Article
STELLAR: A flexible ensemble learning framework integrating rare variants to enhance polygenic risk prediction
2026-06-09
Abstract excerpt
Whole-exome and whole-genome sequencing technology has enabled the discovery of rare genetic variants associated with human health and diseases. However, existing statistical methods used for rare variant association testing are not well-suited for building genetic risk prediction models that jointly incorporate rare and common variants. We propose STELLAR, a flexible ensemble learning-based approach to compute ra...
Topics
Open a Topic to create a Post that cites this publication.
Identifiers and source
- Literature Corpus work
- e6964336-badd-5637-8ad8-b253a7ade5ef
- DOI
- 10.64898/2026.06.07.26355109
