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Cited by 206

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A Hidden Markov Model Combining Linkage and Linkage Disequilibrium Information for Haplotype Reconstruction and Quantitative Trait Locus Fine Mapping

Open access
Druet, Tom, Georges, Michel·2010·Genetics

Abstract

Faithful reconstruction of haplotypes from diploid marker data (phasing) is important for many kinds of genetic analyses, including mapping of trait loci, prediction of genomic breeding values, and identification of signatures of selection. In human genetics, phasing most often exploits population information (linkage disequilibrium), while in animal genetics the primary source of information is familial (Mendelian segregation and linkage). We herein develop and evaluate a method that simultaneously exploits both sources of information. It builds on hidden Markov models that were initially developed to exploit population information only. We demonstrate that the approach improves the accuracy of allele phasing as well as imputation of missing genotypes. Reconstructed haplotypes are assigned to hidden states that are shown to correspond to clusters of genealogically related chromosomes. We show that these cluster states can directly be used to fine map QTL. The method is computationally effective at handling large data sets based on high-density SNP panels.

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Crossref · 10.1534/genetics.109.108431

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Metadata

Authors
Druet, T., & Georges, M.
Venue
Genetics
Published
2010-03-01
Volume
184
Issue
3
Pages
789-798
ISSN
  • 0016-6731 (ISSN-L)
  • 1943-2631
OpenAlex
W2161040839
Cited by
206
References
5
FWCI
7.84
Type
journal article
Language
en
Open access
green

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CoChat. (2026). Citation check: A Hidden Markov Model Combining Linkage and Linkage Disequilibrium Information for Haplotype Reconstruction and Quantitative Trait Locus Fine Mapping. https://app.cochat.ai/papers/10.1534/genetics.109.108431
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Druet, T., & Georges, M. (2010). A Hidden Markov Model Combining Linkage and Linkage Disequilibrium Information for Haplotype Reconstruction and Quantitative Trait Locus Fine Mapping. Genetics. https://doi.org/10.1534/genetics.109.108431

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