In this webinar we describe how current approaches to optimizing vector integrity for gene editing are insufficient and that gene editing protocols can benefit from long read sequencing at multiple…
In this PacBio Virtual Global Summit 2020 presentation, Evan Eichler of the University of Washington discusses approaches to apply long-read sequencing to generate complete telomere-to-telomere assembly of chromosomes. Eichler focuses…
In this PacBio Virtual Global Summit 2020 presentation, Shawn Levy of Discovery Life Sciences shares work on how the ability to reliably detect and characterize the spectrum of sequence variants…
In this PacBio Virtual Global Summit 2020 presentation, Pi-Chuan Chang of Google shares how DeepVariant identifies SNPs and Indels in PacBio HiFi data, starting from the v0.8 release (April 2019)….
In this PacBio Virtual Global Summit 2020 presentation, Neil Miller of Children’s Mercy Hospital in Kansas City describes how third generation sequencing offers sensitive single nucleotide variant detection, variant phasing…
In this PacBio Virtual Global Summit 2020 presentation, Gary Latham of Asuragen shares how high-prevalence carrier genes associated with disorders such as Fragile X Syndrome, SMA, and Hemophilia include GC-rich…
In this PacBio Virtual Global Summit 2020 presentation, Tang Chong of BGI shares work on how single-cell isoform sequencing can reveal transcriptomic dynamics in individual cells invisible to bulk- and…
In this PacBio Virtual Global Summit 2020 presentation, Lori Aro of PacBio shares how scientists are using highly accurate long read-sequencing to target clinically relavent gene and regions of interest.
In this PacBio Virtual Global Summit 2020 presentation, Nicole Newell of PacBio provides an overview of the library preparation kits available for highly accurate long read (HiFi sequencing) applications.
In this PacBio Virtual Global Summit 2020 presentation, Jeremy Schmutz of HudsonAlpha Institute describes applications for PacBio HiFi sequencing to detect structual variations and assembly human genomes, as well as…
Watch this short video to learn about highly accurate long-read sequencing and how HiFi reads can advance scientific discovery.
Watch this short tutorial to learn how to get started with the variant detection application using highly accurate long reads (HiFi reads).
Watch this short tutorial to learn how to get started with the Targeted sequencing application using highly accurate long reads (HiFi reads).
Watch this short tutorial to learn how to get started with the full-length RNA sequencing SMRT Sequencing application using highly accurate long reads (HiFi reads)
In this video, John Harting shares an ASHG 2020 poster entitled: Long-read amplicon sequencing detects a bi-allelic SMN1-SMN2 gene conversion allele that does not guarantee a spinal muscular atrophy (SMA)…
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