates"
#sys.stdout.flush()
#EM.candidates.sort(lambda x,y: cmp(y.MAP,x.MAP))
'''
Compute some metrics
'''
print "#Loading Genome %s"%species ; sys.stdout.flush()
Genome = ProbeSet(species,enrichfact)
ids = Genome.ids_from_file(fastafile)
for C in theEM.candidates:
if not pmax:
C.pssm.pvalue = Genome.p_value(C.pssm,ids,'verbose')
C.pssm.church = Genome.church(C.pssm,ids)
C.pssm.frac = Genome.frac(C.pssm,probes,None,0.7)
else:
(p,frac) = Genome.best_p_value(C.pssm,ids)
C.pssm.pvalue = p
C.pssm.threshold = frac * C.pssm.maxscore
print "Bests:",p,frac
matching = Genome.matching_ids(C.pssm,[],factor=0.7)
matchbound = [x for x in matching if x in probes]
C.pssm.numbound = len(probes)
C.pssm.nummotif = len(matching)
C.pssm.numboundmotif = len(matchbound)
sys.stdout.flush()
'''
Print out all motifs (sorted by Enrichment) in an AlignACE-like form
'''
theEM.candidates.sort(lambda x,y: cmp(x.pssm.pvalue,y.pssm.pvalue))
for C,i in zip(theEM.candidates,range(len(theEM.candidates))):
C.pssm.maxscore = -100 #May have side effects. Recompute when done
if C.pssm.valid: #NOT USED
_t = C.pssm.valid
if not _t[0]:
vstring = "(--- %8.4f %8.4f %s)"%(_t[1],_t[2],_t[3])
else:
vstring = "(HIT %8.4f %8.4f %s)"%(_t[1],_t[2],_t[3])
else:
vstring = ''
C.pssm._maxscore() #Recomputed
MotifTools.print_motif(C.pssm,20,i)
sys.stdout.flush()
continue
#Antiquated stuff -- Remove !!
print "Log-odds matrix for Motif %3d %s"%(i,C)
C.pssm._print_ll()
print "Sequence Logo"
C.pssm._print_bits()
flush()
#print '# %3d matching sequences at 90%%'%len(C.pssm.bestseqs(C.pssm.maxscore * 0.9))
flush()
m = C.pssm
if not m.__dict__.has_key('gamma'): m.gamma = None #Kludge to deal w/ old shelves
if m.seedtxt: print "Seed: %3d %s"%(i,m.seedtxt)
if m.source: print "Source: ",m.source
if m.gamma: print "Gamma: %7.5f"%m.gamma
if m.threshold: print "Threshold: %5.2f"%m.threshold
#if C.pssm.seedtxt:
# print 'Seed %3d %-25s'%(i,C.pssm.seedtxt)
if C.pssm.church != None: vstring = 'ch: %5.2f %s'%(
math.fabs(math.log(C.pssm.church)/math.log(10)), vstring)
print "Motif %3d %-25s nlog(p): %6.3f %s"%(i,C,-math.log(C.pssm.pvalue)/math.log(10),vstring)
if C.pssm.threshold:
print "Threshold: %6.3f %4.1f%%"%(
C.pssm.threshold, 100.0*C.pssm.threshold/C.pssm.maxscore)
C.pssm.maxscore = -1e100 #May have side effects. Recompute when done
for seq in C.wmers:
print seq,i,C.pssm.scan(seq)[2][0]
C.pssm._maxscore() #Recomputed
print '*'*len(seq)
print "MAP Score: %f"%C.MAP
sys.stdout.flush()
sys.stdout.flush()
sys.exit(0) #Avoid ridiculous python cleanup times
def merge_runs_cc(TAMO_file, wdir, height, distance, ancestor, target, genome):
'''This script is used to merge motifs with the PCC matrix of all motifs.
The script was originally written by Cheng Zou, and then converted to a
function by Alex Seddon.
