Webinars
Register now for upcoming educational webinars with industry experts or watch past webinars on-demand any time
Upcoming webinar
HiFi on the brain – advancing Parkinson’s disease research using HiFi sequencing
Americas/Europe broadcast: December 17, 8:00 AM PST | 4:00 PM GMT
Asia-Pacific broadcast: December 18, 9:00 AM SGT
In this webinar, learn about the sequencing technology that is pushing neuroscience research forward, particularly in Parkinson’s disease. Discover how HiFi whole genome sequencing (WGS) and the PacBio Iso-Seq method provide complete visibility into all genomic variants, reveal crucial transcript isoform information, and ultimately enable the potential development of novel therapeutics.
Watch On-Demand Webinars
Detecting cancer fusion transcripts in long-read RNA-Seq data with CTAT-LR-fusion
September 11, 2024 - September 12, 2024
In this webinar, you will learn about CTAT-LR-fusion, a new bioinformatics tool for detecting known and novel fusion transcripts from PacBio long-read isoform sequencing data, with applications to bulk and…
Bioinformatics resources to analyze HiFi cancer genomes
August 06, 2024 - August 07, 2024
PacBio HiFi sequencing enables more complete and accurate characterization of cancer genomes than ever before. However, going from sequences to variant calls requires tools specifically developed to take advantage of…
Bioinformatics resources to analyze PacBio HiFi human genomes
February 21, 2024 - February 22, 2024
Register for our on-demand webinar, Bioinformatics resources to analyze PacBio HiFi human genomes. This session is intricately designed for researchers and professionals who are deeply involved in the exploration and…
Mastering HiFi sequencing: from basics to breakthroughs
October 04, 2023 - October 19, 2023
In this webinar series you can hear from PacBio scientists about all aspects of HiFi sequencing – from experiment planning and sample preparation to sequencing and bioinformatics.
July 06, 2023
Detecting cancer-related RNA dysregulation with long-read sequencing Full-length, single-cell RNA data provides critical insights into the understanding of cancer transcriptomic features, such as isoforms, fusions, and expressed mutations. However, until recently, cell…
Genome and epigenome measured in a single sequencing run
September 21, 2022
Do you need to detect epigenetic modifications in native DNA, even in difficult regions? Then join us virtually for the first webinar in our new bioinformatics series. In this webinar…