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Rapid and highly accurate end-to-end NGS analysis solution for detection of novel inherited disease mutations
Rapid and highly accurate end-to-end NGS analysis solution for detection of novel inherited disease mutations
Presented by Dr. Anika Joecker
September 18, 2015
46:11 minutes
Tags: BxGWB webinar, Causal variants, clc genomics workbench, Rare disease, Solution webinar, webinar
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