Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Roger A, Hoskins"'
Autor:
Sonal Nagarkar-Jaiswal, Pei-Tseng Lee, Megan E Campbell, Kuchuan Chen, Stephanie Anguiano-Zarate, Manuel Cantu Gutierrez, Theodore Busby, Wen-Wen Lin, Yuchun He, Karen L Schulze, Benjamin W Booth, Martha Evans-Holm, Koen JT Venken, Robert W Levis, Allan C Spradling, Roger A Hoskins, Hugo J Bellen
Publikováno v:
eLife, Vol 4 (2015)
Here, we document a collection of ∼7434 MiMIC (Minos Mediated Integration Cassette) insertions of which 2854 are inserted in coding introns. They allowed us to create a library of 400 GFP-tagged genes. We show that 72% of internally tagged proteins
Externí odkaz:
https://doaj.org/article/a360211c69524b5c898cb3e9e9faee55
Autor:
Margaret L Hoang, Frederick J Tan, David C Lai, Sue E Celniker, Roger A Hoskins, Maitreya J Dunham, Yixian Zheng, Douglas Koshland
Publikováno v:
PLoS Genetics, Vol 6, Iss 12, p e1001228 (2010)
Genome rearrangements often result from non-allelic homologous recombination (NAHR) between repetitive DNA elements dispersed throughout the genome. Here we systematically analyze NAHR between Ty retrotransposons using a genome-wide approach that exp
Externí odkaz:
https://doaj.org/article/44485b86523a44119d8fcbbac618ea2d
Autor:
Steven E. Brenner, Changhua Yu, Melissa Ly, Mabel Furutsuki, Roger A. Hoskins, Aashish N. Adhikari, Zhiqiang Hu, Gaia Andreoletti
Publikováno v:
Hum Mutat
Genome sequencing identifies vast number of genetic variants. Predicting these variants' molecular and clinical effects is one of the preeminent challenges in human genetics. Accurate prediction of the impact of genetic variants improves our understa
Autor:
Constantina Bakolitsa, Roger A. Hoskins, Cagi participants, Predrag Radivojac, Steven E. Brenner, John Moult, Gaia Andreoletti
Publikováno v:
Cancer Research. 80:LB-250
Interpretation of genomic variation plays an essential role in the analysis of cancer and monogenic disease, with applications ranging from basic research to clinical decisions. Yet the field lacks a clear consensus on the appropriate level of confid
Autor:
Predrag Radivojac, Yanran Wang, Kunal Kundu, Maggie Haitian Wang, Laksshman Sundaram, Pier Luigi Martelli, Sohela Shah, Steven E. Brenner, Emanuela Leonardi, Yuxiang Jiang, Roxana Daneshjou, Mehdi Pirooznia, Marco Carraro, Rita Casadio, Biao Li, Giulia Babbi, Peter P. Zandi, John Moult, Silvio C. E. Tosatto, Andre Franke, Yanay Ofran, James B. Potash, David T. Jones, Mauno Vihinen, Billy Chang, Sean D. Mooney, Pietro Di Lena, Roger A. Hoskins, Russ B. Altman, David K. Gifford, Rajendra Rana Bhat, Kymberleigh A. Pagel, Carlo Ferrari, Yana Bromberg, Susanna Repo, Britt-Sabina Petersen, Xiaolin Li, Yizhou Yin, Alexander A. Morgan, Teri E. Klein, Lipika R. Pal, Ron Unger, Samuele Bovo, Abhishek Niroula, Richard W. McCombie, Vikas Pejaver, Eran Bachar, Matthew D. Edwards, Alessandra Gasparini, Johnathan Roy Azaria, Manuel Giollo
Publikováno v:
PMC
Precision medicine aims to predict a patient's disease risk and best therapeutic options by using that individual's genetic sequencing data. The Critical Assessment of Genome Interpretation (CAGI) is a community experiment consisting of genotypeâ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7093df1a3254b2b364be645d9ec72274
https://europepmc.org/articles/PMC5600620/
https://europepmc.org/articles/PMC5600620/
Autor:
Nathan Boley, Susan E. Celniker, Kenneth H. Wan, Marcus H. Stoiber, Peter J. Bickel, James B. Brown, Roger A. Hoskins, Benjamin W. Booth
Publikováno v:
Nature biotechnology
