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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2551-2600 / 86044 show all | |||||||||||||||
| cchapple-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.3696 | 99.2268 | 97.5271 | 78.9884 | 28490 | 222 | 28632 | 726 | 57 | 7.8512 | |
| cchapple-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.3696 | 99.2268 | 97.5271 | 78.9884 | 28490 | 222 | 28632 | 726 | 57 | 7.8512 | |
| hfeng-pmm2 | SNP | tv | map_siren | het | 99.5196 | 99.5806 | 99.4588 | 60.5491 | 28489 | 120 | 28484 | 155 | 14 | 9.0323 | |
| jpowers-varprowl | SNP | ti | map_l125_m1_e0 | * | 97.7356 | 97.1093 | 98.3701 | 74.4440 | 28487 | 848 | 28487 | 472 | 165 | 34.9576 | |
| ciseli-custom | INDEL | D1_5 | HG002complexvar | * | 84.6887 | 87.0694 | 82.4348 | 57.7103 | 28483 | 4230 | 28182 | 6005 | 2638 | 43.9301 | |
| ckim-dragen | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.4729 | 99.1955 | 97.7608 | 76.5892 | 28481 | 231 | 28728 | 658 | 53 | 8.0547 | |
| ckim-dragen | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.4729 | 99.1955 | 97.7608 | 76.5892 | 28481 | 231 | 28728 | 658 | 53 | 8.0547 | |
| jlack-gatk | SNP | tv | map_siren | het | 95.9855 | 99.5106 | 92.7015 | 72.5215 | 28469 | 140 | 28464 | 2241 | 108 | 4.8193 | |
| raldana-dualsentieon | SNP | tv | map_siren | het | 99.3697 | 99.4827 | 99.2570 | 59.7589 | 28461 | 148 | 28456 | 213 | 2 | 0.9390 | |
| astatham-gatk | SNP | * | map_l100_m0_e0 | * | 92.7245 | 86.6569 | 99.7057 | 72.7426 | 28459 | 4382 | 28455 | 84 | 35 | 41.6667 | |
| dgrover-gatk | INDEL | * | HG002compoundhet | * | 95.1627 | 94.9733 | 95.3528 | 63.3096 | 28454 | 1506 | 28336 | 1381 | 1370 | 99.2035 | |
| ghariani-varprowl | SNP | tv | map_siren | het | 97.7279 | 99.4512 | 96.0633 | 68.6369 | 28452 | 157 | 28453 | 1166 | 112 | 9.6055 | |
| jli-custom | SNP | tv | map_siren | het | 99.4790 | 99.4407 | 99.5172 | 56.5108 | 28449 | 160 | 28447 | 138 | 26 | 18.8406 | |
| jmaeng-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.6217 | 99.0631 | 98.1843 | 79.0142 | 28443 | 269 | 28443 | 526 | 29 | 5.5133 | |
| jmaeng-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.6217 | 99.0631 | 98.1843 | 79.0142 | 28443 | 269 | 28443 | 526 | 29 | 5.5133 | |
| ckim-dragen | SNP | tv | map_siren | het | 98.4766 | 99.4128 | 97.5580 | 65.5354 | 28441 | 168 | 28444 | 712 | 52 | 7.3034 | |
| ltrigg-rtg2 | INDEL | * | HG002compoundhet | * | 96.7706 | 94.9266 | 98.6878 | 59.5666 | 28440 | 1520 | 28503 | 379 | 309 | 81.5303 | |
| rpoplin-dv42 | SNP | tv | map_siren | het | 99.4388 | 99.4093 | 99.4683 | 57.2644 | 28440 | 169 | 28436 | 152 | 65 | 42.7632 | |
| hfeng-pmm1 | SNP | tv | map_siren | het | 99.6130 | 99.4093 | 99.8175 | 56.2607 | 28440 | 169 | 28435 | 52 | 14 | 26.9231 | |
| cchapple-custom | SNP | ti | map_l125_m1_e0 | * | 97.0755 | 96.9422 | 97.2092 | 72.6876 | 28438 | 897 | 28423 | 816 | 227 | 27.8186 | |
| gduggal-snapplat | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 65.4034 | 58.8863 | 73.5426 | 80.9801 | 28425 | 19846 | 32333 | 11632 | 1955 | 16.8071 | |
| gduggal-bwafb | SNP | tv | map_siren | het | 98.7335 | 99.3254 | 98.1487 | 63.6405 | 28416 | 193 | 28416 | 536 | 69 | 12.8731 | |
| gduggal-snapvard | SNP | * | map_l125_m2_e0 | het | 91.4436 | 96.8927 | 86.5748 | 82.3864 | 28407 | 911 | 28071 | 4353 | 308 | 7.0756 | |
| ltrigg-rtg1 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 97.7774 | 98.9308 | 96.6505 | 72.2034 | 28405 | 307 | 28740 | 996 | 22 | 2.2088 | |
| ltrigg-rtg1 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 97.7774 | 98.9308 | 96.6505 | 72.2034 | 28405 | 307 | 28740 | 996 | 22 | 2.2088 | |
