Skip Navigation


Bioinformatics Advance Access originally published online on February 12, 2004
This Article
Right arrow FREE Full Text (Print PDF) Freely available
Right arrow FREE Full Text (Screen PDF)
Right arrow All Versions of this Article:
20/9/1475    most recent
bth104v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (21)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Robinson, A. J.
Right arrow Articles by Edwards, D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Robinson, A. J.
Right arrow Articles by Edwards, D.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Bioinformatics 20(9) © Oxford University Press 2004; all rights reserved.

Applications Note

Simple sequence repeat marker loci discovery using SSR primer

Andrew J. Robinson 1,2, Christopher G. Love 1,2, Jacqueline Batley 1, Gary Barker 3 and David Edwards 1,2,*

1 Plant Biotechnology Centre, Primary Industries Research Victoria, La Trobe University, Bundoora 3086, Victoria, Australia, 2 Victorian Bioinformatics Consortium, Plant Biotechnology Centre, Primary Industries Research Victoria, La Trobe University, Bundoora 3086, Victoria, Australia and 3 School of Biological Sciences, University of Bristol, BS8 1UG, UK

Received on May 6, 2003; revised on August 10, 2003; accepted on December 17, 2003
Advance Access Publication February 12, 2004

Summary: Simple sequence repeats (SSRs) have become important molecular markers for a broad range of applications, such as genome mapping and characterization, phenotype mapping, marker assisted selection of crop plants and a range of molecular ecology and diversity studies. With the increase in the availability of DNA sequence information, an automated process to identify and design PCR primers for amplification of SSR loci would be a useful tool in plant breeding programs. We report an application that integrates SPUTNIK, an SSR repeat finder, with Primer3, a PCR primer design program, into one pipeline tool, SSR Primer. On submission of multiple FASTA formatted sequences, the script screens each sequence for SSRs using SPUTNIK. The results are parsed to Primer3 for locus-specific primer design. The script makes use of a Web-based interface, enabling remote use.

Availability: This program has been written in PERL and is freely available for non-commercial users by request from the authors. The Web-based version may be accessed at http://hornbill.cspp.latrobe.edu.au/

Contact: Dave.Edwards{at}dpi.vic.gov.au

* To whom correspondence should be addressed.


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Nucleic Acids ResHome page
S. Rudd, H. Schoof, and K. Mayer
PlantMarkers--a database of predicted molecular markers from plants
Nucleic Acids Res., January 1, 2005; 33(suppl_1): D628 - D632.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
C. G. Love, A. J. Robinson, G. A. C. Lim, C. J. Hopkins, J. Batley, G. Barker, G. C. Spangenberg, and D. Edwards
Brassica ASTRA: an integrated database for Brassica genomic research
Nucleic Acids Res., January 1, 2005; 33(suppl_1): D656 - D659.
[Abstract] [Full Text] [PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.