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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.

Register now

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…

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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,…

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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 •…

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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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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…

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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…

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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…

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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…

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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…

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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

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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…

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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…

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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…

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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…

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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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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 –…

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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…

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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

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