Webinar
Bioinformatics resources to analyze HiFi cancer genomes
August 06, 2024 - August 07, 2024
Americas broadcast: Tuesday, August 6, 9:00 AM PDT | 5:00 PM BST
Asia-Pacific broadcast: Wednesday, August 7, 11:00 AM SGT
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 the characteristics of HiFi data. This includes tools for calling somatic single-nucleotide variants, indels, CNVs, structural variants, methylation, and mutational signatures.
In this webinar, we will present bioinformatic solutions for calling these variant types, as well as integrating them into a single, easy-to-use pipeline.