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ATHLATES: accurate typing of human leukocyte antigen through exome sequencing

Human leukocyte antigen (HLA) typing at the allelic level can in theory be achieved using whole exome sequencing (exome-seq) data with no added cost but has been hindered by its computational challenge. We developed ATHLATES, a program that applies assembly, allele identification and allelic pair in...

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Autores principales: Liu, Chang, Yang, Xiao, Duffy, Brian, Mohanakumar, Thalachallour, Mitra, Robi D., Zody, Michael C., Pfeifer, John D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3737559/
https://www.ncbi.nlm.nih.gov/pubmed/23748956
http://dx.doi.org/10.1093/nar/gkt481
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author Liu, Chang
Yang, Xiao
Duffy, Brian
Mohanakumar, Thalachallour
Mitra, Robi D.
Zody, Michael C.
Pfeifer, John D.
author_facet Liu, Chang
Yang, Xiao
Duffy, Brian
Mohanakumar, Thalachallour
Mitra, Robi D.
Zody, Michael C.
Pfeifer, John D.
author_sort Liu, Chang
collection PubMed
description Human leukocyte antigen (HLA) typing at the allelic level can in theory be achieved using whole exome sequencing (exome-seq) data with no added cost but has been hindered by its computational challenge. We developed ATHLATES, a program that applies assembly, allele identification and allelic pair inference to short read sequences, and applied it to data from Illumina platforms. In 15 data sets with adequate coverage for HLA-A, -B, -C, -DRB1 and -DQB1 genes, ATHLATES correctly reported 74 out of 75 allelic pairs with an overall concordance rate of 99% compared with conventional typing. This novel approach should be broadly applicable to research and clinical laboratories.
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spelling pubmed-37375592013-08-08 ATHLATES: accurate typing of human leukocyte antigen through exome sequencing Liu, Chang Yang, Xiao Duffy, Brian Mohanakumar, Thalachallour Mitra, Robi D. Zody, Michael C. Pfeifer, John D. Nucleic Acids Res Methods Online Human leukocyte antigen (HLA) typing at the allelic level can in theory be achieved using whole exome sequencing (exome-seq) data with no added cost but has been hindered by its computational challenge. We developed ATHLATES, a program that applies assembly, allele identification and allelic pair inference to short read sequences, and applied it to data from Illumina platforms. In 15 data sets with adequate coverage for HLA-A, -B, -C, -DRB1 and -DQB1 genes, ATHLATES correctly reported 74 out of 75 allelic pairs with an overall concordance rate of 99% compared with conventional typing. This novel approach should be broadly applicable to research and clinical laboratories. Oxford University Press 2013-08 2013-06-08 /pmc/articles/PMC3737559/ /pubmed/23748956 http://dx.doi.org/10.1093/nar/gkt481 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Methods Online
Liu, Chang
Yang, Xiao
Duffy, Brian
Mohanakumar, Thalachallour
Mitra, Robi D.
Zody, Michael C.
Pfeifer, John D.
ATHLATES: accurate typing of human leukocyte antigen through exome sequencing
title ATHLATES: accurate typing of human leukocyte antigen through exome sequencing
title_full ATHLATES: accurate typing of human leukocyte antigen through exome sequencing
title_fullStr ATHLATES: accurate typing of human leukocyte antigen through exome sequencing
title_full_unstemmed ATHLATES: accurate typing of human leukocyte antigen through exome sequencing
title_short ATHLATES: accurate typing of human leukocyte antigen through exome sequencing
title_sort athlates: accurate typing of human leukocyte antigen through exome sequencing
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3737559/
https://www.ncbi.nlm.nih.gov/pubmed/23748956
http://dx.doi.org/10.1093/nar/gkt481
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