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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
23901-23950 / 86044 show all | |||||||||||||||
| jli-custom | SNP | * | map_l250_m2_e0 | * | 98.2912 | 97.3874 | 99.2119 | 86.5904 | 7679 | 206 | 7679 | 61 | 30 | 49.1803 | |
| gduggal-snapfb | SNP | ti | map_l100_m0_e0 | het | 96.0596 | 96.8390 | 95.2927 | 67.8767 | 13541 | 442 | 13543 | 669 | 329 | 49.1779 | |
| jli-custom | SNP | * | map_l250_m1_e0 | * | 98.1678 | 97.1891 | 99.1664 | 85.6613 | 7019 | 203 | 7019 | 59 | 29 | 49.1525 | |
| ckim-vqsr | SNP | * | HG002complexvar | * | 98.7826 | 97.6098 | 99.9840 | 19.7255 | 736350 | 18031 | 736201 | 118 | 58 | 49.1525 | |
| gduggal-snapvard | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 63.1329 | 71.2580 | 56.6710 | 76.9439 | 895 | 361 | 1304 | 997 | 490 | 49.1474 | |
| gduggal-snapplat | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 58.8151 | 45.7510 | 82.3221 | 66.0165 | 2778 | 3294 | 3772 | 810 | 398 | 49.1358 | |
| jlack-gatk | INDEL | I1_5 | HG002complexvar | het | 99.5954 | 99.5052 | 99.6857 | 57.8787 | 18099 | 90 | 18080 | 57 | 28 | 49.1228 | |
| gduggal-bwaplat | INDEL | * | lowcmp_SimpleRepeat_diTR_51to200 | het | 54.9072 | 42.2449 | 78.4091 | 85.8369 | 207 | 283 | 207 | 57 | 28 | 49.1228 | |
| ghariani-varprowl | INDEL | I1_5 | map_siren | het | 93.1801 | 98.4533 | 88.4430 | 87.0613 | 1655 | 26 | 1653 | 216 | 106 | 49.0741 | |
| qzeng-custom | INDEL | D6_15 | HG002complexvar | homalt | 94.3279 | 97.3482 | 91.4894 | 56.3918 | 1138 | 31 | 1161 | 108 | 53 | 49.0741 | |
| egarrison-hhga | SNP | ti | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 99.3239 | 99.0379 | 99.6116 | 52.2441 | 27690 | 269 | 27695 | 108 | 53 | 49.0741 | |
| gduggal-snapvard | SNP | tv | HG002compoundhet | * | 76.6128 | 76.8912 | 76.3364 | 58.1709 | 6861 | 2062 | 7126 | 2209 | 1084 | 49.0720 | |
| ghariani-varprowl | SNP | * | * | homalt | 99.7891 | 99.9588 | 99.6200 | 19.7823 | 1179670 | 486 | 1179792 | 4500 | 2208 | 49.0667 | |
| gduggal-bwaplat | INDEL | * | map_siren | * | 85.3786 | 75.0202 | 99.0556 | 89.6958 | 5559 | 1851 | 5559 | 53 | 26 | 49.0566 | |
| qzeng-custom | INDEL | * | lowcmp_SimpleRepeat_triTR_51to200 | het | 79.3402 | 78.0000 | 80.7273 | 54.0902 | 39 | 11 | 222 | 53 | 26 | 49.0566 | |
| gduggal-snapfb | INDEL | * | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 98.7954 | 98.2348 | 99.3624 | 57.2660 | 16139 | 290 | 16208 | 104 | 51 | 49.0385 | |
| anovak-vg | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 91.5350 | 93.7209 | 89.4487 | 79.3835 | 6239 | 418 | 6587 | 777 | 381 | 49.0347 | |
| ciseli-custom | INDEL | D1_5 | map_l100_m2_e1 | * | 79.9331 | 76.5859 | 83.5863 | 88.3030 | 1485 | 454 | 1487 | 292 | 143 | 48.9726 | |
| gduggal-snapplat | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 69.9531 | 58.7771 | 86.3768 | 94.4057 | 298 | 209 | 298 | 47 | 23 | 48.9362 | |
| gduggal-snapvard | INDEL | I1_5 | map_siren | * | 90.0863 | 91.7138 | 88.5156 | 83.2677 | 2756 | 249 | 2898 | 376 | 184 | 48.9362 | |
| qzeng-custom | INDEL | D1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 99.4030 | 99.1198 | 99.6877 | 55.5385 | 14640 | 130 | 15005 | 47 | 23 | 48.9362 | |
| ciseli-custom | INDEL | D1_5 | map_l100_m1_e0 | * | 79.6470 | 76.1905 | 83.4320 | 87.8636 | 1408 | 440 | 1410 | 280 | 137 | 48.9286 | |
| gduggal-snapplat | SNP | tv | map_l100_m1_e0 | * | 94.8170 | 93.1840 | 96.5083 | 77.9815 | 22831 | 1670 | 22830 | 826 | 404 | 48.9104 | |
| astatham-gatk | SNP | * | map_siren | * | 93.7139 | 88.2540 | 99.8939 | 58.6796 | 129052 | 17176 | 129029 | 137 | 67 | 48.9051 | |
