PrecisionFDA
Truth Challenge
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Explore HG002 comparison results
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| Entry | Type | Subtype | Subset | Genotype | F-score | Recall | Precision | Frac_NA | Truth TP | Truth FN | Query TP | Query FP | FP gt | % FP ma | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
29351-29400 / 86044 show all | |||||||||||||||
| qzeng-custom | INDEL | I1_5 | lowcmp_SimpleRepeat_triTR_11to50 | het | 98.3975 | 98.7234 | 98.0737 | 43.5889 | 464 | 6 | 1782 | 35 | 13 | 37.1429 | |
| mlin-fermikit | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 97.6709 | 97.2719 | 98.0732 | 76.6321 | 1034 | 29 | 1018 | 20 | 19 | 95.0000 | |
| hfeng-pmm3 | INDEL | D6_15 | HG002compoundhet | * | 95.1894 | 92.4704 | 98.0731 | 32.6928 | 8351 | 680 | 8347 | 164 | 158 | 96.3415 | |
| asubramanian-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 97.6076 | 97.1467 | 98.0729 | 73.4952 | 44398 | 1304 | 44428 | 873 | 38 | 4.3528 | |
| asubramanian-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 97.6076 | 97.1467 | 98.0729 | 73.4952 | 44398 | 1304 | 44428 | 873 | 38 | 4.3528 | |
| qzeng-custom | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 94.7408 | 91.6287 | 98.0717 | 68.7918 | 14273 | 1304 | 54062 | 1063 | 839 | 78.9276 | |
| ghariani-varprowl | INDEL | * | map_l125_m2_e0 | homalt | 95.6347 | 93.3159 | 98.0716 | 83.8343 | 712 | 51 | 712 | 14 | 5 | 35.7143 | |
| eyeh-varpipe | SNP | ti | map_l150_m1_e0 | het | 98.7761 | 99.4907 | 98.0716 | 79.3788 | 12307 | 63 | 12053 | 237 | 11 | 4.6414 | |
| jpowers-varprowl | SNP | ti | map_l150_m2_e1 | * | 97.3682 | 96.6752 | 98.0713 | 80.1400 | 20034 | 689 | 20034 | 394 | 141 | 35.7868 | |
| gduggal-bwaplat | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 73.1343 | 58.3082 | 98.0711 | 75.8578 | 965 | 690 | 966 | 19 | 6 | 31.5789 | |
| jpowers-varprowl | SNP | ti | map_l150_m2_e0 | * | 97.3631 | 96.6654 | 98.0710 | 80.0739 | 19828 | 684 | 19828 | 390 | 140 | 35.8974 | |
| raldana-dualsentieon | INDEL | * | map_l100_m0_e0 | * | 97.7226 | 97.3768 | 98.0707 | 83.8643 | 1522 | 41 | 1525 | 30 | 4 | 13.3333 | |
| astatham-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 97.8006 | 97.5318 | 98.0707 | 78.8291 | 1225 | 31 | 1220 | 24 | 7 | 29.1667 | |
| dgrover-gatk | INDEL | I1_5 | map_l125_m0_e0 | * | 98.0676 | 98.0645 | 98.0707 | 89.6815 | 304 | 6 | 305 | 6 | 2 | 33.3333 | |
| gduggal-bwafb | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 98.8486 | 99.6390 | 98.0706 | 65.3592 | 3864 | 14 | 3863 | 76 | 10 | 13.1579 | |
| gduggal-snapvard | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 95.7435 | 93.5247 | 98.0701 | 82.9494 | 1401 | 97 | 1372 | 27 | 13 | 48.1481 | |
| dgrover-gatk | INDEL | D1_5 | map_l125_m2_e1 | het | 98.3844 | 98.7013 | 98.0695 | 88.5449 | 760 | 10 | 762 | 15 | 2 | 13.3333 | |
| raldana-dualsentieon | SNP | tv | map_l250_m2_e0 | het | 97.4585 | 96.8557 | 98.0689 | 89.2184 | 1879 | 61 | 1879 | 37 | 1 | 2.7027 | |
| asubramanian-gatk | INDEL | D1_5 | map_siren | * | 94.8669 | 91.8674 | 98.0688 | 84.1980 | 3242 | 287 | 3250 | 64 | 8 | 12.5000 | |
| asubramanian-gatk | INDEL | I16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 94.7213 | 91.5952 | 98.0684 | 63.9529 | 534 | 49 | 660 | 13 | 13 | 100.0000 | |
| asubramanian-gatk | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 95.4167 | 92.9048 | 98.0682 | 36.5079 | 1532 | 117 | 1726 | 34 | 29 | 85.2941 | |
| ndellapenna-hhga | INDEL | D6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | hetalt | 66.9692 | 50.8453 | 98.0681 | 41.1478 | 1203 | 1163 | 1066 | 21 | 14 | 66.6667 | |
| rpoplin-dv42 | INDEL | * | map_l100_m2_e1 | het | 97.6450 | 97.2258 | 98.0678 | 84.3523 | 2278 | 65 | 2284 | 45 | 20 | 44.4444 | |
