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Integrity of genome-wide genotype data from low passage lymphoblastoid cell lines

We compared genotype data from the HumanExomeCore Array in peripheral blood mononuclear cells and low passage lymphoblastoid cell lines from the same 24 individuals to test for genotypic errors caused by the Epstein–Barr Virus transformation process. Genotype concordance across the 24 comparisons wa...

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Autores principales: McCarthy, Nina S., Allan, Spencer M., Chandler, David, Jablensky, Assen, Morar, Bharti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909818/
https://www.ncbi.nlm.nih.gov/pubmed/27330997
http://dx.doi.org/10.1016/j.gdata.2016.05.006
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author McCarthy, Nina S.
Allan, Spencer M.
Chandler, David
Jablensky, Assen
Morar, Bharti
author_facet McCarthy, Nina S.
Allan, Spencer M.
Chandler, David
Jablensky, Assen
Morar, Bharti
author_sort McCarthy, Nina S.
collection PubMed
description We compared genotype data from the HumanExomeCore Array in peripheral blood mononuclear cells and low passage lymphoblastoid cell lines from the same 24 individuals to test for genotypic errors caused by the Epstein–Barr Virus transformation process. Genotype concordance across the 24 comparisons was 99.57% for unfiltered genotype data, and 99.63% following standard genotype quality control filters. Mendelian error rates and levels of heterozygosity were not significantly different between lymphoblastoid cell lines and their parent peripheral blood mononuclear cells. These results show that at low passage numbers, genotype discrepancies are minimal even before stringent quality control, and extend current evidence qualifying the use of low-passage lymphoblastoid cell lines as a reliable DNA source for genotype analysis.
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spelling pubmed-49098182016-06-21 Integrity of genome-wide genotype data from low passage lymphoblastoid cell lines McCarthy, Nina S. Allan, Spencer M. Chandler, David Jablensky, Assen Morar, Bharti Genom Data Regular Article We compared genotype data from the HumanExomeCore Array in peripheral blood mononuclear cells and low passage lymphoblastoid cell lines from the same 24 individuals to test for genotypic errors caused by the Epstein–Barr Virus transformation process. Genotype concordance across the 24 comparisons was 99.57% for unfiltered genotype data, and 99.63% following standard genotype quality control filters. Mendelian error rates and levels of heterozygosity were not significantly different between lymphoblastoid cell lines and their parent peripheral blood mononuclear cells. These results show that at low passage numbers, genotype discrepancies are minimal even before stringent quality control, and extend current evidence qualifying the use of low-passage lymphoblastoid cell lines as a reliable DNA source for genotype analysis. Elsevier 2016-05-12 /pmc/articles/PMC4909818/ /pubmed/27330997 http://dx.doi.org/10.1016/j.gdata.2016.05.006 Text en © 2016 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Regular Article
McCarthy, Nina S.
Allan, Spencer M.
Chandler, David
Jablensky, Assen
Morar, Bharti
Integrity of genome-wide genotype data from low passage lymphoblastoid cell lines
title Integrity of genome-wide genotype data from low passage lymphoblastoid cell lines
title_full Integrity of genome-wide genotype data from low passage lymphoblastoid cell lines
title_fullStr Integrity of genome-wide genotype data from low passage lymphoblastoid cell lines
title_full_unstemmed Integrity of genome-wide genotype data from low passage lymphoblastoid cell lines
title_short Integrity of genome-wide genotype data from low passage lymphoblastoid cell lines
title_sort integrity of genome-wide genotype data from low passage lymphoblastoid cell lines
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4909818/
https://www.ncbi.nlm.nih.gov/pubmed/27330997
http://dx.doi.org/10.1016/j.gdata.2016.05.006
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