Supplementary Tables S1-S7 from Whole-Genome Sequencing of Asian Lung Cancers: Second-Hand Smoke Unlikely to Be Responsible for Higher Incidence of Lung Cancer among Asian Never-Smokers

Autor: Pauline C. Ng, Axel M. Hillmer, Patrick Tan, Thomas D. Barber, Geoffrey B. Nilsen, Jason M. Laramie, Dennis G. Ballinger, Stephen E. Lincoln, Brock A. Peters, Daniel S.W. Tan, Christoph Reinhard, Shenli Zhang, Kun Yu, Joanna H.J. Tan, Yuhao Lin, Gary S.L. Loh, Xiwen Ma, Hui-Hoon Chua, Yong G. Yue, Audrey S.M. Teo, Swee-Seong Wong, Elaine Lim, Jason C. Ting, Philip J. Ebert, Vidhya G. Krishnan

Clinical and tissue information on 30 lung cancer patients (S1); Recurrent somatic variants based on presence of the same variant in the COSMIC database or presence of the same variant within the dataset (S2); Variants of the category 'three or more

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51477059a67d33d12c240560c586f66c
https://doi.org/10.1158/0008-5472.22401579.v1

Supplementary Figure Legends from Whole-Genome Sequencing of Asian Lung Cancers: Second-Hand Smoke Unlikely to Be Responsible for Higher Incidence of Lung Cancer among Asian Never-Smokers

Autor: Pauline C. Ng, Axel M. Hillmer, Patrick Tan, Thomas D. Barber, Geoffrey B. Nilsen, Jason M. Laramie, Dennis G. Ballinger, Stephen E. Lincoln, Brock A. Peters, Daniel S.W. Tan, Christoph Reinhard, Shenli Zhang, Kun Yu, Joanna H.J. Tan, Yuhao Lin, Gary S.L. Loh, Xiwen Ma, Hui-Hoon Chua, Yong G. Yue, Audrey S.M. Teo, Swee-Seong Wong, Elaine Lim, Jason C. Ting, Philip J. Ebert, Vidhya G. Krishnan

Legend for Supplementary Figures S1-S2.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a845a616e2bc05351e5429df3d688fd
https://doi.org/10.1158/0008-5472.22401588.v1

A Systematic Comparison of Traditional and Multigene Panel Testing for Hereditary Breast and Ovarian Cancer Genes in More Than 1000 Patients

Autor: Allison W. Kurian, Yuya Kobayashi, Federico A. Monzon, Michael J. Anderson, Andrea Desmond, Leif W. Ellisen, Geoffrey B. Nilsen, Stephen E Lincoln, Kevin B. Jacobs, Shan Yang, Meredith A. Mills, James M. Ford

Publikováno v: The Journal of Molecular Diagnostics. 17:533-544

Gene panels for hereditary breast and ovarian cancer risk assessment are gaining acceptance, even though the clinical utility of these panels is not yet fully defined. Technical questions remain, however, about the performance and clinical interpreta

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cae08f88ec6b77c8c399b0c7307ed146
https://doi.org/10.1016/j.jmoldx.2015.04.009

A public resource facilitating clinical use of genomes

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

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

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https://research.vu.nl/en/publications/6e1a1cef-c7ef-4868-b615-c658b7a3ea72

A sequence-based variation map of 8.27 million SNPs in inbred mouse strains

Autor: Molly A. Bogue, Charit L. Pethiyagoda, Laura L. Stuve, Kelly A. Frazer, David Cox, F. M. Johnson, Geoffrey B. Nilsen, Claire M. Wade, Eleazar Eskin, Hyun Min Kang, Julie Montgomery, Matt Morenzoni, Erica Beilharz, David A. Hinds, Mark J. Daly, Robert V. Gupta

Publikováno v: Nature. 448:1050-1053

A dense map of genetic variation in the laboratory mouse genome will provide insights into the evolutionary history of the species and lead to an improved understanding of the relationship between inter-strain genotypic and phenotypic differences. He

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70e6c6c960b87c2d355dc36d0dbffa06
https://doi.org/10.1038/nature06067