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  • samtools flagstat

    Hello all,

    My merged bam file is about 7.4G,

    "samtools flagtstat" shows that:

    0 QC failure
    0 duplicates
    151038423 mapped (95.66%)
    157886180 paired in sequencing
    78943090 read1
    78943090 read2
    143478844 properly paired (90.87%)
    148750146 with itself and mate mapped
    2288277 singletons (1.45%)
    3935010 with mate mapped to a different chr
    1280027 with mate mapped to a different chr (mapQ>=5)

    After run samtools rmdup, I got 7.2G bam file, there are reads removed.

    Any explanation for this?

    Does "singletons" here mean no paired read in read1 or read2 files?

    Thanks

  • #2
    Originally posted by bair View Post
    Hello all,

    My merged bam file is about 7.4G,

    "samtools flagtstat" shows that:

    0 QC failure
    0 duplicates
    151038423 mapped (95.66%)
    157886180 paired in sequencing
    78943090 read1
    78943090 read2
    143478844 properly paired (90.87%)
    148750146 with itself and mate mapped
    2288277 singletons (1.45%)
    3935010 with mate mapped to a different chr
    1280027 with mate mapped to a different chr (mapQ>=5)

    After run samtools rmdup, I got 7.2G bam file, there are reads removed.

    Any explanation for this?

    Does "singletons" here mean no paired read in read1 or read2 files?

    Thanks
    The author(s) (Heng) specifically recommends moving away from samtools rmdup and use picard.
    -drd

    Comment


    • #3
      Originally posted by drio View Post
      The author(s) (Heng) specifically recommends moving away from samtools rmdup and use picard.
      I marked the duplicates by picard, samtools flagstat can detect the number of duplicates, but still cannot find the number of QC failure.

      Samtools pileup with -m [1796] is said to have the ability to filter out QC failure and duplicates. How can I know reads with QC failur are removed since flagstat does not find one?

      Thanks.

      Comment


      • #4
        Originally posted by bair View Post
        I marked the duplicates by picard, samtools flagstat can detect the number of duplicates, but still cannot find the number of QC failure.

        Samtools pileup with -m [1796] is said to have the ability to filter out QC failure and duplicates. How can I know reads with QC failur are removed since flagstat does not find one?

        Thanks.
        Perhaps you don't have QC failure reads? If the flag is steup properly
        samtools will filter them out for sure.
        -drd

        Comment

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