Dear SEQanswers community,
i would like to ask a more general question about exome sequencing, and mutation analysis. I have mainly analyzed...
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Appropriate methodology for the analysis of whole exome sequencing cancer data
Last edited by mbgventer; 04-26-2018, 01:47 AM.
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Germline Mutations
hi everybody,
i was wondering, if i want to call germline mutations what allele frequency threshold should i choose to filter most of false...
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Filtering steps for VarScan2 somatic and germline calls
What is the proper filtering pipeline for somatic mutation detection using VarScan2, with tumor/normal paired samples?
My understanding of the...