Additional file 2 of Insertion variants missing in the human reference genome are widespread among human populations
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Table S1. Sensitivity and false discovery rate of InserTag, ANISE, MindTheGap and PopIns on simulated data. Table S2. Validation of InserTag by fosmid-clone confirmed insertion variants. Table S3. Number of paired insertion-tags traced to target genomes. Table S4. Phenotype-associated SNPs with high linkage disequilibrium with non-reference insertion variants. Table S5. Ratio of high linkage disequilibrium between phenotype-associated SNPs and non-reference insertion variants. (XLSX 38.7 kb)
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2020-11-14