The identification of full length transcripts entirely from short-read RNA sequencing data (RNA-seq) remains a challenge in genome annotation pipelines. Here we describe an automated pipeline for genome annotation that integrates RNA-seq and gene-bou
Autor:
Gang Fang, LaDeana W. Hillier, Brenton R. Graveley, Ali Mortazavi, Norbert Perrimon, Nathan Boley, Jingyi Jessica Li, William C. Spencer, James B. Brown, Chau Huynh, Roger A. Hoskins, Mark Gerstein, Ann S. Hammonds, Sarah Djebali, Sonali Jha, Kenneth H. Wan, Cédric Howald, Raymond K. Auerbach, Chenghai Xue, Haiyan Huang, Jorg Drenkow, Elise A. Feingold, Julien Lagarde, Daifeng Wang, Dmitri D. Pervouchine, Thomas R. Gingeras, Guilin Wang, Peter Cherbas, Brent Ewing, Chao Di, Gary Saunders, Benjamin W. Booth, Joel Rozowsky, Yan Zhang, Anastasia Samsonova, Dionna M. Kasper, Cristina Sisu, Marcus H. Stoiber, Jiayu Wen, Michael O. Duff, Felix Schlesinger, Gennifer E. Merrihew, Sara Olson, Susan E. Celniker, Burak H. Alver, Chao Cheng, Gemma E. May, Alexandre Reymond, Carrie A. Davis, Alexander Dobin, Max E. Boeck, Roger P. Alexander, Michael J. Pazin, Peter J. Park, Adam Frankish, Lucy Cherbas, Zhi Lu, Kevin Y. Yip, Henry Zheng, Owen Thompson, Jing Leng, Kathie L. Watkins, Andrea Tanzer, Valerie Reinke, Rebecca McWhirter, Eric C. Lai, Steven E. Brenner, Robert H. Waterston, Koon-Kiu Yan, Masaomi Kato, Roderic Guigó, Huaien Wang, Kimberly Bell, Pnina Strasbourger, Baikang Pei, Jen Harrow, Long Hu, Chris Zaleski, Rabi Murad, Thomas C. Kaufman, Erik Ladewig, Robert R. Kitchen, Anurag Sethi, Kejia Wen, Guanjun Gao, Arif Harmanci, Megan Fastuca, Brian Oliver, Frank J. Slack, David M. Miller, Tim Hubbard, Garrett Robinson, Peter J. Good, Peter J. Bickel, Michael J. MacCoss, Li Yang
Publikováno v:
Nature
Recercat. Dipósit de la Recerca de Catalunya
instname
NATURE
Nature, vol 512, iss 7515
Nature, vol. 512, no. 7515, pp. 445-448
Recercat. Dipósit de la Recerca de Catalunya
instname
NATURE
Nature, vol 512, iss 7515
Nature, vol. 512, no. 7515, pp. 445-448
The transcriptome is the readout of the genome. Identifying common features in it across distant species can reveal fundamental principles. To this end, the ENCODE and modENCODE consortia have generated large amounts of matched RNA-sequencing data fo
Autor:
Sohini Sengupta, Marco Carraro, Roger A. Hoskins, Silvio C. E. Tosatto, Jean Fan, Nikki Kiga, Christopher Douville, Binghuang Cai, Steven E. Brenner, Dewey Kim, Mark Diekhans, Susanna Repo, Hannah Carter, Manuel Giollo, Rohit Bhattacharya, John Moult, Lipika R. Pal, Jason Bobe, Biao Li, Sean D. Mooney, Rachel Karchin, Emanuela Leonardi, Jan Zaucha, Julian Gough, Yun-Ching Chen, Timothy Bergquist, Hui Ting Grace Yeo, Violeta Beleva-Guthrie, Carlo Ferrari, Tychele N. Turner, Madeleine Ball, George M. Church, Noushin Niknafs, Melissa S. Cline, Collin Tokheim, Yizhou Yin, Chen Hsin Yu, Chen Cao, Janita Thusberg, Mario Stanke
Publikováno v:
Human mutation, vol 38, iss 9
The advent of next-generation sequencing has dramatically decreased the cost for whole-genome sequencing and increased the viability for its application in research and clinical care. The Personal Genome Project (PGP) provides unrestricted access to
Autor:
Koen J. T. Venken, Michael Buckner, Young Guen Kwon, Frederik Wirtz-Peitz, Ralph A. Neumüller, Norbert Perrimon, Roger A. Hoskins, Stephanie E. Mohr, Hugo J. Bellen, Stella Juhyun Lee
Publikováno v:
Genetics. 190:931-940
In Drosophila collections of green fluorescent protein (GFP) trap lines have been used to probe the endogenous expression patterns of trapped genes or the subcellular localization of their protein products. Here, we describe a method, based on nonove