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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
84101-84150 / 86044 show all | |||||||||||||||
| bgallagher-sentieon | SNP | tv | * | het | 99.8318 | 99.9594 | 99.7045 | 23.0898 | 591456 | 240 | 591385 | 1753 | 53 | 3.0234 | |
| jpowers-varprowl | SNP | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 97.8391 | 98.7777 | 96.9182 | 66.3842 | 54951 | 680 | 55130 | 1753 | 575 | 32.8009 | |
| gduggal-snapfb | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 75.5526 | 81.0392 | 70.7618 | 54.7757 | 5599 | 1310 | 4245 | 1754 | 345 | 19.6693 | |
| ciseli-custom | SNP | ti | map_l100_m0_e0 | het | 78.5726 | 72.8313 | 85.2966 | 78.4054 | 10184 | 3799 | 10181 | 1755 | 57 | 3.2479 | |
| ciseli-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 80.5000 | 97.2526 | 68.6708 | 63.3133 | 3823 | 108 | 3849 | 1756 | 13 | 0.7403 | |
| ciseli-custom | SNP | * | map_l250_m2_e0 | * | 69.1818 | 64.6798 | 74.3575 | 92.1767 | 5100 | 2785 | 5092 | 1756 | 343 | 19.5330 | |
| ndellapenna-hhga | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 80.6222 | 79.0628 | 82.2442 | 83.6336 | 7964 | 2109 | 8143 | 1758 | 1536 | 87.3720 | |
| gduggal-snapvard | SNP | ti | map_l125_m0_e0 | het | 88.1418 | 95.6916 | 81.6961 | 84.2040 | 7907 | 356 | 7851 | 1759 | 129 | 7.3337 | |
| anovak-vg | SNP | ti | map_l250_m2_e1 | * | 75.8245 | 82.3089 | 70.2872 | 91.6096 | 4178 | 898 | 4161 | 1759 | 398 | 22.6265 | |
| ciseli-custom | SNP | tv | lowcmp_SimpleRepeat_quadTR_11to50 | het | 82.5695 | 96.6091 | 72.0927 | 44.6474 | 4530 | 159 | 4544 | 1759 | 24 | 1.3644 | |
| ciseli-custom | INDEL | * | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 92.4417 | 95.1488 | 89.8844 | 58.8124 | 15632 | 797 | 15630 | 1759 | 720 | 40.9323 | |
| gduggal-snapplat | SNP | * | map_l125_m2_e0 | * | 93.9886 | 91.9975 | 96.0678 | 81.8481 | 42984 | 3739 | 42999 | 1760 | 941 | 53.4659 | |
| ghariani-varprowl | SNP | * | map_l100_m2_e1 | * | 98.3564 | 99.0460 | 97.6764 | 72.0101 | 74024 | 713 | 74027 | 1761 | 324 | 18.3986 | |
| gduggal-snapfb | SNP | * | map_l100_m1_e0 | * | 97.6767 | 97.7805 | 97.5731 | 67.6748 | 70796 | 1607 | 70802 | 1761 | 688 | 39.0687 | |
| jpowers-varprowl | SNP | * | map_siren | * | 98.5825 | 98.3751 | 98.7907 | 60.8110 | 143852 | 2376 | 143855 | 1761 | 441 | 25.0426 | |
| jpowers-varprowl | SNP | ti | * | homalt | 99.8713 | 99.9620 | 99.7807 | 18.3988 | 802733 | 305 | 802784 | 1764 | 1014 | 57.4830 | |
| jlack-gatk | SNP | tv | map_l100_m2_e0 | * | 96.1775 | 99.1691 | 93.3612 | 77.4337 | 24825 | 208 | 24821 | 1765 | 100 | 5.6657 | |
| jlack-gatk | SNP | tv | map_l100_m2_e1 | * | 96.2124 | 99.1773 | 93.4195 | 77.4540 | 25075 | 208 | 25071 | 1766 | 100 | 5.6625 | |
| 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 | |
| ckim-isaac | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | * | 92.1428 | 89.6098 | 94.8232 | 41.9297 | 32790 | 3802 | 32348 | 1766 | 1366 | 77.3499 | |
| gduggal-snapplat | SNP | ti | map_siren | * | 97.1306 | 96.0829 | 98.2013 | 65.7243 | 96424 | 3931 | 96473 | 1767 | 855 | 48.3871 | |
| gduggal-snapplat | SNP | * | map_l125_m2_e1 | * | 94.0312 | 92.0554 | 96.0937 | 81.8790 | 43452 | 3750 | 43468 | 1767 | 944 | 53.4239 | |
| gduggal-snapplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 42.2807 | 34.7724 | 53.9244 | 82.6368 | 1780 | 3339 | 2068 | 1767 | 59 | 3.3390 | |
