Zobrazeno 1 - 10
of 54
pro vyhledávání: '"Human genome sequencing"'
Autor:
Liron Ganel, Lei Chen, Ryan Christ, Jagadish Vangipurapu, Erica Young, Indraniel Das, Krishna Kanchi, David Larson, Allison Regier, Haley Abel, Chul Joo Kang, Alexandra Scott, Aki Havulinna, Charleston W. K. Chiang, Susan Service, Nelson Freimer, Aarno Palotie, Samuli Ripatti, Johanna Kuusisto, Michael Boehnke, Markku Laakso, Adam Locke, Nathan O. Stitziel, Ira M. Hall
Publikováno v:
Human Genomics, Vol 15, Iss 1, Pp 1-17 (2021)
Abstract Background Mitochondrial genome copy number (MT-CN) varies among humans and across tissues and is highly heritable, but its causes and consequences are not well understood. When measured by bulk DNA sequencing in blood, MT-CN may reflect a c
Externí odkaz:
https://doaj.org/article/afd0fb03735e45e7af8157b2896c588c
Autor:
Charleston W. K. Chiang, Ira M. Hall, Nelson B. Freimer, Aarno Palotie, Michael Boehnke, David E. Larson, Alexandra J. Scott, Krishna L. Kanchi, Allison A. Regier, Lei Chen, Erica Young, Johanna Kuusisto, Samuli Ripatti, Chul Joo Kang, Nathan O. Stitziel, Ryan Christ, Haley J. Abel, Indraniel Das, Adam E. Locke, Markku Laakso, Jagadish Vangipurapu, Aki S. Havulinna, Liron Ganel
Publikováno v:
Human Genomics
Human Genomics, Vol 15, Iss 1, Pp 1-17 (2021)
Human genomics, vol 15, iss 1
Human Genomics, Vol 15, Iss 1, Pp 1-17 (2021)
Human genomics, vol 15, iss 1
Background Mitochondrial genome copy number (MT-CN) varies among humans and across tissues and is highly heritable, but its causes and consequences are not well understood. When measured by bulk DNA sequencing in blood, MT-CN may reflect a combinatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3571fd60bd62350794f27d98e14101eb
http://hdl.handle.net/10138/333048
http://hdl.handle.net/10138/333048
Autor:
Bauw, G., Van Damme, J., Puype, M., Vandekerckhove, J., Gesser, B., Ratz, G. P., Lauridsen, J. B., Celis, J. E.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America, 1989 Oct . 86(20), 7701-7705.
Externí odkaz:
https://www.jstor.org/stable/35149
Akademický článek
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Publikováno v:
Global Catastrophic Risks, 2008.
Externí odkaz:
https://doi.org/10.1093/oso/9780198570509.003.0027
Autor:
Hatem Zayed
Publikováno v:
Gene. 592:239-243
The 22 Arab nations have a unique genetic structure, which reflects both conserved and diverse gene pools due to the prevalent endogamous and consanguineous marriage culture and the long history of admixture among different ethnic subcultures descend
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fde8d0ca71907cedc31bc774081b7c7c
https://doi.org/10.1016/j.gene.2016.07.007
https://doi.org/10.1016/j.gene.2016.07.007
Autor:
Sapp, Jan, author
Publikováno v:
Genesis : The Evolution of Biology, 2003.
Externí odkaz:
https://doi.org/10.1093/acprof:oso/9780195156195.003.0017
Autor:
Lionel Perrier, Z Zhaomin, Ludovic Lacroix, Etienne Rouleau, Isabelle Durand-Zaleski, Rajae Touzani, Dominique Vaur, Sandrine Baffert, Isabelle Borget, Claude Preudhomme, Dede Sika Kossi, Patricia Marino
Publikováno v:
ISPOR 19th Annual European Congress
ISPOR 19th Annual European Congress, Oct 2016, Vienne, Austria. pp.A693
HAL
ISPOR 19th Annual European Congress, Oct 2016, Vienne, Austria. pp.A693
HAL
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d0998071e3834540352924234f3460c0
https://shs.hal.science/halshs-01446644
https://shs.hal.science/halshs-01446644
Autor:
Baiyu Zhou, Alice S. Whittemore
Publikováno v:
Ann. Appl. Stat. 6, no. 2 (2012), 457-475
Whole and targeted sequencing of human genomes is a promising, increasingly feasible tool for discovering genetic contributions to risk of complex diseases. A key step is calling an individual's genotype from the multiple aligned short read sequences
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3b5f37d3cb8b5cf0187ba4f08938bdd
http://projecteuclid.org/euclid.aoas/1339419603
http://projecteuclid.org/euclid.aoas/1339419603
Autor:
Lindblad-Toh, Kerstin, Garber, Manuel, Zuk, Or, Lin, Michael F, Parker, Brian J, Washietl, Stefan, Kheradpour, Pouya, Ernst, Jason, Jordan, Gregory, Mauceli, Evan, Ward, Lucas D, Lowe, Craig B, Holloway, Alisha K, Clamp, Michele, Gnerre, Sante, Alföldi, Jessica, Beal, Kathryn, Chang, Jean, Clawson, Hiram, Cuff, James, Di Palma, Federica, Fitzgerald, Stephen, Flicek, Paul, Guttman, Mitchell, Hubisz, Melissa J, Jaffe, David B, Jungreis, Irwin, Kent, W James, Kostka, Dennis, Lara, Marcia, Martins, Andre L, Massingham, Tim, Moltke, Ida, Raney, Brian J, Rasmussen, Matthew D, Robinson, Jim, Stark, Alexander, Vilella, Albert J, Wen, Jiayu, Xie, Xiaohui, Zody, Michael C, Broad Institute Sequencing Platform and Whole Genome Assembly Team, Baldwin, Jen, Bloom, Toby, Chin, Chee Whye, Heiman, Dave, Nicol, Robert, Nusbaum, Chad, Young, Sarah, Wilkinson, Jane, Worley, Kim C, Kovar, Christie L, Muzny, Donna M, Gibbs, Richard A, Baylor College of Medicine Human Genome Sequencing Center Sequencing Team, Cree, Andrew, Dihn, Huyen H, Fowler, Gerald, Jhangiani, Shalili, Joshi, Vandita, Lee, Sandra, Lewis, Lora R, Nazareth, Lynne V, Okwuonu, Geoffrey, Santibanez, Jireh, Warren, Wesley C, Mardis, Elaine R, Weinstock, George M, Wilson, Richard K, Genome Institute at Washington University, Delehaunty, Kim, Dooling, David, Fronik, Catrina, Fulton, Lucinda, Fulton, Bob, Graves, Tina, Minx, Patrick, Sodergren, Erica, Birney, Ewan, Margulies, Elliott H, Herrero, Javier, Green, Eric D, Haussler, David, Siepel, Adam, Goldman, Nick, Pollard, Katherine S, Pedersen, Jakob S, Lander, Eric S, Kellis, Manolis
Publikováno v:
Nature, vol 478, iss 7370
The comparison of related genomes has emerged as a powerful lens for genome interpretation. Here we report the sequencing and comparative analysis of 29 eutherian genomes. We confirm that at least 5.5% of the human genome has undergone purifying sele
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::a0d8574d4b46a2745b168a17cdd246c8
https://escholarship.org/uc/item/38v8j6fz
https://escholarship.org/uc/item/38v8j6fz