Detecting the Common and Individual Effects of Rare Variants on Quantitative Traits by Using Extreme Phenotype Sampling
Next-generation sequencing technology has made it possible to detect rare genetic variants associated with complex human traits. In recent literature, various methods specifically designed for rare variants are proposed. These tests can be broadly classified into burden and nonburden tests. In this...
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doaj-e6f434cf211944fa8220ef847816e5c12020-11-24T22:44:11ZengMDPI AGGenes2073-44252016-01-0171210.3390/genes7010002genes7010002Detecting the Common and Individual Effects of Rare Variants on Quantitative Traits by Using Extreme Phenotype SamplingYa-Jing Zhou0Yong Wang1Li-Li Chen2Department of Mathematics, School of Science, Harbin Institute of Technology, Harbin 150001, ChinaDepartment of Mathematics, School of Science, Harbin Institute of Technology, Harbin 150001, ChinaDepartment of Mathematics, School of Science, Harbin Institute of Technology, Harbin 150001, ChinaNext-generation sequencing technology has made it possible to detect rare genetic variants associated with complex human traits. In recent literature, various methods specifically designed for rare variants are proposed. These tests can be broadly classified into burden and nonburden tests. In this paper, we take advantage of the burden and nonburden tests, and consider the common effect and the individual deviations from the common effect. To achieve robustness, we use two methods of combining p-values, Fisher’s method and the minimum-p method. In rare variant association studies, to improve the power of the tests, we explore the advantage of the extreme phenotype sampling. At first, we dichotomize the continuous phenotypes before analysis, and the two extremes are treated as two different groups representing a dichotomous phenotype. We next compare the powers of several methods based on extreme phenotype sampling and random sampling. Extensive simulation studies show that our proposed methods by using extreme phenotype sampling are the most powerful or very close to the most powerful one in various settings of true models when the same sample size is used.http://www.mdpi.com/2073-4425/7/1/2association studyextreme samplingrandom samplingrare variants |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Ya-Jing Zhou Yong Wang Li-Li Chen |
spellingShingle |
Ya-Jing Zhou Yong Wang Li-Li Chen Detecting the Common and Individual Effects of Rare Variants on Quantitative Traits by Using Extreme Phenotype Sampling Genes association study extreme sampling random sampling rare variants |
author_facet |
Ya-Jing Zhou Yong Wang Li-Li Chen |
author_sort |
Ya-Jing Zhou |
title |
Detecting the Common and Individual Effects of Rare Variants on Quantitative Traits by Using Extreme Phenotype Sampling |
title_short |
Detecting the Common and Individual Effects of Rare Variants on Quantitative Traits by Using Extreme Phenotype Sampling |
title_full |
Detecting the Common and Individual Effects of Rare Variants on Quantitative Traits by Using Extreme Phenotype Sampling |
title_fullStr |
Detecting the Common and Individual Effects of Rare Variants on Quantitative Traits by Using Extreme Phenotype Sampling |
title_full_unstemmed |
Detecting the Common and Individual Effects of Rare Variants on Quantitative Traits by Using Extreme Phenotype Sampling |
title_sort |
detecting the common and individual effects of rare variants on quantitative traits by using extreme phenotype sampling |
publisher |
MDPI AG |
series |
Genes |
issn |
2073-4425 |
publishDate |
2016-01-01 |
description |
Next-generation sequencing technology has made it possible to detect rare genetic variants associated with complex human traits. In recent literature, various methods specifically designed for rare variants are proposed. These tests can be broadly classified into burden and nonburden tests. In this paper, we take advantage of the burden and nonburden tests, and consider the common effect and the individual deviations from the common effect. To achieve robustness, we use two methods of combining p-values, Fisher’s method and the minimum-p method. In rare variant association studies, to improve the power of the tests, we explore the advantage of the extreme phenotype sampling. At first, we dichotomize the continuous phenotypes before analysis, and the two extremes are treated as two different groups representing a dichotomous phenotype. We next compare the powers of several methods based on extreme phenotype sampling and random sampling. Extensive simulation studies show that our proposed methods by using extreme phenotype sampling are the most powerful or very close to the most powerful one in various settings of true models when the same sample size is used. |
topic |
association study extreme sampling random sampling rare variants |
url |
http://www.mdpi.com/2073-4425/7/1/2 |
work_keys_str_mv |
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