4 In IDH mutant gliomas in population 4, CpGs hypomethylated in NFKBIA deleted tumors ( Table S3 ) overlapped significantly with those hypomethylated in all NFKBIA deleted gliomas (73.7%) ( Figure S6 E and Table S3 ), and the association of those CpGs, whose presence denotes the G-CIMP-low subtype, remained highly significant ( Figure S7 A).
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Haploinsufficiency of NFKBIA reshapes the epigenome antipodal to the IDH mutation and imparts disease fate in diffuse gliomas.
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