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iPSCORE: A Resource of 222 iPSC Lines Enabling Functional Characterization of Genetic Variation across a Variety of Cell Types

Large-scale collections of induced pluripotent stem cells (iPSCs) could serve as powerful model systems for examining how genetic variation affects biology and disease. Here we describe the iPSCORE resource: a collection of systematically derived and characterized iPSC lines from 222 ethnically dive...

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Autores principales: Panopoulos, Athanasia D., D'Antonio, Matteo, Benaglio, Paola, Williams, Roy, Hashem, Sherin I., Schuldt, Bernhard M., DeBoever, Christopher, Arias, Angelo D., Garcia, Melvin, Nelson, Bradley C., Harismendy, Olivier, Jakubosky, David A., Donovan, Margaret K.R., Greenwald, William W., Farnam, KathyJean, Cook, Megan, Borja, Victor, Miller, Carl A., Grinstein, Jonathan D., Drees, Frauke, Okubo, Jonathan, Diffenderfer, Kenneth E., Hishida, Yuriko, Modesto, Veronica, Dargitz, Carl T., Feiring, Rachel, Zhao, Chang, Aguirre, Aitor, McGarry, Thomas J., Matsui, Hiroko, Li, He, Reyna, Joaquin, Rao, Fangwen, O'Connor, Daniel T., Yeo, Gene W., Evans, Sylvia M., Chi, Neil C., Jepsen, Kristen, Nariai, Naoki, Müller, Franz-Josef, Goldstein, Lawrence S.B., Izpisua Belmonte, Juan Carlos, Adler, Eric, Loring, Jeanne F., Berggren, W. Travis, D'Antonio-Chronowska, Agnieszka, Smith, Erin N., Frazer, Kelly A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5390244/
https://www.ncbi.nlm.nih.gov/pubmed/28410642
http://dx.doi.org/10.1016/j.stemcr.2017.03.012
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author Panopoulos, Athanasia D.
D'Antonio, Matteo
Benaglio, Paola
Williams, Roy
Hashem, Sherin I.
Schuldt, Bernhard M.
DeBoever, Christopher
Arias, Angelo D.
Garcia, Melvin
Nelson, Bradley C.
Harismendy, Olivier
Jakubosky, David A.
Donovan, Margaret K.R.
Greenwald, William W.
Farnam, KathyJean
Cook, Megan
Borja, Victor
Miller, Carl A.
Grinstein, Jonathan D.
Drees, Frauke
Okubo, Jonathan
Diffenderfer, Kenneth E.
Hishida, Yuriko
Modesto, Veronica
Dargitz, Carl T.
Feiring, Rachel
Zhao, Chang
Aguirre, Aitor
McGarry, Thomas J.
Matsui, Hiroko
Li, He
Reyna, Joaquin
Rao, Fangwen
O'Connor, Daniel T.
Yeo, Gene W.
Evans, Sylvia M.
Chi, Neil C.
Jepsen, Kristen
Nariai, Naoki
Müller, Franz-Josef
Goldstein, Lawrence S.B.
Izpisua Belmonte, Juan Carlos
Adler, Eric
Loring, Jeanne F.
Berggren, W. Travis
D'Antonio-Chronowska, Agnieszka
Smith, Erin N.
Frazer, Kelly A.
author_facet Panopoulos, Athanasia D.
D'Antonio, Matteo
Benaglio, Paola
Williams, Roy
Hashem, Sherin I.
Schuldt, Bernhard M.
DeBoever, Christopher
Arias, Angelo D.
Garcia, Melvin
Nelson, Bradley C.
Harismendy, Olivier
Jakubosky, David A.
Donovan, Margaret K.R.
Greenwald, William W.
Farnam, KathyJean
Cook, Megan
Borja, Victor
Miller, Carl A.
Grinstein, Jonathan D.
Drees, Frauke
Okubo, Jonathan
Diffenderfer, Kenneth E.
Hishida, Yuriko
Modesto, Veronica
Dargitz, Carl T.
Feiring, Rachel
Zhao, Chang
Aguirre, Aitor
McGarry, Thomas J.
Matsui, Hiroko
Li, He
Reyna, Joaquin
Rao, Fangwen
O'Connor, Daniel T.
Yeo, Gene W.
Evans, Sylvia M.
Chi, Neil C.
Jepsen, Kristen
Nariai, Naoki
Müller, Franz-Josef
Goldstein, Lawrence S.B.
Izpisua Belmonte, Juan Carlos
Adler, Eric
Loring, Jeanne F.
Berggren, W. Travis
D'Antonio-Chronowska, Agnieszka
Smith, Erin N.
Frazer, Kelly A.
author_sort Panopoulos, Athanasia D.
collection PubMed
description Large-scale collections of induced pluripotent stem cells (iPSCs) could serve as powerful model systems for examining how genetic variation affects biology and disease. Here we describe the iPSCORE resource: a collection of systematically derived and characterized iPSC lines from 222 ethnically diverse individuals that allows for both familial and association-based genetic studies. iPSCORE lines are pluripotent with high genomic integrity (no or low numbers of somatic copy-number variants) as determined using high-throughput RNA-sequencing and genotyping arrays, respectively. Using iPSCs from a family of individuals, we show that iPSC-derived cardiomyocytes demonstrate gene expression patterns that cluster by genetic background, and can be used to examine variants associated with physiological and disease phenotypes. The iPSCORE collection contains representative individuals for risk and non-risk alleles for 95% of SNPs associated with human phenotypes through genome-wide association studies. Our study demonstrates the utility of iPSCORE for examining how genetic variants influence molecular and physiological traits in iPSCs and derived cell lines.
