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Extensive sequencing of seven human genomes to characterize benchmark reference materials

The Genome in a Bottle Consortium, hosted by the National Institute of Standards and Technology (NIST) is creating reference materials and data for human genome sequencing, as well as methods for genome comparison and benchmarking. Here, we describe a large, diverse set of sequencing data for seven...

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Autores principales: Zook, Justin M., Catoe, David, McDaniel, Jennifer, Vang, Lindsay, Spies, Noah, Sidow, Arend, Weng, Ziming, Liu, Yuling, Mason, Christopher E., Alexander, Noah, Henaff, Elizabeth, McIntyre, Alexa B.R., Chandramohan, Dhruva, Chen, Feng, Jaeger, Erich, Moshrefi, Ali, Pham, Khoa, Stedman, William, Liang, Tiffany, Saghbini, Michael, Dzakula, Zeljko, Hastie, Alex, Cao, Han, Deikus, Gintaras, Schadt, Eric, Sebra, Robert, Bashir, Ali, Truty, Rebecca M., Chang, Christopher C., Gulbahce, Natali, Zhao, Keyan, Ghosh, Srinka, Hyland, Fiona, Fu, Yutao, Chaisson, Mark, Xiao, Chunlin, Trow, Jonathan, Sherry, Stephen T., Zaranek, Alexander W., Ball, Madeleine, Bobe, Jason, Estep, Preston, Church, George M., Marks, Patrick, Kyriazopoulou-Panagiotopoulou, Sofia, Zheng, Grace X.Y., Schnall-Levin, Michael, Ordonez, Heather S., Mudivarti, Patrice A., Giorda, Kristina, Sheng, Ying, Rypdal, Karoline Bjarnesdatter, Salit, Marc
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4896128/
https://www.ncbi.nlm.nih.gov/pubmed/27271295
http://dx.doi.org/10.1038/sdata.2016.25
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author Zook, Justin M.
Catoe, David
McDaniel, Jennifer
Vang, Lindsay
Spies, Noah
Sidow, Arend
Weng, Ziming
Liu, Yuling
Mason, Christopher E.
Alexander, Noah
Henaff, Elizabeth
McIntyre, Alexa B.R.
Chandramohan, Dhruva
Chen, Feng
Jaeger, Erich
Moshrefi, Ali
Pham, Khoa
Stedman, William
Liang, Tiffany
Saghbini, Michael
Dzakula, Zeljko
Hastie, Alex
Cao, Han
Deikus, Gintaras
Schadt, Eric
Sebra, Robert
Bashir, Ali
Truty, Rebecca M.
Chang, Christopher C.
Gulbahce, Natali
Zhao, Keyan
Ghosh, Srinka
Hyland, Fiona
Fu, Yutao
Chaisson, Mark
Xiao, Chunlin
Trow, Jonathan
Sherry, Stephen T.
Zaranek, Alexander W.
Ball, Madeleine
Bobe, Jason
Estep, Preston
Church, George M.
Marks, Patrick
Kyriazopoulou-Panagiotopoulou, Sofia
Zheng, Grace X.Y.
Schnall-Levin, Michael
Ordonez, Heather S.
Mudivarti, Patrice A.
Giorda, Kristina
Sheng, Ying
Rypdal, Karoline Bjarnesdatter
Salit, Marc
author_facet Zook, Justin M.
Catoe, David
McDaniel, Jennifer
Vang, Lindsay
Spies, Noah
Sidow, Arend
Weng, Ziming
Liu, Yuling
Mason, Christopher E.
Alexander, Noah
Henaff, Elizabeth
McIntyre, Alexa B.R.
Chandramohan, Dhruva
Chen, Feng
Jaeger, Erich
Moshrefi, Ali
Pham, Khoa
Stedman, William
Liang, Tiffany
Saghbini, Michael
Dzakula, Zeljko
Hastie, Alex
Cao, Han
Deikus, Gintaras
Schadt, Eric
Sebra, Robert
Bashir, Ali
Truty, Rebecca M.
Chang, Christopher C.
Gulbahce, Natali
Zhao, Keyan
Ghosh, Srinka
Hyland, Fiona
Fu, Yutao
Chaisson, Mark
Xiao, Chunlin
Trow, Jonathan
Sherry, Stephen T.
Zaranek, Alexander W.
Ball, Madeleine
Bobe, Jason
Estep, Preston
Church, George M.
Marks, Patrick
Kyriazopoulou-Panagiotopoulou, Sofia
Zheng, Grace X.Y.
Schnall-Levin, Michael
Ordonez, Heather S.
Mudivarti, Patrice A.
Giorda, Kristina
Sheng, Ying
Rypdal, Karoline Bjarnesdatter
Salit, Marc
author_sort Zook, Justin M.
collection PubMed
description The Genome in a Bottle Consortium, hosted by the National Institute of Standards and Technology (NIST) is creating reference materials and data for human genome sequencing, as well as methods for genome comparison and benchmarking. Here, we describe a large, diverse set of sequencing data for seven human genomes; five are current or candidate NIST Reference Materials. The pilot genome, NA12878, has been released as NIST RM 8398. We also describe data from two Personal Genome Project trios, one of Ashkenazim Jewish ancestry and one of Chinese ancestry. The data come from 12 technologies: BioNano Genomics, Complete Genomics paired-end and LFR, Ion Proton exome, Oxford Nanopore, Pacific Biosciences, SOLiD, 10X Genomics GemCode WGS, and Illumina exome and WGS paired-end, mate-pair, and synthetic long reads. Cell lines, DNA, and data from these individuals are publicly available. Therefore, we expect these data to be useful for revealing novel information about the human genome and improving sequencing technologies, SNP, indel, and structural variant calling, and de novo assembly.
