Problem Running Htseq
1
1
Entering edit mode
11.1 years ago
lkmklsmn ▴ 980

Hi I am trying to calculate exon counts from a .bam file using python and HTSeq.
After reading the bam file:

"bam_reader = HTSeq.BAM_Reader( <sorted bam file> )"

I get following error when trying to extract aligned reads

"for alnmt in bam_reader:
...  print alnmt"

"Traceback (most recent call last):
  File "<stdin>", line 1, in <module>
  File "../HTSeq/__init__.py", line 832, in __iter__
    yield SAM_Alignment.from_pysam_AlignedRead( pa, sf )
  File "_HTSeq.pyx", line 1251, in HTSeq._HTSeq.SAM_Alignment.from_pysam_AlignedRead (src/_HTSeq.c:21907)
  File "csamtools.pyx", line 800, in pysam.csamtools.Samfile.getrname (pysam/csamtools.c:8816)
ValueError: tid -1 out of range 0<=tid<25"

Does anyone have an idea what the problem is?

rnaseq htseq python bam alignment • 4.5k views
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1
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A tid of -1 would mean a * in the RNAME column (the 3rd column). I'd need to go through the code, but does your BAM file perhaps have a read with a * in the RNAME column that lacks a 0x4 bit set in the FLAG? I imagine that could cause this error.

Edit: BTW, you can test whether this is the case with something like samtools view foo.bam | awk '{if($3 == "*") { if(!and($2, 0x4)) { print $0; }}}', which should print all reads that might cause this error.

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1
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Thanks. I wasnt able to make that awk statement work but I think you are right. Do you know any efficient way to correct this?

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0
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Hmm, apparently mawk is installed on ubuntu (perhaps that's what you're using, it's what I have in lab) and it lacks awk's bitwise operators (OS X must have gawk installed, since that awk command worked on my laptop last night!). I'll put together a quick script that should work regardless and post that as an answer.

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You can use samtools's built in required filter -f:

samtools view -f 4 xyz.bam | awk '{if($3 == "*") { print $0; }}'

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11.1 years ago

Since the bitwise operators in awk that I used in my comment apparently don't exist on all system (that's good to know!), here's a simply python solution. You could do this with perl to, but I loath the language.

#!/usr/bin/env python
import csv
import sys

f = csv.reader(sys.stdin, dialect="excel-tab")
of = csv.writer(sys.stdout, dialect="excel-tab")
for line in f :
    #Don't try to modify the header!!!
    if(line[1][0] == "@") :
        of.writerow(line)
        continue

    if(line[2] == "*") :
        if((int(line[1]) & 4) != 4) :
            line[1] = "%s" % (int(line[1]) | 4)
    of.writerow(line)

If you saved that as clean.py, then you can probably just samtools view namesorted.bam | python clean.py | htseq-count.py options - annotation.gtf if you want to directly use htseq-count. You can also just try to make a cleaned BAM file with samtools view -h something.bam | python clean.py | samtools view -bS - > something.clean.bam (if you really need that to be faster, you can implement the whole thing in C with the samtools API, but that's likely overkill!).

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Thank you! I just had this exact issue with pysam alone, without HTSeq but this greatly helps me too.

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Good to know. Which aligner did you use that caused this formatting?

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We use RNA-STAR 2.3

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Interesting. I too use STAR, but haven't seen this behavior. Have you reported this to the author yet? If not, please do so, this problem is going to bite a number of people!

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