BatchPrimer3: A high throughput web application for PCR and sequencing primer design

被引:664
作者
You, Frank M. [1 ,2 ]
Huo, Naxin [1 ,2 ]
Gu, Yong Qiang [1 ]
Luo, Ming-cheng [1 ,2 ]
Ma, Yaqin [2 ]
Hane, Dave [1 ,3 ]
Lazo, Gerard R. [1 ]
Dvorak, Jan [2 ]
Anderson, Olin D. [1 ]
机构
[1] ARS, USDA, Western Reg Res Ctr, Albany, CA 94710 USA
[2] Univ Calif Davis, Dept Plant Sci, Davis, CA 95616 USA
[3] Univ Calif Davis, Genet Resources Conservat Program, Davis, CA 95616 USA
基金
美国国家科学基金会;
关键词
D O I
10.1186/1471-2105-9-253
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: Microsatellite (simple sequence repeat - SSR) and single nucleotide polymorphism (SNP) markers are two types of important genetic markers useful in genetic mapping and genotyping. Often, large-scale genomic research projects require high-throughput computer-assisted primer design. Numerous such web-based or standard-alone programs for PCR primer design are available but vary in quality and functionality. In particular, most programs lack batch primer design capability. Such a high-throughput software tool for designing SSR flanking primers and SNP genotyping primers is increasingly demanded. Results: A new web primer design program, BatchPrimer3, is developed based on Primer3. BatchPrimer3 adopted the Primer3 core program as a major primer design engine to choose the best primer pairs. A new score-based primer picking module is incorporated into BatchPrimer3 and used to pick position-restricted primers. BatchPrimer3 v1.0 implements several types of primer designs including generic primers, SSR primers together with SSR detection, and SNP genotyping primers (including single-base extension primers, allele-specific primers, and tetra-primers for tetra-primer ARMS PCR), as well as DNA sequencing primers. DNA sequences in FASTA format can be batch read into the program. The basic information of input sequences, as a reference of parameter setting of primer design, can be obtained by pre-analysis of sequences. The input sequences can be pre-processed and masked to exclude and/or include specific regions, or set targets for different primer design purposes as in Primer3Web and primer3Plus. A tab-delimited or Excel-formatted primer output also greatly facilitates the subsequent primer-ordering process. Thousands of primers, including wheat conserved intron-flanking primers, wheat genome-specific SNP genotyping primers, and Brachypodium SSR flanking primers in several genome projects have been designed using the program and validated in several laboratories. Conclusion: BatchPrimer3 is a comprehensive web primer design program to develop different types of primers in a high-throughput manner. Additional methods of primer design can be easily integrated into future versions of BatchPrimer3. The program with source code and thousands of PCR and sequencing primers designed for wheat and Brachypodium are accessible at http://wheat.pw.usda.gov/demos/BatchPrimer3/.
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页数:13
相关论文
共 44 条
[21]   ANALYSIS OF ANY POINT MUTATION IN DNA - THE AMPLIFICATION REFRACTORY MUTATION SYSTEM (ARMS) [J].
NEWTON, CR ;
GRAHAM, A ;
HEPTINSTALL, LE ;
POWELL, SJ ;
SUMMERS, C ;
KALSHEKER, N ;
SMITH, JC ;
MARKHAM, AF .
NUCLEIC ACIDS RESEARCH, 1989, 17 (07) :2503-2516
[22]   Evaluation of a new efficient procedure for single nucleotide polymorphism genotyping: tetra-primer amplification refractory mutation system polymerase chain reaction [J].
Okayama, N ;
Fujimura, K ;
Nakamura, J ;
Suehiro, Y ;
Hamanaka, Y ;
Hinoda, Y .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2004, 42 (01) :13-16
[23]   Multiplex tetra-primer amplification refractory mutation system PCR to detect 6 common germline mutations of the MUTYH gene associated with polyposis and colorectal cancer [J].
Piccioli, P ;
Sierra, M ;
Gismondi, V ;
Pedemonte, S ;
Loiacono, F ;
Lastraioli, S ;
Bertario, L ;
De Angioletti, M ;
Varcsco, L ;
Notaro, R .
CLINICAL CHEMISTRY, 2006, 52 (04) :739-743
[24]   Polymorphism revealed by simple sequence repeats [J].
Powell, W ;
Machray, GC ;
Provan, J .
TRENDS IN PLANT SCIENCE, 1996, 1 (07) :215-222
[25]   A chromosome bin map of 16,000 expressed sequence tag loci and distribution of genes among the three genomes of polyploid wheat [J].
Qi, LL ;
Echalier, B ;
Chao, S ;
Lazo, GR ;
Butler, GE ;
Anderson, OD ;
Akhunov, ED ;
Dvorak, J ;
Linkiewicz, AM ;
Ratnasiri, A ;
Dubcovsky, J ;
Bermudez-Kandianis, CE ;
Greene, RA ;
Kantety, R ;
La Rota, CM ;
Munkvold, JD ;
Sorrells, SF ;
Sorrells, ME ;
Dilbirligi, M ;
Sidhu, D ;
Erayman, M ;
Randhawa, HS ;
Sandhu, D ;
Bondareva, SN ;
Gill, KS ;
Mahmoud, AA ;
Ma, XF ;
Miftahudin ;
Gustafson, JP ;
Conley, EJ ;
Nduati, V ;
Gonzalez-Hernandez, JL ;
Anderson, JA ;
Peng, JH ;
Lapitan, NLV ;
Hossain, KG ;
Kalavacharla, V ;
Kianian, SF ;
Pathan, MS ;
Zhang, DS ;
Nguyen, HT ;
Choi, DW ;
Fenton, RD ;
Close, TJ ;
McGuire, PE ;
Qualset, CO ;
Gill, BS .
GENETICS, 2004, 168 (02) :701-712
[26]   PrimeArray: genome-scale primer design for DNA-microarray construction [J].
Raddatz, G ;
Dehio, M ;
Meyer, TF ;
Dehio, C .
BIOINFORMATICS, 2001, 17 (01) :98-99
[27]  
Rozen S, 2000, Methods Mol Biol, V132, P365
[28]   Detection of catechol-O-methyltransferase Val158Met polymorphism by a simple one-step tetra-primer amplification refractory mutation system-PCR [J].
Ruiz-Sanz, Jose Ignacio ;
Aurrekoetxea, Igor ;
del Agua, Ainhoa Ruiz ;
Ruiz-Larrea, Maria Begona .
MOLECULAR AND CELLULAR PROBES, 2007, 21 (03) :202-207
[30]   ALLELE SPECIFIC AMPLIFICATION BY TETRA-PRIMER PCR [J].
SHU, Y ;
HUMPHRIES, S ;
GREEN, F .
NUCLEIC ACIDS RESEARCH, 1992, 20 (05) :1152-1152