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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
76701-76750 / 86044 show all | |||||||||||||||
| ciseli-custom | SNP | ti | map_l250_m0_e0 | * | 69.6954 | 66.4234 | 73.3065 | 95.3499 | 910 | 460 | 909 | 331 | 59 | 17.8248 | |
| ciseli-custom | INDEL | D1_5 | map_l125_m2_e0 | homalt | 81.6849 | 82.4176 | 80.9651 | 86.8337 | 300 | 64 | 302 | 71 | 59 | 83.0986 | |
| ciseli-custom | INDEL | D1_5 | map_l125_m2_e1 | homalt | 81.9169 | 82.5269 | 81.3158 | 86.8147 | 307 | 65 | 309 | 71 | 59 | 83.0986 | |
| ciseli-custom | INDEL | D1_5 | segdup | homalt | 89.2779 | 95.5432 | 83.7838 | 94.1865 | 343 | 16 | 341 | 66 | 59 | 89.3939 | |
| ciseli-custom | INDEL | * | map_l150_m2_e0 | homalt | 63.4799 | 54.2620 | 76.4706 | 91.7215 | 261 | 220 | 260 | 80 | 59 | 73.7500 | |
| ciseli-custom | INDEL | * | map_l150_m2_e1 | homalt | 63.5484 | 54.2683 | 76.6571 | 91.7065 | 267 | 225 | 266 | 81 | 59 | 72.8395 | |
| ckim-dragen | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 97.2525 | 95.3621 | 99.2194 | 61.6689 | 8019 | 390 | 8008 | 63 | 59 | 93.6508 | |
| gduggal-snapplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 42.2807 | 34.7724 | 53.9244 | 82.6368 | 1780 | 3339 | 2068 | 1767 | 59 | 3.3390 | |
| gduggal-snapvard | SNP | tv | map_l125_m0_e0 | het | 85.9375 | 96.6599 | 77.3564 | 84.6449 | 4254 | 147 | 4243 | 1242 | 59 | 4.7504 | |
| gduggal-snapfb | INDEL | D6_15 | HG002compoundhet | hetalt | 76.8495 | 65.2926 | 93.3775 | 40.5512 | 5322 | 2829 | 846 | 60 | 59 | 98.3333 | |
| gduggal-snapplat | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 92.9747 | 88.1319 | 98.3807 | 75.7191 | 10181 | 1371 | 10207 | 168 | 59 | 35.1190 | |
| gduggal-snapplat | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 92.9747 | 88.1319 | 98.3807 | 75.7191 | 10181 | 1371 | 10207 | 168 | 59 | 35.1190 | |
| gduggal-snapplat | SNP | tv | lowcmp_SimpleRepeat_diTR_11to50 | het | 75.8773 | 72.5712 | 79.4989 | 87.1649 | 2241 | 847 | 2253 | 581 | 59 | 10.1549 | |
| gduggal-snapvard | INDEL | D6_15 | map_l100_m2_e1 | * | 65.5947 | 59.6364 | 72.8758 | 83.1683 | 164 | 111 | 223 | 83 | 59 | 71.0843 | |
| ghariani-varprowl | SNP | * | lowcmp_SimpleRepeat_homopolymer_6to10 | homalt | 98.9200 | 99.9179 | 97.9418 | 56.8515 | 6083 | 5 | 6091 | 128 | 59 | 46.0938 | |
| hfeng-pmm2 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.1021 | 96.7944 | 99.4457 | 64.3875 | 13316 | 441 | 13275 | 74 | 59 | 79.7297 | |
| hfeng-pmm2 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.1021 | 96.7944 | 99.4457 | 64.3875 | 13316 | 441 | 13275 | 74 | 59 | 79.7297 | |
| hfeng-pmm2 | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | het | 95.8010 | 94.0359 | 97.6336 | 60.3151 | 2570 | 163 | 2558 | 62 | 59 | 95.1613 | |
| hfeng-pmm2 | SNP | * | HG002complexvar | * | 99.8743 | 99.7689 | 99.9799 | 18.8346 | 752638 | 1743 | 752495 | 151 | 59 | 39.0728 | |
| jlack-gatk | SNP | tv | map_l150_m1_e0 | het | 91.9297 | 98.8339 | 85.9271 | 86.1869 | 6865 | 81 | 6863 | 1124 | 59 | 5.2491 | |
| jlack-gatk | SNP | tv | map_l150_m2_e0 | het | 92.1348 | 98.8831 | 86.2488 | 87.0469 | 7171 | 81 | 7169 | 1143 | 59 | 5.1619 | |
| jlack-gatk | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 96.2215 | 96.1718 | 96.2714 | 63.1699 | 1859 | 74 | 1859 | 72 | 59 | 81.9444 | |
| hfeng-pmm1 | INDEL | D16_PLUS | HG002compoundhet | het | 84.9405 | 90.3704 | 80.1262 | 57.0461 | 366 | 39 | 254 | 63 | 59 | 93.6508 | |
| hfeng-pmm1 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 96.5000 | 95.0156 | 98.0316 | 58.6414 | 3050 | 160 | 3038 | 61 | 59 | 96.7213 | |
| hfeng-pmm1 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 96.9690 | 95.8766 | 98.0866 | 62.3435 | 3139 | 135 | 3127 | 61 | 59 | 96.7213 | |
