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High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA

Stored neonatal dried blood spot (DBS) samples from neonatal screening programmes are a valuable diagnostic and research resource. Combined with information from national health registries they can be used in population-based studies of genetic diseases. DNA extracted from neonatal DBSs can be ampli...

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Autores principales: Poulsen, Jesper Buchhave, Lescai, Francesco, Grove, Jakob, Bækvad-Hansen, Marie, Christiansen, Michael, Hagen, Christian Munch, Maller, Julian, Stevens, Christine, Li, Shenting, Li, Qibin, Sun, Jihua, Wang, Jun, Nordentoft, Merete, Werge, Thomas Mears, Mortensen, Preben Bo, Børglum, Anders Dupont, Daly, Mark, Hougaard, David Michael, Bybjerg-Grauholm, Jonas, Hollegaard, Mads Vilhelm
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4835089/
https://www.ncbi.nlm.nih.gov/pubmed/27089011
http://dx.doi.org/10.1371/journal.pone.0153253
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author Poulsen, Jesper Buchhave
Lescai, Francesco
Grove, Jakob
Bækvad-Hansen, Marie
Christiansen, Michael
Hagen, Christian Munch
Maller, Julian
Stevens, Christine
Li, Shenting
Li, Qibin
Sun, Jihua
Wang, Jun
Nordentoft, Merete
Werge, Thomas Mears
Mortensen, Preben Bo
Børglum, Anders Dupont
Daly, Mark
Hougaard, David Michael
Bybjerg-Grauholm, Jonas
Hollegaard, Mads Vilhelm
author_facet Poulsen, Jesper Buchhave
Lescai, Francesco
Grove, Jakob
Bækvad-Hansen, Marie
Christiansen, Michael
Hagen, Christian Munch
Maller, Julian
Stevens, Christine
Li, Shenting
Li, Qibin
Sun, Jihua
Wang, Jun
Nordentoft, Merete
Werge, Thomas Mears
Mortensen, Preben Bo
Børglum, Anders Dupont
Daly, Mark
Hougaard, David Michael
Bybjerg-Grauholm, Jonas
Hollegaard, Mads Vilhelm
author_sort Poulsen, Jesper Buchhave
collection PubMed
description Stored neonatal dried blood spot (DBS) samples from neonatal screening programmes are a valuable diagnostic and research resource. Combined with information from national health registries they can be used in population-based studies of genetic diseases. DNA extracted from neonatal DBSs can be amplified to obtain micrograms of an otherwise limited resource, referred to as whole-genome amplified DNA (wgaDNA). Here we investigate the robustness of exome sequencing of wgaDNA of neonatal DBS samples. We conducted three pilot studies of seven, eight and seven subjects, respectively. For each subject we analysed a neonatal DBS sample and corresponding adult whole-blood (WB) reference sample. Different DNA sample types were prepared for each of the subjects. Pilot 1: wgaDNA of 2x3.2mm neonatal DBSs (DBS_2x3.2) and raw DNA extract of the WB reference sample (WB_ref). Pilot 2: DBS_2x3.2, WB_ref and a WB_ref replica sharing DNA extract with the WB_ref sample. Pilot 3: DBS_2x3.2, WB_ref, wgaDNA of 2x1.6 mm neonatal DBSs and wgaDNA of the WB reference sample. Following sequencing and data analysis, we compared pairwise variant calls to obtain a measure of similarity—the concordance rate. Concordance rates were slightly lower when comparing DBS vs WB sample types than for any two WB sample types of the same subject before filtering of the variant calls. The overall concordance rates were dependent on the variant type, with SNPs performing best. Post-filtering, the comparisons of DBS vs WB and WB vs WB sample types yielded similar concordance rates, with values close to 100%. WgaDNA of neonatal DBS samples performs with great accuracy and efficiency in exome sequencing. The wgaDNA performed similarly to matched high-quality reference—whole-blood DNA—based on concordance rates calculated from variant calls. No differences were observed substituting 2x3.2 with 2x1.6 mm discs, allowing for additional reduction of sample material in future projects.
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spelling pubmed-48350892016-04-29 High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA Poulsen, Jesper Buchhave Lescai, Francesco Grove, Jakob Bækvad-Hansen, Marie Christiansen, Michael Hagen, Christian Munch Maller, Julian Stevens, Christine Li, Shenting Li, Qibin Sun, Jihua Wang, Jun Nordentoft, Merete Werge, Thomas Mears Mortensen, Preben Bo Børglum, Anders Dupont Daly, Mark Hougaard, David Michael Bybjerg-Grauholm, Jonas Hollegaard, Mads Vilhelm PLoS One Research Article Stored neonatal dried blood spot (DBS) samples from neonatal screening programmes are a valuable diagnostic and research resource. Combined with information from national health registries they can be used in population-based studies of genetic diseases. DNA extracted from neonatal DBSs can be amplified to obtain micrograms of an otherwise limited resource, referred to as whole-genome amplified DNA (wgaDNA). Here we investigate the robustness of exome sequencing of wgaDNA of neonatal DBS samples. We conducted three pilot studies of seven, eight and seven subjects, respectively. For each subject we analysed a neonatal DBS sample and corresponding adult whole-blood (WB) reference sample. Different DNA sample types were prepared for each of the subjects. Pilot 1: wgaDNA of 2x3.2mm neonatal DBSs (DBS_2x3.2) and raw DNA extract of the WB reference sample (WB_ref). Pilot 2: DBS_2x3.2, WB_ref and a WB_ref replica sharing DNA extract with the WB_ref sample. Pilot 3: DBS_2x3.2, WB_ref, wgaDNA of 2x1.6 mm neonatal DBSs and wgaDNA of the WB reference sample. Following sequencing and data analysis, we compared pairwise variant calls to obtain a measure of similarity—the concordance rate. Concordance rates were slightly lower when comparing DBS vs WB sample types than for any two WB sample types of the same subject before filtering of the variant calls. The overall concordance rates were dependent on the variant type, with SNPs performing best. Post-filtering, the comparisons of DBS vs WB and WB vs WB sample types yielded similar concordance rates, with values close to 100%. WgaDNA of neonatal DBS samples performs with great accuracy and efficiency in exome sequencing. The wgaDNA performed similarly to matched high-quality reference—whole-blood DNA—based on concordance rates calculated from variant calls. No differences were observed substituting 2x3.2 with 2x1.6 mm discs, allowing for additional reduction of sample material in future projects. Public Library of Science 2016-04-18 /pmc/articles/PMC4835089/ /pubmed/27089011 http://dx.doi.org/10.1371/journal.pone.0153253 Text en © 2016 Poulsen 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Poulsen, Jesper Buchhave
Lescai, Francesco
Grove, Jakob
Bækvad-Hansen, Marie
Christiansen, Michael
Hagen, Christian Munch
Maller, Julian
Stevens, Christine
Li, Shenting
Li, Qibin
Sun, Jihua
Wang, Jun
Nordentoft, Merete
Werge, Thomas Mears
Mortensen, Preben Bo
Børglum, Anders Dupont
Daly, Mark
Hougaard, David Michael
Bybjerg-Grauholm, Jonas
Hollegaard, Mads Vilhelm
High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA
title High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA
title_full High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA
title_fullStr High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA
title_full_unstemmed High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA
title_short High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA
title_sort high-quality exome sequencing of whole-genome amplified neonatal dried blood spot dna
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4835089/
https://www.ncbi.nlm.nih.gov/pubmed/27089011
http://dx.doi.org/10.1371/journal.pone.0153253
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