NIMG-46. RADIOGENOMIC FEATURES PREDICT CLINICALLY RELEVANT GENOME-WIDE ALTERATION SIGNATURES IN GLIOBLASTOMA

BACKGROUND: Previously, we have shown that combined whole-exome sequencing (WES) and genome-wide somatic copy number alteration (SCNA) information can separate IDH1/2-wildtype glioblastoma into two prognostic molecular subtypes (Group 1 and Group 2) and that these subtypes cannot be distinguished by...

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Detaylı Bibliyografya
Yayımlandı:Neuro Oncol
Asıl Yazarlar: Nuechterlein, Nicholas, Li, Beibin, Fink, James, Haynor, David, Holland, Eric, Shapiro, Linda, Cimino, Patrick
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Oxford University Press 2020
Konular:
Neuroimaging
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC7651127/
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/neuonc/noaa215.659
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