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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
83951-84000 / 86044 show all | |||||||||||||||
| gduggal-snapfb | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 75.3468 | 98.8372 | 60.8781 | 62.7229 | 2465 | 29 | 2482 | 1595 | 17 | 1.0658 | |
| gduggal-snapvard | SNP | tv | map_l150_m1_e0 | * | 91.4337 | 96.5909 | 86.7993 | 81.5080 | 10540 | 372 | 10514 | 1599 | 100 | 6.2539 | |
| gduggal-snapplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 38.2939 | 34.3333 | 43.2873 | 81.8899 | 1030 | 1970 | 1222 | 1601 | 26 | 1.6240 | |
| ndellapenna-hhga | INDEL | * | HG002complexvar | * | 97.2866 | 96.6882 | 97.8924 | 67.2163 | 74390 | 2548 | 74363 | 1601 | 1150 | 71.8301 | |
| gduggal-snapvard | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 66.0556 | 65.0014 | 67.1446 | 72.1458 | 2355 | 1268 | 3278 | 1604 | 1089 | 67.8928 | |
| 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 | |
| gduggal-snapvard | SNP | tv | map_l150_m2_e0 | het | 88.6343 | 97.2835 | 81.3975 | 85.0700 | 7055 | 197 | 7036 | 1608 | 95 | 5.9080 | |
| anovak-vg | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 37.7291 | 27.7742 | 58.8070 | 42.9448 | 428 | 1113 | 2297 | 1609 | 1324 | 82.2871 | |
| gduggal-snapfb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 85.1837 | 88.4652 | 82.1369 | 53.6130 | 7401 | 965 | 7403 | 1610 | 1503 | 93.3540 | |
| gduggal-snapvard | SNP | tv | map_l150_m2_e1 | het | 88.7208 | 97.3054 | 81.5281 | 85.1064 | 7150 | 198 | 7128 | 1615 | 97 | 6.0062 | |
| gduggal-snapvard | SNP | tv | map_l150_m2_e0 | * | 91.6223 | 96.6094 | 87.1248 | 82.6892 | 10970 | 385 | 10942 | 1617 | 102 | 6.3080 | |
| gduggal-snapvard | SNP | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 76.2490 | 94.7944 | 63.7727 | 85.1927 | 2859 | 157 | 2850 | 1619 | 31 | 1.9148 | |
| gduggal-bwavard | SNP | ti | map_l125_m1_e0 | het | 94.5411 | 97.6568 | 91.6179 | 81.9499 | 17838 | 428 | 17707 | 1620 | 106 | 6.5432 | |
| qzeng-custom | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 97.3828 | 98.2445 | 96.5360 | 67.1067 | 30221 | 540 | 45147 | 1620 | 1222 | 75.4321 | |
| gduggal-snapvard | SNP | tv | map_l150_m2_e1 | * | 91.6730 | 96.6093 | 87.2166 | 82.7232 | 11112 | 390 | 11080 | 1624 | 104 | 6.4039 | |
| jlack-gatk | SNP | ti | map_l125_m1_e0 | het | 95.2550 | 99.0419 | 91.7470 | 82.2690 | 18091 | 175 | 18087 | 1627 | 140 | 8.6048 | |
| gduggal-snapvard | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 58.8714 | 87.8468 | 44.2696 | 89.1685 | 1330 | 184 | 1294 | 1629 | 74 | 4.5427 | |
| gduggal-bwavard | SNP | * | map_l150_m0_e0 | het | 89.4308 | 97.6574 | 82.4825 | 88.0388 | 7754 | 186 | 7675 | 1630 | 60 | 3.6810 | |
| ciseli-custom | INDEL | D16_PLUS | * | * | 59.6718 | 52.7860 | 68.6237 | 57.6195 | 3581 | 3203 | 3565 | 1630 | 1503 | 92.2086 | |
| gduggal-bwavard | SNP | ti | map_l125_m2_e0 | het | 94.6336 | 97.6319 | 91.8139 | 83.0438 | 18429 | 447 | 18293 | 1631 | 107 | 6.5604 | |
| gduggal-snapfb | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 15.4909 | 90.1316 | 8.4736 | 78.2178 | 137 | 15 | 151 | 1631 | 23 | 1.4102 | |
| ndellapenna-hhga | INDEL | * | * | homalt | 98.8395 | 98.9790 | 98.7005 | 54.9139 | 123894 | 1278 | 123877 | 1631 | 1021 | 62.5996 | |
| mlin-fermikit | SNP | * | HG002compoundhet | * | 92.7673 | 91.9758 | 93.5725 | 42.5829 | 23750 | 2072 | 23759 | 1632 | 1332 | 81.6176 | |
