bioRxiv / medRxiv
open access
A proteome atlas of structural variation and VNTR effects on complex traits and diseases
Structural variants (SVs), including variable number tandem repeats (VNTRs), are a major source of human genetic variation, but their impact on the proteome remains poorly characterized. Using a long-read assembly-based reference panel, we imputed 54,578 general SVs and 15,826 VNTRs in 54,306 UK Bio
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