Joint estimation of gene conversion rates and mean conversion tract lengths from population SNP data.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 19477993.
- Also identified by DOI 10.1093/bioinformatics/btp229 and PMC identifier 2687983.
- Licence recorded as CC BY-NC.
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Abstract
Two known types of meiotic recombination are crossovers and gene conversions. Although they leave behind different footprints in the genome, it is a challenging task to tease apart their relative contributions to the observed genetic variation. In particular, for a given population SNP dataset, the joint estimation of the crossover rate, the gene conversion rate and the mean conversion tract length is widely viewed as a very difficult problem. In this article, we devise a likelihood-based method using an interleaved hidden Markov model (HMM) that can jointly estimate the aforementioned three parameters fundamental to recombination. Our method significantly improves upon a recently proposed method based on a factorial HMM. We show that modeling overlapping gene conversions is crucial for improving the joint estimation of the gene conversion rate and the mean conversion tract length. We test the performance of our method on simulated data. We then apply our method to analyze real biological data from the telomere of the X chromosome of Drosophila melanogaster, and show that the ratio of the gene conversion rate to the crossover rate for the region may not be nearly as high as previously claimed. A software implementation of the algorithms discussed in this article is available at http://www.cs.berkeley.edu/ approximately yss/software.html.
Medical subject headings
- Computational Biology
- Crossing Over, Genetic
- Gene Conversion
- Polymorphism, Single Nucleotide