From somatic variants towards precision oncology: Evidence-driven reporting of treatment options in molecular tumor boards

BACKGROUND: A comprehensive understanding of cancer has been furthered with technological improvements and decreasing costs of next-generation sequencing (NGS). However, the complexity of interpreting genomic data is hindering the implementation of high-throughput technologies in the clinical contex...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Genome Med
Päätekijät: Perera-Bel, Júlia, Hutter, Barbara, Heining, Christoph, Bleckmann, Annalen, Fröhlich, Martina, Fröhling, Stefan, Glimm, Hanno, Brors, Benedikt, Beißbarth, Tim
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: BioMed Central 2018
Aiheet:
Research
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5856211/
https://ncbi.nlm.nih.gov/pubmed/29544535
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13073-018-0529-2
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