Software
Tools for the identification of variable and potentially variable tandem repeats
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* Corresponding author: Colm T O'Dushlaine codushlaine@gmail.com
1 Bioinformatics Core, Molecular and Cellular Therapeutics, Royal College of Surgeons in Ireland, Ireland
2 UCD Conway Institute, University College Dublin, Dublin 4, Ireland
BMC Genomics 2006, 7:290 doi:10.1186/1471-2164-7-290
Published: 15 November 2006Abstract
Background
Tandem repeat arrays showing variation between sequences within a population, between strains or across species may have functional effects. The increasing availability of genomic sequence data makes routine description of observed variation possible, creating a need for tools to describe such variability.
Results
We present a set of programs that facilitate the identification of tandem repeats showing variation across multiple sequences or genomes, and the prediction of potentially polymorphic tandem repeats. The VNTRfinder (Variable Number of Tandem Repeats finder) program enables the detection of sequence length variation between arrays of inter-specific or intra-specific tandem repeats. In the absence of comparable sequences to explore observed variation, predictions are provided describing which tandem repeats are more likely to be variable, to help guide and focus further experimental evaluation.
Conclusion
These tools represent a resource for researchers interested in tandem repeats in nucleotide sequences that are most likely to be of clinical and evolutionary interest. The tools are available at http://bioinformatics.rcsi.ie/vntrfinder/ webcite. Downloadable versions for UNIX/LINUX and WINDOWS which permit the consideration of longer and more numerous sequences are also available.