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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
8301-8350 / 86044 show all | |||||||||||||||
| gduggal-bwafb | SNP | * | map_l100_m1_e0 | het | 98.6881 | 99.0035 | 98.3746 | 69.4458 | 44907 | 452 | 44909 | 742 | 142 | 19.1375 | |
| gduggal-snapvard | SNP | ti | map_l150_m2_e1 | het | 90.0889 | 96.5271 | 84.4559 | 85.0397 | 12563 | 452 | 12464 | 2294 | 173 | 7.5414 | |
| jmaeng-gatk | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 96.0184 | 92.3880 | 99.9457 | 61.4714 | 5486 | 452 | 5522 | 3 | 3 | 100.0000 | |
| jlack-gatk | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 94.8351 | 90.2733 | 99.8824 | 28.4609 | 4195 | 452 | 4248 | 5 | 4 | 80.0000 | |
| hfeng-pmm3 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 97.6110 | 96.3981 | 98.8550 | 60.6748 | 12070 | 451 | 11914 | 138 | 125 | 90.5797 | |
| ciseli-custom | SNP | * | lowcmp_SimpleRepeat_diTR_11to50 | het | 73.8977 | 92.7678 | 61.4068 | 68.2562 | 5785 | 451 | 5919 | 3720 | 112 | 3.0108 | |
| egarrison-hhga | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 94.6023 | 95.2631 | 93.9507 | 47.7088 | 9070 | 451 | 9070 | 584 | 265 | 45.3767 | |
| jpowers-varprowl | SNP | tv | map_l100_m2_e1 | het | 96.9210 | 97.1703 | 96.6729 | 76.0613 | 15487 | 451 | 15487 | 533 | 100 | 18.7617 | |
| mlin-fermikit | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 95.4419 | 95.8245 | 95.0624 | 80.9574 | 10350 | 451 | 10358 | 538 | 336 | 62.4535 | |
| gduggal-snapvard | INDEL | * | map_siren | homalt | 89.9289 | 83.0132 | 98.1015 | 71.6674 | 2204 | 451 | 2377 | 46 | 40 | 86.9565 | |
| gduggal-snapvard | SNP | ti | map_l125_m1_e0 | homalt | 97.8107 | 95.9258 | 99.7712 | 66.1153 | 10595 | 450 | 10464 | 24 | 19 | 79.1667 | |
| hfeng-pmm1 | SNP | * | map_l100_m2_e1 | * | 99.5878 | 99.3979 | 99.7783 | 64.6489 | 74287 | 450 | 74276 | 165 | 49 | 29.6970 | |
| bgallagher-sentieon | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | * | 98.5115 | 98.1663 | 98.8593 | 41.0712 | 24090 | 450 | 24092 | 278 | 270 | 97.1223 | |
| eyeh-varpipe | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 48.4456 | 45.3883 | 51.9444 | 59.2990 | 374 | 450 | 374 | 346 | 337 | 97.3988 | |
| eyeh-varpipe | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | * | 60.5212 | 53.0761 | 70.3956 | 56.0815 | 509 | 450 | 516 | 217 | 206 | 94.9309 | |
| raldana-dualsentieon | SNP | ti | map_siren | * | 99.5625 | 99.5516 | 99.5734 | 52.8084 | 99905 | 450 | 99890 | 428 | 23 | 5.3738 | |
| mlin-fermikit | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_51to200 | * | 69.4588 | 63.4740 | 76.6895 | 52.7315 | 782 | 450 | 783 | 238 | 217 | 91.1765 | |
| mlin-fermikit | INDEL | D1_5 | map_l100_m1_e0 | het | 75.8984 | 62.7792 | 95.9494 | 75.4582 | 759 | 450 | 758 | 32 | 18 | 56.2500 | |
| ndellapenna-hhga | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 93.5407 | 95.2841 | 91.8599 | 48.3177 | 9072 | 449 | 9073 | 804 | 405 | 50.3731 | |
| gduggal-bwafb | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 92.7440 | 88.1997 | 97.7819 | 39.9778 | 3356 | 449 | 1587 | 36 | 36 | 100.0000 | |
| gduggal-bwaplat | INDEL | I1_5 | map_l100_m1_e0 | * | 79.6064 | 66.4675 | 99.2196 | 91.7555 | 890 | 449 | 890 | 7 | 2 | 28.5714 | |
| hfeng-pmm1 | SNP | * | map_l100_m2_e0 | * | 99.5855 | 99.3929 | 99.7787 | 64.6417 | 73515 | 449 | 73504 | 163 | 49 | 30.0613 | |
| gduggal-snapvard | SNP | ti | map_l150_m2_e0 | het | 90.0316 | 96.5142 | 84.3650 | 84.9671 | 12432 | 449 | 12335 | 2286 | 171 | 7.4803 | |
| anovak-vg | INDEL | I16_PLUS | * | homalt | 55.6761 | 71.2364 | 45.6948 | 36.9604 | 1112 | 449 | 1141 | 1356 | 1055 | 77.8024 | |
| raldana-dualsentieon | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 99.0544 | 98.5583 | 99.5556 | 65.3417 | 30694 | 449 | 30694 | 137 | 9 | 6.5693 | |
