亚型
淋巴瘤
基因表达谱
弥漫性大B细胞淋巴瘤
计算生物学
生物
基因
基因表达
计算机科学
遗传学
免疫学
程序设计语言
作者
Robert Ta,David T. Yang,Christian Hirt,Thomas Drago,Richard Flavin
出处
期刊:Diagnostics
[Multidisciplinary Digital Publishing Institute]
日期:2022-04-27
卷期号:12 (5): 1087-1087
被引量:3
标识
DOI:10.3390/diagnostics12051087
摘要
Diffuse large B-cell lymphoma (DLBCL) is the most common non-Hodgkin lymphoma. It is a clinically and morphologically heterogeneous entity that has continued to resist complete subtyping. Molecular subtyping efforts emerged in earnest with the advent of gene expression profiling (GEP). This molecular subtyping approach has continued to evolve simultaneously with others including immunohistochemistry and more modern genomic approaches. Recently, the veritable explosion of genomic data availability and evolving computational methodologies have provided additional avenues, by which further understanding and subclassification of DBLCLs is possible. The goal of this review is to provide a historical overview of the major classification timepoints in the molecular subtyping of DLBCL, from gene expression profiling to present day understanding.
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