Question: How to remove Read Name (1st column) extension from a BAM file?
gravatar for IrK
2.1 years ago by
IrK20 wrote:

Hello everyone,

i have paired-end data, after alignment I have noticed that R1 and R2 have different read names in BAM file, for example:


so read R1 has extension .1 and read R2 has extension .2. This causes a problem when I try to convert BAM to BED file with bedtools bamtobed -bedpe -i. So the only solution I can think of is to remove these extensions. Could anyone please advice on the tool, I would not like to convert data back to SAM, as it is extremely large!!!

Thank you

bam paired-end • 1.1k views
ADD COMMENTlink modified 2.1 years ago by Pierre Lindenbaum118k • written 2.1 years ago by IrK20

I assume you got this data from SRA? You should have used -F|--origfmt Defline contains only original sequence name option to avoid getting these kind of read names.

As for adding /1 /2 to read names you could use from BBMap suite with the addslash=t or addcolon=t options.

ADD REPLYlink written 2.1 years ago by genomax65k

ohhh ok, so you mean when I convert SRA to FATSQ with fastq-dump -F use F option

Thank you

ADD REPLYlink written 2.1 years ago by IrK20
gravatar for Pierre Lindenbaum
2.1 years ago by
France/Nantes/Institut du Thorax - INSERM UMR1087
Pierre Lindenbaum118k wrote:
samtools view -h in.bam | sed '/^[^@]/s/^\(.*\)\.[12]\t/\1\t/' | samtools view -Sb -o out.bam -
ADD COMMENTlink written 2.1 years ago by Pierre Lindenbaum118k

thank you so much, Pierre.

I modified the sed part [12] to [.1.2] and it works. So the final command, which works for me is:

samtools view -h in.bam| sed '/^[^@]/s/^\(.*\)\.[.1.2]\t/\1\t/' | samtools view -Sb -o out.bam

May I clarify for the future reference, how paired-end reads can be annotated with extensions 1 and 2? What software was used for this?

ADD REPLYlink written 2.1 years ago by IrK20
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