| Literature DB >> 27523973 |
Abstract
Application of next-generation sequencing (NGS) on myeloid neoplasms has expanded our knowledge of genomic alterations in this group of diseases. Genomic alterations in myeloid neoplasms are complex, heterogeneous, and not specific to a disease entity. NGS-based panel testing of myeloid neoplasms can complement existing diagnostic modalities and is gaining acceptance in the clinics and diagnostic laboratories. Prospective, randomized trials to evaluate the prognostic significance of genomic markers in myeloid neoplasms are under way in academic medical centers.Entities:
Keywords: Copy number variation; Genomic alterations; Mutations; Myeloid neoplasms; Next-generation sequencing
Mesh:
Substances:
Year: 2016 PMID: 27523973 DOI: 10.1016/j.path.2016.04.010
Source DB: PubMed Journal: Surg Pathol Clin ISSN: 1875-9157