Get the most out of your HiFi sequencing data with expert-led computational biology primers
Whether you’re new to long-read sequencing or looking to expand your analysis toolkit, access our exclusive four-part video series that will guide you through essential computational tools for PacBio HiFi whole genome sequencing data.
Each short, easy-to-follow video, led by PacBio scientists, breaks down complex analysis methods into approachable, practical steps – ideal for researchers, clinicians, and bioinformaticians alike. You’ll discover how to detect and interpret complex variant types, leverage specialized algorithms, and apply these insights to real-world research and clinical scenarios.
Learn about these tools:
✔ WGS Variant Calling Pipeline: Get to know PacBio’s primary WGS pipeline for calling highly accurate SNVs, indels, and structural variants.
✔ TRGT: Detect, size, and analyze tandem repeat expansions with base pair-level precision.
✔ Paraphase: Resolve genes in segmental duplications and homologous regions for improved resolution of challenging loci.
✔ StarPhase: Leverage long-read phasing to accurately and unambiguously determine star (*)-alleles for pharmacogenomics and HLA applications.
Sign up now to access the full series and start getting the most out of your HiFi sequencing data.
