Empirical Evaluation of Oligonucleotide Probe Selection for DNA Microarrays

被引:11
|
作者
Mulle, Jennifer G. [1 ]
Patel, Viren C. [1 ]
Warren, Stephen T. [1 ]
Hegde, Madhuri R. [1 ]
Cutler, David J. [1 ]
Zwick, Michael E. [1 ]
机构
[1] Emory Univ, Sch Med, Dept Human Genet, Atlanta, GA 30322 USA
来源
PLOS ONE | 2010年 / 5卷 / 03期
关键词
SINGLE-NUCLEOTIDE POLYMORPHISMS; COPY NUMBER; GENOME; DESIGN; IDENTIFICATION; MAP;
D O I
10.1371/journal.pone.0009921
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
DNA-based microarrays are increasingly central to biomedical research. Selecting oligonucleotide sequences that will behave consistently across experiments is essential to the design, production and performance of DNA microarrays. Here our aim was to improve on probe design parameters by empirically and systematically evaluating probe performance in a multivariate context. We used experimental data from 19 array CGH hybridizations to assess the probe performance of 385,474 probes tiled in the Duchenne muscular dystrophy (DMD) region of the X chromosome. Our results demonstrate that probe melting temperature, single nucleotide polymorphisms (SNPs), and homocytosine motifs all have a strong effect on probe behavior. These findings, when incorporated into future microarray probe selection algorithms, may improve microarray performance for a wide variety of applications.
引用
收藏
页数:7
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