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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
61551-61600 / 86044 show all | |||||||||||||||
| jlack-gatk | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | het | 99.1117 | 98.9729 | 99.2509 | 77.5593 | 1349 | 14 | 1325 | 10 | 5 | 50.0000 | |
| jlack-gatk | INDEL | I1_5 | map_l250_m1_e0 | het | 88.8889 | 93.3333 | 84.8485 | 97.8138 | 56 | 4 | 56 | 10 | 0 | 0.0000 | |
| jlack-gatk | INDEL | I1_5 | map_l250_m2_e0 | het | 89.8551 | 93.9394 | 86.1111 | 97.9417 | 62 | 4 | 62 | 10 | 0 | 0.0000 | |
| jlack-gatk | INDEL | I1_5 | map_l250_m2_e1 | het | 89.8551 | 93.9394 | 86.1111 | 98.0083 | 62 | 4 | 62 | 10 | 0 | 0.0000 | |
| jlack-gatk | INDEL | I6_15 | map_l100_m1_e0 | * | 92.6407 | 93.8596 | 91.4530 | 88.9934 | 107 | 7 | 107 | 10 | 0 | 0.0000 | |
| jlack-gatk | INDEL | I6_15 | map_l100_m2_e0 | * | 92.7660 | 93.9655 | 91.5966 | 89.8029 | 109 | 7 | 109 | 10 | 0 | 0.0000 | |
| jlack-gatk | INDEL | I6_15 | map_l100_m2_e1 | * | 92.7660 | 93.9655 | 91.5966 | 90.0502 | 109 | 7 | 109 | 10 | 0 | 0.0000 | |
| jlack-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 96.1992 | 95.0777 | 97.3475 | 90.9113 | 367 | 19 | 367 | 10 | 7 | 70.0000 | |
| jlack-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 96.1887 | 96.0145 | 96.3636 | 90.8638 | 265 | 11 | 265 | 10 | 7 | 70.0000 | |
| jlack-gatk | SNP | * | segdup | homalt | 99.8743 | 99.8418 | 99.9069 | 88.3916 | 10726 | 17 | 10726 | 10 | 10 | 100.0000 | |
| jlack-gatk | SNP | ti | * | hetalt | 98.8034 | 99.3127 | 98.2993 | 52.8846 | 578 | 4 | 578 | 10 | 10 | 100.0000 | |
| jlack-gatk | SNP | tv | HG002compoundhet | homalt | 99.7638 | 99.8229 | 99.7048 | 42.2900 | 3382 | 6 | 3377 | 10 | 9 | 90.0000 | |
| jli-custom | INDEL | * | map_l100_m1_e0 | homalt | 99.1850 | 99.1850 | 99.1850 | 82.2765 | 1217 | 10 | 1217 | 10 | 6 | 60.0000 | |
| jli-custom | INDEL | * | map_l150_m0_e0 | het | 97.0674 | 97.0674 | 97.0674 | 91.5678 | 331 | 10 | 331 | 10 | 1 | 10.0000 | |
| hfeng-pmm2 | SNP | * | map_l250_m0_e0 | homalt | 98.8924 | 99.3641 | 98.4252 | 92.6877 | 625 | 4 | 625 | 10 | 5 | 50.0000 | |
| hfeng-pmm2 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 97.9622 | 96.2373 | 99.7500 | 82.0192 | 3990 | 156 | 3990 | 10 | 3 | 30.0000 | |
| hfeng-pmm2 | SNP | tv | map_l150_m0_e0 | homalt | 99.5118 | 99.7741 | 99.2509 | 78.3981 | 1325 | 3 | 1325 | 10 | 3 | 30.0000 | |
| hfeng-pmm3 | INDEL | * | lowcmp_SimpleRepeat_triTR_11to50 | het | 99.2169 | 98.7151 | 99.7238 | 50.1102 | 3611 | 47 | 3611 | 10 | 4 | 40.0000 | |
| hfeng-pmm3 | INDEL | * | map_l100_m2_e0 | homalt | 99.2469 | 99.2863 | 99.2076 | 82.1525 | 1252 | 9 | 1252 | 10 | 4 | 40.0000 | |
| hfeng-pmm3 | INDEL | * | map_l100_m2_e1 | homalt | 99.2587 | 99.2974 | 99.2200 | 82.2364 | 1272 | 9 | 1272 | 10 | 4 | 40.0000 | |
| hfeng-pmm1 | INDEL | * | map_l250_m1_e0 | * | 95.6954 | 94.7541 | 96.6555 | 94.7800 | 289 | 16 | 289 | 10 | 3 | 30.0000 | |
| hfeng-pmm1 | INDEL | * | map_l250_m2_e0 | * | 96.0366 | 95.1662 | 96.9231 | 95.1304 | 315 | 16 | 315 | 10 | 3 | 30.0000 | |
| hfeng-pmm1 | INDEL | * | map_l250_m2_e1 | * | 96.0606 | 95.1952 | 96.9419 | 95.2325 | 317 | 16 | 317 | 10 | 3 | 30.0000 | |
| hfeng-pmm1 | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 99.4714 | 99.0316 | 99.9151 | 48.2190 | 11760 | 115 | 11765 | 10 | 7 | 70.0000 | |
| hfeng-pmm1 | INDEL | D1_5 | map_l100_m1_e0 | het | 98.0780 | 97.0223 | 99.1568 | 79.7611 | 1173 | 36 | 1176 | 10 | 0 | 0.0000 | |
