首页 | 本学科首页   官方微博 | 高级检索  
   检索      

肿瘤表达谱基因芯片数据的混合效应模型分析
引用本文:张杨,张威,曹文君,李运明,李宁霞,陈长生.肿瘤表达谱基因芯片数据的混合效应模型分析[J].现代生物医学进展,2015,15(3):533-537.
作者姓名:张杨  张威  曹文君  李运明  李宁霞  陈长生
作者单位:第四军医大学军事预防医学院卫生统计学教研室;长治医学院基础部;成都军区总医院神经外科;西安医学院第二附属医院检验科
基金项目:国家自然科学基金项目(81172770)
摘    要:目的:研究混合效应模型(Mixed Effects Model)在肿瘤表达谱基因芯片数据分析中的检验效能,并探讨其分析效果。方法:采用混合效应模型分析肿瘤实例基因芯片数据,并以基因集富集分析方法(GSEA)作为参照比较分析结果的有效性和科学性,探讨其检验效果。结果:通过混合效应模型和基因集富集分析(GSEA)两种方法对肿瘤基因芯片数据的分析和比较,两种方法筛选出共同的差异表达通路外,混合效应模型额外地筛选出来GSEA未能检验到的8条差异表达通路,且得到文献支持;混和效应模型筛选出的前10个差异表达通路中有6个已有生物学证明而基因集富集分析方法(GSEA)筛选出的前10个差异表达通路中仅有4个已有生物学证明。结论:混合效应模型作为top-down方法中的典型代表,其优势在于通过构建潜变量达到降维目的,可有效地减少多个复杂的变异来源从而保证了结果的准确性和科学性,其检验效能优于基因集富集分析方法(GSEA),是一种行之有效的筛选肿瘤基因芯片数据的分析方法。

关 键 词:混合效应模型  基因表达谱  肿瘤基因芯片数据  通路分析  统计学意义

Mixed-effects Model Analysis on Cancer Microarray Data
ZHANG Yang;ZHANG Wei;CAO Wen-jun;LI Yun-ming;LI Ning-xia;CHEN Chang-sheng.Mixed-effects Model Analysis on Cancer Microarray Data[J].Progress in Modern Biomedicine,2015,15(3):533-537.
Authors:ZHANG Yang;ZHANG Wei;CAO Wen-jun;LI Yun-ming;LI Ning-xia;CHEN Chang-sheng
Institution:ZHANG Yang;ZHANG Wei;CAO Wen-jun;LI Yun-ming;LI Ning-xia;CHEN Chang-sheng;Department of Health Statistics,Fourth Military Medical University;Changzhi Medical College;Chengdu General hospital of PLA;Department of Clinical Laboratory,Second Hospital of Xi’an Medical University;
Abstract:Objective:To study and evaluate the examine effectiveness of mixed-effects models in cancer microarray data analysis.Methods:The real cancer microarray data was analysed with mixed-effects model, and GSEA was taken as a comparative analysis method to evaluate the testing results.Results:By applying the two analysis methods with the real cancer data, eight differentially expressed pathways were additionally screened by the mixed-effects models other than the common one; Mixed effect models screened six biological pathways out of top ten, however, GSEA only screened four.Conclusion:Asthe typical of top-down approach, mixed effects models reduces the complexity of multiple sources of variations by conceiving a latent variable to ensure the scientific and accuracy of the analysis results. It is better than GSEA in terms of the effectiveness and accuracy and more suitable for cancer gene expression data.
Keywords:Mixed-effects models  Gene Expression Profile  Cancer data  Pathway analysis  Statistical significance
本文献已被 CNKI 万方数据 等数据库收录!
点击此处可从《现代生物医学进展》浏览原始摘要信息
点击此处可从《现代生物医学进展》下载免费的PDF全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号