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Enrichment of sequencing targets from the human genome by solution hybridization

To exploit fully the potential of current sequencing technologies for population-based studies, one must enrich for loci from the human genome. Here we evaluate the hybridization-based approach by using oligonucleotide capture probes in solution to enrich for approximately 3.9 Mb of sequence target....

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Detalles Bibliográficos
Autores principales: Tewhey, Ryan, Nakano, Masakazu, Wang, Xiaoyun, Pabón-Peña, Carlos, Novak, Barbara, Giuffre, Angelica, Lin, Eric, Happe, Scott, Roberts, Doug N, LeProust, Emily M, Topol, Eric J, Harismendy, Olivier, Frazer, Kelly A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2784331/
https://www.ncbi.nlm.nih.gov/pubmed/19835619
http://dx.doi.org/10.1186/gb-2009-10-10-r116
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author Tewhey, Ryan
Nakano, Masakazu
Wang, Xiaoyun
Pabón-Peña, Carlos
Novak, Barbara
Giuffre, Angelica
Lin, Eric
Happe, Scott
Roberts, Doug N
LeProust, Emily M
Topol, Eric J
Harismendy, Olivier
Frazer, Kelly A
author_facet Tewhey, Ryan
Nakano, Masakazu
Wang, Xiaoyun
Pabón-Peña, Carlos
Novak, Barbara
Giuffre, Angelica
Lin, Eric
Happe, Scott
Roberts, Doug N
LeProust, Emily M
Topol, Eric J
Harismendy, Olivier
Frazer, Kelly A
author_sort Tewhey, Ryan
collection PubMed
description To exploit fully the potential of current sequencing technologies for population-based studies, one must enrich for loci from the human genome. Here we evaluate the hybridization-based approach by using oligonucleotide capture probes in solution to enrich for approximately 3.9 Mb of sequence target. We demonstrate that the tiling probe frequency is important for generating sequence data with high uniform coverage of targets. We obtained 93% sensitivity to detect SNPs, with a calling accuracy greater than 99%.
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spelling pubmed-27843312009-11-27 Enrichment of sequencing targets from the human genome by solution hybridization Tewhey, Ryan Nakano, Masakazu Wang, Xiaoyun Pabón-Peña, Carlos Novak, Barbara Giuffre, Angelica Lin, Eric Happe, Scott Roberts, Doug N LeProust, Emily M Topol, Eric J Harismendy, Olivier Frazer, Kelly A Genome Biol Method To exploit fully the potential of current sequencing technologies for population-based studies, one must enrich for loci from the human genome. Here we evaluate the hybridization-based approach by using oligonucleotide capture probes in solution to enrich for approximately 3.9 Mb of sequence target. We demonstrate that the tiling probe frequency is important for generating sequence data with high uniform coverage of targets. We obtained 93% sensitivity to detect SNPs, with a calling accuracy greater than 99%. BioMed Central 2009 2009-10-16 /pmc/articles/PMC2784331/ /pubmed/19835619 http://dx.doi.org/10.1186/gb-2009-10-10-r116 Text en Copyright ©2009 Tewhey; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium provided the original work is properly cited.
spellingShingle Method
Tewhey, Ryan
Nakano, Masakazu
Wang, Xiaoyun
Pabón-Peña, Carlos
Novak, Barbara
Giuffre, Angelica
Lin, Eric
Happe, Scott
Roberts, Doug N
LeProust, Emily M
Topol, Eric J
Harismendy, Olivier
Frazer, Kelly A
Enrichment of sequencing targets from the human genome by solution hybridization
title Enrichment of sequencing targets from the human genome by solution hybridization
title_full Enrichment of sequencing targets from the human genome by solution hybridization
title_fullStr Enrichment of sequencing targets from the human genome by solution hybridization
title_full_unstemmed Enrichment of sequencing targets from the human genome by solution hybridization
title_short Enrichment of sequencing targets from the human genome by solution hybridization
title_sort enrichment of sequencing targets from the human genome by solution hybridization
topic Method
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2784331/
https://www.ncbi.nlm.nih.gov/pubmed/19835619
http://dx.doi.org/10.1186/gb-2009-10-10-r116
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