PacBio HiFi reads can detect single-nucleotide variants (SNVs), small indels (<20 bp in length) and structural variants (SVs), such as insertions, deletions, duplications, inversions, translocations, short tandem repeats (STRs), and copy number variants (CNVs). For more details, please see our Variant detection webpage.
December 13, 2023
What types of genomic variants can be detected from PacBio HiFi data?
Subscribe for blog updates:
Filter by topic
- Bioinformatics
- Gene therapy + editing
- Metagenomics
- Sequencing methods
- Liquid biopsy
- HiFi difference
- Featured
- Computational tools
- Haplotype
- Genomic sequencing
- Repeat expansions
- Multiomics
- Biopharma
- Customer success stories
- Powered by PacBio
- People First
- Human genetics research
- Corporate news
- General
- Events + conferences
- Plant + animal biology
- Products, procedures + protocols
- Infectious disease research
- Microbial sequencing methods
- Sequencing 101
- Agrigenomics
- Pharmacogenomics
- Rare disease
- Microbiome
- Data analysis
- Neurogenomics
- Cancer research
- Biodiversity
- Immunogenomics + HLA
- Public health + surveillance
- Sample + library preparation