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BAMalignmentsPerChromosome.py
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##################################
# #
# Last modified 05/04/2012 #
# #
# Georgi Marinov #
# #
##################################
import sys
import pysam
import string
from sets import Set
def main(argv):
if len(argv) < 3:
print 'usage: python %s BAM chrom.sizes outfilename' % argv[0]
sys.exit(1)
BAM = argv[1]
outputfilename = argv[3]
chrominfo=argv[2]
chromInfoList=[]
ChrDict={}
linelist=open(chrominfo)
for line in linelist:
fields=line.strip().split('\t')
chr=fields[0]
start=0
end=int(fields[1])
chromInfoList.append((chr,start,end))
ChrDict[chr]={}
ChrDict[chr]['unique']=0
ChrDict[chr]['multi']=0
ReadMultiplicity={}
i=0
samfile = pysam.Samfile(BAM, "rb" )
for (chr,start,end) in chromInfoList:
try:
for alignedread in samfile.fetch(chr, 0, 100):
a='b'
except:
continue
for alignedread in samfile.fetch(chr, start, end):
i+=1
if i % 5000000 == 0:
print 'examining read multiplicity and inputting reads', str(i/1000000) + 'M alignments processed processed', chr,start,alignedread.pos,end
ID = alignedread.qname
if alignedread.is_read1:
ID = ID + '/1'
if alignedread.is_read2:
ID = ID + '/2'
if ReadMultiplicity.has_key(ID):
ReadMultiplicity[ID]+=1
else:
ReadMultiplicity[ID]=1
i=0
for (chr,start,end) in chromInfoList:
try:
for alignedread in samfile.fetch(chr, 0, 100):
a='b'
except:
continue
for alignedread in samfile.fetch(chr, start, end):
i+=1
if i % 5000000 == 0:
print 'counting alignments', str(i/1000000) + 'M alignments processed processed', chr,start,alignedread.pos,end
ID = alignedread.qname
if alignedread.is_read1:
ID = ID + '/1'
if alignedread.is_read2:
ID = ID + '/2'
if ReadMultiplicity[ID]==1:
ChrDict[chr]['unique']+=1
else:
ChrDict[chr]['multi']+=1
outfile = open(outputfilename, "w")
outfile.write('#chr\tlength\tunique\tmulti\n')
for (chr,start,end) in chromInfoList:
outline = chr + '\t' + str(end) + '\t' + str(ChrDict[chr]['unique']) + '\t' + str(ChrDict[chr]['multi'])
outfile.write(outline + '\n')
outfile.close()
if __name__ == '__main__':
main(sys.argv)