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  • SWP
    Member
    • Nov 2010
    • 20

    #1

    mpileup SNP detection

    Hello all-

    I've got several full genomes sequenced off a HiSeq. There's good coverage (~30x). Alignments were performed with default parameters in BWA. These are Caucasian individuals.

    Variant detection was performed using mpileup, using almost exact parameters listed on the samtools page:

    samtools mpileup -uf ref.fa output.sorted.bam | bcftools view -bvcg - > var.raw.bcf

    bcftools view var.raw.bcf | vcfutils.pl varFilter -D100000 > var.flt.vcf

    Not a single indel was called, and only ~2 million SNPs. 2 million is well below the >3 million I expected.

    I was wondering if anyone who has aligned a full genome with similar depth of coverage, and called variants using mpileup and got a more reasonable variant number, would be willing to share what parameters were used?

    The raw bcf file has ~3.9 million variants.

    Any ideas/suggestions?
  • colindaven
    Senior Member
    • Oct 2008
    • 417

    #2
    That does seem like a very high coverage you are requiring (-D100000).

    Perhaps try a lower number? Mpileup is pretty good software but I agree with what you are saying.

    Comment

    • SWP
      Member
      • Nov 2010
      • 20

      #3
      The -D option is not a minimum coverage requirement, it's the highest coverage allowed...unless I completely misunderstand something about mpileup. My intention was to have no regions excluded because the coverage was too high, and since I'm a bit OCD I used 10000 as opposed to something like 300 which would probably be adequate.

      I believe I had a corrupted file and I'm running mpileup now and it appears to be working correctly.

      Comment

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