Webinars
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Upcoming webinar
A new age in liquid biopsy research with highly accurate short-read sequencing
Americas/Europe broadcast: Wed., Oct. 18 | 10:00 AM PDT, 6:00 PM BST
Asia-Pacific broadcast: Thurs., Oct. 19 | 11:00 AM SGT
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 to see what they haven’t been able to before.
In this webinar, learn about game-changing liquid biopsy research capabilities made possible by the Onso sequencing system and powered by proprietary sequencing by binding (SBB) chemistry.
Watch On-Demand Webinars
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…
Understanding clonal evolution using game theory and single-cell long-read isoform analysis
April 11, 2023
Dr. Nathan Salomonis of Cincinnati Children’s Hospital Medical Center presented how he used the MAS-Seq kit and sequencing on the PacBio Revio system to provide new insights into leukemia clonal…
Descubra el poder de las secuencias largas y de alta precisión
April 04, 2023
Con este seminario web descubrirá como las secuencias largas y de alta precisión le ayudarán a lograr nuevos descubrimientos en sus investigaciones, y cómo el nuevo sistema Revio está revolucionado…
Metagenome assembly and characterization of a pooled human fecal reference
March 16, 2023
Leading scientists from PacBio and Zymo Research will present state-of-the art HiFi metagenomic sequencing solutions that will enable microbiome researchers to make important discoveries
New methods to characterize VNTR variation in human genomes
February 22, 2023
Variable number tandem repeats (VNTRs) make up almost 3% of the human genome and are difficult to map, due to their repetitive nature. In this webinar, Mark Chaisson, PhD, of…
Tackling challenging genes and their paralogs involved in recessive disorders
February 15, 2023 - February 16, 2023
Effective carrier and newborn screening methods are critical for solving problems in reproductive medicine and launching treatment plans for early-onset genetic diseases. Clinical research faces a number of well-known challenges…
Single-cell RNA sequencing with MAS-Seq
November 16, 2022
Join us for an engaging webinar where PacBio scientists will present the MAS-Seq method, an all-new kitted single-cell transcriptomics solution that delivers exceptional data quality and explanatory power for your next big breakthrough…
Optimizing and confirming AAV designs with PacBio sequencing
November 17, 2022
Find out how to generate and analyze full-length adeno-associated virus (AAV) sequencing data to profile packaged genomes as a single intact molecule, measure impurities, and ensure vectors contain the intended…
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…
Uncovering the unseen in human genomic research sequencing
September 27, 2022 - September 28, 2022
Hear about new tools in human genomics research that will help you do more and further your discoveries. Our speakers will discuss the capabilities of a new PacBio solution –…
Highly Accurate HiFi Reads for Discovery, Design, and Manufacturing of AAV Gene Therapy
June 22, 2022
Join us for this live webinar to learn how experts in the field of gene therapy research are using HiFi reads for better and more efficient vector design and quality…
The RNA Isoform Landscape of Cancer
July 20, 2022
Learn how PacBio’s accurate long-read RNA sequencing provides true discovery power of cancer-related RNA isoforms and allows for the understanding of molecular mechanisms underlying cancer biology