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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
64151-64200 / 86044 show all | |||||||||||||||
| egarrison-hhga | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 98.4400 | 98.0595 | 98.8235 | 76.0788 | 758 | 15 | 756 | 9 | 1 | 11.1111 | |
| eyeh-varpipe | SNP | tv | map_l250_m0_e0 | * | 97.7391 | 99.2157 | 96.3057 | 94.5189 | 759 | 6 | 756 | 29 | 3 | 10.3448 | |
| gduggal-bwavard | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | homalt | 98.9070 | 97.9644 | 99.8679 | 59.9259 | 770 | 16 | 756 | 1 | 0 | 0.0000 | |
| ckim-dragen | INDEL | D1_5 | map_l150_m2_e1 | * | 96.8643 | 97.4293 | 96.3057 | 90.2509 | 758 | 20 | 756 | 29 | 4 | 13.7931 | |
| ndellapenna-hhga | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 92.2021 | 88.9542 | 95.6962 | 86.1888 | 757 | 94 | 756 | 34 | 14 | 41.1765 | |
| ltrigg-rtg2 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 99.3589 | 99.2443 | 99.4737 | 85.1185 | 788 | 6 | 756 | 4 | 0 | 0.0000 | |
| jli-custom | INDEL | D1_5 | map_l125_m2_e0 | het | 98.5651 | 98.8220 | 98.3095 | 85.7566 | 755 | 9 | 756 | 13 | 3 | 23.0769 | |
| hfeng-pmm3 | INDEL | D1_5 | map_l150_m2_e0 | * | 98.6930 | 98.8204 | 98.5658 | 87.1803 | 754 | 9 | 756 | 11 | 3 | 27.2727 | |
| ckim-gatk | INDEL | * | map_l125_m2_e0 | homalt | 99.1487 | 99.2136 | 99.0838 | 87.3090 | 757 | 6 | 757 | 7 | 4 | 57.1429 | |
| egarrison-hhga | INDEL | D1_5 | map_l125_m2_e1 | het | 98.0570 | 98.3117 | 97.8036 | 86.2863 | 757 | 13 | 757 | 17 | 4 | 23.5294 | |
| ckim-vqsr | INDEL | * | map_l125_m2_e0 | homalt | 99.2136 | 99.2136 | 99.2136 | 87.3235 | 757 | 6 | 757 | 6 | 3 | 50.0000 | |
| egarrison-hhga | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 96.6794 | 95.3401 | 98.0570 | 84.9425 | 757 | 37 | 757 | 15 | 9 | 60.0000 | |
| rpoplin-dv42 | INDEL | D1_5 | map_l125_m2_e1 | het | 98.1180 | 98.0519 | 98.1842 | 86.0452 | 755 | 15 | 757 | 14 | 3 | 21.4286 | |
| gduggal-bwavard | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | het | 46.3721 | 79.4421 | 32.7422 | 66.7816 | 769 | 199 | 757 | 1555 | 1454 | 93.5048 | |
| eyeh-varpipe | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 96.3424 | 97.9964 | 94.7434 | 73.1789 | 538 | 11 | 757 | 42 | 37 | 88.0952 | |
| jmaeng-gatk | INDEL | D1_5 | map_l125_m2_e0 | het | 95.1589 | 98.8220 | 91.7576 | 91.8438 | 755 | 9 | 757 | 68 | 4 | 5.8824 | |
| ghariani-varprowl | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 88.0745 | 87.7173 | 88.4346 | 62.4232 | 757 | 106 | 757 | 99 | 93 | 93.9394 | |
| gduggal-snapplat | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 52.6981 | 52.4613 | 52.9371 | 95.3580 | 746 | 676 | 757 | 673 | 56 | 8.3210 | |
| ltrigg-rtg2 | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 97.9977 | 96.8112 | 99.2136 | 36.6279 | 759 | 25 | 757 | 6 | 6 | 100.0000 | |
| qzeng-custom | INDEL | I6_15 | lowcmp_SimpleRepeat_triTR_11to50 | het | 94.3253 | 97.5410 | 91.3148 | 37.7628 | 119 | 3 | 757 | 72 | 4 | 5.5556 | |
| 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 | |
| qzeng-custom | INDEL | I6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 77.6395 | 70.9330 | 85.7466 | 65.4687 | 593 | 243 | 758 | 126 | 94 | 74.6032 | |
| ndellapenna-hhga | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 92.9959 | 91.7476 | 94.2786 | 67.1300 | 756 | 68 | 758 | 46 | 41 | 89.1304 | |
| ndellapenna-hhga | INDEL | D1_5 | map_l150_m2_e1 | * | 97.8696 | 97.4293 | 98.3139 | 88.2398 | 758 | 20 | 758 | 13 | 6 | 46.1538 | |
