Dr. Simonic: Are we good at tailoring our clinical NGS analysis for individual patients or should we optimize more?
Dr. Darbro: Discovery of dual diagnoses and compound genetic events using NxClinical.
Dr. Kanagal-Shamanna: A Comprehensive genomic tool for combined interpretation and reporting of sequence variants and copy number changes assessed using different platforms.
Dr. Wolff: Copy number and sequencing analysis of children and families with heritable retinal dystrophies in Costa Rica: High prevalence of mutations in regions of autozygosity.
|Date: Wednesday, Oct. 18, 2017||Location: Hilton Orlando, FL|
|Time: 7:15am - 8:45am||Room: Lake Florence A & B|
Can't make it to our breakfast talk? Visit us at our booth #935 to learn more about our products and participate in our 20th anniversary activities!