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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
70151-70200 / 86044 show all | |||||||||||||||
| egarrison-hhga | SNP | ti | lowcmp_SimpleRepeat_diTR_11to50 | * | 98.3647 | 97.6018 | 99.1396 | 66.6853 | 4721 | 116 | 4724 | 41 | 16 | 39.0244 | |
| egarrison-hhga | SNP | ti | map_l150_m1_e0 | * | 99.3657 | 98.9448 | 99.7902 | 73.6441 | 19504 | 208 | 19504 | 41 | 20 | 48.7805 | |
| egarrison-hhga | SNP | ti | map_l150_m2_e0 | * | 99.3881 | 98.9811 | 99.7985 | 75.2011 | 20303 | 209 | 20303 | 41 | 20 | 48.7805 | |
| egarrison-hhga | SNP | tv | map_l100_m2_e0 | het | 99.3093 | 98.8845 | 99.7379 | 65.3478 | 15601 | 176 | 15601 | 41 | 13 | 31.7073 | |
| egarrison-hhga | SNP | tv | map_l100_m2_e1 | het | 99.3132 | 98.8894 | 99.7405 | 65.3943 | 15761 | 177 | 15761 | 41 | 13 | 31.7073 | |
| eyeh-varpipe | INDEL | * | segdup | het | 96.4604 | 95.6344 | 97.3009 | 93.4137 | 1402 | 64 | 1478 | 41 | 31 | 75.6098 | |
| eyeh-varpipe | INDEL | C1_5 | HG002compoundhet | hetalt | 95.5961 | 100.0000 | 91.5638 | 80.0247 | 1 | 0 | 445 | 41 | 39 | 95.1220 | |
| ndellapenna-hhga | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 93.6086 | 92.9919 | 94.2335 | 70.5102 | 690 | 52 | 670 | 41 | 20 | 48.7805 | |
| ndellapenna-hhga | SNP | ti | map_l150_m1_e0 | * | 99.0365 | 98.2955 | 99.7888 | 72.3511 | 19376 | 336 | 19376 | 41 | 23 | 56.0976 | |
| ndellapenna-hhga | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 99.5343 | 99.4751 | 99.5935 | 60.5291 | 10044 | 53 | 10045 | 41 | 39 | 95.1220 | |
| ltrigg-rtg2 | SNP | ti | map_l125_m2_e0 | * | 99.0101 | 98.1724 | 99.8622 | 61.4718 | 29705 | 553 | 29707 | 41 | 10 | 24.3902 | |
| ltrigg-rtg2 | SNP | ti | map_l125_m2_e1 | * | 99.0186 | 98.1877 | 99.8636 | 61.5506 | 30015 | 554 | 30018 | 41 | 10 | 24.3902 | |
| mlin-fermikit | INDEL | * | map_l125_m2_e0 | het | 67.2880 | 52.1927 | 94.6684 | 82.7849 | 726 | 665 | 728 | 41 | 17 | 41.4634 | |
| qzeng-custom | INDEL | I6_15 | map_l125_m2_e1 | * | 66.6138 | 66.0377 | 67.2000 | 87.7089 | 35 | 18 | 84 | 41 | 3 | 7.3171 | |
| qzeng-custom | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 98.9647 | 99.8160 | 98.1279 | 69.9341 | 2170 | 4 | 2149 | 41 | 1 | 2.4390 | |
| qzeng-custom | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 98.3855 | 99.7116 | 97.0943 | 71.3328 | 1383 | 4 | 1370 | 41 | 1 | 2.4390 | |
| qzeng-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 95.2623 | 98.5801 | 92.1606 | 58.7214 | 486 | 7 | 482 | 41 | 1 | 2.4390 | |
| qzeng-custom | INDEL | D16_PLUS | map_l125_m2_e0 | het | 52.3636 | 90.0000 | 36.9231 | 94.2376 | 18 | 2 | 24 | 41 | 0 | 0.0000 | |
| qzeng-custom | INDEL | D1_5 | map_l100_m2_e1 | het | 89.9622 | 84.0694 | 96.7434 | 89.9976 | 1066 | 202 | 1218 | 41 | 27 | 65.8537 | |
| qzeng-custom | INDEL | I16_PLUS | map_siren | * | 65.7764 | 70.9302 | 61.3208 | 81.7556 | 61 | 25 | 65 | 41 | 5 | 12.1951 | |
| ltrigg-rtg2 | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 99.1847 | 98.9875 | 99.3827 | 46.8597 | 6648 | 68 | 6601 | 41 | 10 | 24.3902 | |
| ltrigg-rtg2 | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 98.8496 | 98.7433 | 98.9562 | 63.8705 | 3850 | 49 | 3887 | 41 | 14 | 34.1463 | |
| ckim-dragen | INDEL | D6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 96.3915 | 97.1904 | 95.6056 | 75.0334 | 934 | 27 | 892 | 41 | 38 | 92.6829 | |
| ckim-dragen | SNP | * | HG002complexvar | homalt | 99.9551 | 99.9245 | 99.9858 | 19.8995 | 288356 | 218 | 288565 | 41 | 41 | 100.0000 | |
