Abstract
Recent developments in PacBio high-fidelity (HiFi) sequencing technologies have transformed genomic research, with circular consensus sequencing now achieving 99.9% accuracy for long (up to 25 kb) single-molecule reads. This method circumvents biases intrinsic to amplification-based approaches, enabling thorough analysis of complex genomic regions [including tandem repeats, segmental duplications, ribosomal DNA (rDNA) arrays, and centromeres] as well as direct detection of base modifications, furnishing both sequence and epigenetic data concurrently. This has streamlined a number of tasks including genome assembly, variant detection, and full-length transcript analysis. This review provides a comprehensive overview of the applications and challenges of HiFi sequencing across various fields, including genomics, transcriptomics, and epigenetics. By delineating the evolving landscape of HiFi sequencing in multi-omics research, we highlight its potential to deepen our understanding of genetic mechanisms and to advance precision medicine.
| Original language | English |
|---|---|
| Article number | qzaf003 |
| Journal | Genomics, proteomics & bioinformatics / Beijing Genomics Institute |
| Volume | 23 |
| Issue number | 1 |
| DOIs | |
| State | Published - 1 Feb 2025 |
Keywords
- Centromere
- Complex genomic region
- Genome assembly
- Long-read sequencing
- Variant detection
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