| 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-snapfb | INDEL | I1_5 | HG002complexvar | het | 93.2070 | 95.4203 | 91.0940 | 55.8992 | 17356 | 833 | 18135 | 1773 | 467 | 26.3395 | |
| ciseli-custom | SNP | * | map_l250_m2_e1 | * | 69.2947 | 64.8053 | 74.4524 | 92.2088 | 5176 | 2811 | 5167 | 1773 | 350 | 19.7406 | |
| rpoplin-dv42 | INDEL | * | HG002compoundhet | * | 93.3591 | 92.7336 | 93.9930 | 68.4001 | 27783 | 2177 | 27758 | 1774 | 1747 | 98.4780 | |
| gduggal-snapfb | INDEL | D1_5 | * | homalt | 97.4626 | 98.4998 | 96.4470 | 62.9841 | 48192 | 734 | 48237 | 1777 | 1307 | 73.5509 | |
| mlin-fermikit | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 86.2115 | 84.1466 | 88.3803 | 58.2216 | 13503 | 2544 | 13516 | 1777 | 1745 | 98.1992 | |
| 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 | |
| gduggal-snapfb | SNP | * | map_l100_m2_e0 | * | 97.7110 | 97.8206 | 97.6017 | 69.6113 | 72352 | 1612 | 72358 | 1778 | 689 | 38.7514 | |
| gduggal-snapvard | SNP | ti | map_l125_m0_e0 | * | 90.9915 | 95.2045 | 87.1355 | 81.6073 | 12150 | 612 | 12043 | 1778 | 144 | 8.0990 | |
| egarrison-hhga | INDEL | D6_15 | HG002compoundhet | * | 61.1341 | 52.4527 | 73.2591 | 39.3063 | 4737 | 4294 | 4871 | 1778 | 1713 | 96.3442 | |
| 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 | |
| gduggal-snapfb | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | het | 82.5030 | 79.8704 | 85.3152 | 53.3915 | 8872 | 2236 | 10353 | 1782 | 570 | 31.9865 | |
| mlin-fermikit | SNP | ti | map_l125_m2_e1 | homalt | 67.0382 | 58.2650 | 78.9219 | 57.4454 | 6676 | 4782 | 6676 | 1783 | 1698 | 95.2328 | |
| gduggal-bwavard | INDEL | D1_5 | HG002complexvar | het | 94.9162 | 98.4397 | 91.6362 | 58.2975 | 20441 | 324 | 19546 | 1784 | 1236 | 69.2825 | |
| bgallagher-sentieon | SNP | tv | * | * | 99.8908 | 99.9655 | 99.8163 | 21.9055 | 969355 | 335 | 969269 | 1784 | 78 | 4.3722 | |
| mlin-fermikit | SNP | tv | HG002complexvar | homalt | 98.2029 | 98.2799 | 98.1261 | 24.4893 | 93475 | 1636 | 93471 | 1785 | 1729 | 96.8627 | |
| gduggal-snapfb | SNP | * | map_l100_m2_e1 | * | 97.7287 | 97.8404 | 97.6173 | 69.6430 | 73123 | 1614 | 73129 | 1785 | 689 | 38.5994 | |
| gduggal-snapfb | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 19.1559 | 90.9502 | 10.7054 | 81.4012 | 201 | 20 | 214 | 1785 | 28 | 1.5686 | |
| ghariani-varprowl | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 94.4227 | 98.4802 | 90.6863 | 72.2353 | 17301 | 267 | 17390 | 1786 | 11 | 0.6159 | |
| anovak-vg | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 71.6772 | 70.5040 | 72.8901 | 52.2851 | 4281 | 1791 | 4802 | 1786 | 1566 | 87.6820 | |
| ciseli-custom | SNP | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 95.3693 | 99.2326 | 91.7955 | 63.9797 | 20044 | 155 | 20005 | 1788 | 579 | 32.3826 | |
| mlin-fermikit | SNP | tv | map_l100_m1_e0 | * | 70.4651 | 58.3772 | 88.8661 | 53.8051 | 14303 | 10198 | 14295 | 1791 | 1587 | 88.6097 | |
| bgallagher-sentieon | INDEL | * | HG002compoundhet | * | 93.7345 | 93.5147 | 93.9554 | 62.6967 | 28017 | 1943 | 27901 | 1795 | 1783 | 99.3315 | |
| qzeng-custom | INDEL | I1_5 | * | * | 97.7958 | 96.8327 | 98.7782 | 55.3353 | 145892 | 4772 | 145850 | 1804 | 1184 | 65.6319 | |
| raldana-dualsentieon | SNP | * | * | het | 99.8865 | 99.8694 | 99.9036 | 19.2179 | 1871141 | 2446 | 1871016 | 1806 | 43 | 2.3810 | |
| ndellapenna-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 77.1879 | 70.9467 | 84.6330 | 51.0225 | 9780 | 4005 | 9952 | 1807 | 1577 | 87.2717 | |