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  • bioinfosm
    replied
    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

    Leave a comment:


  • bioinfosm
    replied
    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)

    Leave a comment:


  • Artem
    replied
    I am also interested in indel annotation, if you find any good solutions please post.

    Leave a comment:


  • NestorNotabilis
    started a topic Low frequency indel detection

    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.

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