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WEBINAR: Rapid biological interpretation of human NGS data
Join us for a webinar that demonstrates how Ingenuity Variant Analysis combines analytical tools and integrated content to help you rapidly identify a... -
Marking duplicates and comparing 2 WE samples?
Hey,
Two follow-up questions for my WholeExome Analysis:
1) I used Picard "MarkDuplicates" to mark duplicates and...Last edited by angerusso; 02-20-2012, 01:45 PM. -
Missing V600E mutation in WES of A375 cell line? Samtools problem?
I have whole-exome data from A375 cell line generated using Illumina HiSeq. So I created the following pipeline to find SNPs and INDELs. In particular,...