| hfeng-pmm1 | INDEL | D1_5 | map_l100_m2_e0 | het | 98.1096 | 97.0541 | 99.1883 | 80.7169 | 1219 | 37 | 1222 | 10 | 0 | 0.0000 | |
| hfeng-pmm1 | INDEL | D1_5 | map_l100_m2_e1 | het | 98.1277 | 97.0820 | 99.1961 | 80.8880 | 1231 | 37 | 1234 | 10 | 0 | 0.0000 | |
| hfeng-pmm1 | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 94.9244 | 92.1529 | 97.8678 | 75.1983 | 458 | 39 | 459 | 10 | 6 | 60.0000 | |
| hfeng-pmm2 | INDEL | D16_PLUS | HG002compoundhet | homalt | 61.5385 | 100.0000 | 44.4444 | 70.4918 | 8 | 0 | 8 | 10 | 10 | 100.0000 | |
| hfeng-pmm2 | INDEL | D16_PLUS | map_l100_m2_e0 | het | 88.0766 | 95.8333 | 81.4815 | 95.2590 | 46 | 2 | 44 | 10 | 3 | 30.0000 | |
| hfeng-pmm2 | INDEL | D16_PLUS | map_l100_m2_e1 | het | 88.7476 | 96.0784 | 82.4561 | 95.1199 | 49 | 2 | 47 | 10 | 3 | 30.0000 | |
| hfeng-pmm2 | INDEL | D16_PLUS | map_siren | het | 91.1204 | 94.8718 | 87.6543 | 94.8375 | 74 | 4 | 71 | 10 | 1 | 10.0000 | |
| hfeng-pmm2 | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_51to200 | het | 81.1947 | 74.8148 | 88.7640 | 73.9003 | 101 | 34 | 79 | 10 | 8 | 80.0000 | |
| hfeng-pmm2 | INDEL | D1_5 | map_l250_m1_e0 | * | 96.8661 | 99.4152 | 94.4444 | 95.1987 | 170 | 1 | 170 | 10 | 1 | 10.0000 | |
| hfeng-pmm2 | INDEL | D1_5 | map_l250_m1_e0 | het | 95.6897 | 100.0000 | 91.7355 | 95.6159 | 111 | 0 | 111 | 10 | 1 | 10.0000 | |
| hfeng-pmm2 | INDEL | D6_15 | HG002complexvar | homalt | 99.4885 | 99.8289 | 99.1504 | 61.5359 | 1167 | 2 | 1167 | 10 | 9 | 90.0000 | |
| hfeng-pmm2 | INDEL | I16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 96.0630 | 100.0000 | 92.4242 | 86.0759 | 122 | 0 | 122 | 10 | 10 | 100.0000 | |
| hfeng-pmm2 | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 94.5968 | 91.5493 | 97.8541 | 75.8173 | 455 | 42 | 456 | 10 | 7 | 70.0000 | |
| hfeng-pmm2 | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 91.1243 | 93.9024 | 88.5057 | 75.9669 | 77 | 5 | 77 | 10 | 10 | 100.0000 | |
| hfeng-pmm2 | INDEL | I1_5 | map_l100_m0_e0 | * | 98.6285 | 99.0792 | 98.1818 | 85.0543 | 538 | 5 | 540 | 10 | 3 | 30.0000 | |
| hfeng-pmm2 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 99.8615 | 99.7820 | 99.9410 | 72.3104 | 16938 | 37 | 16938 | 10 | 6 | 60.0000 | |
| hfeng-pmm2 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 99.8615 | 99.7820 | 99.9410 | 72.3104 | 16938 | 37 | 16938 | 10 | 6 | 60.0000 | |
| raldana-dualsentieon | SNP | * | lowcmp_SimpleRepeat_triTR_11to50 | het | 99.3909 | 99.0035 | 99.7815 | 31.9351 | 4570 | 46 | 4566 | 10 | 2 | 20.0000 | |
| raldana-dualsentieon | SNP | * | map_l125_m0_e0 | homalt | 99.6192 | 99.3892 | 99.8503 | 65.6627 | 6671 | 41 | 6671 | 10 | 7 | 70.0000 | |
| raldana-dualsentieon | SNP | tv | func_cds | * | 99.8743 | 99.9771 | 99.7716 | 27.8940 | 4370 | 1 | 4369 | 10 | 0 | 0.0000 | |
| raldana-dualsentieon | SNP | tv | func_cds | het | 99.7933 | 99.9624 | 99.6248 | 29.8500 | 2656 | 1 | 2655 | 10 | 0 | 0.0000 | |
| raldana-dualsentieon | SNP | tv | lowcmp_SimpleRepeat_diTR_11to50 | * | 98.6778 | 97.5906 | 99.7894 | 64.3361 | 4739 | 117 | 4739 | 10 | 8 | 80.0000 | |
| rpoplin-dv42 | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | homalt | 97.5510 | 97.1545 | 97.9508 | 60.7085 | 478 | 14 | 478 | 10 | 7 | 70.0000 | |
| rpoplin-dv42 | INDEL | * | map_l250_m1_e0 | * | 96.0396 | 95.4098 | 96.6777 | 99.6478 | 291 | 14 | 291 | 10 | 5 | 50.0000 | |
| rpoplin-dv42 | INDEL | * | map_l250_m2_e0 | * | 96.3526 | 95.7704 | 96.9419 | 99.6591 | 317 | 14 | 317 | 10 | 5 | 50.0000 | |