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 | |||||||||||||||
| mlin-fermikit | SNP | * | map_l250_m2_e1 | het | 43.9700 | 28.3625 | 97.7734 | 83.3895 | 1493 | 3771 | 1493 | 34 | 1 | 2.9412 | |
| gduggal-snapplat | SNP | ti | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 90.1322 | 86.5088 | 94.0725 | 74.1670 | 24187 | 3772 | 24250 | 1528 | 165 | 10.7984 | |
| astatham-gatk | SNP | tv | map_l100_m2_e1 | * | 91.8357 | 85.0651 | 99.7773 | 71.9862 | 21507 | 3776 | 21503 | 48 | 16 | 33.3333 | |
| ghariani-varprowl | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 0.0000 | 0.7096 | 0.0000 | 0.0000 | 27 | 3778 | 0 | 0 | 0 | ||
| gduggal-bwaplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 83.1471 | 72.5516 | 97.3666 | 45.5005 | 9986 | 3778 | 9983 | 270 | 264 | 97.7778 | |
| mlin-fermikit | INDEL | I1_5 | HG002compoundhet | hetalt | 79.4743 | 66.1627 | 99.4916 | 57.4825 | 7395 | 3782 | 7437 | 38 | 38 | 100.0000 | |
| gduggal-snapvard | INDEL | D1_5 | HG002compoundhet | hetalt | 0.0000 | 62.9699 | 0.0000 | 0.0000 | 6433 | 3783 | 0 | 0 | 0 | ||
| jpowers-varprowl | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 0.0000 | 0.5782 | 0.0000 | 0.0000 | 22 | 3783 | 0 | 0 | 0 | ||
| egarrison-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 83.6346 | 82.9843 | 84.2953 | 47.3907 | 18464 | 3786 | 18534 | 3453 | 3234 | 93.6577 | |
| ckim-isaac | SNP | ti | map_l150_m1_e0 | homalt | 65.1458 | 48.3281 | 99.9153 | 66.1412 | 3541 | 3786 | 3541 | 3 | 3 | 100.0000 | |
| mlin-fermikit | INDEL | I1_5 | * | hetalt | 79.4455 | 66.1635 | 99.3997 | 62.4768 | 7407 | 3788 | 7451 | 45 | 45 | 100.0000 | |
| gduggal-bwavard | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 0.0000 | 0.3942 | 0.0000 | 0.0000 | 15 | 3790 | 0 | 0 | 0 | ||
| ndellapenna-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 83.9138 | 82.9573 | 84.8926 | 46.2434 | 18458 | 3792 | 18538 | 3299 | 3068 | 92.9979 | |
| jpowers-varprowl | INDEL | I1_5 | * | het | 91.4249 | 95.2000 | 87.9379 | 62.1984 | 75247 | 3794 | 75259 | 10323 | 10077 | 97.6170 | |
| gduggal-snapvard | INDEL | D1_5 | * | hetalt | 0.0000 | 62.9283 | 0.0000 | 0.0000 | 6447 | 3798 | 0 | 0 | 0 | ||
| ghariani-varprowl | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | hetalt | 0.0000 | 0.6538 | 0.0000 | 0.0000 | 25 | 3799 | 0 | 0 | 0 | ||
| ciseli-custom | SNP | ti | map_l100_m0_e0 | het | 78.5726 | 72.8313 | 85.2966 | 78.4054 | 10184 | 3799 | 10181 | 1755 | 57 | 3.2479 | |
| jpowers-varprowl | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | hetalt | 0.0000 | 0.6015 | 0.0000 | 0.0000 | 23 | 3801 | 0 | 0 | 0 | ||
| ckim-isaac | SNP | * | map_l250_m1_e0 | * | 64.1591 | 47.3553 | 99.4475 | 90.4206 | 3420 | 3802 | 3420 | 19 | 3 | 15.7895 | |
| ckim-isaac | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | * | 92.1428 | 89.6098 | 94.8232 | 41.9297 | 32790 | 3802 | 32348 | 1766 | 1366 | 77.3499 | |
| egarrison-hhga | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 77.4016 | 63.6945 | 98.6259 | 40.8078 | 6672 | 3803 | 6316 | 88 | 82 | 93.1818 | |
| gduggal-snapplat | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 44.5932 | 32.0350 | 73.3458 | 78.2195 | 1793 | 3804 | 1563 | 568 | 142 | 25.0000 | |
| mlin-fermikit | INDEL | I6_15 | HG002compoundhet | hetalt | 71.1432 | 55.4293 | 99.2920 | 28.6902 | 4732 | 3805 | 4768 | 34 | 34 | 100.0000 | |
| mlin-fermikit | INDEL | I6_15 | * | hetalt | 71.1528 | 55.4789 | 99.1705 | 39.8078 | 4744 | 3807 | 4782 | 40 | 40 | 100.0000 | |