| hfeng-pmm1 | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | het | 96.0142 | 94.4383 | 97.6435 | 60.1906 | 2581 | 152 | 2569 | 62 | 59 | 95.1613 | |
| hfeng-pmm1 | INDEL | I16_PLUS | * | * | 97.6402 | 96.6756 | 98.6242 | 68.7700 | 6165 | 212 | 6165 | 86 | 59 | 68.6047 | |
| raldana-dualsentieon | INDEL | D16_PLUS | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 90.7009 | 93.6842 | 87.9017 | 84.8598 | 623 | 42 | 465 | 64 | 59 | 92.1875 | |
| raldana-dualsentieon | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_51to200 | * | 78.0920 | 69.5839 | 88.9706 | 48.6792 | 485 | 212 | 484 | 60 | 59 | 98.3333 | |
| rpoplin-dv42 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 96.5348 | 93.8046 | 99.4286 | 27.8282 | 10417 | 688 | 10441 | 60 | 59 | 98.3333 | |
| rpoplin-dv42 | INDEL | D1_5 | * | hetalt | 96.7748 | 94.2997 | 99.3834 | 61.0557 | 9661 | 584 | 9671 | 60 | 59 | 98.3333 | |
| rpoplin-dv42 | SNP | tv | map_l100_m1_e0 | het | 99.1180 | 99.1503 | 99.0858 | 64.8238 | 15286 | 131 | 15282 | 141 | 59 | 41.8440 | |
| rpoplin-dv42 | SNP | tv | map_l100_m2_e0 | het | 99.1350 | 99.1697 | 99.1004 | 66.6194 | 15646 | 131 | 15642 | 142 | 59 | 41.5493 | |
| rpoplin-dv42 | SNP | tv | map_l100_m2_e1 | het | 99.1406 | 99.1781 | 99.1032 | 66.6722 | 15807 | 131 | 15803 | 143 | 59 | 41.2587 | |
| rpoplin-dv42 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 98.5109 | 97.6402 | 99.3972 | 56.5597 | 11213 | 271 | 11213 | 68 | 60 | 88.2353 | |
| raldana-dualsentieon | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 95.6298 | 98.9362 | 92.5373 | 61.3647 | 744 | 8 | 744 | 60 | 60 | 100.0000 | |
| rpoplin-dv42 | INDEL | I16_PLUS | HG002compoundhet | het | 36.6885 | 59.5745 | 26.5060 | 84.0077 | 28 | 19 | 22 | 61 | 60 | 98.3607 | |
| qzeng-custom | SNP | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 98.7057 | 99.2433 | 98.1739 | 67.8653 | 35151 | 268 | 35268 | 656 | 60 | 9.1463 | |
| qzeng-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 94.7046 | 97.0188 | 92.4983 | 89.7173 | 2636 | 81 | 2762 | 224 | 60 | 26.7857 | |
| qzeng-custom | SNP | tv | map_l100_m1_e0 | homalt | 87.4842 | 78.2705 | 99.1566 | 59.7237 | 7078 | 1965 | 7054 | 60 | 60 | 100.0000 | |
| qzeng-custom | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 88.7617 | 87.5000 | 90.0602 | 60.8952 | 252 | 36 | 598 | 66 | 60 | 90.9091 | |
| qzeng-custom | INDEL | I6_15 | HG002complexvar | het | 94.4892 | 95.7962 | 93.2173 | 56.1507 | 2256 | 99 | 2625 | 191 | 60 | 31.4136 | |
| ndellapenna-hhga | SNP | ti | map_siren | * | 99.5376 | 99.2028 | 99.8746 | 51.9628 | 99555 | 800 | 99557 | 125 | 60 | 48.0000 | |
| ndellapenna-hhga | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 99.4006 | 99.1437 | 99.6587 | 62.2119 | 27441 | 237 | 27449 | 94 | 60 | 63.8298 | |
| qzeng-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 84.7915 | 95.5414 | 76.2159 | 71.9574 | 1200 | 56 | 1426 | 445 | 60 | 13.4831 | |
| mlin-fermikit | INDEL | D1_5 | map_l150_m2_e1 | homalt | 70.9278 | 69.3548 | 72.5738 | 81.4699 | 172 | 76 | 172 | 65 | 60 | 92.3077 | |
| mlin-fermikit | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_51to200 | * | 48.4670 | 39.4052 | 62.9412 | 75.7489 | 106 | 163 | 107 | 63 | 60 | 95.2381 | |
| mlin-fermikit | SNP | tv | map_l250_m0_e0 | * | 37.7799 | 25.3595 | 74.0458 | 82.9427 | 194 | 571 | 194 | 68 | 60 | 88.2353 | |
| mlin-fermikit | SNP | tv | map_l250_m0_e0 | homalt | 47.1642 | 40.9326 | 55.6338 | 80.3051 | 79 | 114 | 79 | 63 | 60 | 95.2381 | |
| ltrigg-rtg2 | SNP | tv | * | het | 99.7405 | 99.8410 | 99.6402 | 19.4900 | 590763 | 941 | 590991 | 2134 | 60 | 2.8116 | |