Goals of this webinar (candidate genes to causal variants):

To understand when it is practical or (just as often) not practical to try to "clone" the gene or nucleotide variant modulating trait variants
To understand that defining the crucial causal nucleotide variant is usually a bonus and often not for the translational or even mechanistic utility of discoveries.
To review new sequence-based methods to identify common and rare variants—the reduced complexity cross and epoch-effects in reference populations

Presented by:

Dr. Rob Williams
Professor and Chair
Department of Genetics, Genomics, and Informatics
University of Tennessee Health Science Center