Comparative analysis of algorithms for signal quantitation from oligonucleotide microarrays

被引:69
作者
Barash, Y
Dehan, E
Krupsky, M
Franklin, W
Geraci, M
Friedman, N
Kaminski, N [1 ]
机构
[1] Univ Pittsburgh, Sch Med, Div Pulm Allergy & Crit Care Med, Pittsburgh, PA 15213 USA
[2] Hebrew Univ Jerusalem, Sch Engn & Comp Sci, IL-91904 Jerusalem, Israel
[3] Chaim Sheba Med Ctr, Funct Gen Unit, Gen Res Ctr, IL-52620 Tel Hashomer, Israel
[4] Univ Colorado, Hlth Sci Ctr, Denver, CO 80262 USA
关键词
D O I
10.1093/bioinformatics/btg487
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Recent years' exponential increase in DNA microarrays experiments has motivated the development of many signal quantitation (SQ) algorithms. These algorithms perform various transformations on the actual measurements aimed to enable researchers to compare readings of different genes quantitatively within one experiment and across separate experiments. However, it is relatively unclear whether there is a 'best' algorithm to quantitate microarray data. The ability to compare and assess such algorithms is crucial for any downstream analysis. In this work, we suggest a methodology for comparing different signal quantitation algorithms for gene expression data. Our aim is to enable researchers to compare the effect of different SQ algorithms on the specific dataset they are dealing with. We combine two kinds of tests to assess the effect of an SQ algorithm in terms of signal to noise ratio. To assess noise, we exploit redundancy within the experimental dataset to test the variability of a given SQ algorithm output. For the effect of the SQ on the signal we evaluate the overabundance of differentially expressed genes using various statistical significance tests. Results: We demonstrate our analysis approach with three SQ algorithms for oligonucleotide microarrays. We compare the results of using the dChip software and the RMAExpress software to the ones obtained by using the standard Affymetrix MAS5 on a dataset containing pairs of repeated hybridizations. Our analysis suggests that dChip is more robust and stable than the MAS5 tools for about 60% of the genes while RMAExpress is able to achieve an even greater improvement in terms of signal to noise, for more than 95% of the genes.
引用
收藏
页码:839 / 846
页数:8
相关论文
共 17 条
[1]  
BENDOR A, 2002, OVERBUNDANCE ANAL CL
[2]  
Cover T. M., 2005, ELEM INF THEORY, DOI 10.1002/047174882X
[3]  
*DCHIP SOFTW, 2001, DNA CHIP AN DCHIP
[4]  
DeGroot M. H., 1989, PROBABILITY STAT
[5]  
DERISI J, 1997, SCIENCE, V282, P699
[6]  
HARTEMINK AJ, 2001, P INT BIOM OPT S SPI
[7]   Summaries of affymetrix GeneChip probe level data [J].
Irizarry, RA ;
Bolstad, BM ;
Collin, F ;
Cope, LM ;
Hobbs, B ;
Speed, TP .
NUCLEIC ACIDS RESEARCH, 2003, 31 (04) :e15
[8]   Analysis of variance for gene expression microarray data [J].
Kerr, MK ;
Martin, M ;
Churchill, GA .
JOURNAL OF COMPUTATIONAL BIOLOGY, 2000, 7 (06) :819-837
[9]   Theoretical and experimental comparisons of gene expression indexes for oligonucleotide arrays [J].
Lemon, WJ ;
Palatini, JJT ;
Krahe, R ;
Wright, FA .
BIOINFORMATICS, 2002, 18 (11) :1470-1476
[10]   Model-based analysis of oligonucleotide arrays: Expression index computation and outlier detection [J].
Li, C ;
Wong, WH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (01) :31-36