YODA: selecting signature oligonucleotides

被引:60
作者
Nordberg, EK [1 ]
机构
[1] Virginia Polytech Inst & State Univ, Virginia Bioinformat Inst, Blacksburg, VA 24061 USA
关键词
D O I
10.1093/bioinformatics/bti182
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Selecting oligonucleotide probes for use in microarray design, and other applications requiring signature sequences, involves identifying sequences which will bind strongly to their intended target, while binding only weakly (or preferably, not at all) to non-target sequences which may be present in the hybridization reaction. While many tools to assist in selection of such sequences exist, all the ones we examined lack important oligo design and software features. Results: YODA is an application for assisting biological researchers in selecting signature sequences. It incorporates a custom sequence similarity search to find potential cross-hybridizing non-target sequences. For this task, most oligo design tools rely on BLAST, which is ill suited for it due to an unacceptable risk of false negatives. YODA supports multiple probe design goals including single-genome, multiple-genome, pathogen-host and species/strain-identification. A graphical interface is provided as well as a command-line interface, both of which support many user-controlled parameters. YODA is easy to install and use and runs on Windows, Mac OS X and Linux platforms.
引用
收藏
页码:1365 / 1370
页数:6
相关论文
共 16 条
[1]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[2]   Expression profiling of the schizont and trophozoite stages of Plasmodium falciparum with a long-oligonucleotide microarray -: art. no. R9 [J].
Bozdech, Z ;
Zhu, JC ;
Joachimiak, MP ;
Cohen, FE ;
Pulliam, B ;
DeRisi, JL .
GENOME BIOLOGY, 2003, 4 (02)
[3]  
Eckart J. Dana, 2003, OMICS A Journal of Integrative Biology, V7, P79, DOI 10.1089/153623103322006661
[4]   Expression profiling using microarrays fabricated by an ink-jet oligonucleotide synthesizer [J].
Hughes, TR ;
Mao, M ;
Jones, AR ;
Burchard, J ;
Marton, MJ ;
Shannon, KW ;
Lefkowitz, SM ;
Ziman, M ;
Schelter, JM ;
Meyer, MR ;
Kobayashi, S ;
Davis, C ;
Dai, HY ;
He, YDD ;
Stephaniants, SB ;
Cavet, G ;
Walker, WL ;
West, A ;
Coffey, E ;
Shoemaker, DD ;
Stoughton, R ;
Blanchard, AP ;
Friend, SH ;
Linsley, PS .
NATURE BIOTECHNOLOGY, 2001, 19 (04) :342-347
[5]   Selecting signature oligonucleotides to identify organisms using DNA arrays [J].
Kaderali, L ;
Schliep, A .
BIOINFORMATICS, 2002, 18 (10) :1340-1349
[6]   Assessment of the sensitivity and specificity of oligonucleotide (50mer) microarrays [J].
Kane, MD ;
Jatkoe, TA ;
Stumpf, CR ;
Lu, J ;
Thomas, JD ;
Madore, SJ .
NUCLEIC ACIDS RESEARCH, 2000, 28 (22) :4552-4557
[7]   Selection of optimal DNA oligos for gene expression arrays [J].
Li, FG ;
Stormo, GD .
BIOINFORMATICS, 2001, 17 (11) :1067-1076
[8]   Design of oligonucleotides for microarrays and perspectives for design of multi-transcriptome arrays [J].
Nielsen, HB ;
Wernersson, R ;
Knudsen, S .
NUCLEIC ACIDS RESEARCH, 2003, 31 (13) :3491-3496
[9]   PrimeArray: genome-scale primer design for DNA-microarray construction [J].
Raddatz, G ;
Dehio, M ;
Meyer, TF ;
Dehio, C .
BIOINFORMATICS, 2001, 17 (01) :98-99
[10]   Optimization of oligonucleotide-based DNA microarrays -: art. no. e51 [J].
Relógio, A ;
Schwager, C ;
Richter, A ;
Ansorge, W ;
Valcárcel, J .
NUCLEIC ACIDS RESEARCH, 2002, 30 (11) :e51