PrecisionFDA
Truth Challenge
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Explore HG002 comparison results
Use this interactive explorer to filter all results across submission entries and multiple dimensions.
| Entry | Type | Subtype | Subset | Genotype | F-score | Recall | Precision | Frac_NA | Truth TP | Truth FN | Query TP | Query FP | FP gt | % FP ma | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
20251-20300 / 86044 show all | |||||||||||||||
| hfeng-pmm3 | SNP | ti | HG002compoundhet | * | 98.2879 | 96.7330 | 99.8937 | 34.5867 | 16907 | 571 | 16909 | 18 | 8 | 44.4444 | |
| hfeng-pmm3 | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 99.2432 | 98.7413 | 99.7502 | 68.4984 | 30751 | 392 | 30752 | 77 | 8 | 10.3896 | |
| hfeng-pmm3 | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 99.2432 | 98.7413 | 99.7502 | 68.4984 | 30751 | 392 | 30752 | 77 | 8 | 10.3896 | |
| hfeng-pmm3 | SNP | ti | map_l125_m1_e0 | het | 99.4436 | 99.3211 | 99.5663 | 71.0299 | 18142 | 124 | 18138 | 79 | 8 | 10.1266 | |
| hfeng-pmm3 | SNP | ti | map_l125_m1_e0 | homalt | 99.8144 | 99.7918 | 99.8370 | 66.0308 | 11022 | 23 | 11022 | 18 | 8 | 44.4444 | |
| hfeng-pmm3 | SNP | ti | map_l125_m2_e0 | het | 99.4510 | 99.3325 | 99.5698 | 72.2770 | 18750 | 126 | 18746 | 81 | 8 | 9.8765 | |
| hfeng-pmm3 | SNP | ti | map_l125_m2_e0 | homalt | 99.8195 | 99.7975 | 99.8415 | 68.5286 | 11335 | 23 | 11335 | 18 | 8 | 44.4444 | |
| hfeng-pmm3 | SNP | ti | map_l125_m2_e1 | het | 99.4518 | 99.3346 | 99.5693 | 72.3168 | 18960 | 127 | 18956 | 82 | 8 | 9.7561 | |
| hfeng-pmm3 | SNP | ti | map_l125_m2_e1 | homalt | 99.8210 | 99.7993 | 99.8428 | 68.5547 | 11435 | 23 | 11435 | 18 | 8 | 44.4444 | |
| hfeng-pmm3 | SNP | ti | map_l150_m1_e0 | het | 99.3161 | 99.2158 | 99.4166 | 75.5923 | 12273 | 97 | 12269 | 72 | 8 | 11.1111 | |
| hfeng-pmm3 | SNP | ti | map_l150_m2_e0 | het | 99.3316 | 99.2392 | 99.4243 | 76.7413 | 12783 | 98 | 12779 | 74 | 8 | 10.8108 | |
| hfeng-pmm3 | SNP | ti | map_l150_m2_e1 | het | 99.3308 | 99.2393 | 99.4225 | 76.8259 | 12916 | 99 | 12912 | 75 | 8 | 10.6667 | |
| hfeng-pmm3 | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 99.4756 | 99.0317 | 99.9234 | 63.0172 | 27410 | 268 | 27401 | 21 | 8 | 38.0952 | |
| hfeng-pmm3 | SNP | tv | map_l100_m0_e0 | * | 99.4268 | 99.3775 | 99.4762 | 69.0933 | 11015 | 69 | 11014 | 58 | 8 | 13.7931 | |
| hfeng-pmm1 | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 99.2017 | 98.7689 | 99.6382 | 66.9061 | 3851 | 48 | 3856 | 14 | 8 | 57.1429 | |
| hfeng-pmm1 | INDEL | I6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 91.9355 | 96.6102 | 87.6923 | 75.7463 | 57 | 2 | 57 | 8 | 8 | 100.0000 | |
| hfeng-pmm1 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 97.8839 | 96.6007 | 99.2017 | 74.1149 | 1904 | 67 | 1864 | 15 | 8 | 53.3333 | |
| hfeng-pmm1 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 97.0946 | 96.0916 | 98.1187 | 71.9562 | 713 | 29 | 678 | 13 | 8 | 61.5385 | |
| hfeng-pmm1 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 97.1748 | 95.9660 | 98.4145 | 72.9224 | 904 | 38 | 869 | 14 | 8 | 57.1429 | |
| hfeng-pmm1 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 97.8839 | 96.6007 | 99.2017 | 74.1149 | 1904 | 67 | 1864 | 15 | 8 | 53.3333 | |
| hfeng-pmm1 | SNP | ti | HG002compoundhet | * | 98.2873 | 96.6987 | 99.9291 | 34.1329 | 16901 | 577 | 16902 | 12 | 8 | 66.6667 | |
| hfeng-pmm1 | SNP | ti | map_l150_m0_e0 | het | 98.8393 | 98.5874 | 99.0925 | 80.9472 | 5025 | 72 | 5023 | 46 | 8 | 17.3913 | |
| hfeng-pmm1 | SNP | ti | map_l250_m1_e0 | het | 98.6671 | 98.5175 | 98.8172 | 88.8014 | 2924 | 44 | 2924 | 35 | 8 | 22.8571 | |
