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本文引用的文献

1
Insights into recombination from patterns of linkage disequilibrium in humans.从人类连锁不平衡模式中洞察重组情况。
Genetics. 2004 May;167(1):387-97. doi: 10.1534/genetics.167.1.387.
2
Intense and highly localized gene conversion activity in human meiotic crossover hot spots.人类减数分裂交叉热点区域强烈且高度局部化的基因转换活性。
Nat Genet. 2004 Feb;36(2):151-6. doi: 10.1038/ng1287. Epub 2004 Jan 4.
3
Modeling linkage disequilibrium and identifying recombination hotspots using single-nucleotide polymorphism data.利用单核苷酸多态性数据对连锁不平衡进行建模并识别重组热点。
Genetics. 2003 Dec;165(4):2213-33. doi: 10.1093/genetics/165.4.2213.
4
Linkage disequilibrium patterns across a recombination gradient in African Drosophila melanogaster.非洲黑腹果蝇中跨越重组梯度的连锁不平衡模式。
Genetics. 2003 Nov;165(3):1289-305. doi: 10.1093/genetics/165.3.1289.
5
Haplotype blocks and linkage disequilibrium in the human genome.人类基因组中的单倍型块与连锁不平衡
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6
An initiation site for meiotic crossing-over and gene conversion in the mouse.小鼠减数分裂交叉和基因转换的起始位点。
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7
Recombination and gene conversion in a 170-kb genomic region of Arabidopsis thaliana.拟南芥170千碱基对基因组区域中的重组与基因转换
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A high-resolution recombination map of the human genome.人类基因组的高分辨率重组图谱。
Nat Genet. 2002 Jul;31(3):241-7. doi: 10.1038/ng917. Epub 2002 Jun 10.
9
A coalescent-based method for detecting and estimating recombination from gene sequences.一种基于溯祖理论从基因序列中检测和估计重组的方法。
Genetics. 2002 Mar;160(3):1231-41. doi: 10.1093/genetics/160.3.1231.
10
Two-locus sampling distributions and their application.两位点抽样分布及其应用。
Genetics. 2001 Dec;159(4):1805-17. doi: 10.1093/genetics/159.4.1805.

使用三位点似然法估计重组率。

Estimating recombination rates using three-site likelihoods.

作者信息

Wall Jeffrey D

机构信息

Program in Molecular and Computational Biology, University of Southern California, Los Angeles, California 90089, USA.

出版信息

Genetics. 2004 Jul;167(3):1461-73. doi: 10.1534/genetics.103.025742.

DOI:10.1534/genetics.103.025742
PMID:15280255
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1470930/
Abstract

We introduce a new method for jointly estimating crossing-over and gene conversion rates using sequence polymorphism data. The method calculates probabilities for subsets of the data consisting of three segregating sites and then forms a composite likelihood by multiplying together the probabilities of many subsets. Simulations show that this new method performs better than previously proposed methods for estimating gene conversion rates, but that all methods require large amounts of data to provide reliable estimates. While existing methods can easily estimate an "average" gene conversion rate over many loci, they cannot reliably estimate gene conversion rates for a single region of the genome.

摘要

我们介绍了一种使用序列多态性数据联合估计交叉率和基因转换率的新方法。该方法计算由三个分离位点组成的数据子集的概率,然后通过将许多子集的概率相乘形成复合似然。模拟表明,这种新方法在估计基因转换率方面比先前提出的方法表现更好,但所有方法都需要大量数据才能提供可靠的估计。虽然现有方法可以轻松估计多个位点上的“平均”基因转换率,但它们无法可靠地估计基因组单个区域的基因转换率。