High-throughput sequencing of frozen and paraffin-embedded tumor and normal tissue

作者: M. Kerick , B. Timmermann , M.-R. Schweiger

DOI: 10.1007/S00292-010-1377-Z

关键词:

摘要: Until now high-throughput sequencing of tumor samples relied on DNA isolated from fresh frozen tissues, the preparation which, however, is relatively laborious. The use preserved material, i.e. tissue banks, could help to avoid this limitation and would enable reanalysis diverse clinical trials. So far we have shown that formalin-fixed paraffin-embedded (FFPE) can be used for genomic re-sequencing processes. FFPE are amply available surgical resections histopathological diagnosis, comprise precursor lesions, primary tumors, lymphogenic and/or hematogenic metastases. To generate models which predict response therapy, also has advantage it a variety Second generation techniques not only applicable snap tissues whole genome analyses but targeted resequencing approaches. In addition, detection copy number variations mutations in obtained within one run. possibility using genome-wide technologies irrespective mode storage facilitates retrieval useful material prerequisite subsequent computational modelling

参考文章(16)
Jay Shendure, Hanlee Ji, Next-generation DNA sequencing. Nature Biotechnology. ,vol. 26, pp. 1135- 1145 ,(2008) , 10.1038/NBT1486
M. Thomas P. Gilbert, Tamara Haselkorn, Michael Bunce, Juan J. Sanchez, Sebastian B. Lucas, Laurence D. Jewell, Eric Van Marck, Michael Worobey, The Isolation of Nucleic Acids from Fixed, Paraffin-Embedded Tissues–Which Methods Are Useful When? PLoS ONE. ,vol. 2, pp. e537- ,(2007) , 10.1371/JOURNAL.PONE.0000537
H. Li, J. Ruan, R. Durbin, Mapping short DNA sequencing reads and calling variants using mapping quality scores Genome Research. ,vol. 18, pp. 1851- 1858 ,(2008) , 10.1101/GR.078212.108
Michael L. Metzker, Sequencing technologies — the next generation Nature Reviews Genetics. ,vol. 11, pp. 31- 46 ,(2010) , 10.1038/NRG2626
Ben Langmead, Cole Trapnell, Mihai Pop, Steven L Salzberg, Ultrafast and memory-efficient alignment of short DNA sequences to the human genome Genome Biology. ,vol. 10, pp. 1- 10 ,(2009) , 10.1186/GB-2009-10-3-R25
Marcel Margulies, Michael Egholm, William E Altman, Said Attiya, Joel S Bader, Lisa A Bemben, Jan Berka, Michael S Braverman, Yi-Ju Chen, Zhoutao Chen, Scott B Dewell, Lei Du, Joseph M Fierro, Xavier V Gomes, Brian C Godwin, Wen He, Scott Helgesen, Chun He Ho, Gerard P Irzyk, Szilveszter C Jando, Maria LI Alenquer, Thomas P Jarvie, Kshama B Jirage, Jong-Bum Kim, James R Knight, Janna R Lanza, John H Leamon, Steven M Lefkowitz, Ming Lei, Jing Li, Kenton L Lohman, Hong Lu, Vinod B Makhijani, Keith E McDade, Michael P McKenna, Eugene W Myers, Elizabeth Nickerson, John R Nobile, Ramona Plant, Bernard P Puc, Michael T Ronan, George T Roth, Gary J Sarkis, Jan Fredrik Simons, John W Simpson, Maithreyan Srinivasan, Karrie R Tartaro, Alexander Tomasz, Kari A Vogt, Greg A Volkmer, Shally H Wang, Yong Wang, Michael P Weiner, Pengguang Yu, Richard F Begley, Jonathan M Rothberg, None, Genome sequencing in microfabricated high-density picolitre reactors Nature. ,vol. 437, pp. 376- 380 ,(2005) , 10.1038/NATURE03959
Scott A Armstrong, Ingo K Mellinghoff, F Stephen Hodi, Glenn Dranoff, Paul S Mischel, Tim F Cloughesy, Stan F Nelson, Linda M Liau, Kirsten Mertz, Mark A Rubin, Holger Moch, Massimo Loda, William Catalona, Jonathan Fletcher, Sabina Signoretti, Frederic Kaye, Kenneth C Anderson, George D Demetri, Reinhard Dummer, Stephan Wagner, Meenhard Herlyn, William R Sellers, Matthew Meyerson, Levi A Garraway, Roman K Thomas, Alissa C Baker, Ralph M DeBiasi, Wendy Winckler, Thomas LaFramboise, William M Lin, Meng Wang, Whei Feng, Thomas Zander, Laura E MacConaill, Jeffrey C Lee, Rick Nicoletti, Charlie Hatton, Mary Goyette, Luc Girard, Kuntal Majmudar, Liuda Ziaugra, Kwok-Kin Wong, Stacey Gabriel, Rameen Beroukhim, Michael Peyton, Jordi Barretina, Amit Dutt, Caroline Emery, Heidi Greulich, Kinjal Shah, Hidefumi Sasaki, Adi Gazdar, John Minna, High-throughput oncogene mutation profiling in human cancer Nature Genetics. ,vol. 39, pp. 347- 351 ,(2007) , 10.1038/NG1975
David A. Eberhard, Bruce E. Johnson, Lukas C. Amler, Audrey D. Goddard, Sherry L. Heldens, Roy S. Herbst, William L. Ince, Pasi A. Jänne, Thomas Januario, David H. Johnson, Pam Klein, Vincent A. Miller, Michael A. Ostland, David A. Ramies, Dragan Sebisanovic, Jeremy A. Stinson, Yu R. Zhang, Somasekar Seshagiri, Kenneth J. Hillan, Mutations in the Epidermal Growth Factor Receptor and in KRAS Are Predictive and Prognostic Indicators in Patients With Non–Small-Cell Lung Cancer Treated With Chemotherapy Alone and in Combination With Erlotinib Journal of Clinical Oncology. ,vol. 23, pp. 5900- 5909 ,(2005) , 10.1200/JCO.2005.02.857
E. R. Mardis, R. K. Wilson, Cancer genome sequencing: a review Human Molecular Genetics. ,vol. 18, ,(2009) , 10.1093/HMG/DDP396
Daphne W Bell, Our changing view of the genomic landscape of cancer The Journal of Pathology. ,vol. 220, pp. 231- 243 ,(2009) , 10.1002/PATH.2645