Cargando…

Genetic Analysis Workshop 13: Simulated longitudinal data on families for a system of oligogenic traits

The Genetic Analysis Workshop 13 simulated data aimed to mimic the major features of the real Framingham Heart Study data that formed Problem 1, but under a known inheritance model and with 100 replicates, so as to allow evaluation of the statistical properties of various methods. The pedigrees used...

Descripción completa

Detalles Bibliográficos
Autores principales:	Daw, E Warwick, Morrison, John, Zhou, Xiaojun, Thomas, Duncan C
Formato:	Texto
Lenguaje:	English
Publicado:	BioMed Central 2003
Materias:	Proceedings
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1866465/ https://www.ncbi.nlm.nih.gov/pubmed/14975071 http://dx.doi.org/10.1186/1471-2156-4-S1-S3

Ejemplares similares

The feasibility of oligogenic combined segregation and linkage analysis in CEPH pedigrees
por: Daw, E Warwick, et al.
Publicado: (2007)

A framework for analyzing both linkage and association: an analysis of Genetic Analysis Workshop 16 simulated data
por: Daw, E Warwick, et al.
Publicado: (2009)

Simulation of a medication and methylation effects on triglycerides in the Genetic Analysis Workshop 20
por: Kraja, Aldi T., et al.
Publicado: (2018)

The Genetic Analysis Workshop 16 Problem 3: simulation of heritable longitudinal cardiovascular phenotypes based on actual genome-wide single-nucleotide polymorphisms in the Framingham Heart Study
por: Kraja, Aldi T, et al.
Publicado: (2009)

Segregation analysis comparing liability and quantitative trait models for hypertension using the Genetic Analysis Workshop 13 simulated data
por: Crockford, GP, et al.
Publicado: (2003)

Description of the Framingham Heart Study data for Genetic Analysis Workshop 13
por: Cupples, L Adrienne, et al.
Publicado: (2003)

Confidence set of putative quantitative trait loci in whole genome scans with application to the Genetic Analysis Workshop 17 simulated data
por: Papachristou, Charalampos
Publicado: (2011)

Single-nucleotide polymorphism versus microsatellite markers in a combined linkage and segregation analysis of a quantitative trait
por: Daw, E Warwick, et al.
Publicado: (2005)

Segregation and linkage analysis for longitudinal measurements of a quantitative trait
por: Gee, Conway, et al.
Publicado: (2003)

Combined linkage and family-based association analysis improves candidate gene detection in Genetic Analysis Workshop 18 simulation data
por: Li, Yi, et al.
Publicado: (2014)

Data for Genetic Analysis Workshop (GAW) 15 Problem 2, genetic causes of rheumatoid arthritis and associated traits
por: Amos, Christopher I, et al.
Publicado: (2007)

Application of collapsing methods for continuous traits to the Genetic Analysis Workshop 17 exome sequence data
por: Sung, Yun Ju, et al.
Publicado: (2011)

Genetic Analysis Workshop 15: simulation of a complex genetic model for rheumatoid arthritis in nuclear families including a dense SNP map with linkage disequilibrium between marker loci and trait loci
por: Miller, Michael B, et al.
Publicado: (2007)

Linkage analysis of a derived glucose phenotype in the Genetic Analysis Workshop 13 simulated data using a variety of Haseman-Elston based regression methods
por: Cordell, Heather J, et al.
Publicado: (2003)

Use of Bayesian networks to dissect the complexity of genetic disease: application to the Genetic Analysis Workshop 17 simulated data
por: Kang, Jia, et al.
Publicado: (2011)

Genetic Analysis Workshop 17 mini-exome simulation
por: Almasy, Laura, et al.
Publicado: (2011)

Successful identification of rare variants using oligogenic segregation analysis as a prioritizing tool for whole-exome sequencing studies
por: Gagnon, France, et al.
Publicado: (2011)

Propensity score analysis in the Genetic Analysis Workshop 17 simulated data set on independent individuals
por: Lin, Chen Min, et al.
Publicado: (2011)