| gduggal-bwavard | SNP | ti | map_l125_m1_e0 | * | 95.9902 | 97.4706 | 94.5540 | 78.3647 | 28593 | 742 | 28335 | 1632 | 115 | 7.0466 | |
| ckim-dragen | INDEL | * | * | homalt | 99.2636 | 99.8234 | 98.7101 | 59.5235 | 124951 | 221 | 124887 | 1632 | 1607 | 98.4681 | |
| qzeng-custom | INDEL | * | HG002complexvar | * | 97.6731 | 97.4200 | 97.9274 | 54.9567 | 74953 | 1985 | 77253 | 1635 | 731 | 44.7095 | |
| mlin-fermikit | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 95.7763 | 96.4226 | 95.1386 | 69.4450 | 32047 | 1189 | 32017 | 1636 | 1576 | 96.3325 | |
| egarrison-hhga | INDEL | D6_15 | HG002compoundhet | het | 59.7254 | 89.0187 | 44.9378 | 47.8055 | 762 | 94 | 1336 | 1637 | 1603 | 97.9230 | |
| 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 | |
| gduggal-bwavard | SNP | ti | map_l125_m2_e1 | het | 94.6705 | 97.6529 | 91.8649 | 83.0811 | 18639 | 448 | 18497 | 1638 | 107 | 6.5324 | |
| jlack-gatk | SNP | ti | map_l125_m1_e0 | * | 96.7083 | 98.8614 | 94.6470 | 78.3386 | 29001 | 334 | 28997 | 1640 | 151 | 9.2073 | |
| eyeh-varpipe | SNP | * | map_l100_m1_e0 | het | 97.9959 | 99.6627 | 96.3839 | 70.0308 | 45206 | 153 | 43739 | 1641 | 34 | 2.0719 | |
| 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 | |
| egarrison-hhga | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 81.4567 | 75.6715 | 88.1998 | 59.8076 | 12143 | 3904 | 12273 | 1642 | 1435 | 87.3934 | |
| gduggal-snapfb | INDEL | D1_5 | HG002complexvar | * | 94.7329 | 94.4337 | 95.0340 | 57.1180 | 30894 | 1821 | 31423 | 1642 | 692 | 42.1437 | |
| ghariani-varprowl | INDEL | D1_5 | HG002complexvar | het | 95.4621 | 98.5649 | 92.5488 | 58.7032 | 20467 | 298 | 20407 | 1643 | 1130 | 68.7766 | |
| gduggal-bwavard | SNP | ti | map_l125_m2_e0 | * | 96.0478 | 97.4585 | 94.6773 | 79.7239 | 29489 | 769 | 29225 | 1643 | 116 | 7.0603 | |
| gduggal-bwavard | SNP | * | map_l150_m0_e0 | * | 92.1711 | 97.2989 | 87.5568 | 86.0626 | 11707 | 325 | 11568 | 1644 | 70 | 4.2579 | |
| ghariani-varprowl | SNP | * | map_l100_m2_e0 | het | 97.8332 | 99.1530 | 96.5480 | 75.0125 | 46006 | 393 | 46009 | 1645 | 255 | 15.5015 | |
| ciseli-custom | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 56.2607 | 88.9328 | 41.1449 | 83.1108 | 1125 | 140 | 1150 | 1645 | 97 | 5.8967 | |
| ghariani-varprowl | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 85.8876 | 95.4769 | 78.0488 | 76.6109 | 5826 | 276 | 5856 | 1647 | 1442 | 87.5531 | |
| gduggal-snapfb | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 72.2413 | 99.3100 | 56.7681 | 68.0924 | 2159 | 15 | 2164 | 1648 | 10 | 0.6068 | |
| ciseli-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 70.4680 | 75.1615 | 66.3261 | 61.3642 | 2908 | 961 | 3246 | 1648 | 1139 | 69.1141 | |
| 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 | |
| anovak-vg | SNP | ti | map_l250_m1_e0 | het | 71.0849 | 85.8491 | 60.6538 | 92.0278 | 2548 | 420 | 2542 | 1649 | 363 | 22.0133 | |
| gduggal-bwavard | SNP | ti | map_l125_m2_e1 | * | 96.0728 | 97.4778 | 94.7076 | 79.7669 | 29798 | 771 | 29527 | 1650 | 116 | 7.0303 | |
| gduggal-snapvard | SNP | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 82.6781 | 95.0672 | 73.1457 | 83.0764 | 4529 | 235 | 4497 | 1651 | 43 | 2.6045 | |
| 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 | |
| mlin-fermikit | INDEL | I6_15 | * | het | 88.6098 | 92.6243 | 84.9289 | 50.1273 | 9293 | 740 | 9315 | 1653 | 1640 | 99.2136 | |