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Multi-Population Classical HLA Type Imputation
Statistical imputation of classical HLA alleles in case-control studies has become established as a valuable tool for identifying and fine-mapping signals of disease association in the MHC. Imputation into diverse populations has, however, remained challenging, mainly because of the additional haplo...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3572961/ https://www.ncbi.nlm.nih.gov/pubmed/23459081 http://dx.doi.org/10.1371/journal.pcbi.1002877 |
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author | Dilthey, Alexander Leslie, Stephen Moutsianas, Loukas Shen, Judong Cox, Charles Nelson, Matthew R. McVean, Gil |
author_facet | Dilthey, Alexander Leslie, Stephen Moutsianas, Loukas Shen, Judong Cox, Charles Nelson, Matthew R. McVean, Gil |
author_sort | Dilthey, Alexander |
collection | PubMed |
description | Statistical imputation of classical HLA alleles in case-control studies has become established as a valuable tool for identifying and fine-mapping signals of disease association in the MHC. Imputation into diverse populations has, however, remained challenging, mainly because of the additional haplotypic heterogeneity introduced by combining reference panels of different sources. We present an HLA type imputation model, HLA*IMP:02, designed to operate on a multi-population reference panel. HLA*IMP:02 is based on a graphical representation of haplotype structure. We present a probabilistic algorithm to build such models for the HLA region, accommodating genotyping error, haplotypic heterogeneity and the need for maximum accuracy at the HLA loci, generalizing the work of Browning and Browning (2007) and Ron et al. (1998). HLA*IMP:02 achieves an average 4-digit imputation accuracy on diverse European panels of 97% (call rate 97%). On non-European samples, 2-digit performance is over 90% for most loci and ethnicities where data available. HLA*IMP:02 supports imputation of HLA-DPB1 and HLA-DRB3-5, is highly tolerant of missing data in the imputation panel and works on standard genotype data from popular genotyping chips. It is publicly available in source code and as a user-friendly web service framework. |
format | Online Article Text |
id | pubmed-3572961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-35729612013-03-01 Multi-Population Classical HLA Type Imputation Dilthey, Alexander Leslie, Stephen Moutsianas, Loukas Shen, Judong Cox, Charles Nelson, Matthew R. McVean, Gil PLoS Comput Biol Research Article Statistical imputation of classical HLA alleles in case-control studies has become established as a valuable tool for identifying and fine-mapping signals of disease association in the MHC. Imputation into diverse populations has, however, remained challenging, mainly because of the additional haplotypic heterogeneity introduced by combining reference panels of different sources. We present an HLA type imputation model, HLA*IMP:02, designed to operate on a multi-population reference panel. HLA*IMP:02 is based on a graphical representation of haplotype structure. We present a probabilistic algorithm to build such models for the HLA region, accommodating genotyping error, haplotypic heterogeneity and the need for maximum accuracy at the HLA loci, generalizing the work of Browning and Browning (2007) and Ron et al. (1998). HLA*IMP:02 achieves an average 4-digit imputation accuracy on diverse European panels of 97% (call rate 97%). On non-European samples, 2-digit performance is over 90% for most loci and ethnicities where data available. HLA*IMP:02 supports imputation of HLA-DPB1 and HLA-DRB3-5, is highly tolerant of missing data in the imputation panel and works on standard genotype data from popular genotyping chips. It is publicly available in source code and as a user-friendly web service framework. Public Library of Science 2013-02-14 /pmc/articles/PMC3572961/ /pubmed/23459081 http://dx.doi.org/10.1371/journal.pcbi.1002877 Text en © 2013 Dilthey et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Dilthey, Alexander Leslie, Stephen Moutsianas, Loukas Shen, Judong Cox, Charles Nelson, Matthew R. McVean, Gil Multi-Population Classical HLA Type Imputation |
title | Multi-Population Classical HLA Type Imputation |
title_full | Multi-Population Classical HLA Type Imputation |
title_fullStr | Multi-Population Classical HLA Type Imputation |
title_full_unstemmed | Multi-Population Classical HLA Type Imputation |
title_short | Multi-Population Classical HLA Type Imputation |
title_sort | multi-population classical hla type imputation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3572961/ https://www.ncbi.nlm.nih.gov/pubmed/23459081 http://dx.doi.org/10.1371/journal.pcbi.1002877 |
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