| astatham-gatk | INDEL | * | HG002compoundhet | * | 95.0088 | 94.7931 | 95.2256 | 62.9264 | 28400 | 1560 | 28282 | 1418 | 1407 | 99.2243 | |
| gduggal-snapvard | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 86.9733 | 91.1887 | 83.1303 | 79.6742 | 28398 | 2744 | 28182 | 5719 | 224 | 3.9168 | |
| gduggal-snapvard | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 86.9733 | 91.1887 | 83.1303 | 79.6742 | 28398 | 2744 | 28182 | 5719 | 224 | 3.9168 | |
| gduggal-snapfb | SNP | ti | map_l125_m1_e0 | * | 96.8890 | 96.7104 | 97.0682 | 71.9792 | 28370 | 965 | 28374 | 857 | 408 | 47.6079 | |
| egarrison-hhga | SNP | tv | map_siren | het | 99.4896 | 99.1331 | 99.8486 | 55.6665 | 28361 | 248 | 28361 | 43 | 15 | 34.8837 | |
| ckim-vqsr | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.9180 | 98.7044 | 99.1325 | 79.1132 | 28340 | 372 | 28340 | 248 | 29 | 11.6935 | |
| ckim-vqsr | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.9180 | 98.7044 | 99.1325 | 79.1132 | 28340 | 372 | 28340 | 248 | 29 | 11.6935 | |
| gduggal-snapfb | SNP | tv | map_siren | het | 97.7974 | 98.9374 | 96.6834 | 63.5849 | 28305 | 304 | 28306 | 971 | 266 | 27.3944 | |
| ltrigg-rtg2 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 97.6510 | 98.5407 | 96.7772 | 70.9827 | 28293 | 419 | 28618 | 953 | 37 | 3.8825 | |
| ltrigg-rtg2 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 97.6510 | 98.5407 | 96.7772 | 70.9827 | 28293 | 419 | 28618 | 953 | 37 | 3.8825 | |
| eyeh-varpipe | SNP | * | map_l125_m1_e0 | het | 98.1718 | 99.6126 | 96.7721 | 75.4925 | 28282 | 110 | 27402 | 914 | 28 | 3.0635 | |
| egarrison-hhga | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.7965 | 98.4954 | 99.0994 | 71.1241 | 28280 | 432 | 28279 | 257 | 56 | 21.7899 | |
| egarrison-hhga | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.7965 | 98.4954 | 99.0994 | 71.1241 | 28280 | 432 | 28279 | 257 | 56 | 21.7899 | |
| ndellapenna-hhga | SNP | tv | map_siren | het | 99.3169 | 98.8465 | 99.7918 | 55.1017 | 28279 | 330 | 28279 | 59 | 19 | 32.2034 | |
| jpowers-varprowl | SNP | * | map_l125_m2_e0 | het | 96.7249 | 96.4527 | 96.9986 | 79.0213 | 28278 | 1040 | 28278 | 875 | 244 | 27.8857 | |
| ltrigg-rtg1 | SNP | tv | map_siren | het | 99.1688 | 98.8255 | 99.5144 | 50.4058 | 28273 | 336 | 28278 | 138 | 6 | 4.3478 | |
| gduggal-snapplat | SNP | ti | map_l125_m2_e1 | * | 94.3667 | 92.4859 | 96.3257 | 81.1411 | 28272 | 2297 | 28287 | 1079 | 590 | 54.6803 | |
| ckim-isaac | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 95.3986 | 91.8696 | 99.2095 | 63.6282 | 28260 | 2501 | 28237 | 225 | 152 | 67.5556 | |
| ckim-isaac | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 94.4491 | 90.7138 | 98.5051 | 60.8883 | 28251 | 2892 | 28401 | 431 | 172 | 39.9072 | |
| ckim-isaac | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 94.4491 | 90.7138 | 98.5051 | 60.8883 | 28251 | 2892 | 28401 | 431 | 172 | 39.9072 | |
| ltrigg-rtg2 | SNP | tv | map_siren | het | 99.1276 | 98.6962 | 99.5628 | 47.7162 | 28236 | 373 | 28241 | 124 | 4 | 3.2258 | |
| gduggal-bwaplat | SNP | * | map_l125_m2_e0 | * | 75.1671 | 60.4306 | 99.4087 | 87.7400 | 28235 | 18488 | 28242 | 168 | 47 | 27.9762 | |
| gduggal-snapvard | SNP | ti | map_l125_m1_e0 | * | 93.7547 | 96.2264 | 91.4068 | 77.7724 | 28228 | 1107 | 27965 | 2629 | 225 | 8.5584 | |
| ciseli-custom | INDEL | I1_5 | HG002complexvar | * | 86.2012 | 84.5873 | 87.8779 | 52.9140 | 28220 | 5142 | 27874 | 3845 | 2974 | 77.3472 | |
| jli-custom | INDEL | * | HG002compoundhet | * | 95.6209 | 94.1822 | 97.1042 | 61.3856 | 28217 | 1743 | 28100 | 838 | 804 | 95.9427 | |