Dear SEQanswers community,
i would like to ask a more general question about exome sequencing, and mutation analysis. I have mainly analyzed...
4 results in 0.0022 seconds.
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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. -
Tolerances for non cells-of-interest for somatic variant calling
Hi,
we are looking at several types on non-solid tumors, so it is difficult to get a 'pure' sample of cancer cells for exome sequencing.... -
VarScan early halt
Hi,
I'm new to VarScan. I was trying to call copynumber from my exome sequencing data.
My script is
samtools mpileup... -
Questions about pathway analyses of genes with somatic mutations
Hi all
!!
I sequenced cancer exomes matched with normal exomes, then after alignment follwed by de-duplication, I extracted significant...
