PrecisionFDA
Truth Challenge
Engage and improve DNA test results with our community challenges
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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
58101-58150 / 86044 show all | |||||||||||||||
| gduggal-bwaplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 73.3800 | 60.1280 | 94.1249 | 85.4676 | 18327 | 12153 | 18328 | 1144 | 321 | 28.0594 | |
| ckim-isaac | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 74.3678 | 72.8507 | 75.9494 | 87.5981 | 161 | 60 | 180 | 57 | 16 | 28.0702 | |
| ckim-gatk | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | het | 99.5405 | 99.5949 | 99.4862 | 63.6798 | 11063 | 45 | 11037 | 57 | 16 | 28.0702 | |
| ciseli-custom | SNP | ti | map_l125_m0_e0 | * | 78.8823 | 74.4554 | 83.8690 | 80.0753 | 9502 | 3260 | 9499 | 1827 | 513 | 28.0788 | |
| hfeng-pmm1 | SNP | * | map_l125_m2_e0 | * | 99.4680 | 99.2509 | 99.6861 | 70.6559 | 46373 | 350 | 46367 | 146 | 41 | 28.0822 | |
| hfeng-pmm1 | SNP | ti | map_l125_m1_e0 | * | 99.4515 | 99.2091 | 99.6951 | 68.8149 | 29103 | 232 | 29099 | 89 | 25 | 28.0899 | |
| jli-custom | SNP | * | map_l100_m2_e0 | * | 99.4726 | 99.3267 | 99.6190 | 63.1033 | 73466 | 498 | 73463 | 281 | 79 | 28.1139 | |
| jli-custom | INDEL | * | map_l100_m2_e0 | het | 98.3050 | 98.0061 | 98.6057 | 84.0570 | 2261 | 46 | 2263 | 32 | 9 | 28.1250 | |
| jli-custom | INDEL | * | map_l100_m2_e1 | het | 98.3311 | 98.0367 | 98.6272 | 84.1536 | 2297 | 46 | 2299 | 32 | 9 | 28.1250 | |
| dgrover-gatk | SNP | ti | map_l250_m2_e1 | * | 98.6193 | 98.5028 | 98.7362 | 90.4249 | 5000 | 76 | 5000 | 64 | 18 | 28.1250 | |
| egarrison-hhga | INDEL | I6_15 | HG002complexvar | het | 96.7518 | 94.9894 | 98.5809 | 56.5929 | 2237 | 118 | 2223 | 32 | 9 | 28.1250 | |
| gduggal-bwafb | SNP | ti | map_l150_m2_e0 | het | 98.3596 | 98.4551 | 98.2644 | 79.4915 | 12682 | 199 | 12682 | 224 | 63 | 28.1250 | |
| eyeh-varpipe | SNP | ti | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 99.7221 | 99.9521 | 99.4931 | 42.7028 | 6265 | 3 | 6281 | 32 | 9 | 28.1250 | |
| gduggal-snapplat | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | het | 61.1186 | 54.5495 | 69.4865 | 69.7213 | 8597 | 7163 | 10095 | 4433 | 1247 | 28.1299 | |
| ltrigg-rtg1 | SNP | ti | map_l100_m2_e1 | * | 99.3168 | 98.8481 | 99.7899 | 59.0336 | 48915 | 570 | 48917 | 103 | 29 | 28.1553 | |
| anovak-vg | SNP | * | map_l150_m0_e0 | * | 77.8146 | 81.9066 | 74.1121 | 85.6738 | 9855 | 2177 | 9745 | 3404 | 959 | 28.1727 | |
| gduggal-bwaplat | SNP | ti | map_l125_m2_e0 | het | 80.5577 | 67.8375 | 99.1492 | 88.7803 | 12805 | 6071 | 12819 | 110 | 31 | 28.1818 | |
| egarrison-hhga | INDEL | * | map_l100_m0_e0 | * | 97.3109 | 97.1209 | 97.5016 | 98.2621 | 1518 | 45 | 1522 | 39 | 11 | 28.2051 | |
| raldana-dualsentieon | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 98.2637 | 96.9355 | 99.6289 | 78.1445 | 10470 | 331 | 10470 | 39 | 11 | 28.2051 | |
| anovak-vg | INDEL | I6_15 | map_siren | het | 45.1108 | 34.9650 | 63.5514 | 79.0607 | 50 | 93 | 68 | 39 | 11 | 28.2051 | |
| asubramanian-gatk | SNP | * | map_siren | het | 78.4554 | 64.6317 | 99.8014 | 73.5808 | 58809 | 32182 | 58800 | 117 | 33 | 28.2051 | |
| qzeng-custom | SNP | tv | HG002complexvar | het | 99.0228 | 98.2997 | 99.7567 | 23.1864 | 148171 | 2563 | 146790 | 358 | 101 | 28.2123 | |
| jlack-gatk | SNP | tv | HG002compoundhet | * | 99.3236 | 99.5965 | 99.0521 | 49.7619 | 8887 | 36 | 8882 | 85 | 24 | 28.2353 | |
| gduggal-bwafb | SNP | ti | map_l125_m2_e0 | * | 98.9368 | 98.8697 | 99.0039 | 73.9957 | 29916 | 342 | 29916 | 301 | 85 | 28.2392 | |
