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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
851-900 / 86044 show all | |||||||||||||||
| gduggal-snapvard | INDEL | I1_5 | * | homalt | 92.2555 | 85.9022 | 99.6235 | 34.4127 | 51909 | 8519 | 51074 | 193 | 178 | 92.2280 | |
| mlin-fermikit | SNP | * | map_l125_m0_e0 | het | 49.1614 | 32.7622 | 98.4323 | 62.8190 | 4149 | 8515 | 4144 | 66 | 3 | 4.5455 | |
| ghariani-varprowl | INDEL | I6_15 | * | hetalt | 0.0000 | 0.5029 | 0.0000 | 0.0000 | 43 | 8508 | 0 | 0 | 0 | ||
| jpowers-varprowl | INDEL | I6_15 | HG002compoundhet | hetalt | 0.0000 | 0.3514 | 0.0000 | 0.0000 | 30 | 8507 | 0 | 0 | 0 | ||
| ghariani-varprowl | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 81.5331 | 72.3481 | 93.3894 | 66.7128 | 22255 | 8506 | 22222 | 1573 | 1272 | 80.8646 | |
| ciseli-custom | SNP | * | map_l125_m2_e0 | het | 76.6942 | 71.0212 | 83.3520 | 81.2570 | 20822 | 8496 | 20798 | 4154 | 134 | 3.2258 | |
| ghariani-varprowl | INDEL | I6_15 | HG002compoundhet | hetalt | 0.0000 | 0.5037 | 0.0000 | 0.0000 | 43 | 8494 | 0 | 0 | 0 | ||
| jpowers-varprowl | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 81.7040 | 72.4326 | 93.6973 | 66.4963 | 22281 | 8480 | 22240 | 1496 | 1307 | 87.3663 | |
| anovak-vg | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 48.9297 | 42.6581 | 57.3634 | 45.6299 | 6307 | 8478 | 6466 | 4806 | 3764 | 78.3188 | |
| jmaeng-gatk | SNP | ti | map_l100_m2_e1 | * | 90.0240 | 82.8837 | 98.5106 | 78.5961 | 41015 | 8470 | 41008 | 620 | 64 | 10.3226 | |
| ckim-gatk | SNP | ti | map_l100_m2_e1 | * | 90.0482 | 82.8877 | 98.5628 | 78.3843 | 41017 | 8468 | 41010 | 598 | 70 | 11.7057 | |
| ciseli-custom | INDEL | I6_15 | * | hetalt | 0.0000 | 1.0291 | 0.0000 | 0.0000 | 88 | 8463 | 0 | 0 | 0 | ||
| gduggal-bwaplat | SNP | ti | map_siren | homalt | 87.4388 | 77.6954 | 99.9762 | 56.7476 | 29459 | 8457 | 29428 | 7 | 6 | 85.7143 | |
| ciseli-custom | INDEL | I6_15 | HG002compoundhet | hetalt | 0.0000 | 1.0308 | 0.0000 | 0.0000 | 88 | 8449 | 0 | 0 | 0 | ||
| jmaeng-gatk | SNP | ti | map_l100_m2_e0 | * | 89.9408 | 82.7455 | 98.5068 | 78.6206 | 40513 | 8448 | 40506 | 614 | 64 | 10.4235 | |
| ckim-gatk | SNP | ti | map_l100_m2_e0 | * | 89.9645 | 82.7516 | 98.5549 | 78.4080 | 40516 | 8445 | 40509 | 594 | 70 | 11.7845 | |
| gduggal-bwafb | INDEL | * | * | het | 97.2465 | 95.6571 | 98.8897 | 54.7010 | 185702 | 8431 | 212773 | 2389 | 1710 | 71.5781 | |
| jmaeng-gatk | SNP | ti | map_l100_m1_e0 | * | 89.7569 | 82.4247 | 98.5209 | 77.3729 | 39507 | 8424 | 39500 | 593 | 63 | 10.6239 | |
| 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 | SNP | * | map_l125_m1_e0 | homalt | 66.8137 | 50.1804 | 99.9411 | 61.4585 | 8483 | 8422 | 8483 | 5 | 5 | 100.0000 | |
| ckim-gatk | SNP | ti | map_l100_m1_e0 | * | 89.7917 | 82.4352 | 98.5900 | 77.1488 | 39512 | 8419 | 39505 | 565 | 68 | 12.0354 | |
| asubramanian-gatk | SNP | tv | map_siren | homalt | 67.6949 | 51.1717 | 99.9773 | 68.4987 | 8822 | 8418 | 8819 | 2 | 2 | 100.0000 | |
| ciseli-custom | SNP | * | map_l150_m2_e1 | * | 78.3942 | 73.8684 | 83.5109 | 81.5923 | 23793 | 8417 | 23753 | 4690 | 1163 | 24.7974 | |
| gduggal-bwaplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 83.5790 | 73.7247 | 96.4741 | 64.8422 | 23586 | 8406 | 23586 | 862 | 511 | 59.2807 | |
| asubramanian-gatk | SNP | tv | map_l150_m1_e0 | * | 37.4814 | 23.0755 | 99.7622 | 94.8394 | 2518 | 8394 | 2517 | 6 | 1 | 16.6667 | |
