Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Lana Sheta"'
Autor:
Kilannin Krysiak, Arpad M Danos, Jason Saliba, Joshua F McMichael, Adam C Coffman, Susanna Kiwala, Erica K Barnell, Lana Sheta, Cameron J Grisdale, Lynzey Kujan, Shahil Pema, Jake Lever, Sarah Ridd, Nicholas C Spies, Veronica Andric, Andreea Chiorean, Damian T Rieke, Kaitlin A Clark, Caralyn Reisle, Ajay C Venigalla, Mark Evans, Payal Jani, Hideaki Takahashi, Avila Suda, Peter Horak, Deborah I Ritter, Xin Zhou, Benjamin J Ainscough, Sean Delong, Chimene Kesserwan, Mario Lamping, Haolin Shen, Alex R Marr, My H Hoang, Kartik Singhal, Mariam Khanfar, Brian V Li, Wan-Hsin Lin, Panieh Terraf, Laura B Corson, Yasser Salama, Katie M Campbell, Kirsten M Farncombe, Jianling Ji, Xiaonan Zhao, Xinjie Xu, Rashmi Kanagal-Shamanna, Ian King, Kelsy C Cotto, Zachary L Skidmore, Jason R Walker, Jinghui Zhang, Aleksandar Milosavljevic, Ronak Y Patel, Rachel H Giles, Raymond H Kim, Lynn M Schriml, Elaine R Mardis, Steven J M Jones, Gordana Raca, Shruti Rao, Subha Madhavan, Alex H Wagner, Malachi Griffith, Obi L Griffith
Publikováno v:
Nucleic Acids Research. 51:D1230-D1241
CIViC (Clinical Interpretation of Variants in Cancer; civicdb.org) is a crowd-sourced, public domain knowledgebase composed of literature-derived evidence characterizing the clinical utility of cancer variants. As clinical sequencing becomes more pre
Autor:
Kilannin Krysiak, Arpad M. Danos, Susanna Kiwala, Joshua F. McMichael, Adam C. Coffman, Erica K. Barnell, Lana Sheta, Jason Saliba, Cameron J. Grisdale, Lynzey Kujan, Shahil Pema, Jake Lever, Nicholas C. Spies, Andreea Chiorean, Damian T. Rieke, Kaitlin A. Clark, Payal Jani, Hideaki Takahashi, Peter Horak, Deborah I. Ritter, Xin Zhou, Benjamin J. Ainscough, Sean Delong, Mario Lamping, Alex R. Marr, Brian V. Li, Wan-Hsin Lin, Panieh Terraf, Yasser Salama, Katie M. Campbell, Kirsten M. Farncombe, Jianling Ji, Xiaonan Zhao, Xinjie Xu, Rashmi Kanagal-Shamanna, Kelsy C. Cotto, Zachary L. Skidmore, Jason R. Walker, Jinghui Zhang, Aleksandar Milosavljevic, Ronak Y. Patel, Rachel H. Giles, Raymond H. Kim, Lynn M. Schriml, Elaine R. Mardis, Steven J. M. Jones, Gordana Raca, Shruti Rao, Subha Madhavan, Alex H. Wagner, Obi L. Griffith, Malachi Griffith
Publikováno v:
Nat Cancer
As guidelines, therapies, and literature on cancer variants expand, the lack of consensus variant interpretations impedes clinical applications. CIViC is a public domain, crowd-sourced, and adaptable knowledgebase of evidence for the Clinical Interpr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ed50e6a9356f3f2f4e3e63d326c2871
https://eprints.gla.ac.uk/279775/1/279775.pdf
https://eprints.gla.ac.uk/279775/1/279775.pdf
Autor:
Andreea Chiorean, Kirsten M. Farncombe, Sean Delong, Veronica Andric, Safa Ansar, Clarissa Chan, Kaitlin Clark, Arpad M. Danos, Yizhuo Gao, Rachel H. Giles, Anna Goldenberg, Payal Jani, Kilannin Krysiak, Lynzey Kujan, Samantha Macpherson, Eamonn R. Maher, Liam G. McCoy, Yasser Salama, Jason Saliba, Lana Sheta, Malachi Griffith, Obi L. Griffith, Lauren Erdman, Arun Ramani, Raymond H. Kim
Publikováno v:
Human mutation. 43(9)
Von Hippel-Lindau (VHL) disease is a hereditary cancer syndrome where individuals are predisposed to tumor development in the brain, adrenal gland, kidney, and other organs. It is caused by pathogenic variants in the VHL tumor suppressor gene. Standa
Autor:
