Webinars
Register now for upcoming educational webinars with industry experts or watch past webinars on-demand any time
Upcoming webinar
AAV Capsid discovery and design – Novel sequencing approaches
Americas/Europe broadcast: Wednesday, May 1, 9 AM PDT | 12 PM EDT | 5 PM BST
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 the potential safety and efficacy of gene therapy products. Our webinar will explore these innovative sequencing approaches, shedding light on their transformative potential in AAV capsid design. Join us and embrace the future with HiFi sequencing, offering game-changing accuracy and visibility essential for groundbreaking gene therapy research.
Upcoming webinar
Understanding full-length single-cell RNA-seq of immune cells in cardiovascular diseases
Europe broadcast: Thursday, May 2 | 4:00 PM CEST
Americas broadcast: Thursday, May 2 | 9:00 AM PDT
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 un-concatenated libraries – without losing accuracy or full-length isoform information.
Upcoming webinar
Comprehensive variant detection in pediatric leukemia research with accurate long-read whole genome sequencing
Americas/Europe broadcast: Wednesday, May 8, 8:00 AM PDT | 4:00 PM BST
Asia-Pacific broadcast: Thursday, May 9, 11:00 AM SGT
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 HiFi sequencing enabled the detection of variants in pediatric leukemia samples that were missed by other technologies, bringing us a step closer to the promise of a single comprehensive assay.
Upcoming webinar
Characterizing C9ORF72 repeat expansions and transcripts using HiFi sequencing
Americas/Europe broadcast: Wednesday, May 22, 8:00 AM PDT | 11:00 AM EDT | 4:00 PM BST
Asia-Pacific broadcast: Thursday, May 23, 11:00 AM SGT
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 repeat expansions, and the Kinnex kit, dedicated to uncovering the spectrum of transcriptomic diversity, represent the forefront of these efforts. Together, they offer a synergistic solution that enables researchers to explore the genetic and epigenetic intricacies of neurodegenerative diseases with unprecedented clarity.
This webinar aims to dive deep into these technologies, showcasing their potential to revolutionize our understanding and treatment of complex genetic conditions.
Watch On-Demand Webinars
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 •…
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…
Streamlined chromosome-scale phasing with HiFi sequencing
June 20, 2023
In human, non-human, and cancer genomic research, there is a pressing need for streamlined, efficient computational approaches that can reconstruct high-quality, chromosome-scale phased sequences at scale. In this webinar, Shilpa…
Shining a light on dark genes in population sequencing
June 20, 2023 - June 22, 2023
Large, diverse datasets are critical to ensuring that the promise of genomics can be realized by more people in more places around the world than ever before. Whether research is focused…
Detecting cancer-related RNA dysregulation with long-read sequencing
May 10, 2023
Full-length RNA data from single cells provides critical insights to better understand the intricacies of cancer transcriptomics. Find out from Arthur Dondi how he uses a high-throughput PacBio sequencing approach…