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  • Basic data extraction on bam files

    I'm trying to get read counts for things like reference normal forward/reverse count, alternative/reference forward/reverse counts from a bam file. I've honestly read through so many forum posts and BioStar and I can't seem to find the answer. Any help would be appreciated.

  • #2
    This should still work thought I have not used it recently: http://genome.sph.umich.edu/wiki/BamUtil:_validate

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    • #3
      I recall running into this site a bit ago. I'll give it another go. Thank you very much.

      Are read counts not something typically used/had? I'm a bit of a novice in the art, but this strikes me as very important, no?

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      • #4
        Forward and reverse counts should be 50/50. You could get counts for all the flags, and tell from that how many go each way.

        That's not a common thing to worry about.

        You can't get "alternate" counts from the bam. If you make a vcf, the vcf is likely to have what you want in the DP4 value

        ##INFO=<ID=DP4,Number=4,Type=Integer,Description="# high-quality ref-forward bases, ref-reverse, alt-forward and alt-reverse bases">

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        • #5
          After consulting with both you guys and a seasoned coworker, I've figured out what I needed I think. Thank you guys for the answers!

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          • #6
            I need suggestion to extract the chromosome or chromosome region (e.g. chr1: 100,000,000-200,000,000) without sorting bam file. Any idea related with this would be appreciated.

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