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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
61751-61800 / 86044 show all | |||||||||||||||
| egarrison-hhga | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 91.7694 | 88.7681 | 94.9807 | 88.6104 | 245 | 31 | 246 | 13 | 6 | 46.1538 | |
| egarrison-hhga | SNP | ti | map_l125_m2_e1 | * | 99.4698 | 99.1135 | 99.8287 | 70.7805 | 30298 | 271 | 30298 | 52 | 24 | 46.1538 | |
| egarrison-hhga | SNP | tv | map_l150_m1_e0 | * | 99.2818 | 98.8087 | 99.7594 | 72.5943 | 10782 | 130 | 10782 | 26 | 12 | 46.1538 | |
| eyeh-varpipe | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | homalt | 9.6515 | 5.2632 | 58.0645 | 68.3673 | 19 | 342 | 18 | 13 | 6 | 46.1538 | |
| ckim-isaac | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 88.4682 | 80.1441 | 98.7217 | 59.1894 | 1001 | 248 | 1004 | 13 | 6 | 46.1538 | |
| ckim-isaac | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 88.4682 | 80.1441 | 98.7217 | 59.1894 | 1001 | 248 | 1004 | 13 | 6 | 46.1538 | |
| egarrison-hhga | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | het | 97.8916 | 97.7256 | 98.0583 | 70.5196 | 1332 | 31 | 1313 | 26 | 12 | 46.1538 | |
| ckim-vqsr | INDEL | D1_5 | HG002complexvar | het | 99.6767 | 99.4799 | 99.8743 | 56.3731 | 20657 | 108 | 20661 | 26 | 12 | 46.1538 | |
| qzeng-custom | SNP | tv | HG002complexvar | * | 99.0948 | 98.4189 | 99.7800 | 23.2771 | 242263 | 3892 | 238613 | 526 | 243 | 46.1977 | |
| qzeng-custom | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_51to200 | het | 74.4676 | 94.6746 | 61.3692 | 51.5690 | 160 | 9 | 502 | 316 | 146 | 46.2025 | |
| gduggal-snapfb | SNP | * | map_l250_m1_e0 | het | 94.0213 | 95.4154 | 92.6675 | 86.7306 | 4537 | 218 | 4537 | 359 | 166 | 46.2396 | |
| gduggal-snapfb | SNP | * | map_l150_m2_e1 | * | 96.3459 | 96.2620 | 96.4300 | 78.3975 | 31006 | 1204 | 31009 | 1148 | 531 | 46.2544 | |
| egarrison-hhga | SNP | ti | map_l100_m1_e0 | * | 99.5648 | 99.2719 | 99.8594 | 62.6430 | 47582 | 349 | 47583 | 67 | 31 | 46.2687 | |
| egarrison-hhga | SNP | tv | map_siren | * | 99.6246 | 99.3686 | 99.8818 | 55.8072 | 45640 | 290 | 45640 | 54 | 25 | 46.2963 | |
| gduggal-snapvard | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 73.8894 | 92.7746 | 61.3924 | 75.7947 | 321 | 25 | 388 | 244 | 113 | 46.3115 | |
| anovak-vg | SNP | ti | * | * | 98.4812 | 98.2960 | 98.6672 | 19.8346 | 2049980 | 35538 | 2043729 | 27607 | 12786 | 46.3143 | |
| gduggal-snapplat | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 70.5199 | 59.6244 | 86.2876 | 93.0181 | 508 | 344 | 516 | 82 | 38 | 46.3415 | |
| gduggal-snapvard | INDEL | I1_5 | map_l100_m2_e0 | het | 89.8150 | 98.4868 | 82.5468 | 88.8499 | 781 | 12 | 1102 | 233 | 108 | 46.3519 | |
| gduggal-snapvard | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 3.4141 | 1.8018 | 32.4590 | 68.7660 | 12 | 654 | 198 | 412 | 191 | 46.3592 | |
| gduggal-snapvard | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 3.4141 | 1.8018 | 32.4590 | 68.7660 | 12 | 654 | 198 | 412 | 191 | 46.3592 | |
| ciseli-custom | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 58.2603 | 63.0693 | 54.1327 | 69.0970 | 2548 | 1492 | 2790 | 2364 | 1096 | 46.3621 | |
| hfeng-pmm3 | INDEL | I1_5 | * | het | 99.7016 | 99.5433 | 99.8604 | 59.2337 | 78680 | 361 | 78661 | 110 | 51 | 46.3636 | |
| gduggal-snapvard | INDEL | * | map_l100_m2_e0 | het | 85.0151 | 94.3650 | 77.3510 | 88.3503 | 2177 | 130 | 3101 | 908 | 421 | 46.3656 | |
| gduggal-snapplat | INDEL | D1_5 | lowcmp_SimpleRepeat_triTR_11to50 | * | 63.8520 | 52.6367 | 81.1407 | 57.2311 | 2146 | 1931 | 3201 | 744 | 345 | 46.3710 | |
