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  • NestorNotabilis
    Member
    • Dec 2011
    • 19

    #1

    Low frequency indel detection

    Hi,
    Can anyone recommend software particularly suited for very low frequency indel detection as might be applied to ultra-deep targeted sequencing (UDT-seq) datasets where coverage exceeds 1000x? Choices seem limited. Am getting the impression scripting around samtools mpileup output might be the most robust strategy. Any thoughts anyone?

    Many thanks.
  • Artem
    Junior Member
    • May 2012
    • 6

    #2
    I am also interested in indel annotation, if you find any good solutions please post.

    Comment

    • bioinfosm
      Senior Member
      • Jan 2008
      • 483

      #3
      I agree .. you would need to parse the pileup file and then use your own thresholds. Perhaps use the simple common filters and start with that indel list.

      For annotation, seattleSEQ (http://snp.gs.washington.edu/SeattleSeqAnnotation/) is an option and so is TREAT (shameless self plug - http://www.ncbi.nlm.nih.gov/pubmed/22088845)
      --
      bioinfosm

      Comment

      • bioinfosm
        Senior Member
        • Jan 2008
        • 483

        #4
        Originally posted by NestorNotabilis View Post
        Hi,
        Can anyone recommend software particularly suited for very low frequency indel detection as might be applied to ultra-deep targeted sequencing (UDT-seq) datasets where coverage exceeds 1000x? Choices seem limited. Am getting the impression scripting around samtools mpileup output might be the most robust strategy. Any thoughts anyone?

        Many thanks.
        ohh well, here is another option, though am not sure if variants includes indels
        Discussion of next-gen sequencing related bioinformatics: resources, algorithms, open source efforts, etc
        --
        bioinfosm

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