Genomics of MPNST (GeM) Consortium: Rationale and Study Design for Multi-Omic Characterization of NF1-Associated and Sporadic MPNSTs - Miller, David T.; Cortés-Ciriano, Isidro; Pillay, Nischalan; Hirbe, Angela C.; Snuderl, Matija; Bui, Marilyn M.; Piculell, Katherine; Al-Ibraheemi, Alyaa; Dickson, Brendan C.; Hart, Jesse; Jones, Kevin; Jordan, Justin T.; et al. (Genes, 2020)
Keywords: Base Sequence; Base Sequence - genetics; Chemotherapy; Chromosomes; clinical genetics; Communication; Computational Biology; Consortia; Copy number; DNA fingerprinting; DNA Methylation; DNA Methylation - genetics; DNA sequencing; Exome; Exome - genetics; Female; Gene expression; Genetic disorders; Genetic Heterogeneity; Genomes; Genomics; Humans; Male; Medical prognosis; MPNST; Mutation; Neurofibromatosis; Neurofibromatosis 1; Neurofibromatosis 1 - complications; Neurofibromatosis 1 - genetics; Neurofibromatosis 1 - pathology; Neurofibromin 1; Neurofibromin 1 - genetics; Neurofibrosarcoma; Neurofibrosarcoma - complications; Neurofibrosarcoma - genetics; Neurofibrosarcoma - pathology; Neurological disorders; next generation sequencing; Pathogenesis; pathology; Peripheral nerves; Proteomics; Proteomics - methods; Recklinghausen's disease; Transcriptome; Transcriptome - genetics; tumor evolution; Tumorigenesis; Tumors; Whole genome sequencing; pathology; next generation sequencing; clinical genetics; genomics; neurofibromatosis; tumor evolution; MPNST