Britt Drogemoller

@brittdrog.bsky.social

🇿🇦🇨🇦 Assistant Professor | Canada Research Chair in Pharmacogenomics & Precision Medicine My lab is using single cell technologies and computational biology to understand the genetics of hearing loss & dementia

What do GWAS and rare variant burden tests discover, and why? Do these studies find the most IMPORTANT genes? If not, how DO they rank genes? Here we present a surprising result: these studies actually test for SPECIFICITY! A 🧵on what this means... (🧪🧬) www.biorxiv.org/content/10.1...

Specificity, length, and luck: How genes are prioritized by rare and common variant association studies

Standard genome-wide association studies (GWAS) and rare variant burden tests are essential tools for identifying trait-relevant genes. Although these methods are conceptually similar, we show by anal...

biorxiv.org

Hello! We are the Pediatric Research in Oncology in #Manitoba: Innovation, Science, Excellence (PROMISE) theme, a dedicated research group established through the Children's Hospital Research Institute of Manitoba (CHRIM) and CancerCare Manitoba (CCMB).