Sequencing Evolved — Highly Accurate Long Reads for Human Genetics
In this online workshop, which is available to watch now on demand, PacBio Chief Scientific Officer Jonas Korlach introduces the new Sequel IIe System as well as our latest applications using highly accurate long reads (HiFi reads), including human WGS for variant detection, de novo genome assembly, single-cell RNA sequencing, and targeted sequencing using PCR and No-Amp methods.
We are also be joined by Emily Farrow (Children’s Mercy Kansas City)—who shares her experience using long-read sequencing to identify novel genetic variations as part of the Genomic Answers for Kids study—and Hagen Tilgner (Cornell University)—who discusses his pioneering work around single-cell isoform analysis in the nervous system.
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Emily G. Farrow, Ph.D., CGC
Director, Laboratory Operations - Genomic Medicine Center, Children’s Mercy Kansas City
Hagen Tilgner, Ph.D.
Assistant Professor of Neuroscience, Weill Medical College of Cornell University
Jonas Korlach, Ph.D.
Chief Scientific Officer, PacBio