'''
print "Here are the parameters you specified in this run "
print "-tamo %s" % TAMO_file
print "-wdir %s" % wdir
print "-h height to cut the tree, %s" % height
print "-ancestor %s" % ancestor
print "-target %s" % target
print "-genome %s" % genome
if TAMO_file == '' or wdir == '':
help()
os.system("cd %s" % wdir)
os.chdir(wdir)
# Get the directory where the script is located.
script_dir = '/'.join(os.path.abspath(__file__).split('/')[:-1])
# This code was in the original clustering script. It has been taken out
# because the processes involved take too long and have been taken up by
# the matrrix creation scripts and the run_UPGMA script.
#if distance==0:
# os.system("python /mnt/home/seddonal/gil scottscripts/5_motif_merging/3.calculate_distance_matrix.py -i %s --dfunc pccrange" % TAMO_file)
#os.system("R --vanilla --slave --args %s.dm %s< /mnt/home/seddonal/scripts/5_motif_merging/UPGMA_final.R> %s.Rout" % (TAMO_file,height,TAMO_file))
cl_dic = {}
n = 0
# The file, TAMO_file.dm_UPGMA_Cl_0.05, is inorder of the motifs that appear
# in the TAMO_file. If two motifs have the same number, they are considered
# a part of the same cluster.
# This loop pulls the clustering information out of this file and creats
# the dictionary cl_dic = {cluster_index:{motif_index:'1'}}
for line in open("%s.dm_UPGMA_Cl_%s" % (TAMO_file, height), "r"):
# Gets the clusterindex of this motif
cl = line.strip()
# Adds the cluster index if it has not been
if not cl_dic.has_key(cl):
cl_dic[cl] = {}
cl_dic[cl][n] = "1" # Adds the motif to that cluster
n += 1 # Increases the motif index for the next motif
#print cl_dic
ml = MotifTools.txt2motifs(TAMO_file)
old = [] # List of motifs that are the sole members of a cluster.
# I think I can divide up this portion of the code to create a series
print ancestor, ancestor == 0
cc_output = open('merge_runs_cc', 'w')
if ancestor == 0:
# This loop Looks at each cluster and attempts to merge the motifs
# in the cluster if there are multiple motifs.
for i in cl_dic.keys():
print i, cl_dic[i]
# If there are multiple motifs in the cluster, it merges the motifs
if len(cl_dic[i]) > 1:
# Adds all of the motifs in the cluster to an object called
# mlist.
mlist = []
for j in cl_dic[i]:
mlist.append(ml[j])
# Saves these motifs to there own TAMO file.
save_motifs(mlist, "%s_sub_%s.tm" % (TAMO_file, i))
cc_output.write(
'module load TAMO; python %s/pcc_merge_CC.py merge_runs_no_ancestor -t %s/%s -i %s -target %s -genome %s\n'
% (script_dir, wdir, TAMO_file, i, target, genome))
# If there is only one motif in the cluster, it leaves it alone,
# And adds it to old
else:
key = cl_dic[i].keys()[0]
old.append(ml[key])
if ancestor == 1:
# This loop Looks at each cluster and attempts to merge the motifs
# in the cluster if there are multiple motifs.
for i in cl_dic.keys():
print i, cl_dic[i]
# If there are multiple motifs in the cluster, it merges the motifs
if len(cl_dic[i]) > 1:
# Adds all of the motifs in the cluster to an object called
# mlist.
mlist = []
for j in cl_dic[i]:
mlist.append(ml[j])
# Saves these motifs to there own TAMO file.
save_motifs(mlist, "%s_sub_%s.tm" % (TAMO_file, i))
cc_output.write(
'module load TAMO; module load STAMPmotif; python %s/pcc_merge_CC.py merge_runs_ancestor -t %s/%s -i %s -target %s -genome %s\n'
% (script_dir, wdir, TAMO_file, i, target, genome))
else:
key = cl_dic[i].keys()[0]
old.append(ml[key])
# Combine together the motifs that are in there own cluster.
#os.system("cat %s_sub_*_sum.tm.tf.tm.TOP > %s_sub_new.tm" % (TAMO_file,TAMO_file))
save_motifs(old, "%s_sub_old.tm" % (TAMO_file))
def combine_distance_matrix(wdir, TAMO_file):
'''Combines the PCC score matricies and outputs them as a single matrix.
Originaly written by Cheng Zou, and converted to a function by Alex Seddon.
