Comprehensive routine diagnostic screening to identify predictive mutations, gene amplifications, and microsatellite instability in FFPE tumor material

Abstract Background Sensitive and reliable molecular diagnostics is needed to guide therapeutic decisions for cancer patients. Although less material becomes available for testing, genetic markers are rapidly expanding. Simultaneous detection of predictive markers, including mutations, gene amplific...

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Bibliografiset tiedot
Päätekijät: Elisabeth M. P. Steeghs, Leonie I. Kroeze, Bastiaan B. J. Tops, Leon C. van Kempen, Arja ter Elst, Annemiek W. M. Kastner-van Raaij, Sandra J. B. Hendriks-Cornelissen, Mandy J. W. Hermsen, Erik A. M. Jansen, Petra M. Nederlof, Ed Schuuring, Marjolijn J. L. Ligtenberg, Astrid Eijkelenboom
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BMC 2020-04-01
Sarja:BMC Cancer
Aiheet:
Predictive analysis
Next-generation sequencing
Mutation
Gene amplification
Microsatellite instability
FFPE
Linkit:http://link.springer.com/article/10.1186/s12885-020-06785-6
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