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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
74801-74850 / 86044 show all | |||||||||||||||
| jmaeng-gatk | INDEL | * | map_siren | het | 97.3536 | 98.6247 | 96.1148 | 86.8437 | 4446 | 62 | 4453 | 180 | 15 | 8.3333 | |
| anovak-vg | SNP | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 92.1744 | 93.3669 | 91.0119 | 70.2375 | 4448 | 316 | 4506 | 445 | 188 | 42.2472 | |
| gduggal-snapplat | SNP | * | map_l250_m2_e1 | het | 87.7421 | 84.4985 | 91.2446 | 94.9087 | 4448 | 816 | 4450 | 427 | 204 | 47.7752 | |
| hfeng-pmm2 | INDEL | * | map_siren | het | 98.6272 | 98.7134 | 98.5411 | 82.4078 | 4450 | 58 | 4458 | 66 | 5 | 7.5758 | |
| ckim-gatk | SNP | * | map_l250_m2_e1 | * | 70.8260 | 55.7155 | 97.1828 | 96.2381 | 4450 | 3537 | 4450 | 129 | 10 | 7.7519 | |
| qzeng-custom | SNP | tv | map_l125_m2_e1 | homalt | 84.2063 | 73.2631 | 98.9926 | 69.1889 | 4450 | 1624 | 4422 | 45 | 45 | 100.0000 | |
| gduggal-bwavard | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 69.3783 | 53.2297 | 99.5922 | 52.1673 | 4450 | 3910 | 4396 | 18 | 16 | 88.8889 | |
| gduggal-bwavard | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 69.3783 | 53.2297 | 99.5922 | 52.1673 | 4450 | 3910 | 4396 | 18 | 16 | 88.8889 | |
| ghariani-varprowl | SNP | ti | map_l250_m1_e0 | * | 96.0095 | 97.2046 | 94.8434 | 90.8840 | 4451 | 128 | 4451 | 242 | 52 | 21.4876 | |
| ltrigg-rtg1 | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 97.7725 | 95.8037 | 99.8239 | 42.4645 | 4452 | 195 | 4535 | 8 | 8 | 100.0000 | |
| jpowers-varprowl | SNP | * | map_l250_m1_e0 | het | 93.2189 | 93.6698 | 92.7723 | 92.0061 | 4454 | 301 | 4454 | 347 | 85 | 24.4957 | |
| ckim-dragen | SNP | ti | map_l125_m0_e0 | homalt | 99.4419 | 99.1761 | 99.7092 | 62.9046 | 4454 | 37 | 4457 | 13 | 12 | 92.3077 | |
| hfeng-pmm3 | INDEL | * | map_siren | het | 98.9897 | 98.8243 | 99.1556 | 80.3605 | 4455 | 53 | 4462 | 38 | 4 | 10.5263 | |
| jli-custom | SNP | ti | map_l250_m1_e0 | * | 98.2684 | 97.2920 | 99.2647 | 86.0135 | 4455 | 124 | 4455 | 33 | 18 | 54.5455 | |
| jmaeng-gatk | SNP | ti | map_l150_m2_e1 | homalt | 73.3394 | 57.9098 | 99.9776 | 80.4132 | 4455 | 3238 | 4455 | 1 | 1 | 100.0000 | |
| mlin-fermikit | SNP | * | lowcmp_SimpleRepeat_triTR_11to50 | het | 98.0092 | 96.5121 | 99.5535 | 31.2615 | 4455 | 161 | 4459 | 20 | 0 | 0.0000 | |
| gduggal-snapfb | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 79.7260 | 75.6106 | 84.3152 | 58.0080 | 4458 | 1438 | 2204 | 410 | 248 | 60.4878 | |
| gduggal-snapfb | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 79.7260 | 75.6106 | 84.3152 | 58.0080 | 4458 | 1438 | 2204 | 410 | 248 | 60.4878 | |
| dgrover-gatk | INDEL | * | map_siren | het | 98.8042 | 98.8909 | 98.7177 | 84.1153 | 4458 | 50 | 4465 | 58 | 7 | 12.0690 | |
| mlin-fermikit | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | * | 85.2297 | 77.7913 | 94.2409 | 52.4466 | 4459 | 1273 | 4451 | 272 | 265 | 97.4265 | |
| bgallagher-sentieon | SNP | ti | map_l125_m0_e0 | homalt | 99.5535 | 99.2875 | 99.8209 | 66.4916 | 4459 | 32 | 4459 | 8 | 6 | 75.0000 | |
| ndellapenna-hhga | SNP | ti | map_l125_m0_e0 | homalt | 99.6092 | 99.3097 | 99.9104 | 66.0377 | 4460 | 31 | 4460 | 4 | 4 | 100.0000 | |
| gduggal-bwavard | SNP | ti | map_l250_m1_e0 | * | 90.9201 | 97.4012 | 85.2478 | 91.8224 | 4460 | 119 | 4438 | 768 | 26 | 3.3854 | |
| jli-custom | SNP | ti | map_l125_m0_e0 | homalt | 99.5980 | 99.3097 | 99.8880 | 64.8868 | 4460 | 31 | 4460 | 5 | 5 | 100.0000 | |
