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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
18651-18700 / 86044 show all | |||||||||||||||
| hfeng-pmm1 | SNP | * | map_siren | homalt | 99.8994 | 99.8803 | 99.9184 | 53.4037 | 55090 | 66 | 55084 | 45 | 26 | 57.7778 | |
| jlack-gatk | INDEL | D1_5 | * | homalt | 99.6645 | 99.8651 | 99.4647 | 59.9060 | 48860 | 66 | 48867 | 263 | 260 | 98.8593 | |
| jlack-gatk | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 94.5847 | 98.2941 | 91.1451 | 66.4714 | 3803 | 66 | 3757 | 365 | 325 | 89.0411 | |
| hfeng-pmm2 | SNP | tv | map_l150_m1_e0 | het | 98.7581 | 99.0498 | 98.4681 | 78.5736 | 6880 | 66 | 6878 | 107 | 10 | 9.3458 | |
| hfeng-pmm2 | SNP | tv | map_l150_m2_e0 | het | 98.7968 | 99.0899 | 98.5054 | 79.5966 | 7186 | 66 | 7184 | 109 | 10 | 9.1743 | |
| hfeng-pmm2 | SNP | tv | map_l150_m2_e1 | het | 98.8125 | 99.1018 | 98.5248 | 79.6036 | 7282 | 66 | 7280 | 109 | 10 | 9.1743 | |
| hfeng-pmm3 | INDEL | * | map_l100_m2_e1 | * | 98.5982 | 98.2428 | 98.9561 | 83.4763 | 3690 | 66 | 3697 | 39 | 9 | 23.0769 | |
| jlack-gatk | SNP | tv | map_l125_m0_e0 | het | 90.4803 | 98.5003 | 83.6680 | 86.8150 | 4335 | 66 | 4334 | 846 | 47 | 5.5556 | |
| jli-custom | INDEL | * | map_l100_m1_e0 | * | 98.4897 | 98.1595 | 98.8222 | 83.0077 | 3520 | 66 | 3524 | 42 | 15 | 35.7143 | |
| jli-custom | INDEL | * | map_siren | het | 98.8982 | 98.5359 | 99.2631 | 80.2992 | 4442 | 66 | 4445 | 33 | 6 | 18.1818 | |
| hfeng-pmm2 | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_11to50 | * | 97.4316 | 96.3170 | 98.5722 | 66.0922 | 1726 | 66 | 1726 | 25 | 17 | 68.0000 | |
| hfeng-pmm1 | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_51to200 | hetalt | 91.8719 | 84.9658 | 100.0000 | 34.9929 | 373 | 66 | 457 | 0 | 0 | ||
| gduggal-snapplat | SNP | tv | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 92.3387 | 87.4046 | 97.8632 | 82.4456 | 458 | 66 | 458 | 10 | 2 | 20.0000 | |
| gduggal-snapvard | INDEL | D16_PLUS | lowcmp_SimpleRepeat_homopolymer_gt10 | * | 5.6818 | 2.9412 | 83.3333 | 90.9091 | 2 | 66 | 5 | 1 | 1 | 100.0000 | |
| gduggal-snapfb | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 0.0000 | 0.0000 | 0.0000 | 0 | 66 | 0 | 0 | 0 | |||
| gduggal-snapfb | INDEL | I1_5 | lowcmp_SimpleRepeat_triTR_11to50 | * | 86.8494 | 93.7143 | 80.9217 | 61.7014 | 984 | 66 | 878 | 207 | 45 | 21.7391 | |
| gduggal-snapplat | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 0.0000 | 0.0000 | 0.0000 | 0 | 66 | 0 | 0 | 0 | |||
| gduggal-snapplat | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | hetalt | 52.9704 | 41.0714 | 74.5763 | 89.3694 | 46 | 66 | 44 | 15 | 4 | 26.6667 | |
| gduggal-snapvard | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 0.0000 | 0.0000 | 36.1111 | 72.9323 | 0 | 66 | 13 | 23 | 11 | 47.8261 | |
| gduggal-snapfb | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 28.4364 | 92.2444 | 16.8091 | 77.5112 | 785 | 66 | 846 | 4187 | 78 | 1.8629 | |
| gduggal-snapfb | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 41.4402 | 94.0217 | 26.5770 | 81.1312 | 1038 | 66 | 1087 | 3003 | 81 | 2.6973 | |
| qzeng-custom | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_51to200 | het | 54.0093 | 51.1111 | 57.2559 | 47.5069 | 69 | 66 | 217 | 162 | 144 | 88.8889 | |
| ltrigg-rtg2 | INDEL | I16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 91.4566 | 84.8624 | 99.1620 | 69.5837 | 370 | 66 | 355 | 3 | 2 | 66.6667 | |
| mlin-fermikit | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 82.0706 | 76.0870 | 89.0756 | 91.1787 | 210 | 66 | 212 | 26 | 7 | 26.9231 | |
