Webinars
Register now for upcoming educational webinars with industry experts or watch past webinars on-demand any time
Upcoming webinar
Benchtop long-read sequencing on Vega: faster + cheaper with SPRQ-Nx
Tuesday, July 28, 8:00 AM PDT | 11:00 AM EDT | 3:00 PM GMT
Wednesday, July 29, 10:00 AM SGT | 12:00 PM AEST
Learn how the new SPRQ-Nx chemistry on the Vega system drives performance up and costs down across applications.
Join PacBio experts to discover how the new SPRQ-Nx chemistry makes HiFi sequencing on the Vega system more accessible than ever. Learn how lower DNA input requirements, higher HiFi yield, faster run times, and lower costs can help accelerate research across biopharma, targeted sequencing, microbiology, and more. See how same-day results and support for regulated workflows are enabling labs to move from sample to answer faster.
Upcoming webinar
HiFi long-read bioinformatic bootcamp
Tuesday, August 11, 8:00 AM PDT | 11:00 AM EDT | 4:00 PM BST
Wednesday, August 12, 10:00 AM SGT | 12:00 PM AEST
Through a curated set of on-demand tutorials and a live Q&A session, you’ll learn how to understand your HiFi data, explore key file formats and quality metrics, choose the right analysis environment, and get started with common bioinformatics workflows.
On-demand webinar + whitepaper
Rare disease panel reopened
One of our favorite rare disease panels is available again, now with access to a newly updated white paper on improving solve rates with HiFi sequencing.
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…