3/8 Webinar: Sequencing SVs for Disease Gene Discovery & Population Genetics

pacbio · 03-05-2018, 09:17 PM

Join us to learn how human geneticists are adding low-coverage, long-read whole genome sequencing to their study designs to fully power genetic variant discovery and ultimately identify disease-causing variants and genes.

During this webcast you will learn about:

Methods for calling and visualizing structural variants from low-coverage, long-read sequencing of human genomes
Optimal study designs to fully power SV detection for gene discovery in rare and Mendelian diseases
Cost-effective population genetics study designs for common SV reporting down to < 1% allele frequency
Case studies demonstrating genetic discovery in rare Mendelian disease subjects

Speakers:

Alexander Hoischen Ph.D., Radboud University Medical Center
Aaron Wenger Ph.D., Principal Scientist, PacBio

Watch Recording

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03-05-2018, 09:17 PM	#1
pacbio Member Location: Menlo Park, CA Join Date: Sep 2011 Posts: 60	Watch Webinar: Sequencing SVs for Disease Gene Discovery & Population Genetics Join us to learn how human geneticists are adding low-coverage, long-read whole genome sequencing to their study designs to fully power genetic variant discovery and ultimately identify disease-causing variants and genes. During this webcast you will learn about: Methods for calling and visualizing structural variants from low-coverage, long-read sequencing of human genomes Optimal study designs to fully power SV detection for gene discovery in rare and Mendelian diseases Cost-effective population genetics study designs for common SV reporting down to < 1% allele frequency Case studies demonstrating genetic discovery in rare Mendelian disease subjects Speakers: Alexander Hoischen Ph.D., Radboud University Medical Center Aaron Wenger Ph.D., Principal Scientist, PacBio Watch Recording Last edited by pacbio; 03-19-2018 at 10:44 AM. Reason: Live webinar has past, now linking to recording