Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Deepali Bhatt"'
Autor:
John D. Minna, Thomas D. Wu, David S. Shames, Stephanie Johnson, Peter Dijkgraaf, Florian Gnad, Deepali Bhatt, Jocelyn Chan, Jeremy Stinson, William Lee, Thomas Holcomb, Zemin Zhang, Kimberly Walter, Steffan Vartanian, Jinfeng Liu, Christiaan Klijn, Adi F. Gazdar, Robert Gentleman, David Stokoe, Peter M. Haverty, Richard M. Neve, Houston Gilbert, Zhaoshi Jiang, Yinghui Guan, Joseph Guillory, Zhongqiang Chen, Klaus P. Hoeflich, Suchit Jhunjhunwala, Zora Modrusan, Julie Koeman, Jeff Settleman, Howard M. Stern, Somasekar Seshagiri, Frederic J. de Sauvage
Publikováno v:
Genome Research. 22:2315-2327
Lung cancer is a highly heterogeneous disease in terms of both underlying genetic lesions and response to therapeutic treatments. We performed deep whole-genome sequencing and transcriptome sequencing on 19 lung cancer cell lines and three lung tumor
Autor:
Frederic J. de Sauvage, James Shin, John T. Poirier, Adi F. Gazdar, Wenlin Yuan, Yinghui Guan, Richard Bourgon, John D. Minna, Thomas D. Wu, Celina Sanchez Rivers, David S. Shames, Bijay S. Jaiswal, Catherine K. Foo, Zora Modrusan, Emily Bergbower, Steffen Durinck, Joseph Guillory, Diego D Paskulin, Florian Gnad, Peter M. Haverty, Somasekar Seshagiri, Peter B. Illei, Jeremy Stinson, Marileila Varella-Garcia, Eric Stawiski, Chaitali Parikh, Zemin Zhang, Kenneth E. Huffman, Howard M. Stern, Subhra Chaudhuri, Hartmut Koeppen, Robert L. Yauch, Deepali Bhatt, Vasantharajan Janakiraman, Malcolm V. Brock, Charles M. Rudin, Robert Gentleman
Small-cell lung cancer (SCLC) is an exceptionally aggressive disease with poor prognosis. Here, we obtained exome, transcriptome and copy-number alteration data from approximately 53 samples consisting of 36 primary human SCLC and normal tissue pairs
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::745bdc7433f8458466e8544058c127f4
https://europepmc.org/articles/PMC3557461/
https://europepmc.org/articles/PMC3557461/
Autor:
Zhengyan Kan, Zora Modrusan, Somasekar Seshagiri, Kenneth Jung, Deepali Bhatt, Celina Sanchez Rivers, Wenlin Yuan, Jeremy Stinson, Serban Nacu, Brock A. Peters, Thomas D. Wu
Publikováno v:
BMC Medical Genomics, Vol 4, Iss 1, p 11 (2011)
BMC Medical Genomics
BMC Medical Genomics
Background Readthrough fusions across adjacent genes in the genome, or transcription-induced chimeras (TICs), have been estimated using expressed sequence tag (EST) libraries to involve 4-6% of all genes. Deep transcriptional sequencing (RNA-Seq) now
Autor:
Serban Nacu1, Wenlin Yuan1, Zhengyan Kan1, Bhatt, Deepali1, Rivers, Celina Sanchez1, Stinson, Jeremy1, Peters, Brock A.1, Modrusan, Zora1, Jung, Kenneth1, Seshagiri, Somasekar1 sekar@gene.com, Wu, Thomas D.1 twu@gene.com
Publikováno v:
BMC Medical Genomics. 2011, Vol. 4 Issue 1, p11-32. 22p.
Autor:
Fedorowicz, Grazyna1 fedorowicz.grazyna@gene.com, Guerrero, Steve2 guerrero.steve@gene.com, Wu, Thomas D.2 wu.thomas@gene.com, Modrusan, Zora1 modrusan.zora@gene.com
Publikováno v:
BMC Medical Genomics. 2009, Vol. 2, p1-11. 11p. 1 Black and White Photograph, 1 Chart, 3 Graphs.
Autor:
Parikh, Chaitali, Janakiraman, Vasantharajan, Wen-I Wu, Foo, Catherine K., Kljavin, Noelyn M., Chaudhuri, Subhra, Stawiski, Eric, Lee, Brian, Jie Lin, Hong Li, Lorenzo, Maria N., Wenlin Yuan, Guillory, Joseph, Jackson, Marlena, Rondon, Jesus, Franke, Yvonne, Bowman, Krista K., Sagolla, Meredith, Stinson, Jeremy, Wu, Thomas D.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America; 11/20/2012, Vol. 109 Issue 47, p19368-19373, 6p