sim1000G: a user-friendly genetic variant simulator in R for unrelated individuals and family-based designs

A comparison of tools for the simulation of genomic next-generation sequencing data

(2016) Merly Escalona et al.   NATURE REVIEWS GENETICS

SNP Set Association Testing for Survival Outcomes in the Presence of Intrafamilial Correlation

(2015) Martin Leclerc et al.   GENETIC EPIDEMIOLOGY

A global reference for human genetic variation

(2015) Richard A. Gibbs et al.   NATURE

Rare-Variant Association Analysis: Study Designs and Statistical Tests

(2014) Seunggeung Lee et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Genetic Data Simulators and their Applications: An Overview

(2014) Bo Peng et al.   GENETIC EPIDEMIOLOGY

Genetic Simulation Tools for Post-Genome Wide Association Studies of Complex Diseases

(2014) Huann-Sheng Chen et al.   GENETIC EPIDEMIOLOGY

Genetic Simulation Resources: a website for the registration and discovery of genetic data simulators

(2013) B. Peng et al.   BIOINFORMATICS

Simulating Realistic Genomic Data With Rare Variants

(2012) Yaji Xu et al.   GENETIC EPIDEMIOLOGY

Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test

(2011) Michael C. Wu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

HAPGEN2: simulation of multiple disease SNPs

(2011) Zhan Su et al.   BIOINFORMATICS

Next generation analytic tools for large scale genetic epidemiology studies of complex diseases

(2011) Leah E. Mechanic et al.   GENETIC EPIDEMIOLOGY

Simulating Sequences of the Human Genome with Rare Variants

(2011) Bo Peng et al.   HUMAN HEREDITY

Forward-time simulation of realistic samples for genome-wide association studies

(2010) Bo Peng et al.   BMC BIOINFORMATICS

The Sequence Alignment/Map format and SAMtools

(2009) H. Li et al.   BIOINFORMATICS

Estimating Disease Risk Associated with Mutated Genes in Family-Based Designs

(2008) Yun-Hee Choi et al.   HUMAN HEREDITY

Assessing the Evolutionary Impact of Amino Acid Mutations in the Human Genome

(2008) Adam R. Boyko et al.   PLoS Genetics