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  • Jerry-cs
    Junior Member
    • Dec 2010
    • 5

    #1

    samtool fixmate drastically decreases the number of properly paired reads

    After samtools namesort + fixmate, the number of properly paired reads decreases from 35.42% to 8%.

    Does anyone know the reason?

    Before namesort and fixmate
    800000 in total
    0 QC failure
    0 duplicates
    331347 mapped (41.42%)
    800000 paired in sequencing
    400000 read1
    400000 read2
    283386 properly paired (35.42%)
    287049 with itself and mate mapped
    44298 singletons (5.54%)
    3314 with mate mapped to a different chr
    1491 with mate mapped to a different chr (mapQ>=5)


    After namesort and fixmate

    800000 in total
    0 QC failure
    0 duplicates
    331347 mapped (41.42%)
    800000 paired in sequencing
    400000 read1
    400000 read2
    64026 properly paired (8.00%)
    64856 with itself and mate mapped
    266491 singletons (33.31%)
    744 with mate mapped to a different chr
    321 with mate mapped to a different chr (mapQ>=5)
  • epigen
    Senior Member
    • May 2010
    • 101

    #2
    Have you found out what went wrong?
    It seems the pairs were matched correctly because the number of singletons increased drastically:
    before:
    287049 with itself and mate mapped
    44298 singletons (5.54%)

    after:
    64856 with itself and mate mapped
    266491 singletons (33.31%)

    Comment

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