Comparison of methods for image analysis on cDNA microarray data

被引:230
作者
Yang, YH
Buckley, MJ
Dudoit, S
Speed, TP
机构
[1] Univ Calif Berkeley, Dept Stat, Berkeley, CA 94720 USA
[2] CSIRO, Dickson, Australia
[3] Univ Calif Berkeley, Div Biostat, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Dept Stat, Berkeley, CA 94720 USA
[5] Walter & Eliza Hall Inst Med Res, Div Genet & Bioinformat, Parkville, Vic, Australia
基金
美国国家卫生研究院;
关键词
automatic addressing; background correction; gene expression; image processing; seeded region growing; segmentation;
D O I
10.1198/106186002317375640
中图分类号
O21 [概率论与数理统计]; C8 [统计学];
学科分类号
020208 ; 070103 ; 0714 ;
摘要
Microarrays are part of a new class of biotechnologies which allow the monitoring of expression levels for thousands of genes simultaneously. Image analysis is an important aspect of microarray experiments, one that can have a potentially large impact on subsequent analyses such as clustering or the identification of differentially expressed genes. This article reviews a number of existing image analysis approaches for cDNA microarray experiments and proposes new addressing, segmentation, and background correction methods for extracting information from microarray scanned images. The segmentation component uses a seeded region growing algorithm which makes provision for spots of different shapes and sizes. The background estimation approach is based on an image analysis technique known as morphological opening. These new image analysis procedures are implemented in a software package named Spot, built on the R environment for statistical computing. The statistical properties of the different segmentation and background adjustment methods are examined using microarray data from a study of lipid metabolism in mice. It is shown that in some cases background adjustment can substantially reduce the precision-that is, increase the variability-of low-intensity spot values. In contrast, the choice of segmentation procedure has a smaller impact. The comparison further suggests that seeded region growing segmentation with morphological background correction provides precise and accurate estimates of foreground and background intensities.
引用
收藏
页码:108 / 136
页数:29
相关论文
共 33 条
[1]   SEEDED REGION GROWING [J].
ADAMS, R ;
BISCHOF, L .
IEEE TRANSACTIONS ON PATTERN ANALYSIS AND MACHINE INTELLIGENCE, 1994, 16 (06) :641-647
[2]   Distinct types of diffuse large B-cell lymphoma identified by gene expression profiling [J].
Alizadeh, AA ;
Eisen, MB ;
Davis, RE ;
Ma, C ;
Lossos, IS ;
Rosenwald, A ;
Boldrick, JG ;
Sabet, H ;
Tran, T ;
Yu, X ;
Powell, JI ;
Yang, LM ;
Marti, GE ;
Moore, T ;
Hudson, J ;
Lu, LS ;
Lewis, DB ;
Tibshirani, R ;
Sherlock, G ;
Chan, WC ;
Greiner, TC ;
Weisenburger, DD ;
Armitage, JO ;
Warnke, R ;
Levy, R ;
Wilson, W ;
Grever, MR ;
Byrd, JC ;
Botstein, D ;
Brown, PO ;
Staudt, LM .
NATURE, 2000, 403 (6769) :503-511
[3]   Broad patterns of gene expression revealed by clustering analysis of tumor and normal colon tissues probed by oligonucleotide arrays [J].
Alon, U ;
Barkai, N ;
Notterman, DA ;
Gish, K ;
Ybarra, S ;
Mack, D ;
Levine, AJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (12) :6745-6750
[4]  
[Anonymous], 1999, MORPHOLOGICAL IMAGE, DOI 10.1007/978-3-662-03939-7_3
[5]  
*AX INSTR INC, 1999, GEN 4000A US GUID
[6]   Development of a toxicological gene array and quantitative assessment of this technology [J].
Bartosiewicz, M ;
Trounstine, M ;
Barker, D ;
Johnston, R ;
Buckpitt, A .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2000, 376 (01) :66-73
[7]  
Beucher S., 2018, Mathematical morphology in image processing, P433, DOI DOI 10.1201/9781482277234-12
[8]  
Buckley M.J., 2000, SPOT USERS GUIDE
[9]   Microarray expression profiling identifies genes with altered expression in HDL-deficient mice [J].
Callow, MJ ;
Dudoit, S ;
Gong, EL ;
Speed, TP ;
Rubin, EM .
GENOME RESEARCH, 2000, 10 (12) :2022-2029
[10]   Profiling expression patterns and isolating differentially expressed genes by cDNA microarray system with colorimetry detection [J].
Chen, JJW ;
Wu, R ;
Yang, PC ;
Huang, JY ;
Sher, YP ;
Han, MH ;
Kao, WC ;
Lee, PJ ;
Chiu, TF ;
Chang, F ;
Chu, YW ;
Wu, CW ;
Peck, K .
GENOMICS, 1998, 51 (03) :313-324