Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Abraham M. Rosenbaum"'
Autor:
John Aach, Euan A. Ashley, Je-Hyuk Lee, Hugh Y. Rienhoff, Matthew T. Wheeler, Jong Bhak, Peter J. Hulick, Joyce L. Yang, Carlos Cano, Radoje Drmanac, Jeong-Sun Seo, Jong Il Kim, Athurva Gore, Anugraha M. Raman, Zhe Li, Xiaodi Wu, Shawn M. Douglas, Michael F. Chou, Daniel B. Vorhaus, Jin Billy Li, Alberto Labarga, Michael F. Murray, Kimberly Robasky, Seong-Jin Kim, Byung Chul Kim, Leonid Peshkin, Luhan Yang, George M. Church, Misha Angrist, Joseph V. Thakuria, Preston W. Estep, Jeantine E. Lunshof, Christine E. Seidman, Madeleine Ball, Tom Clegg, Alexander Wait Zaranek, Abraham M. Rosenbaum, Brock A. Peters, Wendy K. Chung, Ward Vandewege, Heidi L. Rehm, Geoffrey B. Nilsen, Matthew J. Callow, Kun Zhang, Jason Bobe
Publikováno v:
Ball, M P, Thakuria, J V, Zaranek, A W, Clegg, T, Rosenbaum, A M, Wu, X, Angrist, M, Bhak, J, Bobe, J, Callow, M J, Cano, C, Chou, M F, Chung, W K, Douglas, S M, Estep, P W, Gore, A, Hulick, P, Labarga, A, Lee, J-H, Lunshof, J E, Kim, B C, Kim, J L, Li, Z, Murray, M F, Nilsen, G B, Peters, B A, Raman, A M, Rienhoff, H Y, Robasky, K, Wheeler, M T, Vandewege, W, Vorhaus, D B, Yang, Y L, Yang, L, Aach, J, Ashley, E A, Drmanac, R, Kim, S-J, Li, J B, Peshkin, L, Seidman, S E, Seo, J-S, Zhang, K, Rehm, H L & Church, G M 2012, ' A public resource facilitating clinical use of genomes. ', Proceedings of the National Academy of Sciences of the United States of America, vol. 109, no. 30, pp. 11920-11927 . https://doi.org/10.1073/pnas.1201904109
Proceedings of the National Academy of Sciences of the United States of America, 109(30), 11920-11927. National Acad Sciences
Proceedings of the National Academy of Sciences of the United States of America, 109(30), 11920-11927. National Academy of Sciences
Proceedings of the National Academy of Sciences of the United States of America, vol 109, iss 30
Proceedings of the National Academy of Sciences of the United States of America, 109(30), 11920-11927. National Acad Sciences
Proceedings of the National Academy of Sciences of the United States of America, 109(30), 11920-11927. National Academy of Sciences
Proceedings of the National Academy of Sciences of the United States of America, vol 109, iss 30
Rapid advances in DNA sequencing promise to enable new diagnostics and individualized therapies. Achieving personalized medicine, however, will require extensive research on highly reidentifiable, integrated datasets of genomic and health information
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47e2236be047d04a80fe8cbb08175d3e
https://research.vu.nl/en/publications/6e1a1cef-c7ef-4868-b615-c658b7a3ea72
https://research.vu.nl/en/publications/6e1a1cef-c7ef-4868-b615-c658b7a3ea72
Autor:
Matthew T. Wheeler, Stephen R. Quake, Euan A. Ashley, Laura M. Hodges, Joseph V. Thakuria, Joshua W. Knowles, Kelly E. Ormond, Dmitry Pushkarev, Joan M. Hebert, Joel T. Dudley, Mark Woon, Frederick E. Dewey, Katrin Sangkuhl, Alexander A. Morgan, Alexander Wait Zaranek, Dorit S. Berlin, Abraham M. Rosenbaum, Louanne Hudgins, Michael F. Chou, Rong Chen, Atul J. Butte, George M. Church, Aleksandra Pavlovic, Teri E. Klein, Caroline F. Thorn, Henry T. Greely, Li Gong, Ryan Whaley, Russ B. Altman, Norma F. Neff, Hersh Sagreiya
