Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Dilthey, Alexander, Leslie, Stephen, Moutsianas, Loukas, Shen, Judong, Cox, Charles, Nelson, Matthew R., McVean, Gil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
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
_version_ 1782259372529811456
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
work_keys_str_mv AT diltheyalexander multipopulationclassicalhlatypeimputation
AT lesliestephen multipopulationclassicalhlatypeimputation
AT moutsianasloukas multipopulationclassicalhlatypeimputation
AT shenjudong multipopulationclassicalhlatypeimputation
AT coxcharles multipopulationclassicalhlatypeimputation
AT nelsonmatthewr multipopulationclassicalhlatypeimputation
AT mcveangil multipopulationclassicalhlatypeimputation