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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
61801-61850 / 86044 show all | |||||||||||||||
| eyeh-varpipe | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 95.0193 | 92.3530 | 97.8441 | 60.3645 | 12705 | 1052 | 12662 | 279 | 130 | 46.5950 | |
| gduggal-snapfb | SNP | ti | map_l125_m2_e1 | het | 96.4982 | 97.3699 | 95.6419 | 73.0724 | 18585 | 502 | 18588 | 847 | 395 | 46.6352 | |
| gduggal-snapvard | INDEL | I1_5 | map_l100_m2_e1 | het | 89.6492 | 98.3951 | 82.3311 | 88.9834 | 797 | 13 | 1109 | 238 | 111 | 46.6387 | |
| gduggal-snapfb | INDEL | I1_5 | segdup | homalt | 97.4757 | 98.0973 | 96.8619 | 93.7995 | 464 | 9 | 463 | 15 | 7 | 46.6667 | |
| gduggal-snapfb | SNP | ti | map_l150_m0_e0 | homalt | 95.8935 | 92.6114 | 99.4168 | 85.4187 | 2557 | 204 | 2557 | 15 | 7 | 46.6667 | |
| egarrison-hhga | SNP | ti | map_l100_m0_e0 | het | 99.1363 | 98.4982 | 99.7827 | 69.5619 | 13773 | 210 | 13774 | 30 | 14 | 46.6667 | |
| egarrison-hhga | SNP | tv | map_l250_m2_e0 | * | 98.5111 | 97.5711 | 99.4694 | 87.5099 | 2812 | 70 | 2812 | 15 | 7 | 46.6667 | |
| egarrison-hhga | SNP | tv | map_l250_m2_e1 | * | 98.5286 | 97.5995 | 99.4757 | 87.5868 | 2846 | 70 | 2846 | 15 | 7 | 46.6667 | |
| dgrover-gatk | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.6653 | 98.1228 | 99.2138 | 75.9182 | 1934 | 37 | 1893 | 15 | 7 | 46.6667 | |
| dgrover-gatk | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.6653 | 98.1228 | 99.2138 | 75.9182 | 1934 | 37 | 1893 | 15 | 7 | 46.6667 | |
| jmaeng-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 99.4442 | 99.2523 | 99.6368 | 83.0397 | 4115 | 31 | 4115 | 15 | 7 | 46.6667 | |
| jli-custom | SNP | * | map_l250_m0_e0 | het | 96.5658 | 94.2895 | 98.9547 | 90.3152 | 1420 | 86 | 1420 | 15 | 7 | 46.6667 | |
| jmaeng-gatk | INDEL | I1_5 | HG002complexvar | het | 99.6695 | 99.5052 | 99.8344 | 58.2792 | 18099 | 90 | 18081 | 30 | 14 | 46.6667 | |
| ckim-isaac | INDEL | * | map_l100_m2_e1 | * | 81.7169 | 69.9148 | 98.3127 | 84.3697 | 2626 | 1130 | 2622 | 45 | 21 | 46.6667 | |
| hfeng-pmm2 | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 99.1836 | 98.6234 | 99.7502 | 77.6187 | 6018 | 84 | 5989 | 15 | 7 | 46.6667 | |
| jli-custom | INDEL | * | segdup | * | 99.1762 | 98.9437 | 99.4099 | 94.0244 | 2529 | 27 | 2527 | 15 | 7 | 46.6667 | |
| gduggal-bwavard | INDEL | I16_PLUS | HG002complexvar | homalt | 81.9370 | 72.8155 | 93.6709 | 46.7416 | 225 | 84 | 222 | 15 | 7 | 46.6667 | |
| ndellapenna-hhga | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_51to200 | * | 92.8087 | 91.4498 | 94.2085 | 69.3853 | 246 | 23 | 244 | 15 | 7 | 46.6667 | |
| raldana-dualsentieon | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 98.0772 | 96.5750 | 99.6268 | 81.0951 | 4004 | 142 | 4004 | 15 | 7 | 46.6667 | |
| bgallagher-sentieon | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 99.4743 | 99.4428 | 99.5058 | 77.9305 | 6068 | 34 | 6040 | 30 | 14 | 46.6667 | |
| qzeng-custom | INDEL | D6_15 | HG002compoundhet | * | 81.7565 | 82.9255 | 80.6200 | 31.3934 | 7489 | 1542 | 8582 | 2063 | 963 | 46.6796 | |
| gduggal-snapplat | SNP | * | map_siren | het | 96.5899 | 96.2777 | 96.9043 | 72.4626 | 87604 | 3387 | 87710 | 2802 | 1309 | 46.7166 | |
| gduggal-snapvard | INDEL | I1_5 | map_l100_m2_e1 | * | 90.6674 | 93.3333 | 88.1496 | 86.2733 | 1302 | 93 | 1815 | 244 | 114 | 46.7213 | |
| gduggal-snapfb | SNP | * | map_l150_m2_e0 | het | 95.8306 | 96.9701 | 94.7174 | 76.6962 | 19523 | 610 | 19526 | 1089 | 509 | 46.7401 | |
