Open access
Sep 2026
The spectrum of copy number variation in the Pan-Canadian HostSeq databank
The integration of copy number variant (CNV) workflows into genome sequencing (GS) analysis pipelines allows for the identification of CNVs implicated in disease. Here, we generated a novel resource of CNVs identified in the HostSeq population cohort from Canada, identified the prevalence of recurrent CNVs associated w...
Navneet Aujla, B. Thiruvahindrapuram, S. Casalino et al.
· PLoS ONE · 0 citations