| raldana-dualsentieon | INDEL | * | map_l100_m2_e0 | het | 97.6490 | 97.1391 | 98.1643 | 83.4371 | 2241 | 66 | 2246 | 42 | 8 | 19.0476 | |
| raldana-dualsentieon | INDEL | * | map_l100_m2_e1 | het | 97.6853 | 97.1831 | 98.1928 | 83.5574 | 2277 | 66 | 2282 | 42 | 8 | 19.0476 | |
| mlin-fermikit | INDEL | D16_PLUS | * | homalt | 91.6240 | 96.0993 | 87.5470 | 75.8209 | 1626 | 66 | 1631 | 232 | 206 | 88.7931 | |
| mlin-fermikit | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_11to50 | het | 83.9484 | 89.1626 | 79.3103 | 79.1581 | 543 | 66 | 483 | 126 | 115 | 91.2698 | |
| mlin-fermikit | INDEL | D1_5 | lowcmp_SimpleRepeat_triTR_11to50 | het | 96.3317 | 97.1116 | 95.5642 | 35.5358 | 2219 | 66 | 2219 | 103 | 98 | 95.1456 | |
| cchapple-custom | INDEL | I6_15 | HG002complexvar | het | 98.1734 | 97.1975 | 99.1692 | 56.5725 | 2289 | 66 | 3581 | 30 | 25 | 83.3333 | |
| cchapple-custom | SNP | * | lowcmp_SimpleRepeat_diTR_11to50 | het | 99.1314 | 98.9416 | 99.3219 | 67.8823 | 6170 | 66 | 6298 | 43 | 25 | 58.1395 | |
| cchapple-custom | SNP | tv | map_l150_m0_e0 | homalt | 97.4517 | 95.0301 | 100.0000 | 73.1873 | 1262 | 66 | 1261 | 0 | 0 | ||
| ckim-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 96.8901 | 95.6863 | 98.1246 | 84.9192 | 1464 | 66 | 1465 | 28 | 18 | 64.2857 | |
| ckim-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 96.8901 | 95.6863 | 98.1246 | 84.9192 | 1464 | 66 | 1465 | 28 | 18 | 64.2857 | |
| ciseli-custom | SNP | ti | lowcmp_SimpleRepeat_triTR_11to50 | het | 93.1110 | 97.3366 | 89.2370 | 37.3586 | 2412 | 66 | 2421 | 292 | 5 | 1.7123 | |
| ckim-dragen | INDEL | * | map_l100_m2_e0 | het | 96.2796 | 97.1391 | 95.4352 | 88.1801 | 2241 | 66 | 2237 | 107 | 9 | 8.4112 | |
| ckim-dragen | INDEL | * | map_l100_m2_e1 | het | 96.3159 | 97.1831 | 95.4641 | 88.2397 | 2277 | 66 | 2273 | 108 | 10 | 9.2593 | |
| ciseli-custom | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | hetalt | 0.0000 | 10.8108 | 0.0000 | 0.0000 | 8 | 66 | 0 | 0 | 0 | ||
| ciseli-custom | INDEL | D1_5 | map_l250_m1_e0 | * | 66.7446 | 61.4035 | 73.1034 | 97.1877 | 105 | 66 | 106 | 39 | 12 | 30.7692 | |
| ciseli-custom | INDEL | D6_15 | segdup | * | 68.3802 | 65.4450 | 71.5909 | 94.3207 | 125 | 66 | 126 | 50 | 32 | 64.0000 | |
| ciseli-custom | INDEL | I1_5 | map_l250_m1_e0 | * | 43.9560 | 37.7358 | 52.6316 | 97.2333 | 40 | 66 | 40 | 36 | 27 | 75.0000 | |
| ciseli-custom | INDEL | I6_15 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 42.4438 | 56.8627 | 33.8583 | 68.1704 | 87 | 66 | 86 | 168 | 147 | 87.5000 | |
| cchapple-custom | INDEL | D1_5 | map_siren | * | 97.4907 | 98.1298 | 96.8600 | 78.7253 | 3463 | 66 | 3424 | 111 | 14 | 12.6126 | |
| ckim-dragen | SNP | tv | HG002complexvar | homalt | 99.9600 | 99.9306 | 99.9895 | 22.9484 | 95045 | 66 | 95148 | 10 | 10 | 100.0000 | |
| ckim-dragen | SNP | tv | map_l250_m1_e0 | het | 96.1474 | 96.3626 | 95.9331 | 90.7498 | 1722 | 65 | 1722 | 73 | 4 | 5.4795 | |
| ckim-gatk | INDEL | D1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 99.8126 | 99.7437 | 99.8815 | 55.8039 | 25294 | 65 | 25297 | 30 | 17 | 56.6667 | |
| ckim-isaac | INDEL | * | map_l250_m1_e0 | homalt | 57.5163 | 40.3670 | 100.0000 | 93.4621 | 44 | 65 | 44 | 0 | 0 | ||
| ckim-dragen | SNP | ti | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 98.7329 | 97.9988 | 99.4780 | 65.5490 | 3183 | 65 | 3240 | 17 | 5 | 29.4118 | |
| ckim-dragen | SNP | ti | map_l150_m1_e0 | homalt | 99.4455 | 99.1129 | 99.7803 | 65.1947 | 7262 | 65 | 7267 | 16 | 15 | 93.7500 | |
| cchapple-custom | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | het | 95.2285 | 93.2851 | 97.2547 | 53.8987 | 903 | 65 | 3082 | 87 | 61 | 70.1149 | |