Webinars
Register now for upcoming educational webinars with industry experts or watch past webinars on-demand any time
Upcoming Compatible partner webinar
Part 1: Navigating genomic complexities with long-read sequencing in cancer research
Tuesday, May 27, 2025
05:00:00 PM (UTC) – 06:00:00 PM (UTC)
Part one of this two-part webinar series explores how long-read panels are transforming genomic analysis in cancer research. Join us as we lay the groundwork for understanding the complementary nature of long- and short-read sequencing – setting the stage for deeper, integrated analysis in part two of the series.
Upcoming Compatible partner webinar
Part 2: Decoding long-reads with powerful bioinformatics tools
Wednesday, May 28, 2025
05:00:00 PM (UTC) – 06:00:00 PM (UTC)
Building on the foundational knowledge from part one, this session focuses on the critical aspects of secondary analysis for long-read panel data. By the end of this session, you’ll have a clear roadmap for leveraging the full potential of long-read panels in your genomic studies.
On-demand webinar
Streamline and modernize repeat expansion sequencing for neurological disease with the PacBio PureTarget repeat expansion panel
In this webinar, you will learn how HiFi sequencing provides a comprehensive view of the human genome. Hear about the mature product line of PacBio sequencers and the latest kitted solutions for high-throughput sequencing of challenging variants like tandem repeat expansions.
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…