Obi L. Griffith, Nicholas C. Spies, Kelsy C. Cotto, Damian T. Rieke, Malachi Griffith, Kelsi Penewit, Adam Waalkes, Katie M. Campbell, Lana Sheta, Colin Pritchard, Ravindra Uppaluri, Zachary L. Skidmore, Matt C. Mosior, Kilannin Krysiak, Arpad Danos, Stephen J. Salipante, Todd A. Fehniger, Erica K. Barnell, Ramaswamy Govindan
Publikováno v:
JCO Clinical Cancer Informatics
PURPOSE Clinical targeted sequencing panels are important for identifying actionable variants for patients with cancer; however, existing approaches do not provide transparent and rationally designed clinical panels to accommodate the rapidly growing
Autor:
Kilannin Krysiak, Michael Evenson, Jason Saliba, Lana Sheta, Arpad Danos, Obi Griffith, Malachi Griffith
Publikováno v:
Cancer Genetics. :14-15
Autor:
Kilannin C. Krysiak, Adam C. Coffman, Susanna Kiwala, Joshua F. McMichael, Arpad M. Danos, Jason Saliba, Cameron J. Grisdale, Jake Lever, Lana Sheta, Shruti Rao, Alex H. Wagner, Malachi Griffith, Obi L. Griffith
Publikováno v:
Cancer Research. 82:1194-1194
The Clinical Interpretation of Variants in Cancer (CIViC; www.civicdb.org) knowledgebase is a curation platform designed to capture evidence from the published literature which support or refute the significance of genomic variants in various cancer
Autor:
Jason Saliba, Jake Lever, Kilannin Krysiak, Lana Sheta, Arpad Danos, Alex Wagner, Heather Williams, Chimene Kesserwan, Laura Corson, Jianling Ji, Catherine Cottrell, Alanna Church, Laveniya Satgunaseelan, David Meredith, Mark Evans, Wan-Hsin Lin, Kai Lee Yap, Shruti Rao, Lynn Schriml, Angshumoy Roy, Gordana Raca, Malachi Griffith, Obi Griffith
Publikováno v:
Cancer Genetics. :6
Autor:
Arpad Danos, Kilannin Krysiak, Jason Saliba, Lana Sheta, Alex Wagner, Cameron Grisdale, Shruti Rao, Adam Coffman, Joshua McMichael, Susanna Kiwala, Erica Barnell, Shahil Pema, Sydney Anderson, Justin Guerra, Lynzey Kujan, Nick Spies, Malachi Griffith, Obi Griffith
Publikováno v:
Cancer Genetics. :13
Autor:
Shruti Rao, Jason Saliba, Xiaonan Zhao, Rong He, Chimene Kesserwan, Arpad Danos, Lana Sheta, Panieh Terraf, Gordana Raca, Heather Williams, Piers Blombery, David Viswanatha, Celeste Eno, Coumarane Mani, Nan Jiang, Kevin C. Vavra, Liying Zhang, Zonggao Shi, Peng Li, Yuwen Li, Madhu M. Ouseph, Ella Thompson, Yiming Zhong, Kilannin Krysiak, Alex H. Wagner, Matthew McCoy, Mariam T. Matthew, Kristin Deeb, Fengli Zhang, Jie Liu, Xiangqiang Shao, Alejandro Ferrer, Nathan Kopp, Wenying Zhang, Santhi Pondugula, Yasmina Jaufeerally Fakim, David Wu, Sheeja T. Pullarkat, Shashikant Kulkarni, Subha Madhavan, Xinjie Xu, Rashmi Kanagal-Shamana
Publikováno v:
Cancer Genetics. :16
Autor:
Arpad Danos, Shruti Rao, Wan-Hsin Lin, Erica K. Barnell, Cameron J. Grisdale, Shahil Pema, Raymond H. Kim, Dmitriy Sonkin, Joshua F. McMichael, Kaitlin Clark, Malachi Griffith, Susanna Kiwala, Subha Madhavan, Obi L. Griffith, Nicholas C. Spies, Gordana Raca, Lynzey Kujan, Adam C. Coffman, Kilannin Krysiak, Alex H. Wagner, Amber Z. Wollam, Deborah I. Ritter, Lana Sheta
Publikováno v:
Genome Medicine
Genome Medicine, Vol 11, Iss 1, Pp 1-12 (2019)
Genome Medicine, Vol 11, Iss 1, Pp 1-12 (2019)
Manually curated variant knowledgebases and their associated knowledge models are serving an increasingly important role in distributing and interpreting variants in cancer. These knowledgebases vary in their level of public accessibility, and the co