The Genomic Analysis Facility within the Center for Human Genome Variation provides genome sequencing as a service for large scale genomics studies. We specialize in whole genome, whole exome, and custom capture sequencing using our 6 Illumina HiSeq 2000 sequencers. The lab also has one HiSeq 2500 sequencer which can sequence one whole genome or 12 exomes in less than 30 hours. The lab is equipped to handle smaller GWA based studies and can run validation assays using a variety of gold standard techniques including TaqMan, Infinium, and Sanger Sequencing. As a part of the Center for Human Genome Variation we also have a functional core which can provide follow-up molecular characterization of genetic mutations in cell culture or animal models.