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Problems with determination of noncommunicating classes for Monte Carlo Markov chain applications in pedigree analysis.系谱分析中蒙特卡罗马尔可夫链应用的非连通类确定问题。
Biometrics. 1998 Jun;54(2):416-25.
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Bayesian mapping of multiple quantitative trait loci from incomplete inbred line cross data.基于不完全近交系杂交数据的多个数量性状基因座的贝叶斯定位
Genetics. 1998 Mar;148(3):1373-88. doi: 10.1093/genetics/148.3.1373.
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A mixture model approach to the mapping of quantitative trait loci in complex populations with an application to multiple cattle families.一种用于复杂群体中数量性状基因座定位的混合模型方法及其在多个牛家族中的应用。
Genetics. 1998 Jan;148(1):391-9. doi: 10.1093/genetics/148.1.391.
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Genetics. 1997 Nov;147(3):1445-57. doi: 10.1093/genetics/147.3.1445.
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Markov chain Monte Carlo segregation and linkage analysis for oligogenic models.用于寡基因模型的马尔可夫链蒙特卡罗分离与连锁分析
Am J Hum Genet. 1997 Sep;61(3):748-60. doi: 10.1086/515506.
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General formulas for obtaining the MLEs and the asymptotic variance-covariance matrix in mapping quantitative trait loci when using the EM algorithm.在使用期望最大化(EM)算法定位数量性状基因座时,用于获取最大似然估计值(MLEs)和渐近方差 - 协方差矩阵的通用公式。
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Mapping-linked quantitative trait loci using Bayesian analysis and Markov chain Monte Carlo algorithms.使用贝叶斯分析和马尔可夫链蒙特卡罗算法定位连锁数量性状基因座。
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A bayesian approach to detect quantitative trait loci using Markov chain Monte Carlo.一种使用马尔可夫链蒙特卡罗方法检测数量性状位点的贝叶斯方法。
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A general Monte Carlo method for mapping multiple quantitative trait loci.一种用于定位多个数量性状基因座的通用蒙特卡罗方法。
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利用不完全远交后代数据对多个数量性状位点进行贝叶斯定位

Bayesian mapping of multiple quantitative trait loci from incomplete outbred offspring data.

作者信息

Sillanpää M J, Arjas E

机构信息

Rolf Nevanlinna Institute, FIN-00014 University of Helsinki, Finland.

出版信息

Genetics. 1999 Apr;151(4):1605-19. doi: 10.1093/genetics/151.4.1605.

DOI:10.1093/genetics/151.4.1605
PMID:10101181
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1460569/
Abstract

A general fine-scale Bayesian quantitative trait locus (QTL) mapping method for outcrossing species is presented. It is suitable for an analysis of complete and incomplete data from experimental designs of F2 families or backcrosses. The amount of genotyping of parents and grandparents is optional, as well as the assumption that the QTL alleles in the crossed lines are fixed. Grandparental origin indicators are used, but without forgetting the original genotype or allelic origin information. The method treats the number of QTL in the analyzed chromosome as a random variable and allows some QTL effects from other chromosomes to be taken into account in a composite interval mapping manner. A block-update of ordered genotypes (haplotypes) of the whole family is sampled once in each marker locus during every round of the Markov Chain Monte Carlo algorithm used in the numerical estimation. As a byproduct, the method gives the posterior distributions for linkage phases in the family and therefore it can also be used as a haplotyping algorithm. The Bayesian method is tested and compared with two frequentist methods using simulated data sets, considering two different parental crosses and three different levels of available parental information. The method is implemented as a software package and is freely available under the name Multimapper/outbred at URL http://www.rni.helsinki.fi/mjs/.

摘要

本文提出了一种用于杂交物种的精细尺度贝叶斯数量性状基因座(QTL)定位的通用方法。它适用于对F2家系或回交实验设计中的完整和不完整数据进行分析。亲本和祖父母的基因分型数量是可选的,并且杂交品系中的QTL等位基因固定这一假设也是可选的。使用了祖父母起源指标,但不会忘记原始基因型或等位基因起源信息。该方法将分析染色体中的QTL数量视为一个随机变量,并允许以复合区间定位的方式考虑来自其他染色体的一些QTL效应。在数值估计中使用的马尔可夫链蒙特卡罗算法的每一轮中,在每个标记位点对整个家系的有序基因型(单倍型)进行一次块更新抽样。作为一个副产品,该方法给出了家系中连锁相的后验分布,因此它也可以用作单倍型分型算法。使用模拟数据集对贝叶斯方法进行了测试,并与两种频率论方法进行了比较,考虑了两种不同的亲本杂交和三种不同水平的可用亲本信息。该方法被实现为一个软件包,可在网址http://www.rni.helsinki.fi/mjs/ 以Multimapper/outbred的名称免费获取。