Asset Type: Application brochures and briefs
Application brief — Comprehensive human genomic variant detection with HiFi long-read sequencing
Application brief — Microbial genomics at scale with PacBio HiFi sequencing
Application brief — HiFi sequencing enables greater accuracy of somatic variant calling
Application brief — Highly-accurate HiFi reads gene editing
Application brief — Highly-accurate HiFi reads for AAV-research
Application brief — Germline variant detection with the Onso system
Application brief — What can you do with a Revio system
Application brief — Superior sensitivity for ctDNA detection on the Onso System
Application brief — Taxonomic and functional profiling with HiFi metagenomics
Application brief — Scalable HiFi sequencing with Twist Bioscience long-read alliance panels
Application brief — HiFi target enrichment with Twist probes
With HiFi target enrichment you can easily and cost-effectively sequence just the genes you care about at scale. Design custom gene panels with our partners at Twist, sequence them with long and accurate HiFi reads, and get all the benefits you expect from HiFi reads: comprehensive detection of single nucleotide variants, structural variants, and indels. HiFi target enrichment is the only technology that can resolve complex gene families like HLA or Cytochrome P450 genes with haplotype resolution.
Application brief — HIFI WGS at scale on the Sequel IIe system
Scale your whole genome sequencing (WGS) and epigenome workflows with PacBio® HiFi reads employing a single technician working one day a week. Sequence 25 human genomes at ≥ 30-fold coverage each month using four Sequel® II systems.*