Cargando…

SNP Set Association Analysis for Genome-Wide Association Studies

Genome-wide association study (GWAS) is a promising approach for identifying common genetic variants of the diseases on the basis of millions of single nucleotide polymorphisms (SNPs). In order to avoid low power caused by overmuch correction for multiple comparisons in single locus association stud...

Descripción completa

Detalles Bibliográficos
Autores principales:	Cai, Min, Dai, Hui, Qiu, Yongyong, Zhao, Yang, Zhang, Ruyang, Chu, Minjie, Dai, Juncheng, Hu, Zhibin, Shen, Hongbing, Chen, Feng
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2013
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3643925/ https://www.ncbi.nlm.nih.gov/pubmed/23658731 http://dx.doi.org/10.1371/journal.pone.0062495

Ejemplares similares

Weighted SNP Set Analysis in Genome-Wide Association Study
por: Dai, Hui, et al.
Publicado: (2013)

Pathway Analysis for Genome-Wide Association Study of Lung Cancer in Han Chinese Population
por: Zhang, Ruyang, et al.
Publicado: (2013)

Genome-wide analysis of runs of homozygosity identifies new susceptibility regions of lung cancer in Han Chinese
por: Wang, Cheng, et al.
Publicado: (2013)

Genome-wide Association Study on Platinum-induced Hepatotoxicity in Non-Small Cell Lung Cancer Patients
por: Cao, Songyu, et al.
Publicado: (2015)

Comparison of dimension reduction-based logistic regression models for case-control genome-wide association study: principal components analysis vs. partial least squares
por: Yi, Honggang, et al.
Publicado: (2015)

Efficacy assessment of SNP sets for genome-wide disease association studies
por: Wollstein, Andreas, et al.
Publicado: (2007)

Identification of genome-wide SNP-SNP interactions associated with important traits in chicken
por: Zhang, Hui, et al.
Publicado: (2017)

Stability SCAD: a powerful approach to detect interactions in large-scale genomic study
por: Gou, Jianwei, et al.
Publicado: (2014)

Genome wide in silico SNP-tumor association analysis
por: Qiu, Ping, et al.
Publicado: (2004)

RS-SNP: a random-set method for genome-wide association studies
por: D'Addabbo, Annarita, et al.
Publicado: (2011)

Cumulative Effect and Predictive Value of Genetic Variants Associated with Type 2 Diabetes in Han Chinese: A Case-Control Study
por: Qian, Yun, et al.
Publicado: (2015)

On the identification of potential regulatory variants within genome wide association candidate SNP sets
por: Chen, Chih-yu, et al.
Publicado: (2014)

An efficient weighted tag SNP-set analytical method in genome-wide association studies
por: Yan, Bin, et al.
Publicado: (2015)

Importance of SNP Dependency Correction and Association Integration for Gene Set Analysis in Genome-Wide Association Studies
por: Marczyk, Michal, et al.
Publicado: (2021)

Genome-Wide Association Study Identifies a Novel Susceptibility Locus at 12q23.1 for Lung Squamous Cell Carcinoma in Han Chinese
por: Dong, Jing, et al.
Publicado: (2013)

A Large Scale Gene-Centric Association Study of Lung Function in Newly-Hired Female Cotton Textile Workers with Endotoxin Exposure
por: Zhang, Ruyang, et al.
Publicado: (2013)

Genetic variants in regulatory regions of microRNAs are associated with lung cancer risk
por: Xie, Kaipeng, et al.
Publicado: (2016)

Breast cancer risk assessment with five independent genetic variants and two risk factors in Chinese women
por: Dai, Juncheng, et al.
Publicado: (2012)

Genetic variants at 10q23.33 are associated with plasma lipid levels in a Chinese population
por: Liu, Sijun, et al.
Publicado: (2014)

RAINBOW: Haplotype-based genome-wide association study using a novel SNP-set method
por: Hamazaki, Kosuke, et al.
Publicado: (2020)

Genetic variant in fat mass and obesity-associated gene associated with type 2 diabetes risk in Han Chinese
por: Qian, Yun, et al.
Publicado: (2013)

snpGeneSets: An R Package for Genome-Wide Study Annotation
por: Mei, Hao, et al.
Publicado: (2016)

Association of KCTD10, MVK, and MMAB polymorphisms with dyslipidemia and coronary heart disease in Han Chinese population
por: Sun, Jie, et al.
Publicado: (2016)

Statistical analysis for genome-wide association study
por: Zeng, Ping, et al.
Publicado: (2015)

A Comparative Study of Five Association Tests Based on CpG Set for Epigenome-Wide Association Studies
por: Zhang, Qiuyi, et al.
Publicado: (2016)

Fine Mapping in Chromosome 3q28 Identified Two Variants Associated with Lung Cancer Risk in Asian Population
por: Wen, Yang, et al.
Publicado: (2019)

Genetic Variations in the Flanking Regions of miR-101-2 Are Associated with Increased Risk of Breast Cancer
por: Chen, Jiaping, et al.
Publicado: (2014)

Development of the catfish 250K SNP array for genome-wide association studies
por: Liu, Shikai, et al.
Publicado: (2014)

The Development of a Genome Wide SNP Set for the Barnacle Goose Branta leucopsis
por: Jonker, Rudy M., et al.
Publicado: (2012)

How Genome-Wide SNP-SNP Interactions Relate to Nasopharyngeal Carcinoma Susceptibility
por: Su, Wen-Hui, et al.
Publicado: (2013)

Meta-analysis of genome-wide SNP- and pathway-based associations for facets of neuroticism
por: Kim, Song E, et al.
Publicado: (2017)

The eQTL-missense polymorphisms of APOBEC3H are associated with lung cancer risk in a Han Chinese population
por: Zhu, Meng, et al.
Publicado: (2015)

A genome-wide SNP panel for mapping and association studies in the rat
por: Nijman, Isaäc J, et al.
Publicado: (2008)

SNP-based pathway enrichment analysis for genome-wide association studies
por: Weng, Lingjie, et al.
Publicado: (2011)

GStream: Improving SNP and CNV Coverage on Genome-Wide Association Studies
por: Alonso, Arnald, et al.
Publicado: (2013)

snpXplorer: a web application to explore human SNP-associations and annotate SNP-sets
por: Tesi, Niccolo, et al.
Publicado: (2021)

A time-dependent genome-wide SNP-SNP interaction analysis of chicken body weight
por: Li, Fang-Ge, et al.
Publicado: (2019)

Epistatic Effects on Abdominal Fat Content in Chickens: Results from a Genome-Wide SNP-SNP Interaction Analysis
por: Li, Fangge, et al.
Publicado: (2013)

Potentially Functional Polymorphisms in POU5F1 Gene Are Associated with the Risk of Lung Cancer in Han Chinese
por: Niu, Rui, et al.
Publicado: (2015)

Genetic Variations in miR-30 Family Member Regulatory Regions Are Associated with Breast Cancer Risk in a Chinese Population
por: Zhou, Jing, et al.
Publicado: (2020)

Cannot write session to /tmp/vufind_sessions/sess_pfkv1oo3c937f7tb02j2p5m0i9