| cchapple-custom | INDEL | I1_5 | map_siren | * | 98.3102 | 98.0033 | 98.6191 | 79.8398 | 2945 | 60 | 2928 | 41 | 14 | 34.1463 | |
| cchapple-custom | SNP | tv | map_l250_m0_e0 | * | 94.5681 | 94.5098 | 94.6265 | 93.8008 | 723 | 42 | 722 | 41 | 8 | 19.5122 | |
| cchapple-custom | SNP | tv | map_l250_m0_e0 | het | 93.7547 | 94.5804 | 92.9432 | 94.2561 | 541 | 31 | 540 | 41 | 8 | 19.5122 | |
| ciseli-custom | INDEL | C16_PLUS | * | * | 0.0000 | 0.0000 | 22.6415 | 96.3872 | 0 | 0 | 12 | 41 | 15 | 36.5854 | |
| ciseli-custom | INDEL | C1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 0.0000 | 0.0000 | 39.7059 | 96.7006 | 0 | 1 | 27 | 41 | 5 | 12.1951 | |
| ciseli-custom | INDEL | C1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 0.0000 | 0.0000 | 39.7059 | 96.7006 | 0 | 1 | 27 | 41 | 5 | 12.1951 | |
| ciseli-custom | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | het | 63.3990 | 50.8728 | 84.1085 | 55.4404 | 204 | 197 | 217 | 41 | 32 | 78.0488 | |
| ciseli-custom | INDEL | D1_5 | map_l150_m0_e0 | het | 69.0619 | 63.3663 | 75.8824 | 95.3892 | 128 | 74 | 129 | 41 | 7 | 17.0732 | |
| ciseli-custom | INDEL | D1_5 | map_l250_m2_e0 | * | 67.3274 | 61.9565 | 73.7179 | 97.3052 | 114 | 70 | 115 | 41 | 14 | 34.1463 | |
| ckim-dragen | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 99.5645 | 99.8024 | 99.3278 | 58.3031 | 6060 | 12 | 6058 | 41 | 41 | 100.0000 | |
| ckim-gatk | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 96.6054 | 94.5304 | 98.7736 | 51.8161 | 3301 | 191 | 3302 | 41 | 34 | 82.9268 | |
| ckim-gatk | SNP | * | HG002compoundhet | het | 99.3772 | 99.0478 | 99.7088 | 46.6510 | 14043 | 135 | 14041 | 41 | 28 | 68.2927 | |
| ckim-gatk | INDEL | * | map_l250_m1_e0 | het | 88.9423 | 97.3684 | 81.8584 | 97.5127 | 185 | 5 | 185 | 41 | 2 | 4.8781 | |
| ckim-gatk | INDEL | * | map_l250_m2_e0 | het | 89.9123 | 97.6190 | 83.3333 | 97.6273 | 205 | 5 | 205 | 41 | 2 | 4.8781 | |
| ckim-gatk | INDEL | * | map_l250_m2_e1 | het | 89.9563 | 97.6303 | 83.4008 | 97.6831 | 206 | 5 | 206 | 41 | 2 | 4.8781 | |
| cchapple-custom | INDEL | D1_5 | map_l150_m2_e0 | * | 95.7666 | 96.8545 | 94.7028 | 87.9645 | 739 | 24 | 733 | 41 | 6 | 14.6341 | |
| cchapple-custom | INDEL | D1_5 | map_l150_m2_e1 | * | 95.7815 | 96.7866 | 94.7970 | 87.9805 | 753 | 25 | 747 | 41 | 6 | 14.6341 | |
| gduggal-snapfb | INDEL | D1_5 | map_l150_m2_e1 | * | 95.4657 | 96.1440 | 94.7970 | 88.9775 | 748 | 30 | 747 | 41 | 8 | 19.5122 | |
| gduggal-snapfb | INDEL | D6_15 | lowcmp_SimpleRepeat_triTR_11to50 | het | 85.9762 | 77.6671 | 96.2761 | 24.1736 | 546 | 157 | 1060 | 41 | 41 | 100.0000 | |
| gduggal-snapfb | INDEL | I1_5 | map_l100_m0_e0 | * | 94.1894 | 95.7643 | 92.6655 | 86.2889 | 520 | 23 | 518 | 41 | 8 | 19.5122 | |
| gduggal-snapfb | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 41.1854 | 27.9851 | 77.9570 | 49.7297 | 150 | 386 | 145 | 41 | 41 | 100.0000 | |
| gduggal-snapplat | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 69.4882 | 58.7467 | 85.0365 | 91.8258 | 225 | 158 | 233 | 41 | 17 | 41.4634 | |
| gduggal-snapplat | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 71.3745 | 60.3412 | 87.3457 | 93.7848 | 283 | 186 | 283 | 41 | 21 | 51.2195 | |
| ghariani-varprowl | SNP | * | map_l150_m1_e0 | homalt | 98.8738 | 98.1283 | 99.6307 | 72.3027 | 11062 | 211 | 11062 | 41 | 25 | 60.9756 | |
| ghariani-varprowl | SNP | * | map_l150_m2_e0 | homalt | 98.9108 | 98.1879 | 99.6443 | 74.5311 | 11487 | 212 | 11487 | 41 | 25 | 60.9756 | |
| ghariani-varprowl | SNP | * | map_l150_m2_e1 | homalt | 98.9183 | 98.1990 | 99.6482 | 74.5368 | 11614 | 213 | 11614 | 41 | 25 | 60.9756 | |