Efficient primer design algorithms

被引:53
作者
Kämpke, T
Kieninger, M
Mecklenburg, M
机构
[1] Forschungsinst Anwendungsorientierte Wissensverar, D-89081 Ulm, Germany
[2] jSoft GMBH, D-73447 Oberkochen, Germany
[3] INTERACTIVA Biotekn AB & BT Biomed Technol, S-22370 Lund, Sweden
关键词
D O I
10.1093/bioinformatics/17.3.214
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Primer design involves various parameters such as string-based alignment scores, melting temperature, primer length and GC content. This entails a design approach from multicriteria decision making. Values of some of the criteria are easy to compute while others require intense calculations. Results: The reference point method was found to be tractable for trading-off between deviations from ideal Values of all the criteria. Some criteria computations are based on dynamic programs with value iteration whose run time can be bounded by a low-degree polynomial. For designing standard PCR primers, the scheme offers in a relative gain in computing speed of up to 50:1 over ad-hoc computational methods. Single PCR primer pairs have been used as model systems in order to simplify the quantization of the computational acceleration factors. The program has been structured so as to facilitate the analysis of large numbers of primer pairs with minor modifications. The scheme significantly increases primer design throughput which in turn facilitates the use of oligonucleotides in a wide range of applications including: multiplex PCR and other nucleic acid-based amplification systems, as well as in zip code targeting, oligonucleotide microarrays and nucleic acid-based nanoengineering. Availability: A public version of the software DOPRIMER is accessible under http://doprimer.interactiva.de.
引用
收藏
页码:214 / 225
页数:12
相关论文
共 16 条
[1]  
Apostolico A, 1997, Pattern Matching Algorithms
[2]   STABILITY OF RIBONUCLEIC-ACID DOUBLE-STRANDED HELICES [J].
BORER, PN ;
DENGLER, B ;
TINOCO, I ;
UHLENBECK, OC .
JOURNAL OF MOLECULAR BIOLOGY, 1974, 86 (04) :843-853
[3]   PREDICTING DNA DUPLEX STABILITY FROM THE BASE SEQUENCE [J].
BRESLAUER, KJ ;
FRANK, R ;
BLOCKER, H ;
MARKY, LA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (11) :3746-3750
[4]  
EDWARDS MC, 1994, PCR METH APPL, V3, P565
[5]   IMPROVED FREE-ENERGY PARAMETERS FOR PREDICTIONS OF RNA DUPLEX STABILITY [J].
FREIER, SM ;
KIERZEK, R ;
JAEGER, JA ;
SUGIMOTO, N ;
CARUTHERS, MH ;
NEILSON, T ;
TURNER, DH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (24) :9373-9377
[6]  
Hillier L, 1991, PCR Methods Appl, V1, P124
[7]  
Keeney R.L., 1976, DECISIONS MULTIPLE O
[8]  
MECKLENBURG M, 1997, ADV MOL CELL BIOL B, V15, P473
[9]  
Owczarzy R, 1997, BIOPOLYMERS, V44, P217, DOI 10.1002/(SICI)1097-0282(1997)44:3<217::AID-BIP3>3.3.CO
[10]  
2-K