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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1051-1100 / 86044 show all | |||||||||||||||
| gduggal-snapfb | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 76.0331 | 67.0590 | 87.7802 | 43.4475 | 11850 | 5821 | 12686 | 1766 | 1744 | 98.7542 | |
| gduggal-snapfb | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 76.0331 | 67.0590 | 87.7802 | 43.4475 | 11850 | 5821 | 12686 | 1766 | 1744 | 98.7542 | |
| gduggal-snapfb | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 94.5807 | 94.0681 | 95.0990 | 73.7052 | 60609 | 3822 | 61530 | 3171 | 1742 | 54.9354 | |
| gduggal-snapplat | INDEL | D1_5 | HG002compoundhet | homalt | 26.1575 | 72.5086 | 15.9570 | 58.0098 | 211 | 80 | 371 | 1954 | 1741 | 89.0993 | |
| mlin-fermikit | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 86.9120 | 84.3420 | 89.6435 | 36.7917 | 15400 | 2859 | 15390 | 1778 | 1740 | 97.8628 | |
| mlin-fermikit | SNP | tv | HG002complexvar | * | 98.1368 | 97.0653 | 99.2323 | 22.0366 | 238931 | 7224 | 238861 | 1848 | 1739 | 94.1017 | |
| gduggal-snapplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 46.1868 | 42.3753 | 50.7516 | 72.8442 | 6194 | 8423 | 7833 | 7601 | 1738 | 22.8654 | |
| ckim-isaac | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 90.8245 | 87.6365 | 94.2532 | 40.4574 | 33216 | 4686 | 32687 | 1993 | 1737 | 87.1550 | |
| gduggal-snapfb | INDEL | I1_5 | HG002compoundhet | * | 77.3920 | 77.8731 | 76.9169 | 63.1671 | 9622 | 2734 | 10473 | 3143 | 1735 | 55.2020 | |
| mlin-fermikit | SNP | tv | HG002complexvar | homalt | 98.2029 | 98.2799 | 98.1261 | 24.4893 | 93475 | 1636 | 93471 | 1785 | 1729 | 96.8627 | |
| ndellapenna-hhga | INDEL | D6_15 | HG002compoundhet | * | 61.2798 | 52.8513 | 72.9065 | 39.3574 | 4773 | 4258 | 4954 | 1841 | 1725 | 93.6991 | |
| anovak-vg | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 54.7235 | 48.0480 | 63.5530 | 34.9033 | 640 | 692 | 3742 | 2146 | 1725 | 80.3821 | |
| anovak-vg | SNP | ti | map_l125_m2_e1 | het | 77.5988 | 89.9303 | 68.2413 | 78.1425 | 17165 | 1922 | 17046 | 7933 | 1721 | 21.6942 | |
| anovak-vg | SNP | ti | map_l125_m2_e0 | het | 77.5170 | 89.8919 | 68.1370 | 78.1191 | 16968 | 1908 | 16853 | 7881 | 1719 | 21.8120 | |
| gduggal-snapvard | INDEL | D6_15 | HG002compoundhet | * | 59.7955 | 51.4782 | 71.3183 | 33.2912 | 4649 | 4382 | 4896 | 1969 | 1719 | 87.3032 | |
| gduggal-snapvard | INDEL | D6_15 | HG002compoundhet | het | 67.0812 | 63.3178 | 71.3203 | 33.1905 | 542 | 314 | 4894 | 1968 | 1718 | 87.2967 | |
| anovak-vg | SNP | tv | map_siren | het | 83.8130 | 92.8414 | 76.3848 | 65.0646 | 26561 | 2048 | 26517 | 8198 | 1714 | 20.9075 | |
| egarrison-hhga | INDEL | D6_15 | HG002compoundhet | * | 61.1341 | 52.4527 | 73.2591 | 39.3063 | 4737 | 4294 | 4871 | 1778 | 1713 | 96.3442 | |
| ciseli-custom | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | het | 79.9546 | 88.8056 | 72.7080 | 46.5949 | 9242 | 1165 | 9596 | 3602 | 1710 | 47.4736 | |
| gduggal-bwafb | INDEL | * | * | het | 97.2465 | 95.6571 | 98.8897 | 54.7010 | 185702 | 8431 | 212773 | 2389 | 1710 | 71.5781 | |
| eyeh-varpipe | INDEL | D16_PLUS | * | * | 59.3408 | 53.1250 | 67.2039 | 51.2916 | 3604 | 3180 | 3586 | 1750 | 1709 | 97.6571 | |
| gduggal-bwavard | INDEL | I16_PLUS | * | * | 58.4101 | 56.2490 | 60.7439 | 65.3100 | 3587 | 2790 | 3593 | 2322 | 1708 | 73.5573 | |
| anovak-vg | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 90.4686 | 92.4642 | 88.5573 | 75.8297 | 42258 | 3444 | 42999 | 5556 | 1706 | 30.7055 | |
| anovak-vg | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 90.4686 | 92.4642 | 88.5573 | 75.8297 | 42258 | 3444 | 42999 | 5556 | 1706 | 30.7055 | |
| jpowers-varprowl | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 64.7210 | 53.4249 | 82.0746 | 70.9149 | 8322 | 7255 | 8292 | 1811 | 1705 | 94.1469 | |
