Genetic profiles of cervical tumors by high-throughput sequencing for personalized medical care

作者: Etienne Muller , Baptiste Brault , Allyson Holmes , Angelina Legros , Emmanuelle Jeannot

DOI: 10.1002/CAM4.492

关键词:

摘要: … , using high-throughput sequencing. Twenty-nine tumors were sequenced for exons within … It is well-known that some human papillomavirus (HPV) types are the cause of this cancer …

参考文章(45)
Geraldine A. Auwera, Mauricio O. Carneiro, Christopher Hartl, Ryan Poplin, Guillermo del Angel, Ami Levy‐Moonshine, Tadeusz Jordan, Khalid Shakir, David Roazen, Joel Thibault, Eric Banks, Kiran V. Garimella, David Altshuler, Stacey Gabriel, Mark A. DePristo, From FastQ Data to High‐Confidence Variant Calls: The Genome Analysis Toolkit Best Practices Pipeline Current protocols in human genetics. ,vol. 43, ,(2013) , 10.1002/0471250953.BI1110S43
Andreas Wilm, Pauline Poh Kim Aw, Denis Bertrand, Grace Hui Ting Yeo, Swee Hoe Ong, Chang Hua Wong, Chiea Chuen Khor, Rosemary Petric, Martin Lloyd Hibberd, Niranjan Nagarajan, LoFreq: a sequence-quality aware, ultra-sensitive variant caller for uncovering cell-population heterogeneity from high-throughput sequencing datasets Nucleic Acids Research. ,vol. 40, pp. 11189- 11201 ,(2012) , 10.1093/NAR/GKS918
Massimo Tommasino, Rosita Accardi, Sandra Caldeira, Wen Dong, Ilaria Malanchi, Anouk Smet, Ingeborg Zehbe, The role of TP53 in Cervical carcinogenesis Human Mutation. ,vol. 21, pp. 307- 312 ,(2003) , 10.1002/HUMU.10178
A. Carreira, S. C. Kowalczykowski, Two classes of BRC repeats in BRCA2 promote RAD51 nucleoprotein filament function by distinct mechanisms Proceedings of the National Academy of Sciences of the United States of America. ,vol. 108, pp. 10448- 10453 ,(2011) , 10.1073/PNAS.1106971108
Soyeon Kim, Tae Min Kim, Dong-Wan Kim, Heounjeong Go, Bhumsuk Keam, Se-Hoon Lee, Ja-Lok Ku, Doo Hyun Chung, Dae Seog Heo, None, Heterogeneity of Genetic Changes Associated with Acquired Crizotinib Resistance in ALK-Rearranged Lung Cancer Journal of Thoracic Oncology. ,vol. 8, pp. 415- 422 ,(2013) , 10.1097/JTO.0B013E318283DCC0
Claude Houdayer, Virginie Caux-Moncoutier, Sophie Krieger, Michel Barrois, Françoise Bonnet, Violaine Bourdon, Myriam Bronner, Monique Buisson, Florence Coulet, Pascaline Gaildrat, Cédrick Lefol, Mélanie Léone, Sylvie Mazoyer, Danielle Muller, Audrey Remenieras, Françoise Révillion, Etienne Rouleau, Joanna Sokolowska, Jean-Philippe Vert, Rosette Lidereau, Florent Soubrier, Hagay Sobol, Nicolas Sevenet, Brigitte Bressac-de Paillerets, Agnès Hardouin, Mario Tosi, Olga M. Sinilnikova, Dominique Stoppa-Lyonnet, Guidelines for splicing analysis in molecular diagnosis derived from a set of 327 combined in silico/in vitro studies on BRCA1 and BRCA2 variants. Human Mutation. ,vol. 33, pp. 1228- 1238 ,(2012) , 10.1002/HUMU.22101
Huilei Xu, John DiCarlo, Ravi Satya, Quan Peng, Yexun Wang, Comparison of somatic mutation calling methods in amplicon and whole exome sequence data BMC Genomics. ,vol. 15, pp. 244- 244 ,(2014) , 10.1186/1471-2164-15-244
Heidi L. Rehm, Disease-targeted sequencing: a cornerstone in the clinic Nature Reviews Genetics. ,vol. 14, pp. 295- 300 ,(2013) , 10.1038/NRG3463
John B McIntyre, Jackson S Wu, Peter S Craighead, Tien Phan, Martin Köbel, Susan P Lees-Miller, Prafull Ghatage, Anthony M Magliocco, Corinne M Doll, None, PIK3CA mutational status and overall survival in patients with cervical cancer treated with radical chemoradiotherapy. Gynecologic Oncology. ,vol. 128, pp. 409- 414 ,(2013) , 10.1016/J.YGYNO.2012.12.019