Genome-wide prediction of human VNTRs

Abstract

Polymorphic minisatellites, also known as variable number of tandem repeats (VNTRs), are tandem repeat regions that show variation in the number of repeat units among chromosomes in a population. Currently, there are no general methods for predicting which minisatellites have a high probability of being polymorphic, given their sequence characteristics. An earlier approach has focused on potentially highly polymorphic and hypervariable minisatellites, which make up only a small fraction of all minisatellites in the human genome. We have developed a model, based on available minisatellite and VNTR sequence data, that predicts the probability that a minisatellite (unit size 6 bp) identified by the computer program Tandem Repeats Finder is polymorphic (VNTR). According to the model, minisatellites with high copy number and high degree of sequence similarity are most likely to be VNTRs. This approach was used to scan the draft sequence of the human genome for VNTRs. A total of 157,549 minisatellite repeats were found, of which 29,224 are predicted to be VNTRs. Contrary to previous results, VNTRs appear to be widespread and abundant throughout the human genome, with an estimated density of 9.1 VNTRs/Mb. (C) 2004 Elsevier Inc. All rights reserved.

Keywords

minisatellite; VNTR; Tandem repeat

Published in

Genomics
2005, Volume: 85, number: 1, pages: 24-35 Publisher: ACADEMIC PRESS INC ELSEVIER SCIENCE

UKÄ Subject classification

Genetics


Publication identifier

DOI: https://doi.org/10.1016/j.ygeno.2004.10.009

Permanent link to this page (URI)

https://res.slu.se/id/publ/85998