How to remove Duplicates in Sam file using AWK ?
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23 months ago
sunnykevin97 ▴ 980

Hi,

I find a lot of duplicates in my SAM file, how do I remove them? Not by using Picard or samtools are they unable to remove them, any AWK command ?

I found one cmd - every time I had to give a duplicate entry (671) , I had more duplicates in the SAM file. How do I automate the process ?

awk 'BEGIN { i = 0; } /^@/ { if (/671/) { if (i++ < 1) { print; } } else { print } } /^[^@]/ { print }' AvA_.sam > AvA_fixed_.sam

Suggestions.

protein genome gene • 1.8k views
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My 2p - unless you are experienced, don't use sed or awk for manipulating vcf or sam files. There's almost certainly a more robust and less risky package that you could use.

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Any suggestions, I'm unable to find any such packages that do the job. Do you have anything in mind ?

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samtools markup with -r option. You don't need to remove duplicates. If you mark duplicates, that is enough for downstream tools. Bamutil has dedup opion. Try that too.

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Bamutil works fine.

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what's a duplicate for you ? a normal way to remove the FLAG=duplicate would be samtools view -F 1024 in.bam

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might be worth looking in to the BBMap package , there is a sub-program that is called dedupe.sh , or you can even get there by using BBduk I assume.

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dedupe.sh only removes duplicates from fasta or fastq file. Both the programs can't remove duplicates from SAM files.

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that's true indeed. my bad :/

(and yes, from sam to fastq, dedupe is too much work-around )

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All the SAM files generated using BWA mem.

After de novo assembly, I choose assembled contigs as reference and mapped to the trimmed fastq reads.

I found a lot of duplicates only from the Velvet and the Abyss contigs, not from Spades.

My overall objective is to construct a META ASSEMBLY by combining all the assemblies into one, that's why I'm generating a SAM-->BAM file to feed into gam-ngs, which generates the met assembly finally.

I'm generating meta assembly because I had a fragment genome assembly, I'd like to improve the continuity of scaffolds.

With fragmented assembly, it's so troublesome to annotate the genome, it fails.

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