Comparison of parametric and machine methods for variable selection in simulated Genetic Analysis Workshop 19 data
por: Holzinger, Emily R., et al.
Publicado: (2016)

Evaluation of association tests for rare variants using simulated data sets in the Genetic Analysis Workshop 17 data
por: Chen, Wenan, et al.
Publicado: (2011)

A multi-level model for analyzing whole genome sequencing family data with longitudinal traits
por: Chen, Taoye, et al.
Publicado: (2014)

Power of linkage analysis using traits generated from simulated longitudinal data of the Framingham Heart Study
por: Wang, Dai, et al.
Publicado: (2003)

Whole genome sequence analysis of the simulated systolic blood pressure in Genetic Analysis Workshop 18 family data: long-term average and collapsing methods
por: Sung, Yun Ju, et al.
Publicado: (2014)

Comparison of multilevel modeling and the family-based association test for identifying genetic variants associated with systolic and diastolic blood pressure using Genetic Analysis Workshop 18 simulated data
por: Wang, Jian, et al.
Publicado: (2014)

Old lessons learned anew: family-based methods for detecting genes responsible for quantitative and qualitative traits in the Genetic Analysis Workshop 17 mini-exome sequence data
por: Simpson, Claire L, et al.
Publicado: (2011)

Challenges and directions: an analysis of Genetic Analysis Workshop 17 data by collapsing rare variants within family data
por: Lin, Peng, et al.
Publicado: (2011)

Genetic Analysis Workshop 16: Strategies for genome-wide association study analyses
por: Cupples, L Adrienne, et al.
Publicado: (2009)

Accounting for relatedness in family-based association studies: application to Genetic Analysis Workshop 18 data
por: Eu-ahsunthornwattana, Jakris, et al.
Publicado: (2014)

Genome-wide linkage analysis of systolic blood pressure slope using the Genetic Analysis Workshop 13 data sets
por: Pinnaduwage, Dushanthi, et al.
Publicado: (2003)

Methods for detecting methylation by SNP interaction in GAW20 simulation
por: Daw, E. Warwick, et al.
Publicado: (2018)

Genetic Analysis Workshop 15: gene expression analysis and approaches to detecting multiple functional loci
por: Cordell, Heather J, et al.
Publicado: (2007)

Identifying rare disease variants in the Genetic Analysis Workshop 17 simulated data: a comparison of several statistical approaches
por: Fan, Ruixue, et al.
Publicado: (2011)

Data for Genetic Analysis Workshop 18: human whole genome sequence, blood pressure, and simulated phenotypes in extended pedigrees
por: Almasy, Laura, et al.
Publicado: (2014)

A combinatorial approach for detecting gene-gene interaction using multiple traits of Genetic Analysis Workshop 16 rheumatoid arthritis data
por: Cui, Xiaoqi, et al.
Publicado: (2009)

Identifying genetic variation affecting a complex trait in simulated data: a comparison of meta-analysis with pooled data analysis
por: Wu, Xiaodong, et al.
Publicado: (2005)

Bayesian hierarchical modeling of means and covariances of gene expression data within families
por: Pique-Regi, Roger, et al.
Publicado: (2007)

Identifying causal rare variants of disease through family-based analysis of Genetics Analysis Workshop 17 data set
por: Yip, Wai-Ki, et al.
Publicado: (2011)

Longitudinal analytical approaches to genetic data
por: Chiu, Yen-Feng, et al.
Publicado: (2016)

Powerful association test combining rare variant and gene expression using family data from Genetic Analysis Workshop 19
por: Ho, Yen-Yi, et al.
Publicado: (2016)

Genetic Analysis Workshop 19: methods and strategies for analyzing human sequence and gene expression data in extended families and unrelated individuals
por: Engelman, Corinne D., et al.
Publicado: (2016)

Cannot write session to /tmp/vufind_sessions/sess_nkr60nl7g1hevkkn75sqt6cgpe