| hfeng-pmm2 | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 96.6428 | 93.5038 | 100.0000 | 31.5949 | 4462 | 310 | 4512 | 0 | 0 | ||
| ltrigg-rtg2 | SNP | ti | map_l125_m0_e0 | homalt | 99.6428 | 99.3765 | 99.9105 | 65.1370 | 4463 | 28 | 4463 | 4 | 4 | 100.0000 | |
| raldana-dualsentieon | SNP | ti | map_l125_m0_e0 | homalt | 99.6205 | 99.3765 | 99.8657 | 64.9902 | 4463 | 28 | 4463 | 6 | 5 | 83.3333 | |
| ckim-gatk | INDEL | * | map_siren | het | 97.5443 | 99.0018 | 96.1290 | 86.6172 | 4463 | 45 | 4470 | 180 | 15 | 8.3333 | |
| qzeng-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 82.7253 | 89.2979 | 77.0540 | 68.9962 | 4464 | 535 | 4755 | 1416 | 413 | 29.1667 | |
| qzeng-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 82.7253 | 89.2979 | 77.0540 | 68.9962 | 4464 | 535 | 4755 | 1416 | 413 | 29.1667 | |
| bgallagher-sentieon | INDEL | * | map_siren | het | 98.7628 | 99.0683 | 98.4592 | 83.3559 | 4466 | 42 | 4473 | 70 | 8 | 11.4286 | |
| gduggal-bwafb | SNP | ti | map_l250_m1_e0 | * | 97.9068 | 97.5541 | 98.2622 | 89.4468 | 4467 | 112 | 4467 | 79 | 24 | 30.3797 | |
| ltrigg-rtg1 | SNP | ti | map_l125_m0_e0 | homalt | 99.6656 | 99.5324 | 99.7991 | 68.6301 | 4470 | 21 | 4470 | 9 | 9 | 100.0000 | |
| ndellapenna-hhga | SNP | tv | HG002compoundhet | het | 97.5455 | 95.6773 | 99.4882 | 51.9512 | 4471 | 202 | 4471 | 23 | 15 | 65.2174 | |
| ciseli-custom | SNP | tv | map_l150_m1_e0 | het | 70.7269 | 64.3680 | 78.4799 | 84.0134 | 4471 | 2475 | 4471 | 1226 | 46 | 3.7520 | |
| egarrison-hhga | SNP | ti | map_l125_m0_e0 | homalt | 99.7435 | 99.5769 | 99.9106 | 67.7962 | 4472 | 19 | 4472 | 4 | 4 | 100.0000 | |
| ckim-vqsr | SNP | * | map_l150_m0_e0 | het | 71.5668 | 56.3476 | 98.0495 | 94.3303 | 4474 | 3466 | 4474 | 89 | 0 | 0.0000 | |
| hfeng-pmm1 | SNP | ti | map_l125_m0_e0 | homalt | 99.6547 | 99.6215 | 99.6881 | 70.0040 | 4474 | 17 | 4474 | 14 | 5 | 35.7143 | |
| ghariani-varprowl | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 35.3630 | 32.4556 | 38.8425 | 53.3428 | 4474 | 9311 | 4470 | 7038 | 6992 | 99.3464 | |
| ckim-dragen | SNP | ti | map_l250_m1_e0 | * | 97.2516 | 97.7288 | 96.7791 | 88.9718 | 4475 | 104 | 4477 | 149 | 18 | 12.0805 | |
| hfeng-pmm3 | SNP | ti | map_l125_m0_e0 | homalt | 99.6659 | 99.6437 | 99.6881 | 69.8765 | 4475 | 16 | 4475 | 14 | 5 | 35.7143 | |
| anovak-vg | SNP | * | lowcmp_SimpleRepeat_triTR_11to50 | het | 96.8834 | 96.9671 | 96.7998 | 38.7932 | 4476 | 140 | 4507 | 149 | 76 | 51.0067 | |
| hfeng-pmm2 | SNP | ti | map_l125_m0_e0 | homalt | 99.6883 | 99.7105 | 99.6661 | 69.9826 | 4478 | 13 | 4478 | 15 | 6 | 40.0000 | |
| ciseli-custom | SNP | * | lowcmp_SimpleRepeat_triTR_11to50 | het | 91.1740 | 97.0537 | 85.9659 | 38.7403 | 4480 | 136 | 4490 | 733 | 8 | 1.0914 | |
| egarrison-hhga | SNP | ti | map_l250_m1_e0 | * | 98.7333 | 97.8816 | 99.6000 | 88.1610 | 4482 | 97 | 4482 | 18 | 8 | 44.4444 | |
| eyeh-varpipe | SNP | ti | map_l125_m0_e0 | homalt | 99.8314 | 99.7996 | 99.8632 | 71.9880 | 4482 | 9 | 4379 | 6 | 3 | 50.0000 | |
| astatham-gatk | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 96.8567 | 93.9438 | 99.9559 | 31.0125 | 4483 | 289 | 4536 | 2 | 2 | 100.0000 | |
| jlack-gatk | SNP | ti | map_l250_m1_e0 | * | 94.0942 | 97.9472 | 90.5329 | 92.4177 | 4485 | 94 | 4485 | 469 | 43 | 9.1684 | |
| cchapple-custom | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 0.0000 | 94.0067 | 0.0000 | 0.0000 | 4486 | 286 | 0 | 0 | 0 | ||
| anovak-vg | SNP | * | map_l250_m2_e0 | het | 71.8617 | 86.4074 | 61.5077 | 92.1188 | 4488 | 706 | 4455 | 2788 | 641 | 22.9914 | |