The tumor samples we analyzed were from 293 adults with previously untreated lower-grade gliomas (WHO grades II and III), including 100 astrocytomas, 77 oligoastrocytomas, and 116 oligodendrogliomas. Pediatric lower-grade gliomas were excluded; their molecular pathogenesis is distinct from that of lower-grade gliomas in adults.20 (link),21 (link) Diagnoses were established at the contributing institutions; neuropathologists in our consortium reviewed the diagnoses and ensured the quality of the diagnoses and of the tissue for molecular profiling (see Supplementary Appendix 1, available with the full text of this article at NEJM.org, for sample inclusion criteria). Patient characteristics are described in Table 1, and in Table S1 (Supplementary Appendix 2) and Table S2 in Supplementary Appendix 1. We obtained appropriate consent from relevant institutional review boards, which coordinated the consent process at each tissue-source site; written informed consent was obtained from all participants. The patients’ ages, tumor locations, clinical histories and outcomes, tumor histologic classifications, and tumor grades were typical of adults with a diagnosis of diffuse glioma.1 ,2 (link)