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bamCoverage fails in bam files with large number of small contigs in headers

Hi,

I plan to use bamCoverage from Deeptools to get bw files, but it looks like the thread is dead as it never finishes (no errors). I have hundred of thousands of short unlocalized/random contigs in bam files and looks like this can be the reason bamCoverage fails (https://github.com/deeptools/deepTools/issues/662). Using samtools, I removed all the reads except those aligned to chromosomes 1:22 (samtools view -o out.bam in.bamseq 1 22 | sed 's/^/chr/') but of course the tags related to the removed contigs are still available at bam headers and so the problem with bamCoverage persists. Is it reasonable to just naively modify the bam headers (eg samtools reheader) so that only headers related to main chromosomes are retained? I tried samtools reheader newheader.txt out.bam > newbam.bam but the resulting files looks corrupted.

bamcoverage
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updated by colindaven colindaven • written by sarahmanderni sarahmanderni

1 answer

Are you sure the newheader.txt is in sam format ? I re-headered bams successfully using this. Maybe you messed up the sam header somehow with sed etc ?

samtools view -H old_bam.bam > header.sam
samtools reheader header.sam old_bam.bam > new.bam
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written by colindaven colindaven

Probably thats the case. What x.bam refers to in your example? Here is what I did: Retained only reads aligned to chromosomes 1:22:

samtools view -o out.bam in.bam seq 1 22 | sed 's/^/chr/'

Took the header:

samtools view -H out.bam > header.sam

The header.sam still has the '@'SQ line for all the removed contigs. So, manually copy pasted the '@'SQ lines related to chr 1:22 and '@'PQ lines (newheader.sam) and used it for samtools reheader:

samtools reheader newheader.sam outbam.bam >  newbam.bam

Based on your response, the manual modification of header file could be reason. In your example, how x.bam doesnt include the headers from the removed contigs?

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written by sarahmanderni sarahmanderni

Your approach looks fine to me. Maybe just paste the before and after headers (without all the @SQ lines to see if someone sees a mistake. The x.bam is the old_bam.bam, I renamed it.

How do you know the new bam is corrupt ? Just run samtools index on it to see.

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written by colindaven colindaven

Exactly! I know its corrupted as I cant run samtools index:

samtools index newbam.bam
samtools index: failed to create index for "newbam.bam": Numerical result out of range
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written by sarahmanderni sarahmanderni

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