| mlin-fermikit | SNP | ti | map_l250_m2_e0 | homalt | 54.3759 | 43.3391 | 72.9548 | 76.3218 | 758 | 991 | 758 | 281 | 257 | 91.4591 | |
| bgallagher-sentieon | INDEL | D1_5 | map_l150_m2_e0 | * | 98.3127 | 99.0826 | 97.5547 | 89.6483 | 756 | 7 | 758 | 19 | 4 | 21.0526 | |
| hfeng-pmm2 | INDEL | D1_5 | map_l150_m2_e0 | * | 98.0583 | 99.0826 | 97.0551 | 89.2528 | 756 | 7 | 758 | 23 | 3 | 13.0435 | |
| jli-custom | INDEL | * | map_l125_m2_e0 | homalt | 99.2147 | 99.3447 | 99.0850 | 85.6014 | 758 | 5 | 758 | 7 | 4 | 57.1429 | |
| egarrison-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 75.3026 | 95.6815 | 62.0803 | 56.2366 | 709 | 32 | 758 | 463 | 445 | 96.1123 | |
| egarrison-hhga | INDEL | D6_15 | lowcmp_SimpleRepeat_triTR_11to50 | het | 91.9318 | 98.4353 | 86.2344 | 39.0430 | 692 | 11 | 758 | 121 | 116 | 95.8678 | |
| gduggal-snapfb | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 66.4834 | 55.9299 | 81.9459 | 49.8917 | 415 | 327 | 758 | 167 | 160 | 95.8084 | |
| ghariani-varprowl | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 91.3272 | 98.3182 | 85.2643 | 79.7078 | 760 | 13 | 758 | 131 | 122 | 93.1298 | |
| hfeng-pmm1 | INDEL | * | map_l125_m2_e0 | homalt | 99.2796 | 99.3447 | 99.2147 | 85.2510 | 758 | 5 | 758 | 6 | 3 | 50.0000 | |
| gduggal-bwafb | INDEL | D1_5 | map_l150_m2_e1 | * | 97.3667 | 97.4293 | 97.3042 | 89.0328 | 758 | 20 | 758 | 21 | 3 | 14.2857 | |
| gduggal-bwaplat | INDEL | * | map_l100_m1_e0 | homalt | 76.2575 | 61.7767 | 99.6058 | 88.2125 | 758 | 469 | 758 | 3 | 2 | 66.6667 | |
| gduggal-bwaplat | INDEL | I16_PLUS | HG002complexvar | * | 72.2938 | 57.9068 | 96.1929 | 69.4455 | 758 | 551 | 758 | 30 | 22 | 73.3333 | |
| jlack-gatk | INDEL | I1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | hetalt | 89.1544 | 80.6020 | 99.7372 | 41.6858 | 723 | 174 | 759 | 2 | 2 | 100.0000 | |
| jlack-gatk | INDEL | D1_5 | map_l125_m2_e0 | het | 92.0548 | 99.0838 | 85.9570 | 90.8790 | 757 | 7 | 759 | 124 | 5 | 4.0323 | |
| hfeng-pmm2 | INDEL | * | map_l125_m2_e0 | homalt | 99.2157 | 99.4758 | 98.9570 | 85.4238 | 759 | 4 | 759 | 8 | 4 | 50.0000 | |
| hfeng-pmm2 | INDEL | D1_5 | map_l125_m2_e0 | het | 97.9343 | 99.0838 | 96.8112 | 87.3344 | 757 | 7 | 759 | 25 | 2 | 8.0000 | |
| hfeng-pmm3 | INDEL | * | map_l125_m2_e0 | homalt | 99.2806 | 99.4758 | 99.0862 | 84.5627 | 759 | 4 | 759 | 7 | 3 | 42.8571 | |
| hfeng-pmm3 | INDEL | D1_5 | map_l125_m2_e0 | het | 98.7626 | 99.0838 | 98.4436 | 84.5181 | 757 | 7 | 759 | 12 | 2 | 16.6667 | |
| hfeng-pmm3 | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | hetalt | 97.0178 | 94.3253 | 99.8684 | 24.7525 | 748 | 45 | 759 | 1 | 1 | 100.0000 | |
| ltrigg-rtg2 | INDEL | I1_5 | map_l100_m2_e0 | het | 97.3799 | 96.2169 | 98.5714 | 78.0188 | 763 | 30 | 759 | 11 | 1 | 9.0909 | |
| ckim-gatk | INDEL | D1_5 | map_l125_m2_e0 | het | 94.8739 | 99.0838 | 91.0072 | 91.6037 | 757 | 7 | 759 | 75 | 4 | 5.3333 | |
| ckim-dragen | INDEL | * | map_l125_m2_e1 | homalt | 98.4458 | 98.3204 | 98.5714 | 86.6180 | 761 | 13 | 759 | 11 | 6 | 54.5455 | |
| raldana-dualsentieon | INDEL | D1_5 | map_l150_m2_e1 | * | 97.8058 | 97.3008 | 98.3161 | 87.6421 | 757 | 21 | 759 | 13 | 4 | 30.7692 | |
| bgallagher-sentieon | INDEL | * | map_l125_m2_e0 | homalt | 99.1509 | 99.4758 | 98.8281 | 86.7266 | 759 | 4 | 759 | 9 | 4 | 44.4444 | |
| astatham-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 97.4326 | 95.5919 | 99.3455 | 89.4983 | 759 | 35 | 759 | 5 | 5 | 100.0000 | |
| astatham-gatk | INDEL | * | map_l125_m2_e0 | homalt | 99.2806 | 99.4758 | 99.0862 | 86.9395 | 759 | 4 | 759 | 7 | 4 | 57.1429 | |