gravatar for jrleary

3 hours ago by

Lineberger Comprehensive Cancer Center

My lab is looking to get into Whole Genome Sequencing, and we of course need a processing and analysis pipeline for the data we generate. I've been reading up on WGS / WES, and I understand the basics but I haven't seen any "best practices" type documents / tutorials like those that exist for single cell and bulk RNAseq (my typical work). Since this is the first time I'll have analyzed WGS data I'm less familiar with the literature surrounding the topic, and would greatly appreciate if someone could point me in the right direction.

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