背景(考古学)
计算机科学
特征(语言学)
光学(聚焦)
样品(材料)
数据科学
生物
古生物学
哲学
语言学
化学
色谱法
物理
光学
作者
David Axelrod,Naomi Miller,Judith‐Anne W. Chapman
出处
期刊:Biomedical informatics insights
[SAGE]
日期:2009-01-01
卷期号:2: BII.S2222-BII.S2222
被引量:11
摘要
Information about tumors is usually obtained from a single assessment of a tumor sample, performed at some point in the course of the development and progression of the tumor, with patient characteristics being surrogates for natural history context. Differences between cells within individual tumors (intratumor heterogeneity) and between tumors of different patients (intertumor heterogeneity) may mean that a small sample is not representative of the tumor as a whole, particularly for solid tumors which are the focus of this paper. This issue is of increasing importance as high-throughput technologies generate large multi-feature data sets in the areas of genomics, proteomics, and image analysis. Three potential pitfalls in statistical analysis are discussed (sampling, cut-points, and validation) and suggestions are made about how to avoid these pitfalls.
科研通智能强力驱动
Strongly Powered by AbleSci AI