Lessons learned from Genetic Analysis Workshop 17: transitioning from genome-wide association studies to whole-genome statistical genetic analysis

Dealing with high dimensionality for the identification of common and rare variants as main effects and for gene-environment interaction

(2011) Heike Bickeböller et al.   GENETIC EPIDEMIOLOGY

Effect of linkage disequilibrium on the identification of functional variants

(2011) Alun Thomas et al.   GENETIC EPIDEMIOLOGY

Joint analyses of disease and correlated quantitative phenotypes using next-generation sequencing data

(2011) Phillip E. Melton et al.   GENETIC EPIDEMIOLOGY

Incorporating biological information into association studies of sequencing data

(2011) Gary Chen et al.   GENETIC EPIDEMIOLOGY

Detecting rare variant associations: methods for testing haplotypes and multiallelic genotypes

(2011) Rita M. Cantor et al.   GENETIC EPIDEMIOLOGY

Quality control issues and the identification of rare functional variants with next-generation sequencing data

(2011) Claudia Hemmelmann et al.   GENETIC EPIDEMIOLOGY

Detecting multiple causal rare variants in exome sequence data

(2011) Kenny Q. Ye et al.   GENETIC EPIDEMIOLOGY

Rare variants, common markers: synthetic association and beyond

(2011) Jack W. Kent   GENETIC EPIDEMIOLOGY

Multiple testing in high-throughput sequence data: experiences from Group 8 of Genetic Analysis Workshop 17

(2011) Inke R. König et al.   GENETIC EPIDEMIOLOGY

Analysis of exome sequences with and without incorporating prior biological knowledge

(2011) Junghyun Namkung et al.   GENETIC EPIDEMIOLOGY

Inflated type I error rates when using aggregation methods to analyze rare variants in the 1000 Genomes Project exon sequencing data in unrelated individuals: summary results from Group 7 at Genetic Analysis Workshop 17

(2011) Nathan Tintle et al.   GENETIC EPIDEMIOLOGY

Population-based and family-based designs to analyze rare variants in complex diseases

(2011) Rémi Kazma et al.   GENETIC EPIDEMIOLOGY

Incorporating linkage information into a common disease/rare variant framework

(2011) Anthony L. Hinrichs et al.   GENETIC EPIDEMIOLOGY

Regression and data mining methods for analyses of multiple rare variants in the Genetic Analysis Workshop 17 mini-exome data

(2011) Joan E. Bailey-Wilson et al.   GENETIC EPIDEMIOLOGY

Identification of genetic association of multiple rare variants using collapsing methods

(2011) Yan V. Sun et al.   GENETIC EPIDEMIOLOGY

The ClinSeq Project: Piloting large-scale genome sequencing for research in genomic medicine

(2009) L. G. Biesecker et al.   GENOME RESEARCH