Combined targeted DNA and RNA sequencing of advanced NSCLC in routine molecular diagnostics: analysis of the first 3000 Heidelberg cases
Here, we demonstrate the feasibility and clinical utility of comprehensive, NGS-based genetic profiling for routine workup of advanced NSCLC based on the first 3000 patients analyzed in our department
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| Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , |
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| Format: | Article (Journal) |
| Language: | English |
| Published: |
17 January 2019
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| In: |
International journal of cancer
Year: 2019, Volume: 145, Issue: 3, Pages: 649-661 |
| ISSN: | 1097-0215 |
| DOI: | 10.1002/ijc.32133 |
| Online Access: | Resolving-System, Volltext: http://dx.doi.org/10.1002/ijc.32133 Verlag, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/ijc.32133 
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| Author Notes: | Anna-Lena Volckmar, Jonas Leichsenring, Martina Kirchner, Petros Christopoulos, Olaf Neumann, Jan Budczies, Cristiano Manuel Morais de Oliveira, Eugen Rempel, Ivo Buchhalter, Regine Brandt, Michael Allgäuer, Suranand Babu Talla, Moritz von Winterfeld, Esther Herpel, Benjamin Goeppert, Amelie Lier, Hauke Winter, Tilman Brummer, Stefan Fröhling, Martin Faehling, Jürgen R. Fischer, Claus Peter Heußel, Felix Herth, Felix Lasitschka, Peter Schirmacher, Michael Thomas, Volker Endris, Roland Penzel and Albrecht Stenzinger |
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