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Upcoming webinar - APAC region

Welcome to the accuracy era: Introducing Onso

June 06, 2023
8:30 – 9:30 am (India)
11:00 am – 12:00 pm (Singapore)
12:00 – 1:00 pm (Seoul, Tokyo)
2:00 – 3:00 pm (Melbourne)

The broad adoption of next-generation sequencing technologies (NGS) has been driven by technological advances, resulting in increased throughput and lowered costs, akin to Moore’s Law in the semiconductor industry. However, a significant sequencing metric, accuracy, has made little progress over the years, hindering efforts to adopt important applications such as liquid biopsy, which require detection of low variant allele frequency events. Register now to hear how the Onso system, a benchtop short-read system, can provide exceptional accuracy to propel the next phase of discoveries in applications traditionally underserved by existing on-market NGS platforms.

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Upcoming bioinformatics webinar

Streamlined chromosome-scale phasing with HiFi sequencing

Tuesday, June 20, 2023
10.00 AM EDT | 3.00 PM BST | 4.00 PM CEST

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 Garg, PhD discusses innovative methods for efficient and accurate haplotype-resolved genome assembly that enable new, unbiased studies of haplotype variation.

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Upcoming webinar

Shining a light on dark genes in population sequencing

 Americas broadcast: Tuesday, June 20 | 9:00 am PDT
 Europe broadcast: Thursday, June 22 | 3:00 pm BST
 Asia-Pacific broadcast: Thursday, June 22 | 11:00 am SGT

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 on discovering novel variants, determining frequencies, or empowering precision health for the greater good, having the most comprehensive and accurate sequencing technology is vitally important. HiFi long-read sequencing allows scientists to study populations in incredible detail to drive discovery and democratize findings for maximum global impact—far into the future.

Join us for this exciting digital event where Fritz Sedlazeck, PhD from Baylor College of Medicine and Kiran Garimella, PhD from the Broad Institute and All of Us program will explain how HiFi long-read sequencing is energizing the potential of population genomics by enabling scientists to:

  • Catalogue all genetic variation, reflecting a population’s true diversity.
  • Maximize discovery potential to enable the most accurate insights possible.

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Watch On-Demand Webinars

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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HiFi Metagenomics: More Samples, More Species, More MAGs

April 27, 2022

PacBio HiFi sequencing is setting a new standard for quality and resolution in metagenome sequencing thanks to significant strides in data analysis tools. Learn from expert bioinformaticians how using the…

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Unlocking the Genome with Long-Read Sequencing in Genetic Disease Research

April 07, 2022

Follow two scientists on their journey of discovery using whole genome sequencing and single-cell RNA sequencing to shed light on previously unresolved medical mysteries.

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Pediatric Rare Disease Genomes and the Role of Long-Read Sequencing

March 30, 2022

Join us for this live webinar to hear how Children’s Mercy Kansas City successfully analyzed samples from 960 families with suspected genetic disorders and prior negative genetic tests. Using HiFi…

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Getting the Most Out of Your Breeding Program with DNA & RNA Sequencing

September 21, 2021

Join us for this webinar to understand the evolution of sequencing technologies and where they stand today, the experiences of three plant biologists incorporating sequencing into their work, and how…

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Revealing Mechanisms of Bacterial Virulence and Adaptation with PacBio SMRT Sequencing

September 02, 2021

Learn how scientists are using highly accurate long-read sequencing to make new discoveries about bacteria, viruses, and the complex systems they inhabit and influence in this, the fourth of a…

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Identifying Key Players in Host-Microbiome Interactions with High Resolution 16S Sequencing

August 19, 2021

Learn how scientists are using highly accurate long-read sequencing to make new discoveries about bacteria, viruses, and the complex systems they inhabit and influence in this, the third of a…

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