NGS-dataset of putative driver mutations associated with benign peritoneal strumosis

A rare case of benign peritoneal strumosis was screened for driver mutations in genes relevant to currently approved cancer therapies. Therefore, three formalin fixed paraffin embedded issue sections were screened with the GeneReader Actionable Insights NGS panel (Qiagen, Hilden, Germany) for the oc...

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Salvato in:
Dettagli Bibliografici
Pubblicato in:Data Brief
Autori principali: Brockmann, Michael, Schildgen, Verena, Schildgen, Oliver, Lüsebrink, Jessica, Pieper, Monika, Gudima, Alexandru
Natura: Artigo
Lingua:Inglês
Pubblicazione: Elsevier 2018
Soggetti:
Philosophy
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6122335/
https://ncbi.nlm.nih.gov/pubmed/30186896
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.dib.2018.08.006
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