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Detecting PCOS susceptibility loci from genome-wide association studies via iterative trend correlation based feature screening
BACKGROUND: Feature screening plays a critical role in handling ultrahigh dimensional data analyses when the number of features exponentially exceeds the number of observations. It is increasingly common in biomedical research to have case-control (binary) response and an extremely large-scale categ...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7199379/ https://www.ncbi.nlm.nih.gov/pubmed/32366216 http://dx.doi.org/10.1186/s12859-020-3492-z |
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author | Dai, Xiaotian Fu, Guifang Reese, Randall |
author_facet | Dai, Xiaotian Fu, Guifang Reese, Randall |
author_sort | Dai, Xiaotian |
collection | PubMed |
description | BACKGROUND: Feature screening plays a critical role in handling ultrahigh dimensional data analyses when the number of features exponentially exceeds the number of observations. It is increasingly common in biomedical research to have case-control (binary) response and an extremely large-scale categorical features. However, the approach considering such data types is limited in extant literature. In this article, we propose a new feature screening approach based on the iterative trend correlation (ITC-SIS, for short) to detect important susceptibility loci that are associated with the polycystic ovary syndrome (PCOS) affection status by screening 731,442 SNP features that were collected from the genome-wide association studies. RESULTS: We prove that the trend correlation based screening approach satisfies the theoretical strong screening consistency property under a set of reasonable conditions, which provides an appealing theoretical support for its outperformance. We demonstrate that the finite sample performance of ITC-SIS is accurate and fast through various simulation designs. CONCLUSION: ITC-SIS serves as a good alternative method to detect disease susceptibility loci for clinic genomic data. |
format | Online Article Text |
id | pubmed-7199379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-71993792020-05-08 Detecting PCOS susceptibility loci from genome-wide association studies via iterative trend correlation based feature screening Dai, Xiaotian Fu, Guifang Reese, Randall BMC Bioinformatics Methodology Article BACKGROUND: Feature screening plays a critical role in handling ultrahigh dimensional data analyses when the number of features exponentially exceeds the number of observations. It is increasingly common in biomedical research to have case-control (binary) response and an extremely large-scale categorical features. However, the approach considering such data types is limited in extant literature. In this article, we propose a new feature screening approach based on the iterative trend correlation (ITC-SIS, for short) to detect important susceptibility loci that are associated with the polycystic ovary syndrome (PCOS) affection status by screening 731,442 SNP features that were collected from the genome-wide association studies. RESULTS: We prove that the trend correlation based screening approach satisfies the theoretical strong screening consistency property under a set of reasonable conditions, which provides an appealing theoretical support for its outperformance. We demonstrate that the finite sample performance of ITC-SIS is accurate and fast through various simulation designs. CONCLUSION: ITC-SIS serves as a good alternative method to detect disease susceptibility loci for clinic genomic data. BioMed Central 2020-05-04 /pmc/articles/PMC7199379/ /pubmed/32366216 http://dx.doi.org/10.1186/s12859-020-3492-z Text en © The Author(s) 2020 Open Access This 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 Dai, Xiaotian Fu, Guifang Reese, Randall Detecting PCOS susceptibility loci from genome-wide association studies via iterative trend correlation based feature screening |
title | Detecting PCOS susceptibility loci from genome-wide association studies via iterative trend correlation based feature screening |
title_full | Detecting PCOS susceptibility loci from genome-wide association studies via iterative trend correlation based feature screening |
title_fullStr | Detecting PCOS susceptibility loci from genome-wide association studies via iterative trend correlation based feature screening |
title_full_unstemmed | Detecting PCOS susceptibility loci from genome-wide association studies via iterative trend correlation based feature screening |
title_short | Detecting PCOS susceptibility loci from genome-wide association studies via iterative trend correlation based feature screening |
title_sort | detecting pcos susceptibility loci from genome-wide association studies via iterative trend correlation based feature screening |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7199379/ https://www.ncbi.nlm.nih.gov/pubmed/32366216 http://dx.doi.org/10.1186/s12859-020-3492-z |
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