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Detecting cancer fusion transcripts in long-read RNA-Seq data with CTAT-LR-fusion

September 11, 2024 - September 12, 2024

In this webinar, you will learn about CTAT-LR-fusion, a new bioinformatics tool for detecting known and novel fusion transcripts from PacBio long-read isoform sequencing data, with applications to bulk and…

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Bioinformatics resources to analyze HiFi cancer genomes

August 06, 2024 - August 07, 2024

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…

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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…

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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.

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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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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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