Algorithms to estimate the lower bounds of recombination with or without recurrent mutations

<p>Abstract</p> <p>Background</p> <p>An important method to quantify the effects of recombination on populations is to estimate the minimum number of recombination events, <it>R<sub>min</sub></it>, in the history of a DNA sample. People have focu...

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Main Authors: Fu Yun-Xin, Liu Xiaoming
Format: Article
Language:English
Published: BMC 2008-03-01
Series:BMC Genomics
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spelling doaj-dbe073fd799b43ceb08cf476323891cc2020-11-25T00:42:10ZengBMCBMC Genomics1471-21642008-03-019Suppl 1S2410.1186/1471-2164-9-S1-S24Algorithms to estimate the lower bounds of recombination with or without recurrent mutationsFu Yun-XinLiu Xiaoming<p>Abstract</p> <p>Background</p> <p>An important method to quantify the effects of recombination on populations is to estimate the minimum number of recombination events, <it>R<sub>min</sub></it>, in the history of a DNA sample. People have focused on estimating the lower bound of <it>R<sub>min</sub></it>, because it is also a valid lower bound for the true number of recombination events occurred. Current approaches for estimating the lower bound are under the assumption of the infinite site model and do not allow for recurrent mutations. However, recurrent mutations are relatively common in genes with high mutation rates or mutation hot-spots, such as those in the genomes of bacteria or viruses.</p> <p>Results</p> <p>In this paper two new algorithms were proposed for estimating the lower bound of <it>R<sub>min</sub></it> under the infinite site model. Their performances were compared to other bounds currently in use. The new lower bounds were further extended to allow for recurrent mutations. Application of these methods were demonstrated with two haplotype data sets.</p> <p>Conclusions</p> <p>These new algorithms would help to obtain a better estimation of the lower bound of <it>R<sub>min</sub></it> under the infinite site model. After extension to allow for recurrent mutations, they can produce robust estimations with the existence of high mutation rate or mutation hot-spots. They can also be used to show different combinations of recurrent mutations and recombinations that can produce the same polymorphic pattern in the sample.</p>
collection DOAJ
language English
format Article
sources DOAJ
author Fu Yun-Xin
Liu Xiaoming
spellingShingle Fu Yun-Xin
Liu Xiaoming
Algorithms to estimate the lower bounds of recombination with or without recurrent mutations
BMC Genomics
author_facet Fu Yun-Xin
Liu Xiaoming
author_sort Fu Yun-Xin
title Algorithms to estimate the lower bounds of recombination with or without recurrent mutations
title_short Algorithms to estimate the lower bounds of recombination with or without recurrent mutations
title_full Algorithms to estimate the lower bounds of recombination with or without recurrent mutations
title_fullStr Algorithms to estimate the lower bounds of recombination with or without recurrent mutations
title_full_unstemmed Algorithms to estimate the lower bounds of recombination with or without recurrent mutations
title_sort algorithms to estimate the lower bounds of recombination with or without recurrent mutations
publisher BMC
series BMC Genomics
issn 1471-2164
publishDate 2008-03-01
description <p>Abstract</p> <p>Background</p> <p>An important method to quantify the effects of recombination on populations is to estimate the minimum number of recombination events, <it>R<sub>min</sub></it>, in the history of a DNA sample. People have focused on estimating the lower bound of <it>R<sub>min</sub></it>, because it is also a valid lower bound for the true number of recombination events occurred. Current approaches for estimating the lower bound are under the assumption of the infinite site model and do not allow for recurrent mutations. However, recurrent mutations are relatively common in genes with high mutation rates or mutation hot-spots, such as those in the genomes of bacteria or viruses.</p> <p>Results</p> <p>In this paper two new algorithms were proposed for estimating the lower bound of <it>R<sub>min</sub></it> under the infinite site model. Their performances were compared to other bounds currently in use. The new lower bounds were further extended to allow for recurrent mutations. Application of these methods were demonstrated with two haplotype data sets.</p> <p>Conclusions</p> <p>These new algorithms would help to obtain a better estimation of the lower bound of <it>R<sub>min</sub></it> under the infinite site model. After extension to allow for recurrent mutations, they can produce robust estimations with the existence of high mutation rate or mutation hot-spots. They can also be used to show different combinations of recurrent mutations and recombinations that can produce the same polymorphic pattern in the sample.</p>
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AT liuxiaoming algorithmstoestimatethelowerboundsofrecombinationwithorwithoutrecurrentmutations
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