Webinars
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Upcoming webinar
Bioinformatics resources to analyze HiFi cancer genomes
Americas broadcast: Tuesday, August 6, 9:00 AM PDT | 5:00 PM BST
Asia-Pacific broadcast: Wednesday, August 7, 11:00 AM SGT
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 the characteristics of HiFi data. This includes tools for calling somatic single-nucleotide variants, indels, CNVs, structural variants, methylation, and mutational signatures.
In this webinar, we will present bioinformatic solutions for calling these variant types, as well as integrating them into a single, easy-to-use pipeline.
Watch On-Demand Webinars
Characterizing C9ORF72 repeat expansions and transcripts using HiFi sequencing
May 22, 2024 - May 23, 2024
HiFi sequencing’s precision and comprehensive coverage make it an invaluable tool in the genetic researcher’s arsenal. The PureTarget repeat expansion panel, with its tailored approach to sequencing regions known for…
May 08, 2024 - May 09, 2024
Accurate long-read sequencing from PacBio (HiFi sequencing) offers whole-genome and transcriptome sequencing for the detection of DNA and RNA variants, including methylation. In this webinar you will hear about how…
Understanding full-length single-cell RNA-seq of immune cells in cardiovascular diseases
May 02, 2024
Full-length isoform sequencing enables you to robustly identify new isoforms and study isoform dynamics in single-cell populations. Find out how concatenating isoforms can deliver a 16-fold throughput increase compared to…
AAV Capsid discovery and design – Novel sequencing approaches
May 01, 2024
HiFi sequencing emerges as a critical technology in this quest, offering exceptional accuracy in sequencing the full-length AAV capsid gene. This capability is crucial for enabling whole-capsid engineering, thereby enhancing…
More samples, lower costs, less time: New PacBio HIFI prep kits + microbial WGS and AMR
April 17, 2024 - April 18, 2024
New, high-throughput library preparation solutions from PacBio, combined with highly accurate long-read sequencing, are enabling researchers to achieve deeper genomic insights more efficiently than ever before. In this webinar, our…
March 14, 2024
Join us for our webinar, Transcript detection and quantification using Kinnex full-length RNA sequencing data, where we will evaluate the prowess of long-read RNA sequencing (lrRNA-Seq) in the realm of isoform…
Assessing HiFi genomes as first-tier analysis in rare disease genetic research
March 13, 2024
Discover how highly accurate long-read sequencing (HiFi sequencing) on the PacBio Revio system is reshaping human genetics, uncovering variants inaccessible with short-read sequencing. A group of clinical researchers from Radboudumc…
Leveraging isoform-level RNA sequencing to understand rare disease pathogenesis
February 28, 2024 - February 29, 2024
Our webinar, Leveraging isoform-level RNA sequencing to understand rare disease pathogenesis, is a next-level exploration of the latest advancements in RNA sequencing technology and its application in the study of rare…
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…
Increasing the throughput of full-length 16s and RNA-Seq with Kinnex kits
December 12, 2023 - December 13, 2023
Explore the transformative capabilities of Kinnex kits from PacBio, in reshaping the landscape of microbiome community profiling and RNA-Seq in plant and animal research. This webinar will guide you through…
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.
Advancing cardiology research with long-read RNA sequencing
November 15, 2023 - November 16, 2023
In this webinar, learn how long-read transcriptomics at full-length isoform resolution is transforming our understanding of heart development, function, and disease. Hear two researchers discuss their use of bulk and…
A new age in liquid biopsy research with highly accurate short-read sequencing
October 18, 2023 - October 19, 2023
New, proprietary technology from PacBio delivers a 10 to 100-fold increase in accuracy over traditional short-read sequencing platforms. With enhanced sensitivity and reduced sequencing depth, PacBio short-read sequencing technology empowers cancer researchers…
Understanding SMRT Link run QC and on-instrument analysis on the PacBio Revio system
September 28, 2023
In this webinar, PacBio scientists Nancy Francoeur, PhD and Caroline Storer, PhD take a closer look at QC metrics and on-instrument analysis pipelines in SMRT Link. Primary run QC metrics…
More comprehensive variant detection at scale in rare disease research
September 26, 2023
Higher throughput and lower costs of long-read sequencing are now available on the Revio system with its trusted highly accurate long-read chemistry (HiFi chemistry). In this webinar, Adam Ameur, PhD,…
Library preparation and HiFi sequencing applications for AAV
September 20, 2023
Gene therapy is experiencing unprecedented growth. Accurate, comprehensive data is crucial for successful vector discovery, design, and characterization. HiFi sequencing offers a unique solution, enabling the sequencing of full-length AAV…
Long-read RNA Neurology Symposium
September 12, 2023
In this virtual symposium, hear from a variety of researchers who are using the PacBio Iso-Seq method for bulk and single-cell transcriptomics to drive cutting-edge research in neurology, neurodegenerative diseases,…
The Full-Length Transcriptomic Atlas of Human Colorectal Cancer from Single-Cell Isoform Sequencing
August 14, 2023
In this webinar Zhongxiao Li will discuss: • Building the first isoform-resolution colorectal cancer (CRC) transcriptomic atlas • Characterizing genes and isoforms associated with different epithelial lineages and subpopulations •…