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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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81951-82000 / 86044 show all | |||||||||||||||
| anovak-vg | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 89.7688 | 92.5437 | 87.1556 | 81.5735 | 3922 | 316 | 4207 | 620 | 247 | 39.8387 | |
| bgallagher-sentieon | INDEL | I1_5 | * | * | 99.4227 | 99.2586 | 99.5873 | 58.2134 | 149547 | 1117 | 149597 | 620 | 500 | 80.6452 | |
| jmaeng-gatk | SNP | ti | map_l100_m2_e1 | * | 90.0240 | 82.8837 | 98.5106 | 78.5961 | 41015 | 8470 | 41008 | 620 | 64 | 10.3226 | |
| jmaeng-gatk | SNP | * | segdup | het | 97.9514 | 99.4283 | 96.5177 | 95.0045 | 17218 | 99 | 17212 | 621 | 2 | 0.3221 | |
| anovak-vg | INDEL | D6_15 | HG002complexvar | het | 77.7392 | 75.0641 | 80.6119 | 50.1246 | 2342 | 778 | 2582 | 621 | 443 | 71.3366 | |
| gduggal-snapfb | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 72.1995 | 97.7700 | 57.2314 | 91.8059 | 833 | 19 | 831 | 621 | 50 | 8.0515 | |
| gduggal-bwavard | SNP | tv | map_l250_m2_e1 | het | 85.2663 | 97.9135 | 75.5126 | 92.7832 | 1924 | 41 | 1915 | 621 | 13 | 2.0934 | |
| ckim-isaac | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 89.4763 | 93.5448 | 85.7470 | 50.2621 | 4159 | 287 | 3742 | 622 | 558 | 89.7106 | |
| rpoplin-dv42 | INDEL | D1_5 | * | * | 99.4429 | 99.3110 | 99.5751 | 58.2332 | 145734 | 1011 | 145779 | 622 | 549 | 88.2637 | |
| gduggal-bwafb | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 92.3938 | 89.4378 | 95.5519 | 45.2869 | 12329 | 1456 | 13383 | 623 | 612 | 98.2343 | |
| gduggal-bwavard | SNP | tv | map_l250_m2_e0 | * | 88.8754 | 97.3629 | 81.7490 | 91.8702 | 2806 | 76 | 2795 | 624 | 17 | 2.7244 | |
| ndellapenna-hhga | SNP | ti | * | het | 99.8668 | 99.7824 | 99.9512 | 16.9483 | 1279102 | 2789 | 1279103 | 624 | 83 | 13.3013 | |
| ltrigg-rtg1 | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.5512 | 99.0752 | 98.0327 | 69.1780 | 30855 | 288 | 31094 | 624 | 24 | 3.8462 | |
| ltrigg-rtg1 | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.5512 | 99.0752 | 98.0327 | 69.1780 | 30855 | 288 | 31094 | 624 | 24 | 3.8462 | |
| gduggal-snapplat | INDEL | I1_5 | lowcmp_SimpleRepeat_triTR_11to50 | * | 31.4068 | 29.5238 | 33.5463 | 77.9887 | 310 | 740 | 315 | 624 | 44 | 7.0513 | |
| jmaeng-gatk | INDEL | D1_5 | * | het | 99.4941 | 99.6997 | 99.2893 | 60.9724 | 87311 | 263 | 87316 | 625 | 129 | 20.6400 | |
| ciseli-custom | SNP | * | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 96.0994 | 97.6994 | 94.5510 | 57.2127 | 10829 | 255 | 10845 | 625 | 21 | 3.3600 | |
| raldana-dualsentieon | SNP | * | map_siren | het | 99.3673 | 99.4219 | 99.3127 | 56.6962 | 90465 | 526 | 90451 | 626 | 10 | 1.5974 | |
| anovak-vg | SNP | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 97.4699 | 97.9603 | 96.9843 | 55.7493 | 19787 | 412 | 20132 | 626 | 469 | 74.9201 | |
| jli-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.2520 | 97.4920 | 99.0239 | 63.2840 | 63712 | 1639 | 63508 | 626 | 529 | 84.5048 | |
| jli-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.2520 | 97.4920 | 99.0239 | 63.2840 | 63712 | 1639 | 63508 | 626 | 529 | 84.5048 | |
| gduggal-snapplat | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 45.4362 | 49.0690 | 42.3041 | 95.5909 | 448 | 465 | 459 | 626 | 33 | 5.2716 | |
| gduggal-snapvard | INDEL | * | map_l125_m1_e0 | het | 83.6174 | 95.9551 | 74.0909 | 89.7946 | 1281 | 54 | 1793 | 627 | 240 | 38.2775 | |
| gduggal-snapvard | INDEL | C1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 35.0259 | 100.0000 | 21.2312 | 82.4631 | 1 | 0 | 169 | 627 | 43 | 6.8581 | |
