نتایج جستجو برای: genome wide association study

تعداد نتایج: 4629884  

Journal: :Human heredity 2011
Chengyin Ye Yuehua Cui Changshuai Wei Robert C Elston Jun Zhu Qing Lu

OBJECTIVE Predictive tests that capitalize on emerging genetic findings hold great promise for enhanced personalized healthcare. With the emergence of a large amount of data from genome-wide association studies (GWAS), interest has shifted towards high-dimensional risk prediction. METHODS To form predictive genetic tests on high-dimensional data, we propose a non-parametric method, called the...

Journal: :AMIA ... Annual Symposium proceedings. AMIA Symposium 2010
Xia Jiang Richard E Neapolitan M Michael Barmada Shyam Visweswaran Gregory F Cooper

Genetic epidemiologists strive to determine the genetic profile of diseases. Epistasis is the interaction between two or more genes to affect phenotype. Due to the often non-linearity of the interaction, it is difficult to detect statistical patterns of epistasis. Combinatorial methods for detecting epistasis investigate a subset of combinations of genes without employing a search strategy. The...

2017
Sophie Hackinger Eleftheria Zeggini

In recent years pleiotropy, the phenomenon of one genetic locus influencing several traits, has become a widely researched field in human genetics. With the increasing availability of genome-wide association study summary statistics, as well as the establishment of deeply phenotyped sample collections, it is now possible to systematically assess the genetic overlap between multiple traits and d...

2016
Simo Kitanovski

2 Conducting GWAS with genphen 2 2.1 Input . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2 2.2 Methods . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3 2.2.1 runGenphenRf and runGenphenSvm . . . . . . . . . . 3 2.2.2 runGenphenBayes . . . . . . . . . . . . . . . . . . . . 5 2.3 Case studies . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6 2.3.1 SNP-phenot...

2012
Joshua Mark Galanter Juan Carlos Fernandez-Lopez Christopher R. Gignoux Jill Barnholtz-Sloan Ceres Fernandez-Rozadilla Marc Via Alfredo Hidalgo-Miranda Alejandra V. Contreras Laura Uribe Figueroa Paola Raska Gerardo Jimenez-Sanchez Irma Silva Zolezzi Maria Torres Clara Ruiz Ponte Yarimar Ruiz Antonio Salas Elizabeth Nguyen Celeste Eng Lisbeth Borjas William Zabala Guillermo Barreto Fernando Rondón González Adriana Ibarra Patricia Taboada Liliana Porras Fabián Moreno Abigail Bigham Gerardo Gutierrez Tom Brutsaert Fabiola León-Velarde Lorna G. Moore Enrique Vargas Miguel Cruz Jorge Escobedo José Rodriguez-Santana William Rodriguez-Cintrón Rocio Chapela Jean G. Ford Carlos Bustamante Daniela Seminara Mark Shriver Elad Ziv Esteban Gonzalez Burchard Robert Haile Esteban Parra Angel Carracedo

Most individuals throughout the Americas are admixed descendants of Native American, European, and African ancestors. Complex historical factors have resulted in varying proportions of ancestral contributions between individuals within and among ethnic groups. We developed a panel of 446 ancestry informative markers (AIMs) optimized to estimate ancestral proportions in individuals and populatio...

2011
Gengxin Li John Ferguson Wei Zheng Joon Sang Lee Xianghua Zhang Lun Li Jia Kang Xiting Yan Hongyu Zhao

We consider the application of Efron's empirical Bayes classification method to risk prediction in a genome-wide association study using the Genetic Analysis Workshop 17 (GAW17) data. A major advantage of using this method is that the effect size distribution for the set of possible features is empirically estimated and that all subsequent parameter estimation and risk prediction is guided by t...

2012
Fuencisla Matesanz Antonio González-Pérez Miguel Lucas Serena Sanna Javier Gayán Elena Urcelay Ilenia Zara Maristella Pitzalis María L. Cavanillas Rafael Arroyo Magdalena Zoledziewska Marisa Marrosu Oscar Fernández Laura Leyva Antonio Alcina Maria Fedetz Concha Moreno-Rey Juan Velasco Luis M. Real Juan Luis Ruiz-Peña Francesco Cucca Agustín Ruiz Guillermo Izquierdo

Multiple Sclerosis (MS) is the most common progressive and disabling neurological condition affecting young adults in the world today. From a genetic point of view, MS is a complex disorder resulting from the combination of genetic and non-genetic factors. We aimed to identify previously unidentified loci conducting a new GWAS of Multiple Sclerosis (MS) in a sample of 296 MS cases and 801 contr...

Journal: :BMC Proceedings 2007
Soonil Kwon Dai Wang Xiuqing Guo

Genome-wide association studies usually involve several hundred thousand of single-nucleotide polymorphisms (SNPs). Conventional approaches face challenges when there are enormous number of SNPs but a relatively small number of samples and, in some cases, are not feasible. We introduce here an iterative Bayesian variable selection method that provides a unique tool for association studies with ...

Journal: :Current opinion in genetics & development 2009
Scott T Weiss Benjamin A Raby Angela Rogers

Asthma Genetic Association studies have been plagued by methodologic problems that are common in all studies of complex traits: small sample size, lack of replication, and lack of control of population stratification. Despite this, the field has identified 43 replicated genes from association studies. The most frequently replicated are: TNF alpha, IL4, FCERB, Adam 33, and GSTP1. Several genes h...

Journal: :Arteriosclerosis, thrombosis, and vascular biology 2017
Jacqueline S Dron Rosettia Ho Robert A Hegele

Over the past 2 years, the pace of scientific discovery in human genetics related to atherothrombotic disease and vascular biology has been rapid, with no shortage of innovative articles published in ATVB. Several studies have identified novel loci by genetic association approaches, whereas others focused on validating genome-wide association study (GWAS) data functionally. Strides were also ma...

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