ArticleAmerican journal of human genetics2006
A comparison of phasing algorithms for trios and unrelated individuals.
Article in American journal of human genetics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 137 papers, 1 of them a synthesis that pooled it.
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137 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Genome-Wide Association Study Identifies African-Specific Susceptibility Loci in African Americans With Inflammatory Bowel Disease.Gastroenterology · 2017Pooled it
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- KnockoffHybrid: A knockoff framework for hybrid analysis of trio and population designs in genome-wide association studies.American journal of human genetics · 2024Article
- Direct Comparative Analysis of a Pharmacogenomics Panel with PacBio HifiJournal of personalized medicine · 2023Article
- Imputation of ancient human genomes.Nature communications · 2023Article
- Haplotyping-Assisted Diploid Assembly and Variant Detection with Linked Reads.Methods in molecular biology (Clifton, N.J.) · 2023Review
- KnockoffTrio: A knockoff framework for the identification of putative causal variants in genome-wide association studies with trio design.American journal of human genetics · 2022Article
- North Asian population relationships in a global context.Scientific reports · 2022Article
- Benchmarking phasing software with a whole-genome sequenced cattle pedigree.BMC genomics · 2022Article
- Accurate haplotype-resolved assembly reveals the origin of structural variants for human trios.Bioinformatics (Oxford, England) · 2021Article
- Plant-ImputeDB: an integrated multiple plant reference panel database for genotype imputation.Nucleic acids research · 2021Article
- Causal inference in genetic trio studies.Proceedings of the National Academy of Sciences of the United States of America · 2020Article
- Oligonucleotide hybridization with magnetic separation assay for multiple SNP phasing.Analytica chimica acta: X · 2020Article
- Exploring effective approaches for haplotype block phasing.BMC bioinformatics · 2019Article
- Evaluating the quality of the 1000 genomes project data.BMC genomics · 2019Article
- A New Fast Phasing Method Based On Haplotype Subtraction.The Journal of molecular diagnostics : JMD · 2019Article
- Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans.Human molecular genetics · 2018Article
- Enhanced Contribution of HLA in Pediatric Onset Ulcerative Colitis.Inflammatory bowel diseases · 2018Article
77 more citing papers are in PubMed but not listed here.
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12 authors.
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Abstract
Knowledge of haplotype phase is valuable for many analysis methods in the study of disease, population, and evolutionary genetics. Considerable research effort has been devoted to the development of statistical and computational methods that infer haplotype phase from genotype data. Although a substantial number of such methods have been developed, they have focused principally on inference from unrelated individuals, and comparisons between methods have been rather limited. Here, we describe the extension of five leading algorithms for phase inference for handling father-mother-child trios. We performed a comprehensive assessment of the methods applied to both trios and to unrelated individuals, with a focus on genomic-scale problems, using both simulated data and data from the HapMap project. The most accurate algorithm was PHASE (v2.1). For this method, the percentages of genotypes whose phase was incorrectly inferred were 0.12%, 0.05%, and 0.16% for trios from simulated data, HapMap Centre d'Etude du Polymorphisme Humain (CEPH) trios, and HapMap Yoruban trios, respectively, and 5.2% and 5.9% for unrelated individuals in simulated data and the HapMap CEPH data, respectively. The other methods considered in this work had comparable but slightly worse error rates. The error rates for trios are similar to the levels of genotyping error and missing data expected. We thus conclude that all the methods considered will provide highly accurate estimates of haplotypes when applied to trio data sets. Running times differ substantially between methods. Although it is one of the slowest methods, PHASE (v2.1) was used to infer haplotypes for the 1 million-SNP HapMap data set. Finally, we evaluated methods of estimating the value of r(2) between a pair of SNPs and concluded that all methods estimated r(2) well when the estimated value was >or=0.8.
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