Question: Pileup Analysis
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gravatar for Andrea Edwards
7.5 years ago by
Andrea Edwards • 30 wrote:
Hello I was wondering if there was anything available within galaxy that would let you do the following with pileup files: 1) filter for homozygous SNVs (i.e. that do not contain the reference genome allele in the genotype) 2) compare the pileup files for 2 (or more) individuals to find SNVs unique to each individual and to further limit this to homozygous SNPs unique to each individual 3) compare the pileup files for 2 (or more) individuals to find shared SNVs and to further limit to this to shared SNVs where the individuals have different alleles (rare as would assume triallelic snv) and then group the individuals according to the allele for each SNV. I could only see the filter pileup tool but nothing for comparing pileup files thanks
galaxy • 977 views
ADD COMMENT • link • modified 7.4 years ago by Anton Nekrutenko ♦ 1.7k • written 7.5 years ago by Andrea Edwards • 30
0
gravatar for Anton Nekrutenko
7.4 years ago by
Penn State
Anton Nekrutenko ♦ 1.7k wrote:
Dear Andrea: Many apologies for a delay answering this. We are currently in the process of shifting genotyping pipelines to use VCF format, which, combined with a set of VCF manipulation utilities, will make it quite easy to perform operations you request. These should be ready for use by the end of Summer. Thanks for using Galaxy, anton galaxy team Anton Nekrutenko http://nekrut.bx.psu.edu http://usegalaxy.org
ADD COMMENT • link written 7.4 years ago by Anton Nekrutenko ♦ 1.7k
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