| anovak-vg | INDEL | I1_5 | map_l100_m1_e0 | * | 58.0113 | 59.2233 | 56.8479 | 83.7016 | 793 | 546 | 826 | 627 | 447 | 71.2919 | |
| mlin-fermikit | SNP | tv | map_l125_m0_e0 | homalt | 55.7975 | 49.6173 | 63.7363 | 55.1608 | 1102 | 1119 | 1102 | 627 | 574 | 91.5470 | |
| gduggal-bwavard | SNP | tv | map_l250_m2_e1 | * | 88.9493 | 97.3937 | 81.8524 | 91.9441 | 2840 | 76 | 2828 | 627 | 17 | 2.7113 | |
| mlin-fermikit | INDEL | I16_PLUS | * | * | 82.9403 | 77.8109 | 88.7937 | 66.6528 | 4962 | 1415 | 4976 | 628 | 607 | 96.6561 | |
| hfeng-pmm1 | SNP | * | * | het | 99.9238 | 99.8812 | 99.9665 | 18.1036 | 1871361 | 2226 | 1871236 | 628 | 48 | 7.6433 | |
| gduggal-bwaplat | SNP | * | map_siren | het | 92.3406 | 86.3635 | 99.2066 | 74.9301 | 78583 | 12408 | 78653 | 629 | 157 | 24.9603 | |
| gduggal-snapvard | INDEL | C1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 38.6341 | 100.0000 | 23.9420 | 83.0324 | 1 | 0 | 198 | 629 | 44 | 6.9952 | |
| ghariani-varprowl | SNP | tv | map_l125_m1_e0 | * | 97.4146 | 98.6888 | 96.1728 | 76.4417 | 15806 | 210 | 15806 | 629 | 115 | 18.2830 | |
| gduggal-snapfb | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 96.6878 | 99.4355 | 94.0878 | 74.6352 | 10040 | 57 | 10026 | 630 | 84 | 13.3333 | |
| eyeh-varpipe | SNP | * | map_l125_m0_e0 | het | 97.2776 | 99.5499 | 95.1068 | 80.0626 | 12607 | 57 | 12245 | 630 | 17 | 2.6984 | |
| cchapple-custom | SNP | ti | map_l100_m0_e0 | het | 96.2084 | 96.8676 | 95.5581 | 74.9532 | 13545 | 438 | 13553 | 630 | 172 | 27.3016 | |
| cchapple-custom | SNP | ti | map_l100_m0_e0 | * | 96.8619 | 96.6377 | 97.0872 | 70.6515 | 21039 | 732 | 21032 | 631 | 173 | 27.4168 | |
| jpowers-varprowl | SNP | ti | map_l100_m2_e0 | * | 98.2207 | 97.7472 | 98.6987 | 70.3702 | 47858 | 1103 | 47860 | 631 | 192 | 30.4279 | |
| gduggal-bwafb | INDEL | D1_5 | HG002compoundhet | homalt | 46.3350 | 95.8763 | 30.5495 | 82.2716 | 279 | 12 | 278 | 632 | 615 | 97.3101 | |
| gduggal-bwafb | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 93.5778 | 91.1697 | 96.1165 | 54.9134 | 14630 | 1417 | 15642 | 632 | 605 | 95.7278 | |
| gduggal-snapvard | INDEL | D16_PLUS | * | het | 17.6734 | 11.3960 | 39.3474 | 71.0797 | 360 | 2799 | 410 | 632 | 372 | 58.8608 | |
| anovak-vg | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 49.6401 | 47.9452 | 51.4593 | 46.5298 | 420 | 456 | 670 | 632 | 480 | 75.9494 | |
| mlin-fermikit | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 82.5092 | 75.5024 | 90.9494 | 56.1947 | 6349 | 2060 | 6351 | 632 | 617 | 97.6266 | |
| mlin-fermikit | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 95.3085 | 94.9832 | 95.6360 | 75.7457 | 13840 | 731 | 13850 | 632 | 351 | 55.5380 | |
| mlin-fermikit | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 95.3085 | 94.9832 | 95.6360 | 75.7457 | 13840 | 731 | 13850 | 632 | 351 | 55.5380 | |
| qzeng-custom | INDEL | I16_PLUS | * | het | 85.2063 | 89.5879 | 81.2333 | 62.0542 | 2435 | 283 | 2740 | 633 | 156 | 24.6445 | |
| jmaeng-gatk | SNP | * | segdup | * | 98.5236 | 99.2803 | 97.7783 | 93.6584 | 27865 | 202 | 27859 | 633 | 14 | 2.2117 | |
| gduggal-bwafb | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 87.4269 | 95.5834 | 80.5530 | 88.6814 | 2597 | 120 | 2622 | 633 | 90 | 14.2180 | |
| eyeh-varpipe | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 92.1748 | 98.3088 | 86.7613 | 48.1654 | 3604 | 62 | 4155 | 634 | 622 | 98.1073 | |
| gduggal-snapplat | SNP | * | HG002complexvar | homalt | 98.9173 | 98.0729 | 99.7763 | 21.2516 | 283014 | 5561 | 282787 | 634 | 338 | 53.3123 | |
| gduggal-snapvard | INDEL | D16_PLUS | * | * | 10.7850 | 6.2058 | 41.1492 | 71.3717 | 421 | 6363 | 444 | 635 | 373 | 58.7402 | |