Rare Variant Analysis Workflows: Analyzing NGS Data in Large Cohorts

Knowing Your NGS Upstream: Alignment and Variants

Mixed Models: How to Effectively Account for Inbreeding and Population Structure in GWAS

Insights: Identification of Candidate Variants using Exome Data in Ophthalmic Genetics

Making NGS Data Analysis Clinically Practical: Repeatable and Time-Effective Workflows

Advancing Agrigenomic Discoveries with Sequencing and GWAS Research

Using Public Access Clinical Databases to Interpret NGS Variants

AGBT 2013: Home Brewed Personalized Genomics - The Quest for Meaningful Analysis Results of a 23andMe Exome Pilot Trio of Myself, Wife, and Son

Performing Small-N Sequencing Workflows: Approaches to Analyzing Trio NGS Data

Back to Basics: Using GWAS to Drive Discovery for Complex Diseases

New Study Identifies High-Risk Variants Associated with Autism Spectrum Disorders

Knowing Your NGS Downstream: Functional Predictions

Exploring DNA/RNA-Seq Analysis Results with Golden Helix GenomeBrowse and SVS

Examining the Genetic Underpinnings of Commonly Comorbid Language Disorders: Dyslexia and Language Impairment

Maximizing Public Data Sources for Sequencing and GWAS Studies

Population Structure & Genetic Improvement in Livestock

MM - KBAC: Using mixed models to adjust for population structure in a rare-variant burden test

GWAS in a model organism: Arabidopsis thaliana

Tips and Tricks for Genomic Analysis

A Walk Through GWAS