| hfeng-pmm1 | SNP | ti | map_l250_m2_e0 | het | 98.7844 | 98.6478 | 98.9214 | 88.9993 | 3210 | 44 | 3210 | 35 | 8 | 22.8571 | |
| hfeng-pmm1 | SNP | ti | map_l250_m2_e1 | het | 98.7703 | 98.6056 | 98.9355 | 89.0938 | 3253 | 46 | 3253 | 35 | 8 | 22.8571 | |
| hfeng-pmm1 | SNP | tv | map_siren | homalt | 99.8956 | 99.8898 | 99.9014 | 56.0205 | 17221 | 19 | 17219 | 17 | 8 | 47.0588 | |
| hfeng-pmm2 | INDEL | * | map_l100_m0_e0 | * | 97.7482 | 98.4645 | 97.0422 | 86.4304 | 1539 | 24 | 1542 | 47 | 8 | 17.0213 | |
| hfeng-pmm2 | SNP | * | map_l150_m0_e0 | homalt | 99.5726 | 99.7065 | 99.4390 | 76.7349 | 4077 | 12 | 4077 | 23 | 8 | 34.7826 | |
| hfeng-pmm2 | SNP | ti | map_l150_m0_e0 | het | 98.5736 | 98.9994 | 98.1514 | 83.2987 | 5046 | 51 | 5044 | 95 | 8 | 8.4211 | |
| hfeng-pmm2 | SNP | tv | HG002complexvar | het | 99.7540 | 99.5389 | 99.9700 | 20.7785 | 150036 | 695 | 149957 | 45 | 8 | 17.7778 | |
| hfeng-pmm3 | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_51to200 | * | 96.9392 | 95.2922 | 98.6441 | 64.3073 | 587 | 29 | 582 | 8 | 8 | 100.0000 | |
| hfeng-pmm3 | INDEL | D1_5 | HG002complexvar | homalt | 99.8962 | 99.8773 | 99.9151 | 58.2388 | 10585 | 13 | 10590 | 9 | 8 | 88.8889 | |
| hfeng-pmm2 | SNP | ti | HG002complexvar | het | 99.8373 | 99.6928 | 99.9822 | 16.6591 | 313799 | 967 | 313749 | 56 | 7 | 12.5000 | |
| hfeng-pmm2 | SNP | ti | HG002compoundhet | * | 98.2110 | 96.5843 | 99.8935 | 34.1246 | 16881 | 597 | 16883 | 18 | 7 | 38.8889 | |
| hfeng-pmm2 | SNP | ti | map_l100_m0_e0 | homalt | 99.7813 | 99.7685 | 99.7941 | 63.0398 | 7756 | 18 | 7756 | 16 | 7 | 43.7500 | |
| hfeng-pmm2 | SNP | ti | map_l150_m1_e0 | homalt | 99.7953 | 99.8089 | 99.7817 | 70.9972 | 7313 | 14 | 7313 | 16 | 7 | 43.7500 | |
| hfeng-pmm2 | SNP | ti | map_l150_m2_e0 | homalt | 99.8031 | 99.8162 | 99.7900 | 73.1902 | 7602 | 14 | 7602 | 16 | 7 | 43.7500 | |
| hfeng-pmm2 | SNP | ti | map_l150_m2_e1 | homalt | 99.8050 | 99.8180 | 99.7921 | 73.2339 | 7679 | 14 | 7679 | 16 | 7 | 43.7500 | |
| hfeng-pmm2 | SNP | ti | map_l250_m1_e0 | het | 98.2909 | 98.8208 | 97.7667 | 90.5159 | 2933 | 35 | 2933 | 67 | 7 | 10.4478 | |
| hfeng-pmm2 | SNP | ti | map_l250_m2_e0 | het | 98.4404 | 98.9244 | 97.9610 | 90.8174 | 3219 | 35 | 3219 | 67 | 7 | 10.4478 | |
| hfeng-pmm2 | SNP | ti | map_l250_m2_e1 | het | 98.4165 | 98.9088 | 97.9292 | 90.8817 | 3263 | 36 | 3263 | 69 | 7 | 10.1449 | |
| hfeng-pmm2 | SNP | tv | HG002compoundhet | * | 96.9561 | 94.2396 | 99.8337 | 46.6519 | 8409 | 514 | 8407 | 14 | 7 | 50.0000 | |
| hfeng-pmm2 | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 99.3792 | 98.9089 | 99.8541 | 63.0972 | 27376 | 302 | 27367 | 40 | 7 | 17.5000 | |
| hfeng-pmm2 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.8596 | 98.1676 | 99.5615 | 75.0651 | 14304 | 267 | 14304 | 63 | 7 | 11.1111 | |
| hfeng-pmm2 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.8596 | 98.1676 | 99.5615 | 75.0651 | 14304 | 267 | 14304 | 63 | 7 | 11.1111 | |
| hfeng-pmm2 | SNP | tv | map_l250_m2_e0 | * | 98.3016 | 98.4039 | 98.1994 | 89.7037 | 2836 | 46 | 2836 | 52 | 7 | 13.4615 | |
| hfeng-pmm2 | SNP | tv | map_l250_m2_e1 | * | 98.3213 | 98.4225 | 98.2204 | 89.7650 | 2870 | 46 | 2870 | 52 | 7 | 13.4615 | |
| hfeng-pmm3 | INDEL | * | HG002complexvar | hetalt | 97.4347 | 95.2149 | 99.7604 | 68.3328 | 3522 | 177 | 3748 | 9 | 7 | 77.7778 | |
| hfeng-pmm3 | INDEL | D16_PLUS | HG002complexvar | het | 96.3171 | 94.3089 | 98.4127 | 66.5304 | 1044 | 63 | 806 | 13 | 7 | 53.8462 | |
| hfeng-pmm1 | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 99.4714 | 99.0316 | 99.9151 | 48.2190 | 11760 | 115 | 11765 | 10 | 7 | 70.0000 | |