Mathematical tools to optimize the design of oligonucleotide probes and primers

被引:15
|
作者
Noguera, Daniel R. [1 ,2 ]
Wright, Erik S. [3 ,4 ]
Camejo, Pamela [1 ]
Yilmaz, L. Safak [5 ]
机构
[1] Univ Wisconsin, Dept Civil & Environm Engn, Madison, WI 53706 USA
[2] Univ Wisconsin, Great Lakes Bioenergy Res Ctr, Madison, WI USA
[3] Univ Wisconsin, Wisconsin Inst Discovery, Madison, WI USA
[4] Univ Wisconsin, Dept Bacteriol, Madison, WI 53706 USA
[5] Univ Massachusetts, Sch Med, Program Syst Biol, Worcester, MA USA
关键词
Oligonucleotides; DNA probes; FISH; PCR; Microarrays; Mismatch stability; Microbial diversity; Primer design; 16S RIBOSOMAL-RNA; IN-SITU HYBRIDIZATION; AMMONIA-OXIDIZING ARCHAEA; POLYMERASE-CHAIN-REACTION; REAL-TIME; THERMODYNAMIC PARAMETERS; DOMAINS BACTERIA; GENE DATABASE; MICROARRAYS; PCR;
D O I
10.1007/s00253-014-6165-x
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The identification and quantification of specific organisms in mixed microbial communities often relies on the ability to design oligonucleotide probes and primers with high specificity and sensitivity. The design of these oligonucleotides (or "oligos" for short) shares many of the same principles in spite of their widely divergent applications. Three common molecular biology technologies that require oligonucleotide design are polymerase chain reaction (PCR), fluorescence in situ hybridization (FISH), and DNA microarrays. This article reviews techniques and software available for the design and optimization of oligos with the goal of targeting a specific group of organisms within mixed microbial communities. Strategies for enhancing specificity without compromising sensitivity are described, as well as design tools well suited for this purpose.
引用
收藏
页码:9595 / 9608
页数:14
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