| anovak-vg | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | * | 69.0612 | 65.8068 | 72.6543 | 37.5809 | 16149 | 8391 | 16741 | 6301 | 4632 | 73.5121 | |
| qzeng-custom | SNP | ti | map_siren | het | 92.2591 | 86.5538 | 98.7696 | 67.2335 | 53994 | 8388 | 53703 | 669 | 449 | 67.1151 | |
| ciseli-custom | INDEL | * | HG002complexvar | het | 83.6520 | 81.8863 | 85.4955 | 58.3237 | 37838 | 8370 | 38019 | 6450 | 2732 | 42.3566 | |
| mlin-fermikit | SNP | tv | map_l125_m2_e1 | * | 62.9750 | 49.8289 | 85.5434 | 62.7659 | 8300 | 8357 | 8296 | 1402 | 1229 | 87.6605 | |
| qzeng-custom | SNP | ti | map_l125_m2_e1 | * | 83.3343 | 72.6815 | 97.6462 | 82.9373 | 22218 | 8351 | 22070 | 532 | 443 | 83.2707 | |
| ciseli-custom | SNP | * | map_l125_m1_e0 | het | 76.3493 | 70.6009 | 83.1168 | 80.0504 | 20045 | 8347 | 20022 | 4067 | 129 | 3.1719 | |
| astatham-gatk | SNP | tv | * | het | 99.2722 | 98.5893 | 99.9647 | 23.3815 | 583349 | 8347 | 583282 | 206 | 35 | 16.9903 | |
| ciseli-custom | SNP | * | map_l150_m2_e0 | * | 78.3493 | 73.8101 | 83.4833 | 81.5713 | 23510 | 8342 | 23473 | 4644 | 1150 | 24.7631 | |
| gduggal-snapvard | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 22.0793 | 12.5407 | 92.2309 | 57.4591 | 1194 | 8327 | 1294 | 109 | 93 | 85.3211 | |
| qzeng-custom | SNP | ti | map_l125_m2_e0 | * | 83.2073 | 72.4998 | 97.6254 | 82.9474 | 21937 | 8321 | 21790 | 530 | 441 | 83.2075 | |
| anovak-vg | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 53.3229 | 48.2739 | 59.5513 | 59.8591 | 7761 | 8316 | 10724 | 7284 | 5656 | 77.6496 | |
| anovak-vg | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 53.3229 | 48.2739 | 59.5513 | 59.8591 | 7761 | 8316 | 10724 | 7284 | 5656 | 77.6496 | |
| anovak-vg | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 45.9396 | 39.7316 | 54.4469 | 43.4180 | 5477 | 8308 | 5626 | 4707 | 3701 | 78.6276 | |
| mlin-fermikit | SNP | tv | map_l125_m2_e0 | * | 62.7919 | 49.6210 | 85.4813 | 62.5997 | 8182 | 8307 | 8178 | 1389 | 1218 | 87.6890 | |
| ciseli-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 47.4490 | 43.8282 | 51.7219 | 54.7342 | 6480 | 8305 | 6518 | 6084 | 5189 | 85.2893 | |
| ckim-isaac | SNP | * | map_l150_m2_e1 | het | 74.2817 | 59.2251 | 99.6036 | 80.2344 | 12060 | 8303 | 12061 | 48 | 9 | 18.7500 | |
| gduggal-snapvard | SNP | ti | * | homalt | 99.4493 | 98.9663 | 99.9370 | 16.0694 | 794738 | 8301 | 790421 | 498 | 326 | 65.4618 | |
| asubramanian-gatk | SNP | ti | map_l125_m2_e1 | homalt | 43.2344 | 27.5790 | 100.0000 | 87.5507 | 3160 | 8298 | 3160 | 0 | 0 | ||
| gduggal-snapvard | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 59.6473 | 59.7203 | 59.5745 | 39.9758 | 12300 | 8296 | 17724 | 12027 | 10545 | 87.6777 | |
| mlin-fermikit | SNP | ti | map_l100_m0_e0 | het | 57.7466 | 40.8496 | 98.4828 | 55.5044 | 5712 | 8271 | 5712 | 88 | 4 | 4.5455 | |
| anovak-vg | SNP | * | map_l100_m2_e1 | * | 84.3316 | 88.9439 | 80.1741 | 71.0026 | 66474 | 8263 | 65661 | 16237 | 3582 | 22.0607 | |
| jpowers-varprowl | INDEL | D6_15 | HG002compoundhet | * | 9.9769 | 8.5262 | 12.0225 | 38.0227 | 770 | 8261 | 768 | 5620 | 5568 | 99.0747 | |
| gduggal-bwafb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 91.1270 | 87.3774 | 95.2128 | 60.8815 | 57102 | 8249 | 63963 | 3216 | 2822 | 87.7488 | |
| gduggal-bwafb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 91.1270 | 87.3774 | 95.2128 | 60.8815 | 57102 | 8249 | 63963 | 3216 | 2822 | 87.7488 | |
| ckim-vqsr | SNP | * | HG002complexvar | het | 99.0965 | 98.2281 | 99.9803 | 19.3098 | 457249 | 8248 | 457124 | 90 | 32 | 35.5556 | |