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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
77301-77350 / 86044 show all | |||||||||||||||
| cchapple-custom | INDEL | D1_5 | * | homalt | 99.7503 | 99.8385 | 99.6622 | 57.7109 | 48847 | 79 | 48389 | 164 | 151 | 92.0732 | |
| ciseli-custom | INDEL | C1_5 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 0.0000 | 0.0000 | 16.7513 | 92.3465 | 0 | 0 | 33 | 164 | 45 | 27.4390 | |
| ckim-dragen | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_51to200 | * | 82.6739 | 80.2710 | 85.2252 | 43.8259 | 948 | 233 | 946 | 164 | 164 | 100.0000 | |
| gduggal-bwafb | INDEL | D1_5 | HG002complexvar | homalt | 98.4856 | 98.5186 | 98.4525 | 57.9745 | 10441 | 157 | 10434 | 164 | 151 | 92.0732 | |
| gduggal-bwafb | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 93.8831 | 89.7436 | 98.4229 | 41.9180 | 3990 | 456 | 10235 | 164 | 145 | 88.4146 | |
| gduggal-bwaplat | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 83.9877 | 74.1728 | 96.7962 | 69.7744 | 4954 | 1725 | 4955 | 164 | 54 | 32.9268 | |
| gduggal-bwaplat | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 86.6565 | 78.2921 | 97.0220 | 41.1897 | 5345 | 1482 | 5343 | 164 | 163 | 99.3902 | |
| rpoplin-dv42 | SNP | ti | map_siren | het | 99.5664 | 99.3973 | 99.7362 | 53.8516 | 62006 | 376 | 61997 | 164 | 94 | 57.3171 | |
| rpoplin-dv42 | SNP | tv | map_l100_m1_e0 | * | 99.2751 | 99.2204 | 99.3298 | 64.0760 | 24310 | 191 | 24306 | 164 | 80 | 48.7805 | |
| ndellapenna-hhga | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_51to200 | het | 61.1681 | 90.3704 | 46.2295 | 44.2413 | 122 | 13 | 141 | 164 | 161 | 98.1707 | |
| ltrigg-rtg2 | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 99.4910 | 99.5737 | 99.4084 | 59.3516 | 27560 | 118 | 27559 | 164 | 14 | 8.5366 | |
| ltrigg-rtg2 | SNP | ti | HG002complexvar | het | 99.8501 | 99.7528 | 99.9475 | 16.9710 | 313988 | 778 | 313992 | 165 | 46 | 27.8788 | |
| qzeng-custom | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_51to200 | * | 41.5478 | 32.1377 | 58.7500 | 48.1865 | 224 | 473 | 235 | 165 | 147 | 89.0909 | |
| qzeng-custom | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 79.4289 | 78.4553 | 80.4270 | 61.9241 | 193 | 53 | 678 | 165 | 80 | 48.4848 | |
| ckim-vqsr | SNP | tv | map_l100_m2_e1 | * | 75.3037 | 60.7839 | 98.9375 | 85.6609 | 15368 | 9915 | 15365 | 165 | 1 | 0.6061 | |
| dgrover-gatk | SNP | ti | map_l125_m2_e0 | het | 99.2165 | 99.3060 | 99.1273 | 77.0589 | 18745 | 131 | 18741 | 165 | 34 | 20.6061 | |
| ckim-isaac | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 81.2534 | 85.2901 | 77.5815 | 56.2165 | 632 | 109 | 571 | 165 | 144 | 87.2727 | |
| egarrison-hhga | INDEL | I6_15 | * | het | 97.7387 | 97.1494 | 98.3352 | 52.6628 | 9747 | 286 | 9746 | 165 | 103 | 62.4242 | |
| egarrison-hhga | SNP | ti | * | homalt | 99.9365 | 99.8935 | 99.9794 | 16.8582 | 802183 | 855 | 802203 | 165 | 113 | 68.4848 | |
| anovak-vg | INDEL | I1_5 | map_l150_m2_e0 | homalt | 68.6340 | 94.0299 | 54.0390 | 86.8015 | 189 | 12 | 194 | 165 | 148 | 89.6970 | |
| asubramanian-gatk | INDEL | * | lowcmp_SimpleRepeat_diTR_51to200 | homalt | 79.7448 | 96.1003 | 68.1467 | 47.3577 | 345 | 14 | 353 | 165 | 141 | 85.4545 | |
| cchapple-custom | INDEL | * | HG002complexvar | homalt | 99.4073 | 99.4302 | 99.3845 | 51.9433 | 26873 | 154 | 26641 | 165 | 156 | 94.5455 | |
| jpowers-varprowl | SNP | tv | map_l250_m1_e0 | * | 94.0667 | 94.3332 | 93.8017 | 91.6023 | 2497 | 150 | 2497 | 165 | 33 | 20.0000 | |
| ltrigg-rtg1 | SNP | * | map_l100_m2_e0 | * | 99.3059 | 98.8413 | 99.7748 | 59.2762 | 73107 | 857 | 73104 | 165 | 38 | 23.0303 | |
