Uploaded August 2024 | Updated September 2026, 28 minutes ago

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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 present bioinformatic solutions for calling these variant types, as well as integrating them into a single, easy-to-use pipeline.

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