| gduggal-snapfb | SNP | ti | map_l125_m2_e1 | * | 96.9811 | 96.8334 | 97.1293 | 73.9180 | 29601 | 968 | 29605 | 875 | 409 | 46.7429 | |
| qzeng-custom | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | het | 91.0906 | 96.0483 | 86.6196 | 46.4616 | 2625 | 108 | 7477 | 1155 | 540 | 46.7532 | |
| ckim-isaac | SNP | ti | lowcmp_SimpleRepeat_diTR_11to50 | * | 93.1299 | 89.8491 | 96.6594 | 59.1348 | 4346 | 491 | 4456 | 154 | 72 | 46.7532 | |
| anovak-vg | SNP | tv | lowcmp_SimpleRepeat_triTR_11to50 | het | 96.7565 | 97.0533 | 96.4614 | 41.7715 | 2075 | 63 | 2099 | 77 | 36 | 46.7532 | |
| gduggal-bwavard | INDEL | I1_5 | map_l100_m1_e0 | * | 93.9837 | 93.8013 | 94.1667 | 85.5706 | 1256 | 83 | 1243 | 77 | 36 | 46.7532 | |
| ghariani-varprowl | INDEL | * | map_l100_m1_e0 | het | 90.5454 | 98.1655 | 84.0230 | 89.3321 | 2194 | 41 | 2193 | 417 | 195 | 46.7626 | |
| gduggal-snapvard | INDEL | * | map_siren | het | 85.6604 | 93.9663 | 78.7036 | 86.4515 | 4236 | 272 | 4978 | 1347 | 630 | 46.7706 | |
| ckim-gatk | INDEL | D1_5 | * | * | 99.4755 | 99.4262 | 99.5247 | 61.4945 | 145903 | 842 | 145958 | 697 | 326 | 46.7719 | |
| rpoplin-dv42 | INDEL | * | map_l100_m2_e1 | * | 97.9158 | 97.4973 | 98.3378 | 98.2252 | 3662 | 94 | 3668 | 62 | 29 | 46.7742 | |
| gduggal-snapfb | SNP | * | map_l250_m1_e0 | * | 94.5000 | 94.2121 | 94.7896 | 89.4714 | 6804 | 418 | 6804 | 374 | 175 | 46.7914 | |
| gduggal-snapfb | SNP | ti | map_l125_m2_e0 | het | 96.4670 | 97.3405 | 95.6090 | 72.9883 | 18374 | 502 | 18377 | 844 | 395 | 46.8009 | |
| egarrison-hhga | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 94.9868 | 95.2804 | 94.6949 | 56.1929 | 10942 | 542 | 10942 | 613 | 287 | 46.8189 | |
| gduggal-snapvard | INDEL | * | map_l100_m1_e0 | * | 85.9341 | 89.2080 | 82.8920 | 85.9643 | 3199 | 387 | 4414 | 911 | 427 | 46.8716 | |
| qzeng-custom | INDEL | * | map_l150_m2_e0 | het | 81.2179 | 72.2958 | 92.6521 | 95.0610 | 655 | 251 | 807 | 64 | 30 | 46.8750 | |
| ckim-gatk | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 99.6249 | 99.5200 | 99.7301 | 51.4696 | 11818 | 57 | 11823 | 32 | 15 | 46.8750 | |
| ciseli-custom | INDEL | C16_PLUS | HG002complexvar | * | 0.0000 | 0.0000 | 23.8095 | 92.5926 | 0 | 0 | 10 | 32 | 15 | 46.8750 | |
| egarrison-hhga | SNP | * | map_l250_m1_e0 | * | 98.6376 | 97.7430 | 99.5487 | 87.7148 | 7059 | 163 | 7059 | 32 | 15 | 46.8750 | |
| hfeng-pmm3 | SNP | * | HG002compoundhet | * | 97.8284 | 95.8679 | 99.8709 | 39.6499 | 24755 | 1067 | 24755 | 32 | 15 | 46.8750 | |
| jmaeng-gatk | INDEL | I1_5 | * | * | 99.2409 | 99.0383 | 99.4444 | 59.6817 | 149215 | 1449 | 149263 | 834 | 391 | 46.8825 | |
| gduggal-snapfb | SNP | * | map_l150_m1_e0 | * | 96.2111 | 96.1025 | 96.3199 | 76.8067 | 29416 | 1193 | 29419 | 1124 | 527 | 46.8861 | |
| ghariani-varprowl | INDEL | I1_5 | map_siren | * | 92.4494 | 93.3444 | 91.5714 | 83.4764 | 2805 | 200 | 2803 | 258 | 121 | 46.8992 | |
| gduggal-snapfb | SNP | ti | map_l125_m2_e0 | * | 96.9548 | 96.8008 | 97.1093 | 73.8651 | 29290 | 968 | 29294 | 872 | 409 | 46.9037 | |
| gduggal-snapvard | INDEL | * | map_l100_m2_e1 | * | 85.8099 | 88.8445 | 82.9757 | 86.6598 | 3337 | 419 | 4601 | 944 | 443 | 46.9280 | |
| ndellapenna-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 95.3132 | 95.4134 | 95.2131 | 38.5261 | 4535 | 218 | 4535 | 228 | 107 | 46.9298 | |
| mlin-fermikit | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 98.1375 | 97.9385 | 98.3373 | 54.7451 | 2898 | 61 | 2898 | 49 | 23 | 46.9388 | |
| jpowers-varprowl | INDEL | D1_5 | map_l100_m0_e0 | * | 93.8918 | 93.5110 | 94.2757 | 85.2184 | 807 | 56 | 807 | 49 | 23 | 46.9388 | |