'''
ml = MotifTools.txt2motifs(TAMO_file)
n_split = len(ml) / 100
##
# Change to the working directory.
os.system("cd %s" % wdir)
os.chdir(wdir)
#
##
##
# The following loop keeps counts the number of lines in the each of the
# PCC matricies for a comparison of a TAMO file with itself.
lendic = {} # Dictionary with the length of PCC matricies.
for i in range(n_split + 1):
lendic[i] = line_count("%s_n%s.dm" % (TAMO_file, i))
print lendic
#
##
##
# This loop creates files with blanks. The files are used to ensure that
# the PCC-distance matrix is square. The blank files will be created to take
# the place of files that would have been left blank
for i in range(n_split + 1):
for j in range(0, i):
# open the file to add blanks
oup = open("%s_n%s-%s_n%s.dm" % (TAMO_file, i, TAMO_file, j), "w")
print lendic[j], lendic[i]
list = []
# Add a number of "-" to the list equal to the number of lines in
# the self comparison files.
for y in range(lendic[j]):
list.append("-")
for x in range(lendic[i]):
oup.write("%s\n" % "\t".join(list))
oup.close()
#
##
##
# Creates a copy of the self comparison file so that it can be easily picked
# out by the function.
for i in range(n_split + 1):
os.system("cp %s_n%s.dm %s_n%s-%s_n%s.dm" %
(TAMO_file, i, TAMO_file, i, TAMO_file, i))
#
##
##
# This loop will look at each
for i in range(n_split + 1):
com = "paste "
for j in range(n_split + 1):
com += "%s_n%s-%s_n%s.dm " % (TAMO_file, i, TAMO_file, j)
com += "> distance_%s" % i
print com
os.system(com)
com = "cat "
for i in range(n_split + 1):
com += "distance_%s " % i
com += "> %s.dm" % TAMO_file
print com
# Concatonate all the matricies
os.system(com)
# My embarisingly ad hoc way of removing double tabs
remove_double_tabs("%s.dm" % TAMO_file)
#!/usr/bin/python
'''
This opens a general TAMO cluster list and outputs **TO STANDARD OUT** the probability matrices of all
items there. Separated by a line with the name of each cluster. *It is recommended to be used in a
bash pipeline where the standard out can be written into a file.*
Has 1 argument:
- motiflist: a TAMO motif list that will be outputed
Returns:
- A series of strings that represet the probability matrices of all motifs in the input list
Author: Hector Galvez
'''
from sys import argv
from TAMO import MotifTools
# Open list
motiflist = MotifTools.load(argv[1])
# Start printing information for each motif
for num in range(len(motiflist)):
print '>Cluster_' + str(num + 1)
motiflist[num]._print_p()
# Create a general list with all the motifs from all algorithms
genlist = []
genlist.extend(seederlist)
genlist.extend(memelist)
genlist.extend(weederlist)
# Perform clustering on the general list of motifs
clusterinf = clusterinfo(genlist)
averages = clusteravg(genlist,clusterinf)
# Trim the final average list
# averages = trim(averages,0.5)
# print clusterinf
# Save new list of cluster averages
MotifTools.save_motifs(averages,tamooutput)
# WEBLOGO IMAGE GENERATION
# Generate giflogos of all average motifs
for index in range(len(averages)):
cluster = 'Cluster ' + str(index + 1)
clustergif = argv[1] + '/other/cluster' + str(index + 1)
averages[index].giflogo(clustergif,title=cluster,scale=2)
# SUMMARY REPORT
# Determine location of the markdown file for the summary report
reportout = open(str(argv[1] + '/final/' + listname + '_cluster_report.md'), 'w')
# Write the header of the report
rundate = date.today()
header = "# Summary report for `" + listname + "`\nThis analysis was run on: " + str(rundate) + \
