Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Virginie Petitjean"'
Autor:
Yongmei Zhao, Li Tai Fang, Tsai-wei Shen, Sulbha Choudhari, Keyur Talsania, Xiongfong Chen, Jyoti Shetty, Yuliya Kriga, Bao Tran, Bin Zhu, Zhong Chen, Wanqiu Chen, Charles Wang, Erich Jaeger, Daoud Meerzaman, Charles Lu, Kenneth Idler, Luyao Ren, Yuanting Zheng, Leming Shi, Virginie Petitjean, Marc Sultan, Tiffany Hung, Eric Peters, Jiri Drabek, Petr Vojta, Roberta Maestro, Daniela Gasparotto, Sulev Kõks, Ene Reimann, Andreas Scherer, Jessica Nordlund, Ulrika Liljedahl, Jonathan Foox, Christopher E. Mason, Chunlin Xiao, Huixiao Hong, Wenming Xiao
Publikováno v:
Scientific Data, Vol 8, Iss 1, Pp 1-14 (2021)
Measurement(s) Somatic Mutation Analysis Technology Type(s) whole genome sequencing • Whole Exome Sequencing Factor Type(s) sequencing platform • sample prepration • library preparation • bioinformatics method Sample Characteristic - Organism
Externí odkaz:
https://doaj.org/article/df99660883fb470bb2307f5ae2b58917
Autor:
Sven Schuierer, Walter Carbone, Judith Knehr, Virginie Petitjean, Anita Fernandez, Marc Sultan, Guglielmo Roma
Publikováno v:
BMC Genomics, Vol 18, Iss 1, Pp 1-13 (2017)
Abstract Background RNA-sequencing (RNA-seq) has emerged as one of the most sensitive tool for gene expression analysis. Among the library preparation methods available, the standard poly(A) + enrichment provides a comprehensive, detailed, and accura
Externí odkaz:
https://doaj.org/article/6e9e42e60d93451c828fca0695250937
Autor:
Kenneth Idler, Andreas Scherer, Charles Lu, Timothy K. McDaniel, Penelope Duerken-Hughes, K J. Langenbach, Seta Stanbouly, Charles Wang, Victoria Zismann, Keyur Talsania, Leming Shi, Margaret C. Cam, Shamoni Maheshwari, Zhipan Li, Luyao Ren, Petr Vojta, Mehdi Pirooznia, Jonathan J Keats, Rasika Kalamegham, Howard Jacob, Bao Tran, Liz Kerrigan, Baitang Ning, Ene Reimann, Jiri Drabek, Eric F. Donaldson, Zhaowei Yang, Sayed Mohammad Ebrahim Sahraeian, Daoud Meerzaman, Marc Sultan, Jessica Nordlund, Tsai-wei Shen, Sulev Kõks, Christopher E. Mason, Yunfei Guo, Winnie S. Liang, Claudia Catalanotti, Jeffrey M. Trent, Ying Yu, Roderick V. Jensen, Huixiao Hong, Malcolm Moos, Wenming Xiao, Stephen T. Sherry, Jonathan Foox, Joe Shuga, Hugo Y. K. Lam, Chunlin Xiao, Lijing Yao, Li Tai Fang, Wanqiu Chen, Marghoob Mohiyuddin, Monika Mehta, Rebecca Kusko, Roberta Maestro, Yongmei Zhao, Jonathan Adkins, Gary P. Schroth, Daniel Butler, Yuliya Kriga, Ogan D Abaan, Erich Jaeger, Yuanting Zheng, Daniela Gasparotto, Ulrika Liljedahl, Tiffany Hung, Eric Peters, Erica Tassone, Maryellen de Mars, Cu Nguyen, Lei Song, Bin Zhu, Weida Tong, Zivana Tezak, Justin B. Lack, Virginie Petitjean, Jyoti Shetty, Jing Li, Zhong Chen
Publikováno v:
Nat Biotechnol
The lack of samples for generating standardized DNA datasets for setting up a sequencing pipeline or benchmarking the performance of different algorithms limits the implementation and uptake of cancer genomics. Here, we describe reference call sets o
Autor:
