Analysis of simulated disease architecture with 180 causal 1Mbp loci yielding a true . In each locus, 1–10 causal variants were sampled from either low-frequency () of common (MAF) WTCCC2 SNPs. For ea
Additional file 3. DMS data. Contains all raw read counts, experimental scores, and the final imputed and refined data for each variant in each condition.
General Information Title: Fabry Disease: AI-Extracted Clinical Dataset from Published Case Reports Version: 1.0.0 Date of export: 2026-02-27 Created by: Silene Systems (AI-powered clinical data