def GetKmerFromMotifFromPWM(pwm, seq): m = MotifTools.toDict(pwm) #print m motif = MotifTools.Motif_from_counts(m) return motif.bestscanseq(seq);
#
# Compare motifs in tamo format
#
from TAMO import MotifTools
from TAMO.MotifMetrics import ProbeSet
from TAMO.Clustering import MotifCompare
from TAMO.Clustering import Kmedoids
import sys
import pickle
import pprint
file_unknown = sys.argv[1]# Unknown
file_tfbs = sys.argv[2]# TF db
motifs_unknown = MotifTools.load(file_unknown)
motifs_tfbs = MotifTools.load(file_tfbs)
match_dict = {}
for unknown in motifs_unknown:
tf_list = []
for tfbs in motifs_tfbs:
#print
#print "Comparing motifs:"
#print " %s vs %s" % (unknown.source, tfbs.source)
#print " Unknown motif ( %s ) vs TFBS ( %s ) " % (unknown, tfbs)
#print
joined_motifs = []
joined_motifs.append(unknown)
joined_motifs.append(tfbs)
print joined_motifs
def probOvlp(A,B,thresh=0.7,verbose=None):
if A.width >= B.width:
Wide, Narrow = A, B
else:
Wide, Narrow = B, A
RC = MotifTools.revcomplement
if 1:
newWide = Wide[-1,Wide.width+1]
if Wide.__dict__.has_key('bestWide'):
bestWide = Wide.bestWide
else:
bestWideD = {}
for x in newWide.bestseqs(thresh*newWide.maxscore):
bestWideD[x] = 1
for x in bestWideD.keys():
bestWideD[RC(x)] = 1
Wide.bestWide = bestWideD.keys()
bestWide = Wide.bestWide
Wide = newWide
if Narrow.__dict__.has_key('bestNarrow'):
bestNarrow = Narrow.bestNarrow
else:
bestNarrowD = {}
for x in Narrow.bestseqs(thresh*Narrow.maxscore):
bestNarrowD[x] = 1
for x in bestNarrowD.keys():
bestNarrowD[RC(x)] = 1
bestNarrow = bestNarrowD.keys()
Narrow.bestNarrow = bestNarrow
#bestWide = [x[1] for x in Wide.bestseqs (thresh*Wide.maxscore) ]
#bestNarrow = [x[1] for x in Narrow.bestseqs(thresh*Narrow.maxscore)]
countNarrow = len(bestNarrow)
countWide = len(bestWide)
numtotal = math.pow(4,Wide.width)
fudgefactor = math.pow(4,Wide.width - Narrow.width)
bestWideTups = [(x,MotifTools.revcomplement(x)) for x in bestWide]
countBoth = 0
for i in range(len(bestNarrow)):
m_narrow = bestNarrow[i]
delj = []
for j in range(len(bestWideTups)):
if (bestWideTups[j][0].find(m_narrow) >= 0) or (bestWideTups[j][1].find(m_narrow) >= 0):
countBoth += 1
delj.append(j)
delj.reverse() #Chew in from the back
for j in delj:
del(bestWideTups[j])
if verbose: print '%10d %10d %10d %10d | %10d %5d '%(
countWide, numtotal, countNarrow *fudgefactor , countBoth , countNarrow, Wide.width - Narrow.width),
p = Arith.hypgeomsummore(countWide, #Num Interesting
numtotal, #All k-mers
countNarrow * fudgefactor, #Number picked
countBoth ) #Number found
return p
import os,sys,string
from TAMO import MotifTools
from TAMO.seq import Fasta
from TAMO.MotifMetrics import ProbeSet
promoters = ProbeSet(sys.argv[1])
geneset_ids = open(sys.argv[2]).read().split('\n')[:-1]
match_ids = []
prom_ids = promoters.probes.keys()
for id in geneset_ids:
if id in prom_ids:
match_ids.append(id)
motifs = MotifTools.load(sys.argv[3])
church = 0.05
rocauc = 0.1
pvalue = 0.05
print "Name\tMotif\tChurch\tRoc-auc\tP-value"
for m in motifs:
m.church = promoters.church (m, match_ids)
# m.ROC_auc = promoters.ROC_AUC (m, match_ids)
m.pvalue = promoters.p_value (m, match_ids)
if m.church <= church and m.pvalue <= pvalue:
print "%s\t%s\t%s\t%s" %\
(m.source, m, m.church, m.pvalue)
from gusPyCode.MDAP_proj.MDAP_defs import alignAndCombineMotifs
from TAMO import MotifTools
Motif = MotifTools.Motif
outFile = '/Users/biggus/Documents/James/Collaborations/Campbell/data/Results_HyperGeoScreen/masked/Results_gGEMS/CCupAt4Days.6-8mers.gGEMS.top6PlusCombos.motifs.stdThresh.tmo'
