Ando Tomohiro, Imoto Seiya, Miyano Satoru
Human Genome Center, Institute of Medical Science, University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.
Genome Inform. 2004;15(2):201-10.
One important application of microarray gene expression data is to study the relationship between the clinical phenotype of cancer patients and gene expression profiles on the whole-genome scale. The clinical phenotype includes several different types of cancers, survival times, relapse times, drug responses and so on. Under the situation that the subtypes of cancer have not been previously identified or known to exist, we develop a new kernel mixture modeling method that performs simultaneously identification of the subtype of cancer, prediction of the probabilities of both cancer type and patient's survival, and detection of a set of marker genes on which to base a diagnosis. The proposed method is successfully performed on real data analysis and simulation studies.
微阵列基因表达数据的一个重要应用是在全基因组规模上研究癌症患者的临床表型与基因表达谱之间的关系。临床表型包括几种不同类型的癌症、生存时间、复发时间、药物反应等。在癌症亚型此前未被识别或未知存在的情况下,我们开发了一种新的核混合建模方法,该方法可同时进行癌症亚型的识别、癌症类型和患者生存概率的预测,以及一组用于诊断的标记基因的检测。所提出的方法在实际数据分析和模拟研究中均成功实施。