WEBINAR
The detection of genomic variants in cancer depends on an array of complementary and overlapping methods including fluorescence in situ hybridization (FISH), karyotyping, and DNA and/or RNA sequencing. The need for an "all-in-one," comprehensive genomic assay that captures all variants accurately is needed to improve variant detection, as well as reduce cost and maximize precious samples.
Accurate long-read sequencing from PacBio (HiFi sequencing) offers whole-genome and transcriptome sequencing for the detection of DNA and RNA variants, including methylation. In this webinar you will hear about how HiFi sequencing enabled the detection of variants in pediatric leukemia samples that were missed by other technologies, bringing us a step closer to the promise of a single comprehensive assay.
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Don’t forget to stick around and have your questions answered during the live Q&A session at the end of the event!
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Director, Molecular Oncology, Children’s Mercy Hospital
Assistant Director, Molecular Genetics, Children’s Mercy Hospital
Associate Director, Cancer Genomics, PacBio
Manager, Oncology & Cancer Research, PacBio
Host and moderator