Rank Aggregation for Candidate Gene Identification

被引:3
作者
Burkovski, Andre [1 ,2 ]
Lausser, Ludwig [1 ]
Kraus, Johann M. [1 ]
Kestler, Hans A. [1 ]
机构
[1] Univ Ulm, Inst Neural Informat Proc, Res Grp Bioinformat & Syst Biol, D-89069 Ulm, Germany
[2] Univ Ulm, Int Grad Sch Mol Med, Ulm, Germany
来源
DATA ANALYSIS, MACHINE LEARNING AND KNOWLEDGE DISCOVERY | 2014年
关键词
CANCER;
D O I
10.1007/978-3-319-01595-8_31
中图分类号
TP [自动化技术、计算机技术];
学科分类号
0812 ;
摘要
Differences of molecular processes are reflected, among others, by differences in gene expression levels of the involved cells. High-throughput methods such as microarrays and deep sequencing approaches are increasingly used to obtain these expression profiles. Often differences of gene expression across different conditions such as tumor vs inflammation are investigated. Top scoring differential genes are considered as candidates for further analysis. Measured differences may not be related to a biological process as they can also be caused by variation in measurement or by other sources of noise. A method for reducing the influence of noise is to combine the available samples. Here, we analyze different types of combination methods, early and late aggregation and compare these statistical and positional rank aggregation methods in a simulation study and by experiments on real microarray data.
引用
收藏
页码:285 / 293
页数:9
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