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spelling pubmed-53902442017-04-21 iPSCORE: A Resource of 222 iPSC Lines Enabling Functional Characterization of Genetic Variation across a Variety of Cell Types Panopoulos, Athanasia D. D'Antonio, Matteo Benaglio, Paola Williams, Roy Hashem, Sherin I. Schuldt, Bernhard M. DeBoever, Christopher Arias, Angelo D. Garcia, Melvin Nelson, Bradley C. Harismendy, Olivier Jakubosky, David A. Donovan, Margaret K.R. Greenwald, William W. Farnam, KathyJean Cook, Megan Borja, Victor Miller, Carl A. Grinstein, Jonathan D. Drees, Frauke Okubo, Jonathan Diffenderfer, Kenneth E. Hishida, Yuriko Modesto, Veronica Dargitz, Carl T. Feiring, Rachel Zhao, Chang Aguirre, Aitor McGarry, Thomas J. Matsui, Hiroko Li, He Reyna, Joaquin Rao, Fangwen O'Connor, Daniel T. Yeo, Gene W. Evans, Sylvia M. Chi, Neil C. Jepsen, Kristen Nariai, Naoki Müller, Franz-Josef Goldstein, Lawrence S.B. Izpisua Belmonte, Juan Carlos Adler, Eric Loring, Jeanne F. Berggren, W. Travis D'Antonio-Chronowska, Agnieszka Smith, Erin N. Frazer, Kelly A. Stem Cell Reports Resource Large-scale collections of induced pluripotent stem cells (iPSCs) could serve as powerful model systems for examining how genetic variation affects biology and disease. Here we describe the iPSCORE resource: a collection of systematically derived and characterized iPSC lines from 222 ethnically diverse individuals that allows for both familial and association-based genetic studies. iPSCORE lines are pluripotent with high genomic integrity (no or low numbers of somatic copy-number variants) as determined using high-throughput RNA-sequencing and genotyping arrays, respectively. Using iPSCs from a family of individuals, we show that iPSC-derived cardiomyocytes demonstrate gene expression patterns that cluster by genetic background, and can be used to examine variants associated with physiological and disease phenotypes. The iPSCORE collection contains representative individuals for risk and non-risk alleles for 95% of SNPs associated with human phenotypes through genome-wide association studies. Our study demonstrates the utility of iPSCORE for examining how genetic variants influence molecular and physiological traits in iPSCs and derived cell lines. Elsevier 2017-04-06 /pmc/articles/PMC5390244/ /pubmed/28410642 http://dx.doi.org/10.1016/j.stemcr.2017.03.012 Text en http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Resource
Panopoulos, Athanasia D.
D'Antonio, Matteo
Benaglio, Paola
Williams, Roy
Hashem, Sherin I.
Schuldt, Bernhard M.
DeBoever, Christopher
Arias, Angelo D.
Garcia, Melvin
Nelson, Bradley C.
Harismendy, Olivier
Jakubosky, David A.
Donovan, Margaret K.R.
Greenwald, William W.
Farnam, KathyJean
Cook, Megan
Borja, Victor
Miller, Carl A.
Grinstein, Jonathan D.
Drees, Frauke
Okubo, Jonathan
Diffenderfer, Kenneth E.
Hishida, Yuriko
Modesto, Veronica
Dargitz, Carl T.
Feiring, Rachel
Zhao, Chang
Aguirre, Aitor
McGarry, Thomas J.
Matsui, Hiroko
Li, He
Reyna, Joaquin
Rao, Fangwen
O'Connor, Daniel T.
Yeo, Gene W.
Evans, Sylvia M.
Chi, Neil C.
Jepsen, Kristen
Nariai, Naoki
Müller, Franz-Josef
Goldstein, Lawrence S.B.
Izpisua Belmonte, Juan Carlos
Adler, Eric
Loring, Jeanne F.
Berggren, W. Travis
D'Antonio-Chronowska, Agnieszka
Smith, Erin N.
Frazer, Kelly A.
iPSCORE: A Resource of 222 iPSC Lines Enabling Functional Characterization of Genetic Variation across a Variety of Cell Types
title iPSCORE: A Resource of 222 iPSC Lines Enabling Functional Characterization of Genetic Variation across a Variety of Cell Types
title_full iPSCORE: A Resource of 222 iPSC Lines Enabling Functional Characterization of Genetic Variation across a Variety of Cell Types
title_fullStr iPSCORE: A Resource of 222 iPSC Lines Enabling Functional Characterization of Genetic Variation across a Variety of Cell Types
title_full_unstemmed iPSCORE: A Resource of 222 iPSC Lines Enabling Functional Characterization of Genetic Variation across a Variety of Cell Types
title_short iPSCORE: A Resource of 222 iPSC Lines Enabling Functional Characterization of Genetic Variation across a Variety of Cell Types
title_sort ipscore: a resource of 222 ipsc lines enabling functional characterization of genetic variation across a variety of cell types
topic Resource
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5390244/
https://www.ncbi.nlm.nih.gov/pubmed/28410642
http://dx.doi.org/10.1016/j.stemcr.2017.03.012
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