m = MotifTools.load('/Users/biggus/Documents/James/Collaborations/Campbell/data/Results_HyperGeoScreen/masked/Results_gGEMS/CCupAt4Days.6-8mers.gGEMS.top6.motifs.stdThresh.tmo')
w = [5.8952,
5.6523,
5.0585,
4.9788,
4.9678,
4.7688]
toTmo = []
toTmo.append(alignAndCombineMotifs([m[0],m[1]],[w[0],w[1]]))
toTmo.append(alignAndCombineMotifs([m[0],m[4]],[w[0],w[4]]))
toTmo.append(alignAndCombineMotifs([m[1],m[4]],[w[1],w[4]]))
toTmo.append(alignAndCombineMotifs([m[2],m[3]],[w[2],w[3]]))
toTmo.append(alignAndCombineMotifs([m[2],m[5]],[w[2],w[5]]))
for e in toTmo:
print e.oneletter
MotifTools.save_motifs(m+toTmo,outFile)
None
filename = sys.argv[1]
motif_list = open(filename).read().split('\nMOTIF')[1:]
tamo_list = []
motif_counter = 1
nsites_pat = re.compile("(w= [0-9]+)")
for motif in motif_list:
m_info1, m_info2 = motif.split('letter-probability matrix: ')
m_mat = m_info2.split('--------------------------------------------------------------------------------', 1)[0]
m_mat_header, m_prob_mat = m_mat.split('\n', 1)
nsites = int(nsites_pat.findall(m_mat_header)[0].split('= ')[1])
count_pos = m_prob_mat.split('\n')[:-1]
count_mat = []
site_list = []
for count in count_pos:
sites = [float(i) for i in count.split()]
site_list.append(sites)
count_dict = {'A': int(sites[0] * nsites),
'C': int(sites[1] * nsites),
'G': int(sites[2] * nsites),
'T': int(sites[3] * nsites)}
count_mat.append(count_dict)
m = MotifTools.Motif_from_counts(count_mat)
m.source = "Motif%s | %s" % (motif_counter, m_mat_header)
tamo_list.append(m)
motif_counter += 1
MotifTools.save_motifs(tamo_list, "MEME_motifs_%s.tamo" % filename.split('.')[0])
def motif_matrix(fsa, motif, outfile, genome='mm9'):
if genome == 'hg18':
markov = "/nfs/genomes/human_gp_mar_06/hg18_promoters_3000_1000.markov"
else:
markov = "/nfs/data/cwng/chipseq/hypotheses/Mouse.markov"
#Load motif and background adjust PSSM
m = MotifTools.load(motif)
EM.loadMarkovBackground(markov)
bg = EM.theMarkovBackground.zeroth()
F = Fasta.load(fsa, key_func=lambda x: x)
seqs = F.values()
n_seqs = len(seqs)
n_motifs = len(m)
SCORES = np.zeros((n_motifs, n_seqs), dtype='float')
#SHIFTS=np.zeros((n_motifs,n_seqs))
#out=open(outfile,'w')
for i, M in enumerate(m):
ll = M.logP
EM.loadMarkovBackground(markov)
bg = EM.theMarkovBackground.zeroth()
for pos in ll:
for letter in pos.keys():
pos[letter] = pos[letter] - math.log(
bg[letter]) / math.log(2.0)
AM = MotifTools.Motif_from_ll(ll)
#adj_model = MotifTools.Motif_from_ll(ll)
#adj_model.source = M.source
#pssm = MDsupport.Motif2c_PSSM(adj_model)
#w=pssm.width
#shift=[]
#scores=[]
mi, ma = AM.minscore, AM.maxscore
#F_m={}
#Search every seq for given motif above threshold t and print motif centered results
for j, seq in enumerate(seqs):
seq_fwd = seq.upper()
#seq_rev = str(MotifTools.revcomplement(seq_fwd))[::-1]
#scores_fwd = pssm.score_probe(seq_fwd)
#scores_rev = pssm.score_probe(seq_rev)
#max_score=mi
#max_ind=0
#for ind,s in enumerate(scores_fwd):
# if s> max_score:
# max_score=s
# max_ind=ind
# strand='+'
#for ind,s in enumerate(scores_rev):
# if s> max_score:
# max_score=s
# max_ind=ind
# strand='-'
max_score = AM.bestscore(seq_fwd)
mscore = (max_score - mi) / (ma - mi)
#orig=len(seq_fwd)/2
#bind=max_ind+w//2
#d=abs(orig-bind)
SCORES[i, j] = mscore
#SHIFTS[i,j]=d
#out.write('%1.3f\t'%mscore)
#out.write('\n')
#out.close()
#del F
np.savetxt(outfile, SCORES, fmt='%1.3f')