Maryellen de Mars, Cu Nguyen, Tiffany Hung, Eric Peters, Charles Lu, Meijian Guan, Bao Tran, Maurizio Polano, Bin Zhu, Samir Lababidi, Wendell D. Jones, Chunlin Xiao, Andreas Scherer, K J. Langenbach, Zhipan Li, Luyao Ren, Weida Tong, Erich Jaeger, Rebecca Kusko, Zivana Tezak, Ying Yu, Ulrika Liljedahl, Louis M. Staudt, Huixiao Hong, Jing Wang, Yuanting Zheng, Ali Moshrefi, Cristobal Juan Vera, Chris Miller, Rasika Kalamegham, Arati Raziuddin, Howard Jacob, Roberta Maestro, Bindu Swapna Madala, Petr Vojta, Jessica Nordlund, Li Tai Fang, Jiri Drabek, Xuelu Liu, Corey Miles, Gary P. Schroth, Fayaz Seifuddin, Tim R. Mercer, Chunhua Yan, Leihong Wu, Sulev Kõks, Roderick V. Jensen, Jennifer A Hipp, Yun-Ching Chen, Malcolm Moos, Yongmei Zhao, Baitang Ning, Aparna Natarajan, Brian N. Papas, Xin Chen, Ashley Walton, Stephen T. Sherry, Christopher E. Mason, Liz Kerrigan, Ogan D Abaan, Wanqiu Chen, Kenneth Idler, Jingya Wang, Tsai-wei Shen, James C. Willey, Ene Reimann, Justin B. Lack, Virginie Petitjean, Jyoti Shetty, Daoud Meerzaman, Charles Wang, Jian-Liang Li, Tiffany Truong, Keyur Talsania, Mehdi Pirooznia, Marc Sultan, Urvashi Mehra, Wenming Xiao, Zhong Chen, Ana Granat, Leming Shi, Margaret C. Cam, Qing-Rong Chen, Eric F. Donaldson, Wolfgang Resch, Ben Ernest, Yuliya Kriga, Gokhan Yavas, Thomas M. Blomquist, Parthav Jailwala
Publikováno v:
Nat Biotechnol
Clinical applications of precision oncology require accurate tests that can distinguish true cancer-specific mutations from errors introduced at each step of next-generation sequencing (NGS). To date, no bulk sequencing study has addressed the effect
Autor:
Bao Tran, Erich Jaeger, Sulbha Choudhari, Daniela Gasparotto, Yuliya Kriga, Sulev Kõks, Kenneth Idler, Keyur Talsania, Petr Vojta, Zhong Chen, Charles Wang, Jiri Drabek, Wanqiu Chen, Yuanting Zheng, Daoud Meerzaman, Christopher E. Mason, Roberta Maestro, Leming Shi, Ene Reimann, Tsai-wei Shen, Charles Lu, Jonathan Foox, Xiongfong Chen, Chunlin Xiao, Luyao Ren, Wenming Xiao, Tiffany Hung, Eric Peters, Marc Sultan, Andreas Scherer, Bin Zhu, Yongmei Zhao, Virginie Petitjean, Jyoti Shetty, Huixiao Hong, Jessica Nordlund, Ulrika Liljedahl, Li Tai Fang
Publikováno v:
Scientific Data, Vol 8, Iss 1, Pp 1-14 (2021)
Scientific Data
Scientific Data
With the rapid advancement of sequencing technologies, next generation sequencing (NGS) analysis has been widely applied in cancer genomics research. More recently, NGS has been adopted in clinical oncology to advance personalized medicine. Clinical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::50da38baf6dea5f68d7766a7d6f0bfc0
http://hdl.handle.net/10138/336358
http://hdl.handle.net/10138/336358
Autor:
Ene Reimann, Marc Sultan, Andreas Scherer, Yuliya Kriga, Ulrika Liljedahl, Wangqiu Chen, Li Tai Fang, Bin Zhu, Daoud Meerzaman, Zhong Chen, Bao Tran, Leming Shi, Christopher E. Mason, Sulbha Choudhari, Keyur Talsania, Jessica Nordlund, Virginie Petitjean, Chunlin Xiao, Xiongfong Chen, Jyoti Shetty, Jiri Drabek, Wenming Xiao, Charles Wang, Yongmei Zhao, Daniela Gasparotto, Charles W. Lu, Petr Vojta, Erich Jaeger, Yuanting Zheng, Sulev Kõks, Roberta Maestro, Tsai-wei Shen, Kenneth Idler, Tiffany Hung, Eric Peters, Jonathan Foox