| rpoplin-dv42 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 97.5962 | 97.1292 | 98.0676 | 74.3176 | 203 | 6 | 203 | 4 | 3 | 75.0000 | |
| gduggal-snapplat | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 86.1165 | 76.7619 | 98.0676 | 77.3770 | 403 | 122 | 406 | 8 | 2 | 25.0000 | |
| gduggal-bwafb | INDEL | I1_5 | map_l150_m2_e1 | homalt | 98.7835 | 99.5098 | 98.0676 | 89.3683 | 203 | 1 | 203 | 4 | 1 | 25.0000 | |
| gduggal-bwafb | INDEL | * | map_l125_m1_e0 | * | 96.9083 | 95.7760 | 98.0676 | 85.9889 | 2018 | 89 | 2030 | 40 | 8 | 20.0000 | |
| gduggal-bwafb | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 92.8504 | 88.1608 | 98.0670 | 34.4871 | 3552 | 477 | 1522 | 30 | 30 | 100.0000 | |
| hfeng-pmm3 | SNP | tv | map_l250_m0_e0 | het | 97.8089 | 97.5524 | 98.0668 | 92.4426 | 558 | 14 | 558 | 11 | 0 | 0.0000 | |
| gduggal-bwaplat | SNP | ti | lowcmp_SimpleRepeat_diTR_11to50 | * | 87.8326 | 79.5328 | 98.0666 | 79.9980 | 3847 | 990 | 3855 | 76 | 43 | 56.5789 | |
| ckim-dragen | SNP | ti | map_l100_m2_e1 | * | 98.6777 | 99.2968 | 98.0664 | 68.9837 | 49137 | 348 | 49145 | 969 | 108 | 11.1455 | |
| eyeh-varpipe | INDEL | C1_5 | HG002complexvar | het | 91.4751 | 85.7143 | 98.0661 | 74.9495 | 6 | 1 | 1217 | 24 | 16 | 66.6667 | |
| ckim-dragen | SNP | * | map_l100_m1_e0 | * | 98.6742 | 99.2901 | 98.0660 | 67.7530 | 71889 | 514 | 71900 | 1418 | 151 | 10.6488 | |
| jli-custom | INDEL | * | map_l125_m0_e0 | * | 97.8989 | 97.7324 | 98.0660 | 88.3592 | 862 | 20 | 862 | 17 | 6 | 35.2941 | |
| gduggal-bwafb | INDEL | I1_5 | map_l150_m2_e1 | * | 96.7557 | 95.4802 | 98.0658 | 89.8148 | 507 | 24 | 507 | 10 | 2 | 20.0000 | |
| ghariani-varprowl | SNP | tv | * | * | 98.9190 | 99.7874 | 98.0655 | 30.2667 | 967620 | 2062 | 967900 | 19093 | 1348 | 7.0602 | |
| hfeng-pmm2 | INDEL | I1_5 | map_l150_m2_e0 | het | 97.8993 | 97.7346 | 98.0645 | 91.3359 | 302 | 7 | 304 | 6 | 0 | 0.0000 | |
| jpowers-varprowl | INDEL | * | map_l150_m0_e0 | homalt | 95.2978 | 92.6829 | 98.0645 | 90.6514 | 152 | 12 | 152 | 3 | 2 | 66.6667 | |
| eyeh-varpipe | SNP | ti | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 99.0228 | 100.0000 | 98.0645 | 81.3926 | 6 | 0 | 152 | 3 | 2 | 66.6667 | |
| mlin-fermikit | SNP | * | map_l150_m2_e0 | het | 55.5672 | 38.7672 | 98.0639 | 69.9736 | 7805 | 12328 | 7800 | 154 | 5 | 3.2468 | |
| eyeh-varpipe | INDEL | D1_5 | map_l100_m0_e0 | het | 98.0166 | 97.9695 | 98.0636 | 83.8904 | 579 | 12 | 709 | 14 | 4 | 28.5714 | |
| hfeng-pmm1 | SNP | tv | map_l250_m0_e0 | het | 97.7193 | 97.3776 | 98.0634 | 92.6176 | 557 | 15 | 557 | 11 | 1 | 9.0909 | |
| raldana-dualsentieon | INDEL | * | map_l125_m2_e1 | het | 97.4295 | 96.8040 | 98.0631 | 86.2674 | 1363 | 45 | 1367 | 27 | 3 | 11.1111 | |
| eyeh-varpipe | INDEL | I1_5 | map_l150_m2_e1 | * | 97.7120 | 97.3635 | 98.0630 | 88.1407 | 517 | 14 | 810 | 16 | 10 | 62.5000 | |
| hfeng-pmm1 | INDEL | D16_PLUS | HG002complexvar | het | 96.2431 | 94.4896 | 98.0630 | 66.6532 | 1046 | 61 | 810 | 16 | 6 | 37.5000 | |
| asubramanian-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 92.7463 | 87.9765 | 98.0630 | 55.8289 | 300 | 41 | 405 | 8 | 8 | 100.0000 | |
| ndellapenna-hhga | INDEL | D1_5 | map_l150_m2_e1 | het | 97.4952 | 96.9349 | 98.0620 | 87.9355 | 506 | 16 | 506 | 10 | 3 | 30.0000 | |
| ltrigg-rtg2 | INDEL | D6_15 | map_l100_m2_e1 | * | 96.0828 | 94.1818 | 98.0620 | 81.0294 | 259 | 16 | 253 | 5 | 0 | 0.0000 | |
| ltrigg-rtg1 | INDEL | * | HG002complexvar | hetalt | 94.3098 | 90.8354 | 98.0606 | 74.9985 | 3360 | 339 | 4045 | 80 | 79 | 98.7500 | |
| gduggal-bwaplat | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 85.9154 | 76.4472 | 98.0606 | 64.1454 | 2879 | 887 | 2882 | 57 | 53 | 92.9825 | |