瓦片
雌激素受体
生物
表皮生长因子受体
人口
乳腺癌
稳健性(进化)
医学
癌症
生物标志物
肿瘤科
计算生物学
遗传学
基因
艺术
视觉艺术
环境卫生
作者
Robert L. Camp,Marisa Dolled‐Filhart,David L. Rimm
标识
DOI:10.1158/1078-0432.ccr-04-0713
摘要
Abstract The ability to parse tumors into subsets based on biomarker expression has many clinical applications; however, there is no global way to visualize the best cut-points for creating such divisions. We have developed a graphical method, the X-tile plot that illustrates the presence of substantial tumor subpopulations and shows the robustness of the relationship between a biomarker and outcome by construction of a two dimensional projection of every possible subpopulation. We validate X-tile plots by examining the expression of several established prognostic markers (human epidermal growth factor receptor-2, estrogen receptor, p53 expression, patient age, tumor size, and node number) in cohorts of breast cancer patients and show how X-tile plots of each marker predict population subsets rooted in the known biology of their expression.
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