Friday, November 25, 2016

Fwd: Confirmed - Keynote Speaker for Clinical Genomics Track at BioITWorld 2017 this May 23-25 in Boston

I discuss how we interpret and prioritize the many variants in a personal genome. I concentrate on rare and somatic variants and discuss ways of assessing their impact in coding regions using protein structure. For non-coding regions, I present ways to analyze the overall burden of mutations, finding allelic elements differentially affected by variants in paternal and maternal chromosomes and using network connectivity to prioritize variants.

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