PrecisionFDA
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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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1101-1150 / 86044 show all | |||||||||||||||
| mlin-fermikit | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 90.3770 | 92.9127 | 87.9760 | 55.1468 | 12782 | 975 | 12731 | 1740 | 1664 | 95.6322 | |
| mlin-fermikit | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 90.3770 | 92.9127 | 87.9760 | 55.1468 | 12782 | 975 | 12731 | 1740 | 1664 | 95.6322 | |
| gduggal-bwavard | INDEL | I1_5 | HG002complexvar | het | 93.6787 | 97.5535 | 90.0999 | 57.7758 | 17744 | 445 | 17310 | 1902 | 1663 | 87.4343 | |
| eyeh-varpipe | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 54.1237 | 72.0257 | 43.3492 | 26.9375 | 224 | 87 | 1271 | 1661 | 1654 | 99.5786 | |
| mlin-fermikit | SNP | ti | map_l125_m1_e0 | * | 63.1485 | 49.0745 | 88.5410 | 56.6927 | 14396 | 14939 | 14395 | 1863 | 1654 | 88.7815 | |
| mlin-fermikit | INDEL | D6_15 | * | het | 90.4589 | 94.5825 | 86.6799 | 51.7766 | 10964 | 628 | 10952 | 1683 | 1653 | 98.2175 | |
| ghariani-varprowl | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 36.5445 | 33.8941 | 39.6445 | 65.7686 | 1088 | 2122 | 1093 | 1664 | 1651 | 99.2188 | |
| anovak-vg | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 37.5716 | 28.2822 | 55.9480 | 46.5176 | 1788 | 4534 | 2582 | 2033 | 1650 | 81.1608 | |
| anovak-vg | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 37.5716 | 28.2822 | 55.9480 | 46.5176 | 1788 | 4534 | 2582 | 2033 | 1650 | 81.1608 | |
| gduggal-bwafb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 92.2413 | 93.5539 | 90.9650 | 64.4972 | 16995 | 1171 | 16995 | 1688 | 1649 | 97.6896 | |
| gduggal-bwafb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 92.2413 | 93.5539 | 90.9650 | 64.4972 | 16995 | 1171 | 16995 | 1688 | 1649 | 97.6896 | |
| mlin-fermikit | SNP | ti | map_l125_m1_e0 | homalt | 66.1427 | 57.1480 | 78.4977 | 52.8912 | 6312 | 4733 | 6312 | 1729 | 1647 | 95.2574 | |
| anovak-vg | SNP | tv | HG002compoundhet | * | 74.6577 | 75.2101 | 74.1133 | 50.0629 | 6711 | 2212 | 7063 | 2467 | 1646 | 66.7207 | |
| anovak-vg | INDEL | * | lowcmp_SimpleRepeat_triTR_11to50 | * | 72.6300 | 71.4689 | 73.8294 | 38.5577 | 4812 | 1921 | 5913 | 2096 | 1645 | 78.4828 | |
| mlin-fermikit | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 67.9552 | 65.9379 | 70.1000 | 59.0467 | 4011 | 2072 | 3927 | 1675 | 1645 | 98.2090 | |
| egarrison-hhga | INDEL | D6_15 | * | het | 92.3399 | 97.9037 | 87.3745 | 56.6927 | 11349 | 243 | 11924 | 1723 | 1642 | 95.2989 | |
| egarrison-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 86.5434 | 96.4420 | 78.4876 | 62.7159 | 5638 | 208 | 6217 | 1704 | 1642 | 96.3615 | |
| egarrison-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 86.5434 | 96.4420 | 78.4876 | 62.7159 | 5638 | 208 | 6217 | 1704 | 1642 | 96.3615 | |
| jpowers-varprowl | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 35.0251 | 32.1184 | 38.5102 | 64.1905 | 1031 | 2179 | 1034 | 1651 | 1642 | 99.4549 | |
| eyeh-varpipe | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 52.5500 | 71.5640 | 41.5188 | 24.1862 | 151 | 60 | 1170 | 1648 | 1641 | 99.5752 | |
| mlin-fermikit | INDEL | I6_15 | * | het | 88.6098 | 92.6243 | 84.9289 | 50.1273 | 9293 | 740 | 9315 | 1653 | 1640 | 99.2136 | |
| ckim-isaac | INDEL | I1_5 | * | * | 96.6542 | 94.9085 | 98.4652 | 49.5628 | 142993 | 7671 | 142942 | 2228 | 1638 | 73.5189 | |
| raldana-dualsentieon | INDEL | * | * | * | 99.1095 | 98.7566 | 99.4648 | 57.7282 | 340258 | 4284 | 340120 | 1830 | 1626 | 88.8525 | |
| anovak-vg | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 81.2064 | 88.9071 | 74.7333 | 41.7707 | 5971 | 745 | 6655 | 2250 | 1626 | 72.2667 | |
