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Upcoming webinar

Filling the gaps in rare disease research with long-read sequencing: stories from undiagnosed cohorts

Thursday, May 21, 8:00 AM PDT | 11:00 AM EDT | 5:00 PM CEST

Friday, May 22, 9:00 AM SGT | 11:00 AM AEST

In this webinar, learn how long-read sequencing is helping researchers find explanations in rare disease cases that remain unresolved with traditional approaches.

Featuring real-world examples from undiagnosed cohorts, you’ll discover how HiFi sequencing detects complex genetic variation and integrates multiomic data to help resolve challenging cases. Find out how these advances are shaping the future of rare disease research by moving toward more comprehensive genomic characterization and advancing long-read sequencing toward standard of care.

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Upcoming webinar

Unlocking human microbiome clarity with PacBio HiFi sequencing

Thursday, June 18, 8:00 AM PDT | 11:00 AM EDT | 4:00 PM BST

Join a live rebroadcast of this popular session on PacBio HiFi sequencing for human microbiome research, followed by a new live Q&A with PacBio microbial genomics expert Jeremy Wilkinson, PhD.

In this session, you’ll hear how PacBio HiFi sequencing supports full-length 16S and shotgun metagenomics approaches for human microbiome research, helping researchers resolve species- and strain-level variation, uncover novel taxa, generate more complete MAGs, and improve pathway and functional annotation in complex microbial communities.

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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.

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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…

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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…

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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…

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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.

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APAC Bioinformatics webinar

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…

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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…

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