2025/01/01 by Ulrich Hartmann, Eran Shaham, Dafna Nathan +2 · 1 voice
Biochemistry, Genetics and Molecular Biology · #Genetic Associations and Epidemiology #Genomics and Rare Diseases #Genomic variations and chromosomal abnormalities
paper · pdf · doi:10.1093/gigascience/giaf138
openalex publication_date 2025/01/01 · openalex created_date 2025/10/28 · openalex updated_date 2026/07/29
BACKGROUND: Phasing, the assignment of alleles to their respective parental chromosomes, is fundamental to studying genetic variation and identifying disease-causing variants. Traditional approaches, including statistical, pedigree-based, and read-based phasing, face challenges such as limited accuracy for rare variants and reliance on external reference panels. RESULTS: To address these limitations, we developed TinkerHap, a novel phasing algorithm that integrates a read-based phaser, based on a pairwise distance-based unsupervised classification, with external phased data, such as statistical or pedigree phasing. We evaluated TinkerHap's performance against other phasing algorithms using 1,040 parent-offspring trios from the UK Biobank (Illumina short reads) and GIAB Ashkenazi trio (PacBio long reads). TinkerHap's read-based phaser alone achieved higher phasing accuracies than all other algorithms with 95.1% for short reads (second best: 94.8%) and 97.5% for long reads (second best: 95.5%). Its hybrid approach further enhanced short-read performance to 96.3% accuracy and was able to phase 99.5% of all heterozygous sites. TinkerHap also extended haplotype block sizes to a median of 79,449 bp for long reads (second best: 68,303 bp) and demonstrated higher accuracy for both single-nucleotide polymorphisms and indels. CONCLUSIONS: The combination of a robust read-based algorithm and a hybrid integration strategy makes TinkerHap a powerful and versatile tool for genomic analysis, enabling more accurate, contiguous, and comprehensive phasing across diverse sequencing platforms and variant types.