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首页> 外文期刊>Journal of Bioinformatics and Computational Biology >Regression based fast multi-trait genome-wide QTL analysis
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Regression based fast multi-trait genome-wide QTL analysis

机译:基于回归的快速多特征基因组宽QTL分析

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摘要

Multivariate simple interval mapping (SIM) is one of the most popular approaches for multiple quantitative trait locus (QTL) analysis. Both maximum likelihood (ML) and least squares (LS) multivariate regression (MVR) are widely used methods for multi-trait SIM. ML-based MVR (MVR-ML) is an expectation maximization (EM) algorithm based iterative and complex time-consuming approach. Although the LS-based MVR (MVR-LS) approach is not an iterative process, the calculation of likelihood ratio (LR) statistic in MVR-LS is also a time-consuming complex process. We have introduced a new approach (called FastMtQTL) for multi-trait QTL analysis based on the assumption of multivariate normal distribution of phenotypic observations. Our proposed method can identify almost the same QTL positions as those identified by the existing methods. Moreover, the proposed method takes comparatively less computation time because of the simplicity in the calculation of LR statistic by this method. In the proposed method, LR statistic is calculated only using the sample variance-covariance matrix of phenotypes and the conditional probability of QTL genotype given the marker genotypes. This improvement in computation time is advantageous when the numbers of phenotypes and individuals are larger, and the markers are very dense resulting in a QTL mapping with a bigger dataset.
机译:多元简单区间作图(SIM)是多数量性状位点(QTL)分析中最常用的方法之一。最大似然(ML)和最小二乘(LS)多元回归(MVR)都是广泛应用于多性状SIM的方法。基于ML的MVR(MVR-ML)是一种基于期望最大化(EM)算法的迭代复杂耗时方法。尽管基于LS的MVR(MVR-LS)方法不是一个迭代过程,但MVR-LS中似然比(LR)统计量的计算也是一个耗时复杂的过程。基于表型观察的多元正态分布假设,我们引入了一种新的多性状QTL分析方法(称为FastMtQTL)。我们提出的方法可以识别与现有方法几乎相同的QTL位置。此外,由于该方法计算LR统计量的简单性,该方法所需的计算时间相对较少。在该方法中,仅使用表型的样本方差协方差矩阵和给定标记基因型的QTL基因型的条件概率来计算LR统计量。当表型和个体的数量较大时,这种计算时间的改进是有利的,并且标记非常密集,导致QTL作图具有更大的数据集。

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