Fully automatic quantification of microarray image data

被引:255
作者
Jain, AN
Tokuyasu, TA
Snijders, AM
Segraves, R
Albertson, DG
Pinkel, D
机构
[1] Univ Calif San Francisco, Ctr Comprehens Canc, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Canc Res Inst, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Lab Med, San Francisco, CA 94143 USA
关键词
D O I
10.1101/gr.210902
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
DNA microarrays are now widely used to measure expression levels and DNA copy number in biological samples. Ratios of relative abundance of nucleic acids are derived from images of regular arrays of spots containing target genetic material to which fluorescently labeled samples are hybridized. Whereas there are a number of methods in use for the quantification of images, many of the software systems in wide use either encourage or require extensive human interaction at the level of individual spots on arrays. We present a fully automatic system for microarray image quantification. The system automatically locates both subarray grids and individual spots, requiring no user identification of any image coordinates. Ratios are computed based on explicit segmentation of each spot. On a typical image of 6000 spots, the entire process takes less than 20 sec. We present a quantitative assessment of performance on multiple replicates of genome-wide array-based comparative genomic hybridization experiments. By explicitly identifying the pixels in each spot, the system yields more accurate estimates of ratios than systems assuming spot circularity. The software, called UCSF spot, runs on Windows platforms and is available free of charge for academic use.
引用
收藏
页码:325 / 332
页数:8
相关论文
共 6 条
[1]   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
[2]  
*AX INSTR INC, 2001, GEN PRO 3 0
[3]   Molecular classification of cancer: Class discovery and class prediction by gene expression monitoring [J].
Golub, TR ;
Slonim, DK ;
Tamayo, P ;
Huard, C ;
Gaasenbeek, M ;
Mesirov, JP ;
Coller, H ;
Loh, ML ;
Downing, JR ;
Caligiuri, MA ;
Bloomfield, CD ;
Lander, ES .
SCIENCE, 1999, 286 (5439) :531-537
[4]   Molecular portraits of human breast tumours [J].
Perou, CM ;
Sorlie, T ;
Eisen, MB ;
van de Rijn, M ;
Jeffrey, SS ;
Rees, CA ;
Pollack, JR ;
Ross, DT ;
Johnsen, H ;
Akslen, LA ;
Fluge, O ;
Pergamenschikov, A ;
Williams, C ;
Zhu, SX ;
Lonning, PE ;
Borresen-Dale, AL ;
Brown, PO ;
Botstein, D .
NATURE, 2000, 406 (6797) :747-752
[5]   High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays [J].
Pinkel, D ;
Seagraves, R ;
Sudar, D ;
Clark, S ;
Poole, I ;
Kowbel, D ;
Collins, C ;
Kuo, WL ;
Chen, C ;
Zhai, Y ;
Dairkee, SH ;
Ljung, BM ;
Gray, JW ;
Albertson, DG .
NATURE GENETICS, 1998, 20 (02) :207-211
[6]   Assembly of microarrays for genome-wide measurement of DNA copy number. [J].
Snijders, AM ;
Nowak, N ;
Segraves, R ;
Blackwood, S ;
Brown, N ;
Conroy, J ;
Hamilton, G ;
Hindle, AK ;
Huey, B ;
Kimura, K ;
Law, S ;
Myambo, K ;
Palmer, J ;
Ylstra, B ;
Yue, JP ;
Gray, JW ;
Jain, AN ;
Pinkel, D ;
Albertson, DG .
NATURE GENETICS, 2001, 29 (03) :263-264