Reputation: 99
I am trying to get the reverse sequences orientated correctly in a file. This is the code:
import os
import sys import pysam
from Bio import SeqIO, Seq, SeqRecord
def main(in_file):
out_file = "%s.fa" % os.path.splitext(in_file)[0]
with open(out_file, "w") as out_handle:
# Write records from the BAM file one at a time to the output file.
# Works lazily as BAM sequences are read so will handle large files.
SeqIO.write(bam_to_rec(in_file), out_handle, "fasta")
def bam_to_rec(in_file):
"""Generator to convert BAM files into Biopython SeqRecords.
"""
bam_file = pysam.Samfile(in_file, "rb")
for read in bam_file:
seq = Seq.Seq(read.seq)
if read.is_reverse:
seq = seq.reverse_complement()
rec = SeqRecord.SeqRecord(seq, read.qname, "", "")
yield rec
if __name__ == "__main__":
main(*sys.argv[1:])`
When I print out the reverse sequences, the code works. But when in the file it is printed out as a reverse sequence. Can anyone help me to find out what is going wrong? Here is the link to my infile: https://www.dropbox.com/sh/68ui8l7nh5fxatm/AABUr82l01qT1nL8I_XgJaeTa?dl=0
Upvotes: 0
Views: 387
Reputation: 1574
Note the ugly counter is just to print 10000 sequences, not more.
comparing one without ever reversing with one that reverses if needed Here's the output on a couple of seqs, feel free to test it, I think your issue is that yield returns an iterator but you are not iterating it, unless I am missunderstanding what you are doing:
Original:
SOLEXA-1GA-2:2:93:1281:961#0 GGGTTAGGTTAGGGTTAGGGTTAGGGTTAGGGTTAG
Becomes:
SOLEXA-1GA-2:2:93:1281:961#0 CTAACCCTAACCCTAACCCTAACCCTAACCTAACCC
And if not reverse:
Original:
SOLEXA-1GA-2:2:12:96:1547#0 ACACACAAACACACACACACACACACACACACCCCC
Becomes:
SOLEXA-1GA-2:2:12:96:1547#0 ACACACAAACACACACACACACACACACACACCCCC Here's my code:
import os
import sys
import pysam
from Bio import SeqIO, Seq, SeqRecord
def main(in_file):
out_file = "%s.fa" % os.path.splitext(in_file)[0]
with open('test_non_reverse.txt', 'w') as non_reverse:
with open(out_file, "w") as out_handle:
# Write records from the BAM file one at a time to the output file.
# Works lazily as BAM sequences are read so will handle large files.
i = 0
for s in bam_to_rec(in_file):
if i == 10000:
break
i +=1
SeqIO.write(s, out_handle, "fasta")
i = 0
for s in convert_to_seq(in_file):
if i == 10000:
break
i +=1
SeqIO.write(s, non_reverse, 'fasta')
def convert_to_seq(in_file):
bam_file = pysam.Samfile(in_file, "rb")
for read in bam_file:
seq = Seq.Seq(read.seq)
rec = SeqRecord.SeqRecord(seq, read.qname, "", "")
yield rec
def bam_to_rec(in_file):
"""Generator to convert BAM files into Biopython SeqRecords.
"""
bam_file = pysam.Samfile(in_file, "rb")
for read in bam_file:
seq = Seq.Seq(read.seq)
if read.is_reverse:
seq = seq.reverse_complement()
rec = SeqRecord.SeqRecord(seq, read.qname, "", "")
yield rec
if __name__ == "__main__":
main(*sys.argv[1:])
Upvotes: 1