| egarrison-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 63.1996 | 46.4567 | 98.8107 | 36.5459 | 3304 | 3808 | 2908 | 35 | 31 | 88.5714 | |
| mlin-fermikit | SNP | tv | map_siren | homalt | 81.9952 | 77.9060 | 86.5373 | 48.2163 | 13431 | 3809 | 13428 | 2089 | 1999 | 95.6917 | |
| gduggal-snapplat | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 40.2264 | 28.2838 | 69.6252 | 65.8356 | 1503 | 3811 | 1412 | 616 | 90 | 14.6104 | |
| ciseli-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 39.2362 | 37.2842 | 41.4038 | 61.8887 | 2268 | 3815 | 2336 | 3306 | 2550 | 77.1325 | |
| gduggal-bwavard | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | hetalt | 0.0000 | 0.1831 | 0.0000 | 0.0000 | 7 | 3817 | 0 | 0 | 0 | ||
| mlin-fermikit | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 85.8694 | 82.8315 | 89.1386 | 45.6102 | 18430 | 3820 | 18400 | 2242 | 2180 | 97.2346 | |
| 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 | |
| egarrison-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 63.3593 | 46.6406 | 98.7609 | 37.5052 | 3346 | 3828 | 2949 | 37 | 33 | 89.1892 | |
| asubramanian-gatk | SNP | * | map_l250_m1_e0 | het | 32.3296 | 19.3060 | 99.3506 | 98.5655 | 918 | 3837 | 918 | 6 | 1 | 16.6667 | |
| gduggal-bwavard | SNP | tv | HG002complexvar | het | 98.2582 | 97.4538 | 99.0760 | 23.1907 | 146896 | 3838 | 144431 | 1347 | 888 | 65.9243 | |
| ciseli-custom | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 0.0000 | 4.6910 | 0.0000 | 0.0000 | 189 | 3840 | 0 | 0 | 0 | ||
| jmaeng-gatk | SNP | ti | map_siren | het | 96.0962 | 93.8396 | 98.4641 | 69.3151 | 58539 | 3843 | 58530 | 913 | 76 | 8.3242 | |
| gduggal-bwaplat | SNP | tv | map_l100_m1_e0 | homalt | 73.0094 | 57.4920 | 100.0000 | 72.7511 | 5199 | 3844 | 5198 | 0 | 0 | ||
| anovak-vg | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 58.8351 | 54.0163 | 64.5980 | 47.2721 | 4519 | 3847 | 5600 | 3069 | 2397 | 78.1036 | |
| qzeng-custom | SNP | ti | map_l100_m1_e0 | homalt | 87.7858 | 78.5523 | 99.4792 | 55.9352 | 14108 | 3852 | 13944 | 73 | 71 | 97.2603 | |
| gduggal-bwaplat | SNP | tv | map_l100_m2_e0 | homalt | 73.5296 | 58.1398 | 100.0000 | 74.6665 | 5357 | 3857 | 5356 | 0 | 0 | ||
| gduggal-snapvard | SNP | ti | map_siren | * | 96.3076 | 96.1556 | 96.4600 | 63.8276 | 96497 | 3858 | 95534 | 3506 | 409 | 11.6657 | |
| qzeng-custom | SNP | ti | map_l100_m2_e0 | homalt | 87.9965 | 78.9175 | 99.4361 | 59.4553 | 14449 | 3860 | 14284 | 81 | 75 | 92.5926 | |
| ndellapenna-hhga | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 81.5223 | 75.9394 | 87.9912 | 60.0478 | 12186 | 3861 | 12361 | 1687 | 1429 | 84.7066 | |
| qzeng-custom | SNP | ti | map_l150_m1_e0 | het | 79.9066 | 68.7551 | 95.3758 | 89.6012 | 8505 | 3865 | 8477 | 411 | 348 | 84.6715 | |
| qzeng-custom | SNP | ti | map_l100_m2_e1 | homalt | 88.0999 | 79.0797 | 99.4428 | 59.4081 | 14625 | 3869 | 14457 | 81 | 75 | 92.5926 | |
| anovak-vg | SNP | ti | map_l125_m1_e0 | * | 81.2273 | 86.8110 | 76.3184 | 74.3923 | 25466 | 3869 | 25253 | 7836 | 1746 | 22.2818 | |
| ciseli-custom | SNP | * | HG002compoundhet | * | 73.2436 | 85.0050 | 64.3413 | 46.5864 | 21950 | 3872 | 21988 | 12186 | 1203 | 9.8720 | |
| anovak-vg | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 47.9368 | 36.5290 | 69.7055 | 72.0207 | 2229 | 3873 | 9137 | 3971 | 2851 | 71.7955 | |
| ltrigg-rtg2 | INDEL | * | * | * | 99.2539 | 98.8759 | 99.6347 | 56.1284 | 340668 | 3873 | 340411 | 1248 | 516 | 41.3462 | |
| ciseli-custom | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | * | 45.4191 | 32.4145 | 75.8496 | 67.6203 | 1858 | 3874 | 1674 | 533 | 342 | 64.1651 | |