| ndellapenna-hhga | SNP | * | map_l100_m0_e0 | het | 98.6808 | 97.7128 | 99.6681 | 67.9602 | 20720 | 485 | 20721 | 69 | 32 | 46.3768 | |
| egarrison-hhga | SNP | * | map_l150_m2_e1 | * | 99.3609 | 98.9413 | 99.7840 | 74.9205 | 31869 | 341 | 31869 | 69 | 32 | 46.3768 | |
| gduggal-snapfb | INDEL | * | HG002complexvar | * | 90.4920 | 87.9994 | 93.1300 | 55.3026 | 67705 | 9233 | 69298 | 5112 | 2371 | 46.3811 | |
| ciseli-custom | INDEL | D1_5 | map_siren | * | 83.6317 | 82.1196 | 85.2005 | 84.5008 | 2898 | 631 | 2890 | 502 | 233 | 46.4143 | |
| gduggal-snapplat | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 76.9680 | 69.6854 | 85.9503 | 79.9286 | 44899 | 19532 | 52067 | 8511 | 3951 | 46.4223 | |
| egarrison-hhga | INDEL | * | map_l100_m1_e0 | * | 97.4160 | 97.1835 | 97.6497 | 97.4833 | 3485 | 101 | 3490 | 84 | 39 | 46.4286 | |
| ndellapenna-hhga | SNP | tv | map_l125_m0_e0 | * | 98.6916 | 97.8284 | 99.5702 | 72.2163 | 6487 | 144 | 6487 | 28 | 13 | 46.4286 | |
| astatham-gatk | SNP | * | map_l100_m2_e1 | * | 92.0052 | 85.3219 | 99.8246 | 70.5612 | 63767 | 10970 | 63756 | 112 | 52 | 46.4286 | |
| gduggal-snapvard | INDEL | I1_5 | map_l100_m2_e0 | * | 90.7740 | 93.4211 | 88.2728 | 86.1304 | 1278 | 90 | 1799 | 239 | 111 | 46.4435 | |
| gduggal-snapfb | SNP | * | map_l150_m2_e0 | * | 96.3250 | 96.2326 | 96.4176 | 78.3427 | 30652 | 1200 | 30655 | 1139 | 529 | 46.4442 | |
| ghariani-varprowl | INDEL | * | map_l100_m2_e1 | * | 90.3178 | 92.5453 | 88.1950 | 92.4782 | 3476 | 280 | 3474 | 465 | 216 | 46.4516 | |
| ghariani-varprowl | INDEL | * | map_l100_m2_e0 | het | 90.5891 | 98.0928 | 84.1518 | 89.9495 | 2263 | 44 | 2262 | 426 | 198 | 46.4789 | |
| egarrison-hhga | INDEL | I1_5 | * | het | 99.4365 | 99.3775 | 99.4956 | 58.7039 | 78549 | 492 | 78511 | 398 | 185 | 46.4824 | |
| gduggal-snapvard | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 1.5317 | 0.7843 | 32.5163 | 68.9024 | 12 | 1518 | 199 | 413 | 192 | 46.4891 | |
| gduggal-snapvard | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 1.5317 | 0.7843 | 32.5163 | 68.9024 | 12 | 1518 | 199 | 413 | 192 | 46.4891 | |
| egarrison-hhga | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 94.3344 | 92.7536 | 95.9700 | 83.7025 | 1024 | 80 | 1024 | 43 | 20 | 46.5116 | |
| ckim-vqsr | SNP | tv | HG002complexvar | * | 98.6339 | 97.3216 | 99.9820 | 22.8566 | 239559 | 6593 | 239468 | 43 | 20 | 46.5116 | |
| ndellapenna-hhga | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 90.5095 | 98.0519 | 84.0445 | 60.8569 | 453 | 9 | 453 | 86 | 40 | 46.5116 | |
| gduggal-snapvard | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 71.2817 | 75.3968 | 67.5926 | 74.1362 | 475 | 155 | 511 | 245 | 114 | 46.5306 | |
| gduggal-snapfb | SNP | * | map_l150_m2_e1 | het | 95.8511 | 96.9945 | 94.7343 | 76.7883 | 19751 | 612 | 19754 | 1098 | 511 | 46.5392 | |
| egarrison-hhga | INDEL | * | map_siren | het | 97.9497 | 98.4472 | 97.4573 | 81.1814 | 4438 | 70 | 4446 | 116 | 54 | 46.5517 | |
| ciseli-custom | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 78.1562 | 80.3015 | 76.1225 | 51.8771 | 9535 | 2339 | 9494 | 2978 | 1387 | 46.5749 | |
| gduggal-bwavard | INDEL | I1_5 | map_l100_m1_e0 | het | 94.4243 | 97.9408 | 91.1515 | 88.7786 | 761 | 16 | 752 | 73 | 34 | 46.5753 | |
| ltrigg-rtg2 | INDEL | * | HG002complexvar | het | 99.0269 | 98.6108 | 99.4465 | 53.1360 | 45570 | 642 | 44739 | 249 | 116 | 46.5863 | |
| egarrison-hhga | SNP | * | map_l125_m2_e1 | * | 99.4493 | 99.0890 | 99.8122 | 70.5609 | 46772 | 430 | 46772 | 88 | 41 | 46.5909 | |
| eyeh-varpipe | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 95.0193 | 92.3530 | 97.8441 | 60.3645 | 12705 | 1052 | 12662 | 279 | 130 | 46.5950 | |