| gduggal-bwafb | SNP | ti | map_l125_m2_e1 | * | 98.9476 | 98.8812 | 99.0140 | 74.0560 | 30227 | 342 | 30227 | 301 | 85 | 28.2392 | |
| ciseli-custom | SNP | ti | map_siren | * | 90.7989 | 89.0429 | 92.6255 | 57.4504 | 89359 | 10996 | 89077 | 7092 | 2003 | 28.2431 | |
| hfeng-pmm1 | SNP | tv | map_l125_m0_e0 | * | 99.1084 | 98.9142 | 99.3035 | 75.2093 | 6559 | 72 | 6558 | 46 | 13 | 28.2609 | |
| gduggal-snapfb | INDEL | * | segdup | het | 92.4787 | 90.9277 | 94.0836 | 94.1056 | 1333 | 133 | 1463 | 92 | 26 | 28.2609 | |
| bgallagher-sentieon | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 99.5462 | 99.5186 | 99.5739 | 79.3195 | 10749 | 52 | 10749 | 46 | 13 | 28.2609 | |
| hfeng-pmm1 | SNP | * | map_l125_m1_e0 | * | 99.4583 | 99.2389 | 99.6786 | 68.9911 | 44982 | 345 | 44976 | 145 | 41 | 28.2759 | |
| jpowers-varprowl | SNP | ti | map_l250_m2_e1 | het | 94.1266 | 94.2407 | 94.0127 | 92.2458 | 3109 | 190 | 3109 | 198 | 56 | 28.2828 | |
| gduggal-bwaplat | SNP | ti | map_l125_m1_e0 | het | 79.9258 | 66.9495 | 99.1416 | 88.1040 | 12229 | 6037 | 12243 | 106 | 30 | 28.3019 | |
| anovak-vg | INDEL | * | map_l100_m2_e1 | het | 70.6838 | 66.8374 | 75.0000 | 86.9385 | 1566 | 777 | 1653 | 551 | 156 | 28.3122 | |
| gduggal-bwafb | SNP | ti | map_l150_m2_e1 | het | 98.3690 | 98.4710 | 98.2671 | 79.5893 | 12816 | 199 | 12816 | 226 | 64 | 28.3186 | |
| ghariani-varprowl | INDEL | * | map_l150_m2_e0 | het | 90.1781 | 97.7925 | 83.6638 | 93.5954 | 886 | 20 | 886 | 173 | 49 | 28.3237 | |
| ghariani-varprowl | INDEL | D1_5 | map_l100_m2_e1 | * | 91.5085 | 94.4817 | 88.7167 | 87.2602 | 1832 | 107 | 1832 | 233 | 66 | 28.3262 | |
| gduggal-bwaplat | SNP | tv | lowcmp_SimpleRepeat_diTR_11to50 | * | 84.3374 | 74.7117 | 96.8102 | 79.6075 | 3628 | 1228 | 3642 | 120 | 34 | 28.3333 | |
| ciseli-custom | INDEL | C1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 0.0000 | 0.0000 | 20.2658 | 93.8269 | 0 | 0 | 61 | 240 | 68 | 28.3333 | |
| ciseli-custom | INDEL | C1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 0.0000 | 0.0000 | 20.2658 | 93.8269 | 0 | 0 | 61 | 240 | 68 | 28.3333 | |
| hfeng-pmm1 | SNP | tv | map_l100_m2_e0 | * | 99.6119 | 99.4647 | 99.7596 | 65.8235 | 24899 | 134 | 24895 | 60 | 17 | 28.3333 | |
| anovak-vg | INDEL | * | map_l100_m2_e0 | het | 70.9065 | 67.2735 | 74.9542 | 86.8513 | 1552 | 755 | 1637 | 547 | 155 | 28.3364 | |
| jpowers-varprowl | SNP | * | map_l100_m1_e0 | * | 98.0599 | 97.7308 | 98.3912 | 69.8054 | 70760 | 1643 | 70762 | 1157 | 328 | 28.3492 | |
| gduggal-bwavard | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 85.0584 | 88.4799 | 81.8917 | 87.8767 | 2404 | 313 | 2329 | 515 | 146 | 28.3495 | |
| gduggal-snapplat | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 57.2793 | 53.5509 | 61.5656 | 80.5733 | 7367 | 6390 | 10114 | 6314 | 1790 | 28.3497 | |
| gduggal-snapplat | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 57.2793 | 53.5509 | 61.5656 | 80.5733 | 7367 | 6390 | 10114 | 6314 | 1790 | 28.3497 | |
| jli-custom | SNP | tv | map_l150_m1_e0 | het | 98.7145 | 98.4020 | 99.0291 | 72.7212 | 6835 | 111 | 6834 | 67 | 19 | 28.3582 | |
| ciseli-custom | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 91.8329 | 98.7645 | 85.8105 | 79.7572 | 5356 | 67 | 5352 | 885 | 251 | 28.3616 | |
| ciseli-custom | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 91.8329 | 98.7645 | 85.8105 | 79.7572 | 5356 | 67 | 5352 | 885 | 251 | 28.3616 | |
| ghariani-varprowl | INDEL | D1_5 | map_l100_m2_e0 | * | 91.5803 | 94.5692 | 88.7745 | 87.1803 | 1811 | 104 | 1811 | 229 | 65 | 28.3843 | |
| anovak-vg | SNP | tv | map_l125_m0_e0 | het | 76.8817 | 88.8434 | 67.7587 | 83.1340 | 3910 | 491 | 3909 | 1860 | 528 | 28.3871 | |