| raldana-dualsentieon | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 99.0544 | 98.5583 | 99.5556 | 65.3417 | 30694 | 449 | 30694 | 137 | 9 | 6.5693 | |
| ltrigg-rtg1 | INDEL | D1_5 | HG002complexvar | * | 99.1020 | 98.6275 | 99.5810 | 54.4390 | 32266 | 449 | 32088 | 135 | 85 | 62.9630 | |
| gduggal-snapvard | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 21.6154 | 16.4179 | 31.6279 | 50.5178 | 88 | 448 | 136 | 294 | 156 | 53.0612 | |
| gduggal-bwavard | SNP | ti | map_l125_m2_e1 | het | 94.6705 | 97.6529 | 91.8649 | 83.0811 | 18639 | 448 | 18497 | 1638 | 107 | 6.5324 | |
| ciseli-custom | INDEL | D16_PLUS | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 42.6022 | 32.6316 | 61.3466 | 68.7695 | 217 | 448 | 246 | 155 | 138 | 89.0323 | |
| ciseli-custom | INDEL | D1_5 | map_l100_m2_e0 | * | 79.9976 | 76.6057 | 83.7037 | 88.2507 | 1467 | 448 | 1469 | 286 | 139 | 48.6014 | |
| ckim-gatk | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | * | 98.6306 | 98.1744 | 99.0911 | 41.2071 | 24092 | 448 | 24094 | 221 | 211 | 95.4751 | |
| jli-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 97.7497 | 95.9658 | 99.6012 | 27.0945 | 10657 | 448 | 10739 | 43 | 42 | 97.6744 | |
| asubramanian-gatk | INDEL | I1_5 | HG002complexvar | * | 99.2344 | 98.6572 | 99.8183 | 57.3625 | 32915 | 448 | 32967 | 60 | 50 | 83.3333 | |
| asubramanian-gatk | INDEL | * | map_l100_m2_e0 | * | 92.1174 | 87.8960 | 96.7646 | 96.1178 | 3246 | 447 | 3260 | 109 | 17 | 15.5963 | |
| anovak-vg | SNP | ti | map_l250_m2_e0 | homalt | 85.1522 | 74.4425 | 99.4611 | 88.0122 | 1302 | 447 | 1292 | 7 | 5 | 71.4286 | |
| ckim-gatk | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 97.1837 | 96.7573 | 97.6138 | 51.8740 | 13338 | 447 | 13336 | 326 | 319 | 97.8528 | |
| jpowers-varprowl | SNP | tv | map_l100_m2_e0 | het | 96.9118 | 97.1668 | 96.6583 | 76.0137 | 15330 | 447 | 15330 | 530 | 100 | 18.8679 | |
| ndellapenna-hhga | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 60.0653 | 42.9847 | 99.6711 | 45.3237 | 337 | 447 | 303 | 1 | 1 | 100.0000 | |
| mlin-fermikit | INDEL | D1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 98.6770 | 98.2373 | 99.1206 | 53.5009 | 24912 | 447 | 24909 | 221 | 216 | 97.7376 | |
| ndellapenna-hhga | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.8647 | 98.5647 | 99.1665 | 69.0402 | 30696 | 447 | 30695 | 258 | 94 | 36.4341 | |
| ndellapenna-hhga | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.8647 | 98.5647 | 99.1665 | 69.0402 | 30696 | 447 | 30695 | 258 | 94 | 36.4341 | |
| gduggal-bwavard | SNP | * | lowcmp_SimpleRepeat_diTR_11to50 | * | 95.4182 | 95.3879 | 95.4484 | 71.2860 | 9245 | 447 | 9143 | 436 | 182 | 41.7431 | |
| gduggal-bwavard | SNP | ti | map_l125_m2_e0 | het | 94.6336 | 97.6319 | 91.8139 | 83.0438 | 18429 | 447 | 18293 | 1631 | 107 | 6.5604 | |
| gduggal-snapfb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 77.5741 | 66.9623 | 92.1827 | 77.2517 | 906 | 447 | 908 | 77 | 24 | 31.1688 | |
| ckim-isaac | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 81.6460 | 74.6599 | 90.0744 | 85.4526 | 1317 | 447 | 1452 | 160 | 15 | 9.3750 | |
| ckim-isaac | SNP | ti | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 97.6487 | 95.5751 | 99.8142 | 40.4145 | 9655 | 447 | 9670 | 18 | 11 | 61.1111 | |
| ckim-isaac | SNP | tv | lowcmp_SimpleRepeat_quadTR_11to50 | * | 96.4572 | 94.0150 | 99.0295 | 31.3640 | 7006 | 446 | 7041 | 69 | 48 | 69.5652 | |
| raldana-dualsentieon | INDEL | * | lowcmp_SimpleRepeat_diTR_51to200 | * | 82.1683 | 78.7720 | 85.8708 | 53.3827 | 1655 | 446 | 1568 | 258 | 253 | 98.0620 | |
| ciseli-custom | INDEL | * | map_l100_m1_e0 | homalt | 69.2990 | 63.6512 | 76.0467 | 84.7739 | 781 | 446 | 781 | 246 | 199 | 80.8943 | |