Publikováno v:
The Lancet. 375:1525-1535
Summary Background The cost of genomic information has fallen steeply, but the clinical translation of genetic risk estimates remains unclear. We aimed to undertake an integrated analysis of a complete human genome in a clinical context. Methods We a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8d4f54bf2e1f647abdda37f15e523a5
https://doi.org/10.1016/s0140-6736(10)60452-7
https://doi.org/10.1016/s0140-6736(10)60452-7
Autor:
Robert Hartlage, Brock A. Peters, Igor Nazarenko, Jonathan Baccash, Calvin Kong, Vitali Karpinchyk, Andres Fernandez, Abraham M. Rosenbaum, Ryan J. Cedeno, Paolo Carnevali, Celeste E. McBride, Norman L. Burns, Shaunak Roy, Karen W. Shannon, George M. Church, Snezana Drmanac, Daniel F. Chernikoff, Radoje Drmanac, Geoffrey B. Nilsen, Claudia Richter, Coleen R. Hacker, Jay Shafto, William C. Banyai, Kaliprasad Pothuraju, Helena Perazich, Bruce L. Martin, Dennis G. Ballinger, Benjamin Curson, Linsu Chen, Brian Hauser, Steve Huang, Alexander Wait Zaranek, Anushka Brownley, Dylan Vu, Matt Morenzoni, Andrew B. Sparks, Matthew J. Callow, Alex Cheung, Clifford Reid, Adam P. Borcherding, George Yeung, Xiaodi Wu, Catherine Le, Tom Landers, Aaron L. Halpern, Bahram G. Kermani, Kimberly Perry, Arnold R. Oliphant, Mark Koenig, Charit L. Pethiyagoda, Michel Sun, Joseph V. Thakuria, Conrad G. Sheppy, Anne Tran, Robert E. Morey, Fredrik A. Dahl, Krishna Pant, Karl Mutch, Bryan Staker, Joe Peterson, Jessica Ebert, Yuan Jiang, Jia Liu, Razvan Chirita, Uladzislau Sharanhovich
Publikováno v:
Science. 327:78-81
Toward $1000 Genomes The ability to generate human genome sequence data that is complete, accurate, and inexpensive is a necessary prerequisite to perform genome-wide disease association studies. Drmanac et al. (p. 78 , published online 5 November) p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bfc5b869194526e702f24446172ea13f
https://doi.org/10.1126/science.1181498
https://doi.org/10.1126/science.1181498
Autor:
Yuan Gao, Shamil R. Sunyaev, Jin Billy Li, Annika Ahlford, Abraham M. Rosenbaum, Kun Zhang, Jung-Ki Yoon, Bin Xie, John Aach, Gregory V. Kryukov, Alexander Wait Zaranek, George M. Church, Emily M LeProust
Publikováno v:
Genome Research. 19:1606-1615
Utilizing the full power of next-generation sequencing often requires the ability to perform large-scale multiplex enrichment of many specific genomic loci in multiple samples. Several technologies have been recently developed but await substantial i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::984034a8d25607dfccf9cf970083993d
https://doi.org/10.1101/gr.092213.109
https://doi.org/10.1101/gr.092213.109
Autor:
Robi D. Mitra, George M. Church, Kun Zhang, Xiaoxia Lin, Nikos Reppas, John P. McCutcheon, Abraham M. Rosenbaum, Michael D. Wang, Jay Shendure, Gregory J. Porreca
Publikováno v:
Science. 309:1728-1732
We describe a DNA sequencing technology in which a commonly available, inexpensive epifluorescence microscope is converted to rapid nonelectrophoretic DNA sequencing automation. We apply this technology to resequence an evolved strain of Escherichia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed192a5052f1654e61fc4bfe96de7593
https://doi.org/10.1126/science.1117389
https://doi.org/10.1126/science.1117389