| mlin-fermikit | SNP | ti | map_l125_m2_e1 | * | 64.3036 | 50.3876 | 88.8389 | 61.3583 | 15403 | 15166 | 15402 | 1935 | 1705 | 88.1137 | |
| gduggal-bwavard | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 65.1709 | 54.2531 | 81.5900 | 69.4864 | 8451 | 7126 | 8323 | 1878 | 1704 | 90.7348 | |
| ckim-isaac | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 94.7847 | 94.6676 | 94.9020 | 63.1937 | 45697 | 2574 | 44659 | 2399 | 1704 | 71.0296 | |
| gduggal-bwavard | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 84.1187 | 95.1327 | 75.3903 | 72.1991 | 5805 | 297 | 5747 | 1876 | 1702 | 90.7249 | |
| gduggal-snapplat | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 68.7702 | 67.0305 | 70.6027 | 63.8943 | 3808 | 1873 | 5471 | 2278 | 1700 | 74.6269 | |
| mlin-fermikit | SNP | ti | map_l125_m2_e1 | homalt | 67.0382 | 58.2650 | 78.9219 | 57.4454 | 6676 | 4782 | 6676 | 1783 | 1698 | 95.2328 | |
| anovak-vg | SNP | ti | map_l125_m1_e0 | het | 77.2287 | 89.8883 | 67.6948 | 76.8145 | 16419 | 1847 | 16307 | 7782 | 1697 | 21.8067 | |
| mlin-fermikit | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | * | 90.5721 | 88.6430 | 92.5871 | 36.0947 | 21753 | 2787 | 21720 | 1739 | 1695 | 97.4698 | |
| gduggal-bwavard | INDEL | I16_PLUS | * | het | 66.4433 | 91.0228 | 52.3161 | 67.5288 | 2474 | 244 | 2496 | 2275 | 1694 | 74.4615 | |
| ciseli-custom | INDEL | I1_5 | HG002complexvar | het | 88.5454 | 89.7735 | 87.3504 | 57.1664 | 16328 | 1860 | 16352 | 2368 | 1692 | 71.4527 | |
| mlin-fermikit | SNP | ti | map_l125_m2_e0 | * | 64.0610 | 50.1091 | 88.7802 | 61.1948 | 15162 | 15096 | 15161 | 1916 | 1690 | 88.2046 | |
| gduggal-snapplat | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 68.6126 | 67.6959 | 69.5544 | 59.1226 | 3464 | 1653 | 5010 | 2193 | 1686 | 76.8810 | |
| mlin-fermikit | SNP | ti | map_l125_m2_e0 | homalt | 66.8459 | 58.0120 | 78.8535 | 57.3303 | 6589 | 4769 | 6589 | 1767 | 1683 | 95.2462 | |
| gduggal-bwavard | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 47.8303 | 45.4143 | 50.5177 | 68.7660 | 1847 | 2220 | 1854 | 1816 | 1681 | 92.5661 | |
| gduggal-snapvard | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 38.8587 | 37.6192 | 40.1826 | 50.2147 | 907 | 1504 | 1584 | 2358 | 1680 | 71.2468 | |
| ghariani-varprowl | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 65.9654 | 55.6526 | 80.9698 | 74.3202 | 8669 | 6908 | 8633 | 2029 | 1680 | 82.7994 | |
| mlin-fermikit | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 73.6558 | 85.1238 | 64.9109 | 67.0798 | 3439 | 601 | 3241 | 1752 | 1680 | 95.8904 | |
| mlin-fermikit | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 91.3029 | 96.6649 | 86.5044 | 61.6244 | 11101 | 383 | 11089 | 1730 | 1680 | 97.1098 | |
| gduggal-snapvard | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 50.1574 | 67.0715 | 40.0560 | 49.5050 | 497 | 244 | 1573 | 2354 | 1678 | 71.2829 | |
| gduggal-bwavard | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 56.4307 | 91.8797 | 40.7201 | 70.5769 | 1222 | 108 | 1244 | 1811 | 1677 | 92.6008 | |
| anovak-vg | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 54.2561 | 49.7820 | 59.6139 | 54.7156 | 1941 | 1958 | 3057 | 2071 | 1674 | 80.8305 | |
| anovak-vg | INDEL | D1_5 | HG002complexvar | * | 91.1523 | 90.0107 | 92.3232 | 54.8532 | 29447 | 3268 | 29789 | 2477 | 1674 | 67.5818 | |
| gduggal-snapplat | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 82.6699 | 77.1496 | 89.0409 | 77.8450 | 16895 | 5004 | 19914 | 2451 | 1673 | 68.2579 | |
| anovak-vg | INDEL | D1_5 | HG002compoundhet | homalt | 30.3224 | 87.2852 | 18.3482 | 73.7981 | 254 | 37 | 431 | 1918 | 1670 | 87.0699 | |
| gduggal-bwavard | INDEL | I1_5 | HG002complexvar | * | 92.2209 | 90.6273 | 93.8716 | 50.7362 | 30236 | 3127 | 29241 | 1909 | 1668 | 87.3756 | |