Genomic-Enabled Medicine for Recurrent Glioblastoma

Study ID Alternative Stable ID Type
phs001460 Case Set

Study Description

In this prospective study, we performed genome-wide tumor/normal exome sequencing and tumor RNA-sequencing for recurrent glioblastoma patients. A subset of patients had both enhancing tumor and non-enhancing tissue sequenced to investigate spatial heterogeneity of this disease. Together, this information builds our understanding of the genomic underpinnings of glioblastoma, and contributes toward the knowledge base for identifying and developing more effective treatments for patients with glioblastoma.

Archive Link Archive Accession
dbGaP phs001460

Who archives the data?

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