| hfeng-pmm1 | SNP | * | map_l100_m2_e1 | * | 99.5878 | 99.3979 | 99.7783 | 64.6489 | 74287 | 450 | 74276 | 165 | 49 | 29.6970 | |
| hfeng-pmm2 | INDEL | D1_5 | * | het | 99.5604 | 99.3114 | 99.8107 | 56.3200 | 86971 | 603 | 86977 | 165 | 71 | 43.0303 | |
| hfeng-pmm2 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 97.1094 | 95.4346 | 98.8440 | 49.6543 | 14110 | 675 | 14108 | 165 | 157 | 95.1515 | |
| gduggal-snapvard | INDEL | I1_5 | map_l125_m2_e1 | het | 88.5797 | 98.8189 | 80.2632 | 90.8843 | 502 | 6 | 671 | 165 | 69 | 41.8182 | |
| gduggal-snapvard | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 65.7441 | 83.6158 | 54.1667 | 62.4609 | 148 | 29 | 195 | 165 | 113 | 68.4848 | |
| rpoplin-dv42 | SNP | tv | map_l100_m2_e0 | * | 99.2885 | 99.2370 | 99.3401 | 66.0825 | 24842 | 191 | 24838 | 165 | 80 | 48.4848 | |
| raldana-dualsentieon | SNP | tv | map_l100_m2_e1 | het | 99.1544 | 99.3412 | 98.9684 | 69.6842 | 15833 | 105 | 15829 | 165 | 1 | 0.6061 | |
| raldana-dualsentieon | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 97.4422 | 96.4266 | 98.4794 | 49.9423 | 10686 | 396 | 10686 | 165 | 162 | 98.1818 | |
| ciseli-custom | INDEL | D1_5 | map_l100_m1_e0 | het | 79.1153 | 74.3590 | 84.5216 | 89.5868 | 899 | 310 | 901 | 165 | 39 | 23.6364 | |
| ciseli-custom | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 44.5054 | 31.6677 | 74.8476 | 75.2826 | 488 | 1053 | 491 | 165 | 135 | 81.8182 | |
| gduggal-bwaplat | SNP | * | map_l125_m2_e0 | het | 79.9285 | 66.9418 | 99.1669 | 89.4354 | 19626 | 9692 | 19640 | 165 | 44 | 26.6667 | |
| gduggal-bwavard | INDEL | * | * | homalt | 93.4187 | 87.7664 | 99.8491 | 40.7725 | 109859 | 15313 | 109214 | 165 | 92 | 55.7576 | |
| gduggal-bwaplat | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | * | 81.2908 | 70.4641 | 96.0486 | 65.7173 | 4039 | 1693 | 4035 | 166 | 29 | 17.4699 | |
| gduggal-bwafb | SNP | tv | segdup | * | 98.7191 | 99.3671 | 98.0796 | 93.0076 | 8478 | 54 | 8478 | 166 | 14 | 8.4337 | |
| eyeh-varpipe | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 98.8642 | 99.2036 | 98.5271 | 69.1157 | 11460 | 92 | 11104 | 166 | 51 | 30.7229 | |
| eyeh-varpipe | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 98.8642 | 99.2036 | 98.5271 | 69.1157 | 11460 | 92 | 11104 | 166 | 51 | 30.7229 | |
| gduggal-bwafb | SNP | ti | * | homalt | 99.9234 | 99.8676 | 99.9793 | 17.0184 | 801976 | 1063 | 801993 | 166 | 111 | 66.8675 | |
| gduggal-bwavard | INDEL | * | map_l125_m0_e0 | * | 88.9737 | 95.2381 | 83.4826 | 91.4946 | 840 | 42 | 839 | 166 | 31 | 18.6747 | |
| gduggal-bwavard | INDEL | C1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 64.3489 | 66.6667 | 62.1868 | 95.0669 | 2 | 1 | 273 | 166 | 40 | 24.0964 | |
| hfeng-pmm2 | SNP | ti | map_l150_m2_e1 | * | 99.3155 | 99.4306 | 99.2007 | 77.6747 | 20605 | 118 | 20601 | 166 | 20 | 12.0482 | |
| hfeng-pmm3 | INDEL | D1_5 | * | * | 99.5137 | 99.1441 | 99.8861 | 56.7122 | 145489 | 1256 | 145542 | 166 | 109 | 65.6627 | |
| hfeng-pmm1 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 97.3881 | 95.8010 | 99.0287 | 53.0662 | 16929 | 742 | 16924 | 166 | 154 | 92.7711 | |
| hfeng-pmm1 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 97.3881 | 95.8010 | 99.0287 | 53.0662 | 16929 | 742 | 16924 | 166 | 154 | 92.7711 | |
| hfeng-pmm2 | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 93.8555 | 92.3515 | 95.4093 | 77.3915 | 3731 | 309 | 3450 | 166 | 128 | 77.1084 | |
| anovak-vg | SNP | ti | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 94.0474 | 96.9194 | 91.3406 | 62.4853 | 1636 | 52 | 1751 | 166 | 130 | 78.3133 | |
| qzeng-custom | INDEL | D16_PLUS | map_l100_m1_e0 | het | 38.9095 | 89.1304 | 24.8869 | 85.7327 | 41 | 5 | 55 | 166 | 1 | 0.6024 | |