Originally posted by GenoMax
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Hi @GenoMax, could you be more specific on what tags you'd like featureCounts to support?
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It is written in C (not C++ or java).Originally posted by dpryan View PostfeatureCounts is part of the subRead package, which is written in either java or C++ (I'd have to look). We script this in python as well. Since it's a regular executable it's not a problem to do.
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featureCounts is part of the subRead package, which is written in either java or C++ (I'd have to look). We script this in python as well. Since it's a regular executable it's not a problem to do.
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It seems your bam file is encoded with v1.4, there the CIGAR string distinguishes between matches and missmatches. You can use reformat.sh from the bbmap suite in order to convert from SAM1.4 to SAM1.3. See https://www.biostars.org/p/182156/#182160 and http://seqanswers.com/forums/showthread.php?t=46174
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which package is featureCounts from? I need to script, preferably in python, to handle a large number of bam files, so its hard to interact with R (can't script in R). I guess I will have to learn R!
s.
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featureCounts is much faster. I'm a little surprised that htseq-count was never updated to support the = and X cigar operators.
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HTseq error
Hi,
anyone know how to solve these cigar type errors in HTseq? Seems ti is unusable until its solved..
python -m HTSeq.scripts.count in_sorted.bam ref.gff -f bam -s no -t CDS -m union -i locus_tag
Error occured when reading beginning of SAM/BAM file.
Unknown CIGAR code '=' encountered.
[Exception type: ValueError, raised in _HTSeq.pyx:1163]
Or better yet, another progam to get raw counts from bam and gff files. Don't say 'bedtools' because that doesn't work either.. endlessly gives '0' as all the counts.
Thanks,
S.
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