| jmaeng-gatk | INDEL | * | * | * | 99.1098 | 99.0216 | 99.1981 | 60.9184 | 341171 | 3371 | 341038 | 2757 | 1621 | 58.7958 | |
| mlin-fermikit | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 83.0571 | 91.0366 | 76.3636 | 59.1295 | 5322 | 524 | 5292 | 1638 | 1616 | 98.6569 | |
| mlin-fermikit | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 83.0571 | 91.0366 | 76.3636 | 59.1295 | 5322 | 524 | 5292 | 1638 | 1616 | 98.6569 | |
| mlin-fermikit | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 90.3706 | 96.6600 | 84.8496 | 55.8282 | 9203 | 318 | 9196 | 1642 | 1614 | 98.2948 | |
| rpoplin-dv42 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 96.7786 | 96.2480 | 97.3151 | 87.4466 | 62899 | 2452 | 62814 | 1733 | 1611 | 92.9602 | |
| rpoplin-dv42 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 96.7786 | 96.2480 | 97.3151 | 87.4466 | 62899 | 2452 | 62814 | 1733 | 1611 | 92.9602 | |
| ckim-dragen | INDEL | * | * | homalt | 99.2636 | 99.8234 | 98.7101 | 59.5235 | 124951 | 221 | 124887 | 1632 | 1607 | 98.4681 | |
| gduggal-snapfb | INDEL | I1_5 | * | het | 94.5346 | 97.1091 | 92.0931 | 57.7460 | 76756 | 2285 | 82322 | 7068 | 1603 | 22.6797 | |
| egarrison-hhga | INDEL | D6_15 | HG002compoundhet | het | 59.7254 | 89.0187 | 44.9378 | 47.8055 | 762 | 94 | 1336 | 1637 | 1603 | 97.9230 | |
| gduggal-snapvard | SNP | ti | HG002complexvar | het | 97.7415 | 96.8929 | 98.6052 | 20.9330 | 304985 | 9780 | 300448 | 4250 | 1602 | 37.6941 | |
| jpowers-varprowl | SNP | * | HG002complexvar | * | 99.4683 | 99.2937 | 99.6435 | 20.7160 | 749051 | 5328 | 749404 | 2681 | 1602 | 59.7538 | |
| ckim-isaac | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 90.5655 | 92.3733 | 88.8270 | 56.6366 | 16460 | 1359 | 15479 | 1947 | 1601 | 82.2291 | |
| jpowers-varprowl | INDEL | I1_5 | HG002complexvar | * | 92.7158 | 90.8192 | 94.6934 | 52.3150 | 30300 | 3063 | 30175 | 1691 | 1600 | 94.6186 | |
| mlin-fermikit | SNP | tv | map_l100_m2_e1 | * | 71.2430 | 59.3165 | 89.1725 | 57.7345 | 14997 | 10286 | 14989 | 1820 | 1600 | 87.9121 | |
| gduggal-bwavard | SNP | ti | HG002complexvar | * | 98.2991 | 97.1039 | 99.5241 | 18.2603 | 493712 | 14725 | 485576 | 2322 | 1599 | 68.8630 | |
| mlin-fermikit | SNP | tv | map_l100_m2_e1 | homalt | 72.1476 | 66.6523 | 78.6303 | 53.6694 | 6200 | 3102 | 6200 | 1685 | 1598 | 94.8368 | |
| mlin-fermikit | SNP | tv | map_l100_m2_e0 | * | 71.0756 | 59.1180 | 89.0970 | 57.6083 | 14799 | 10234 | 14791 | 1810 | 1594 | 88.0663 | |
| ndellapenna-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 78.5723 | 72.6344 | 85.5675 | 52.9869 | 10739 | 4046 | 10909 | 1840 | 1594 | 86.6304 | |
| ghariani-varprowl | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 48.4627 | 89.8402 | 33.1807 | 64.3673 | 787 | 89 | 797 | 1605 | 1594 | 99.3146 | |
| cchapple-custom | INDEL | * | * | * | 99.1388 | 98.8448 | 99.4346 | 57.2260 | 340562 | 3980 | 363520 | 2067 | 1592 | 77.0198 | |
| mlin-fermikit | SNP | tv | map_l100_m2_e0 | homalt | 72.0127 | 66.5183 | 78.4964 | 53.5791 | 6129 | 3085 | 6129 | 1679 | 1592 | 94.8183 | |
| mlin-fermikit | SNP | tv | map_l100_m1_e0 | * | 70.4651 | 58.3772 | 88.8661 | 53.8051 | 14303 | 10198 | 14295 | 1791 | 1587 | 88.6097 | |
| egarrison-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 78.5618 | 72.3842 | 85.8922 | 52.6470 | 10702 | 4083 | 10825 | 1778 | 1586 | 89.2013 | |
| ghariani-varprowl | INDEL | I1_5 | HG002complexvar | * | 92.9673 | 92.2577 | 93.6879 | 54.6199 | 30779 | 2583 | 30650 | 2065 | 1585 | 76.7554 | |
| mlin-fermikit | SNP | tv | map_l100_m1_e0 | homalt | 71.5194 | 65.9516 | 78.1139 | 49.8226 | 5964 | 3079 | 5964 | 1671 | 1585 | 94.8534 | |
| jpowers-varprowl | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 45.9328 | 83.4475 | 31.6874 | 62.3505 | 731 | 145 | 738 | 1591 | 1584 | 99.5600 | |