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Quantitative Trait Loci Identification by Estimating the Genetic Model based on the Extremal Samples
BACKGROUND: In genetic association studies with quantitative trait loci (QTL), the association between a candidate genetic marker and the trait of interest is commonly examined by the omnibus F test or by the t-test corresponding to a given genetic model or mode of inheritance. It is known that the...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Bentham Science Publishers
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844942/ https://www.ncbi.nlm.nih.gov/pubmed/35283669 http://dx.doi.org/10.2174/1389202922666210625161602 |
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author | Yang, Zining Yang, Yaning Xu, Xu Steven Yuan, Min |
author_facet | Yang, Zining Yang, Yaning Xu, Xu Steven Yuan, Min |
author_sort | Yang, Zining |
collection | PubMed |
description | BACKGROUND: In genetic association studies with quantitative trait loci (QTL), the association between a candidate genetic marker and the trait of interest is commonly examined by the omnibus F test or by the t-test corresponding to a given genetic model or mode of inheritance. It is known that the t-test with a correct model specification is more powerful than the F test. However, since the underlying genetic model is rarely known in practice, the use of a model-specific t-test may incur substantial power loss. Robust-efficient tests, such as the Maximin Efficiency Robust Test (MERT) and MAX3 have been proposed in the literature. METHODS: In this paper, we propose a novel two-step robust-efficient approach, namely, the genetic model selection (GMS) method for quantitative trait analysis. GMS selects a genetic model by testing Hardy-Weinberg disequilibrium (HWD) with extremal samples of the population in the first step and then applies the corresponding genetic model-specific t-test in the second step. RESULTS: Simulations show that GMS is not only more efficient than MERT and MAX3, but also has comparable power to the optimal t-test when the genetic model is known. CONCLUSION: Application to the data from Alzheimer’s Disease Neuroimaging Initiative (ADNI) cohort demonstrates that the proposed approach can identify meaningful biological SNPs on chromosome 19. |
format | Online Article Text |
id | pubmed-8844942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Bentham Science Publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-88449422022-06-30 Quantitative Trait Loci Identification by Estimating the Genetic Model based on the Extremal Samples Yang, Zining Yang, Yaning Xu, Xu Steven Yuan, Min Curr Genomics Article BACKGROUND: In genetic association studies with quantitative trait loci (QTL), the association between a candidate genetic marker and the trait of interest is commonly examined by the omnibus F test or by the t-test corresponding to a given genetic model or mode of inheritance. It is known that the t-test with a correct model specification is more powerful than the F test. However, since the underlying genetic model is rarely known in practice, the use of a model-specific t-test may incur substantial power loss. Robust-efficient tests, such as the Maximin Efficiency Robust Test (MERT) and MAX3 have been proposed in the literature. METHODS: In this paper, we propose a novel two-step robust-efficient approach, namely, the genetic model selection (GMS) method for quantitative trait analysis. GMS selects a genetic model by testing Hardy-Weinberg disequilibrium (HWD) with extremal samples of the population in the first step and then applies the corresponding genetic model-specific t-test in the second step. RESULTS: Simulations show that GMS is not only more efficient than MERT and MAX3, but also has comparable power to the optimal t-test when the genetic model is known. CONCLUSION: Application to the data from Alzheimer’s Disease Neuroimaging Initiative (ADNI) cohort demonstrates that the proposed approach can identify meaningful biological SNPs on chromosome 19. Bentham Science Publishers 2021-12-30 2021-12-30 /pmc/articles/PMC8844942/ /pubmed/35283669 http://dx.doi.org/10.2174/1389202922666210625161602 Text en © 2021 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/ This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited. |
spellingShingle | Article Yang, Zining Yang, Yaning Xu, Xu Steven Yuan, Min Quantitative Trait Loci Identification by Estimating the Genetic Model based on the Extremal Samples |
title | Quantitative Trait Loci Identification by Estimating the Genetic Model based on the Extremal Samples |
title_full | Quantitative Trait Loci Identification by Estimating the Genetic Model based on the Extremal Samples |
title_fullStr | Quantitative Trait Loci Identification by Estimating the Genetic Model based on the Extremal Samples |
title_full_unstemmed | Quantitative Trait Loci Identification by Estimating the Genetic Model based on the Extremal Samples |
title_short | Quantitative Trait Loci Identification by Estimating the Genetic Model based on the Extremal Samples |
title_sort | quantitative trait loci identification by estimating the genetic model based on the extremal samples |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8844942/ https://www.ncbi.nlm.nih.gov/pubmed/35283669 http://dx.doi.org/10.2174/1389202922666210625161602 |
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