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Identifying rare variants for quantitative traits in extreme samples of population via Kullback-Leibler distance

BACKGROUND: The rapid development of sequencing technology and simultaneously the availability of large quantities of sequence data has facilitated the identification of rare variant associated with quantitative traits. However, existing statistical methods depend on certain assumptions and thus lac...

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Autores principales: Xiang, Yang, Xiang, Xinrong, Li, Yumei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7687851/
https://www.ncbi.nlm.nih.gov/pubmed/33234108
http://dx.doi.org/10.1186/s12863-020-00951-2
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author Xiang, Yang
Xiang, Xinrong
Li, Yumei
author_facet Xiang, Yang
Xiang, Xinrong
Li, Yumei
author_sort Xiang, Yang
collection PubMed
description BACKGROUND: The rapid development of sequencing technology and simultaneously the availability of large quantities of sequence data has facilitated the identification of rare variant associated with quantitative traits. However, existing statistical methods depend on certain assumptions and thus lacking uniform power. The present study focuses on mapping rare variant associated with quantitative traits. RESULTS: In the present study, we proposed a two-stage strategy to identify rare variant of quantitative traits using phenotype extreme selection design and Kullback-Leibler distance, where the first stage was association analysis and the second stage was fine mapping. We presented a statistic and a linkage disequilibrium measure for the first stage and the second stage, respectively. Theory analysis and simulation study showed that (1) the power of the proposed statistic for association analysis increased with the stringency of the sample selection and was affected slightly by non-causal variants and opposite effect variants, (2) the statistic here achieved higher power than three commonly used methods, and (3) the linkage disequilibrium measure for fine mapping was independent of the frequencies of non-causal variants and simply dependent on the frequencies of causal variants. CONCLUSIONS: We conclude that the two-stage strategy here can be used effectively to mapping rare variant associated with quantitative traits.
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spelling pubmed-76878512020-11-30 Identifying rare variants for quantitative traits in extreme samples of population via Kullback-Leibler distance Xiang, Yang Xiang, Xinrong Li, Yumei BMC Genet Methodology Article BACKGROUND: The rapid development of sequencing technology and simultaneously the availability of large quantities of sequence data has facilitated the identification of rare variant associated with quantitative traits. However, existing statistical methods depend on certain assumptions and thus lacking uniform power. The present study focuses on mapping rare variant associated with quantitative traits. RESULTS: In the present study, we proposed a two-stage strategy to identify rare variant of quantitative traits using phenotype extreme selection design and Kullback-Leibler distance, where the first stage was association analysis and the second stage was fine mapping. We presented a statistic and a linkage disequilibrium measure for the first stage and the second stage, respectively. Theory analysis and simulation study showed that (1) the power of the proposed statistic for association analysis increased with the stringency of the sample selection and was affected slightly by non-causal variants and opposite effect variants, (2) the statistic here achieved higher power than three commonly used methods, and (3) the linkage disequilibrium measure for fine mapping was independent of the frequencies of non-causal variants and simply dependent on the frequencies of causal variants. CONCLUSIONS: We conclude that the two-stage strategy here can be used effectively to mapping rare variant associated with quantitative traits. BioMed Central 2020-11-24 /pmc/articles/PMC7687851/ /pubmed/33234108 http://dx.doi.org/10.1186/s12863-020-00951-2 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Methodology Article
Xiang, Yang
Xiang, Xinrong
Li, Yumei
Identifying rare variants for quantitative traits in extreme samples of population via Kullback-Leibler distance
title Identifying rare variants for quantitative traits in extreme samples of population via Kullback-Leibler distance
title_full Identifying rare variants for quantitative traits in extreme samples of population via Kullback-Leibler distance
title_fullStr Identifying rare variants for quantitative traits in extreme samples of population via Kullback-Leibler distance
title_full_unstemmed Identifying rare variants for quantitative traits in extreme samples of population via Kullback-Leibler distance
title_short Identifying rare variants for quantitative traits in extreme samples of population via Kullback-Leibler distance
title_sort identifying rare variants for quantitative traits in extreme samples of population via kullback-leibler distance
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7687851/
https://www.ncbi.nlm.nih.gov/pubmed/33234108
http://dx.doi.org/10.1186/s12863-020-00951-2
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