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spelling pubmed-48961282016-06-08 Extensive sequencing of seven human genomes to characterize benchmark reference materials Zook, Justin M. Catoe, David McDaniel, Jennifer Vang, Lindsay Spies, Noah Sidow, Arend Weng, Ziming Liu, Yuling Mason, Christopher E. Alexander, Noah Henaff, Elizabeth McIntyre, Alexa B.R. Chandramohan, Dhruva Chen, Feng Jaeger, Erich Moshrefi, Ali Pham, Khoa Stedman, William Liang, Tiffany Saghbini, Michael Dzakula, Zeljko Hastie, Alex Cao, Han Deikus, Gintaras Schadt, Eric Sebra, Robert Bashir, Ali Truty, Rebecca M. Chang, Christopher C. Gulbahce, Natali Zhao, Keyan Ghosh, Srinka Hyland, Fiona Fu, Yutao Chaisson, Mark Xiao, Chunlin Trow, Jonathan Sherry, Stephen T. Zaranek, Alexander W. Ball, Madeleine Bobe, Jason Estep, Preston Church, George M. Marks, Patrick Kyriazopoulou-Panagiotopoulou, Sofia Zheng, Grace X.Y. Schnall-Levin, Michael Ordonez, Heather S. Mudivarti, Patrice A. Giorda, Kristina Sheng, Ying Rypdal, Karoline Bjarnesdatter Salit, Marc Sci Data Data Descriptor The Genome in a Bottle Consortium, hosted by the National Institute of Standards and Technology (NIST) is creating reference materials and data for human genome sequencing, as well as methods for genome comparison and benchmarking. Here, we describe a large, diverse set of sequencing data for seven human genomes; five are current or candidate NIST Reference Materials. The pilot genome, NA12878, has been released as NIST RM 8398. We also describe data from two Personal Genome Project trios, one of Ashkenazim Jewish ancestry and one of Chinese ancestry. The data come from 12 technologies: BioNano Genomics, Complete Genomics paired-end and LFR, Ion Proton exome, Oxford Nanopore, Pacific Biosciences, SOLiD, 10X Genomics GemCode WGS, and Illumina exome and WGS paired-end, mate-pair, and synthetic long reads. Cell lines, DNA, and data from these individuals are publicly available. Therefore, we expect these data to be useful for revealing novel information about the human genome and improving sequencing technologies, SNP, indel, and structural variant calling, and de novo assembly. Nature Publishing Group 2016-06-07 /pmc/articles/PMC4896128/ /pubmed/27271295 http://dx.doi.org/10.1038/sdata.2016.25 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0 This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0 Metadata associated with this Data Descriptor is available at http://www.nature.com/sdata/ and is released under the CC0 waiver to maximize reuse.
spellingShingle Data Descriptor
Zook, Justin M.
Catoe, David
McDaniel, Jennifer
Vang, Lindsay
Spies, Noah
Sidow, Arend
Weng, Ziming
Liu, Yuling
Mason, Christopher E.
Alexander, Noah
Henaff, Elizabeth
McIntyre, Alexa B.R.
Chandramohan, Dhruva
Chen, Feng
Jaeger, Erich
Moshrefi, Ali
Pham, Khoa
Stedman, William
Liang, Tiffany
Saghbini, Michael
Dzakula, Zeljko
Hastie, Alex
Cao, Han
Deikus, Gintaras
Schadt, Eric
Sebra, Robert
Bashir, Ali
Truty, Rebecca M.
Chang, Christopher C.
Gulbahce, Natali
Zhao, Keyan
Ghosh, Srinka
Hyland, Fiona
Fu, Yutao
Chaisson, Mark
Xiao, Chunlin
Trow, Jonathan
Sherry, Stephen T.
Zaranek, Alexander W.
Ball, Madeleine
Bobe, Jason
Estep, Preston
Church, George M.
Marks, Patrick
Kyriazopoulou-Panagiotopoulou, Sofia
Zheng, Grace X.Y.
Schnall-Levin, Michael
Ordonez, Heather S.
Mudivarti, Patrice A.
Giorda, Kristina
Sheng, Ying
Rypdal, Karoline Bjarnesdatter
Salit, Marc
Extensive sequencing of seven human genomes to characterize benchmark reference materials
title Extensive sequencing of seven human genomes to characterize benchmark reference materials
title_full Extensive sequencing of seven human genomes to characterize benchmark reference materials
title_fullStr Extensive sequencing of seven human genomes to characterize benchmark reference materials
title_full_unstemmed Extensive sequencing of seven human genomes to characterize benchmark reference materials
title_short Extensive sequencing of seven human genomes to characterize benchmark reference materials
title_sort extensive sequencing of seven human genomes to characterize benchmark reference materials
topic Data Descriptor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4896128/
https://www.ncbi.nlm.nih.gov/pubmed/27271295
http://dx.doi.org/10.1038/sdata.2016.25
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