Multicenter validation of cancer gene panel-based next-generation sequencing for translational research and molecular diagnostics
-
Published:2018-01-27
Issue:4
Volume:472
Page:557-565
-
ISSN:0945-6317
-
Container-title:Virchows Archiv
-
language:en
-
Short-container-title:Virchows Arch
Author:
Hirsch B.ORCID, Endris V., Lassmann S., Weichert W., Pfarr N., Schirmacher P., Kovaleva V., Werner M., Bonzheim I., Fend F., Sperveslage J., Kaulich K., Zacher A., Reifenberger G., Köhrer K., Stepanow S., Lerke S., Mayr T., Aust D. E., Baretton G., Weidner S., Jung A., Kirchner T., Hansmann M. L., Burbat L., von der Wall E., Dietel M., Hummel M.
Funder
German Consortium for Translational Cancer Research
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Molecular Biology,General Medicine,Pathology and Forensic Medicine
Reference29 articles.
1. Alioto TS, Buchhalter I, Derdak S, Hutter B, Eldridge MD, Hovig E, Heisler LE, Beck TA, Simpson JT, Tonon L, Sertier AS, Patch AM, Jager N, Ginsbach P, Drews R, Paramasivam N, Kabbe R, Chotewutmontri S, Diessl N, Previti C, Schmidt S, Brors B, Feuerbach L, Heinold M, Grobner S, Korshunov A, Tarpey PS, Butler AP, Hinton J, Jones D, Menzies A, Raine K, Shepherd R, Stebbings L, Teague JW, Ribeca P, Giner FC, Beltran S, Raineri E, Dabad M, Heath SC, Gut M, Denroche RE, Harding NJ, Yamaguchi TN, Fujimoto A, Nakagawa H, Quesada V, Valdes-Mas R, Nakken S, Vodak D, Bower L, Lynch AG, Anderson CL, Waddell N, Pearson JV, Grimmond SM, Peto M, Spellman P, He M, Kandoth C, Lee S, Zhang J, Letourneau L, Ma S, Seth S, Torrents D, Xi L, Wheeler DA, Lopez-Otin C, Campo E, Campbell PJ, Boutros PC, Puente XS, Gerhard DS, Pfister SM, McPherson JD, Hudson TJ, Schlesner M, Lichter P, Eils R, Jones DT, Gut IG (2015) A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing. Nat Commun 6:10001.
https://doi.org/10.1038/ncomms10001 2. Aziz N, Zhao Q, Bry L, Driscoll DK, Funke B, Gibson JS, Grody WW, Hegde MR, Hoeltge GA, Leonard DG, Merker JD, Nagarajan R, Palicki LA, Robetorye RS, Schrijver I, Weck KE, Voelkerding KV (2015) College of American Pathologists’ laboratory standards for next-generation sequencing clinical tests. Archives of pathology & laboratory medicine 139(4):481–493.
https://doi.org/10.5858/arpa.2014-0250-CP 3. Bamford S, Dawson E, Forbes S, Clements J, Pettett R, Dogan A, Flanagan A, Teague J, Futreal PA, Stratton MR, Wooster R (2004) The COSMIC (Catalogue of Somatic Mutations in Cancer) database and website. Br J Cancer 91(2):355–358.
https://doi.org/10.1038/sj.bjc.6601894 4. Bonin S, Hlubek F, Benhattar J, Denkert C, Dietel M, Fernandez PL, Hofler G, Kothmaier H, Kruslin B, Mazzanti CM, Perren A, Popper H, Scarpa A, Soares P, Stanta G, Groenen PJ (2010) Multicentre validation study of nucleic acids extraction from FFPE tissues. Virchows Arch 457(3):309–317.
https://doi.org/10.1007/s00428-010-0917-5 5. Chen X, Shi X, Hilakivi-Clarke L, Shajahan-Haq AN, Clarke R, Xuan J (2017) PSSV: a novel pattern-based probabilistic approach for somatic structural variation identification. Bioinformatics 33(2):177–183.
https://doi.org/10.1093/bioinformatics/btw605
Cited by
19 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|