| ndellapenna-hhga | SNP | tv | map_l125_m2_e0 | * | 99.1430 | 98.5687 | 99.7239 | 69.3029 | 16253 | 236 | 16253 | 45 | 22 | 48.8889 | |
| qzeng-custom | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 91.6770 | 95.2628 | 88.3513 | 55.6869 | 1468 | 73 | 6227 | 821 | 401 | 48.8429 | |
| ckim-isaac | INDEL | * | map_l100_m2_e0 | * | 81.7339 | 69.9161 | 98.3594 | 84.3176 | 2582 | 1111 | 2578 | 43 | 21 | 48.8372 | |
| ckim-dragen | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 97.7158 | 97.4490 | 97.9841 | 76.9231 | 2101 | 55 | 2090 | 43 | 21 | 48.8372 | |
| jlack-gatk | SNP | * | lowcmp_SimpleRepeat_diTR_11to50 | het | 99.4314 | 99.5510 | 99.3121 | 70.6126 | 6208 | 28 | 6208 | 43 | 21 | 48.8372 | |
| astatham-gatk | INDEL | D1_5 | * | het | 99.6974 | 99.6803 | 99.7145 | 58.9760 | 87294 | 280 | 87301 | 250 | 122 | 48.8000 | |
| hfeng-pmm1 | SNP | tv | HG002complexvar | * | 99.8458 | 99.7087 | 99.9833 | 21.6860 | 245435 | 717 | 245349 | 41 | 20 | 48.7805 | |
| gduggal-snapvard | INDEL | I1_5 | map_siren | het | 89.5229 | 97.5610 | 82.7085 | 86.5938 | 1640 | 41 | 1765 | 369 | 180 | 48.7805 | |
| egarrison-hhga | SNP | ti | map_l150_m1_e0 | * | 99.3657 | 98.9448 | 99.7902 | 73.6441 | 19504 | 208 | 19504 | 41 | 20 | 48.7805 | |
| egarrison-hhga | SNP | ti | map_l150_m2_e0 | * | 99.3881 | 98.9811 | 99.7985 | 75.2011 | 20303 | 209 | 20303 | 41 | 20 | 48.7805 | |
| ciseli-custom | INDEL | * | map_l250_m1_e0 | * | 57.5139 | 51.1475 | 65.6904 | 97.4137 | 156 | 149 | 157 | 82 | 40 | 48.7805 | |
| ckim-isaac | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 88.4335 | 83.8126 | 93.5937 | 65.9030 | 1807 | 349 | 1797 | 123 | 60 | 48.7805 | |
| ndellapenna-hhga | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 93.6086 | 92.9919 | 94.2335 | 70.5102 | 690 | 52 | 670 | 41 | 20 | 48.7805 | |
| rpoplin-dv42 | SNP | tv | map_l100_m1_e0 | * | 99.2751 | 99.2204 | 99.3298 | 64.0760 | 24310 | 191 | 24306 | 164 | 80 | 48.7805 | |
| qzeng-custom | INDEL | * | map_l150_m2_e0 | * | 81.1578 | 71.3778 | 94.0432 | 94.0095 | 1005 | 403 | 1263 | 80 | 39 | 48.7500 | |
| anovak-vg | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 76.6177 | 84.7222 | 69.9283 | 81.0889 | 1098 | 198 | 1365 | 587 | 286 | 48.7223 | |
| astatham-gatk | SNP | ti | map_l150_m2_e0 | het | 86.0268 | 75.7084 | 99.6015 | 83.8910 | 9752 | 3129 | 9748 | 39 | 19 | 48.7179 | |
| astatham-gatk | SNP | ti | map_l150_m2_e1 | het | 86.0111 | 75.6819 | 99.6055 | 83.9600 | 9850 | 3165 | 9846 | 39 | 19 | 48.7179 | |
| qzeng-custom | INDEL | * | map_l150_m0_e0 | * | 78.8292 | 68.8716 | 92.1529 | 96.4092 | 354 | 160 | 458 | 39 | 19 | 48.7179 | |
| ciseli-custom | INDEL | I16_PLUS | HG002complexvar | het | 19.4609 | 11.4286 | 65.4867 | 81.3223 | 76 | 589 | 74 | 39 | 19 | 48.7179 | |
| ghariani-varprowl | SNP | tv | * | homalt | 99.6533 | 99.9547 | 99.3538 | 23.4817 | 376950 | 171 | 377023 | 2452 | 1194 | 48.6949 | |
| egarrison-hhga | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 98.5257 | 98.5798 | 98.4716 | 73.3734 | 21588 | 311 | 21584 | 335 | 163 | 48.6567 | |
| qzeng-custom | INDEL | * | map_l150_m1_e0 | * | 80.7260 | 70.7025 | 94.0610 | 93.9470 | 946 | 392 | 1172 | 74 | 36 | 48.6486 | |
| qzeng-custom | INDEL | I16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | * | 83.1523 | 78.6082 | 88.2540 | 57.7370 | 305 | 83 | 834 | 111 | 54 | 48.6486 | |
| ndellapenna-hhga | INDEL | I1_5 | * | het | 99.3796 | 99.2245 | 99.5353 | 57.8169 | 78428 | 613 | 78394 | 366 | 178 | 48.6339 | |
| gduggal-bwaplat | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | het | 79.1172 | 68.0571 | 94.4698 | 74.1440 | 1860 | 873 | 1862 | 109 | 53 | 48.6239 | |