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  • chris
    Member
    • Apr 2008
    • 52

    #1

    On/off target rate for whole exome data

    Hi all,

    I've some human exome data, which I've aligned with bowtie2 as bwa doesn't work (see this post).

    Using samtools flagstat I can see ~98% of reads map to the genome. However, only about 60% of those are on-target with 40% off-target. That doesn't seem great.

    What kind of on/off-target rates do others see?
  • swbarnes2
    Senior Member
    • May 2008
    • 910

    #2
    Originally posted by chris View Post
    Hi all,

    I've some human exome data, which I've aligned with bowtie2 as bwa doesn't work (see this post).

    Using samtools flagstat I can see ~98% of reads map to the genome. However, only about 60% of those are on-target with 40% off-target. That doesn't seem great.

    What kind of on/off-target rates do others see?
    Actually, that's about what the people selling the kits promise, so you are fine.

    Comment

    • Bukowski
      Senior Member
      • Jan 2010
      • 388

      #3
      Originally posted by chris View Post
      Hi all,

      I've some human exome data, which I've aligned with bowtie2 as bwa doesn't work (see this post).

      Using samtools flagstat I can see ~98% of reads map to the genome. However, only about 60% of those are on-target with 40% off-target. That doesn't seem great.

      What kind of on/off-target rates do others see?
      Don't worry - perfectly acceptable figures there.

      Comment

      • chris
        Member
        • Apr 2008
        • 52

        #4
        Great. Thanks.

        Comment

        • desaila
          Junior Member
          • Oct 2010
          • 7

          #5
          @chris -- would you care to share your command line for bowtie2? I'm running into a slightly worse issue, performance wise, and am curious how you're doing it!

          Comment

          • chris
            Member
            • Apr 2008
            • 52

            #6
            Sure, its:

            Code:
            bowtie2 --threads 4 -q --sensitive --end-to-end --phred33 -x /db/bowtie2/Hsapiens68 -1 fastq_file1 -2 fastq_file1 -S out.sam

            Comment

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