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  • ynwh
    Member
    • Jul 2011
    • 16

    #1

    inconsistency between samtools mpileup and igvtools

    Hi all,
    I'm checking reads mapping coverage on rice genome using IGV but find something strange:
    (1) I generate .tdf file for IGV using the following command:
    igvtools count -z 10 -w 1 a.sorted.bam a.tdf rice.genome
    where rice.genome is the genome file generated by igv

    (2) I generate coverage file using samtools using the following command:
    samtools mpileup -BQ0 -d10000000 -f rice.fasta a.sorted.bam >a.mpileup

    However, I find regions where a.tdf shows reads mapped but a.mpileup does not. The following is an example:

    a.mpileup (mpileup.jpg) suggests no reads mapped between 16097520 and 16103121

    a.tdf (igvtools.jpg) suggests several regions between 16097520 and 16103121 are covered by reads.

    Can anybody explain and solve this problem?

    Many thanks

    Hao
    Attached Files
  • swbarnes2
    Senior Member
    • May 2008
    • 910

    #2
    IGV and mpileup are two different tools, they are probably filtering things differently.

    For starters, I bet mpileup is not showing anomalous pairs, and I bet IGV is.

    So start by getting some read names from IGV, and seeing what their sam entry looks like. Maybe then you can figure out why mpileup isn't putting them where IGV does.

    Comment

    • dariober
      Senior Member
      • May 2010
      • 311

      #3
      I don't if it is relevant to your case... I think mpileup is hard-coded to skip reads with flag 1024 (duplicates).

      Dario

      Comment

      • ynwh
        Member
        • Jul 2011
        • 16

        #4
        Thanks for your advices. Now what I want is to get accurate coverage on each base, what tools and what parameter settings should I use?

        Comment

        • GenoMax
          Senior Member
          • Feb 2008
          • 7142

          #5
          Originally posted by ynwh View Post
          Thanks for your advices. Now what I want is to get accurate coverage on each base, what tools and what parameter settings should I use?
          http://www.biostars.org/p/5165/

          Discussion of next-gen sequencing related bioinformatics: resources, algorithms, open source efforts, etc

          Comment

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