Go Back   SEQanswers > Sequencing Technologies/Companies > Pacific Biosciences

Similar Threads
Thread Thread Starter Forum Replies Last Post
Webinar: Combined NGS Analysis for Genomic Variation, Gene Expression & Gene Regul... DNASTAR Events / Conferences 0 10-12-2016 04:38 AM
population genetics parameter estimation of solexa population sequencing baohua100 Bioinformatics 1 07-16-2008 10:53 AM

Thread Tools
Old 03-05-2018, 09:17 PM   #1
Location: Menlo Park, CA

Join Date: Sep 2011
Posts: 76
Default 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


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
pacbio is offline   Reply With Quote

Thread Tools

Posting Rules
You may not post new threads
You may not post replies
You may not post attachments
You may not edit your posts

BB code is On
Smilies are On
[IMG] code is On
HTML code is Off

All times are GMT -8. The time now is 04:32 AM.

Powered by vBulletin® Version 3.8.9
Copyright ©2000 - 2020, vBulletin Solutions, Inc.
Single Sign On provided by vBSSO