With the rapid advancement of sequencing technologies in the past decade, next generation sequencing (NGS) analysis has been widely applied in cancer genomics research. More recently, NGS has been adopted in clinical oncology to advance personalized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50416f0113399c37c54d442c795408af
https://doi.org/10.1101/2021.02.27.433136
https://doi.org/10.1101/2021.02.27.433136
Autor:
Wenming Xiao, Roderick V. Jensen, Yuanting Zheng, Daoud Meerzaman, Wanqiu Chen, Marghoob Mohiyuddin, Roberta Maestro, Charles Wang, Andreas Scherer, Kenneth Idler, Zhong Chen, Stephen T. Sherry, Seta Stanbouly, P. Duerken-Hughes, Keyur Talsania, S.M. Ebrahim Sahraeian, Yongmei Zhao, Leming Shi, Chunlin Xiao, K J. Langenbach, Ene Reimann, Mehdi Pirooznia, Liz Kerrigan, Margaret C. Cam, Charles Lu, Gary P. Schroth, Zhaowei Yang, Marc Sultan, Tiffany Hung, Eric Peters, Rebecca Kusko, Bing-Mei Zhu, Zhipan Li, Huixiao Hong, Bao Tran, Yunfei Guo, Cu Nguyen, Jiri Drabek, Long-Sheng Song, Malcolm Moos, Lingshuang Ren, T-W Shen, Yonghao Yu, Ulrika Liljedahl, Li Tai Fang, Justin B. Lack, Hugo Y. K. Lam, Virginie Petitjean, Jyoti Shetty, Zivana Tezak, Rasika Kalamegham, Howard Jacob, Daniela Gasparotto, Jessica Nordlund, Jian Li, Lijing Yao, Erich Jaeger, Sulev Kõks, Baitang Ning, Eric F. Donaldson, Ogan D Abaan, M. de Mars
We characterized two reference samples for NGS technologies: a human triple-negative breast cancer cell line and a matched normal cell line. Leveraging several whole-genome sequencing (WGS) platforms, multiple sequencing replicates, and orthogonal mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6eb40aaefe2c60f2a2156ec78a1c7fff
https://doi.org/10.1101/625624
https://doi.org/10.1101/625624
Autor:
Mathias Frederiksen, Uwe Plikat, Sven Schuierer, Marc Altorfer, Bhupinder Bhullar, Esther K. Schmitt, David Estoppey, Thomas Aust, Sophie Brachat, John A. Tallarico, Britta Knapp, Ireos Filipuzzi, Juerg Eichenberger, Nicole Hartmann, Christian Studer, Ralph Riedl, Annika Hohendahl, Lukas Baeriswyl, Frank Staedtler, Edward J. Oakeley, Florian Nigsch, Raffaele Cerino, Stefan Wetzel, Yann Abraham, Heather Sadlish, Stephen B. Helliwell, Jeffrey A. Porter, N. Rao Movva, Mark C. Fishman, Frank Petersen, Virginie Petitjean, Nicolas Melin, Philipp Krastel, Lena Chang, Dominic Hoepfner
Publikováno v:
Microbiological Research. 169:107-120
Due to evolutionary conservation of biology, experimental knowledge captured from genetic studies in eukaryotic model organisms provides insight into human cellular pathways and ultimately physiology. Yeast chemogenomic profiling is a powerful approa
Autor:
Virginie Petitjean
Le developpement du câble et du satellite, et de la TNT a accentue la concurrence entre les chaines. Celles-ci, qui vivent principalement ou uniquement des recettes publicitaires, se doivent de mettre en place des strategies de programmation efficac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b9496cd8e153fce012f6be2299bf413
http://entrelacs.revues.org/276
http://entrelacs.revues.org/276