7 research outputs found
Additional file 2: of Identification of missing variants by combining multiple analytic pipelines
Table S2. The composition of Tier 1, 2 and 3 variants in BWA-unique, Novo-unique and shared variants. (DOCX 13 kb
Additional file 3: of Identification of missing variants by combining multiple analytic pipelines
Table S3. The percentage of known and novel variants in BWA-unique, Novo-unique and shared variants. (DOCX 13 kb
Additional file 4: of Identification of missing variants by combining multiple analytic pipelines
Table S4. The genomic location and GC content of multi-unique, single-unique and shared variants. (DOCX 14 kb
Additional file 1: of Identification of missing variants by combining multiple analytic pipelines
Table S1. The genomic location and GC content of BWA-unique, Novo-unique and shared variants. (DOCX 14 kb
Additional file 7: of Identification of missing variants by combining multiple analytic pipelines
Table S7. The full list of variants identified in APP, PSEN1 and PSEN2 by each workflow. (XLSX 14 kb
Additional file 5: of Identification of missing variants by combining multiple analytic pipelines
Table S5. The composition of Tier 1, 2 and 3 variants in multi-unique, single-unique and shared variants. (DOCX 14 kb
Additional file 6: of Identification of missing variants by combining multiple analytic pipelines
Table S6. The percentage of known and novel variants in multi-unique, single-unique and shared variants. (DOCX 13 kb