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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
55351-55400 / 86044 show all | |||||||||||||||
| gduggal-bwavard | INDEL | C1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 0.0000 | 0.0000 | 62.3288 | 90.0950 | 0 | 1 | 91 | 55 | 10 | 18.1818 | |
| gduggal-bwavard | INDEL | C1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 0.0000 | 0.0000 | 55.6452 | 90.5847 | 0 | 1 | 69 | 55 | 10 | 18.1818 | |
| eyeh-varpipe | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | homalt | 99.4785 | 99.4671 | 99.4898 | 52.4587 | 2240 | 12 | 2145 | 11 | 2 | 18.1818 | |
| gduggal-bwavard | INDEL | D16_PLUS | map_l125_m2_e0 | het | 73.4694 | 90.0000 | 62.0690 | 95.9441 | 18 | 2 | 18 | 11 | 2 | 18.1818 | |
| bgallagher-sentieon | INDEL | I1_5 | map_l125_m1_e0 | * | 98.7373 | 98.7952 | 98.6795 | 85.8454 | 820 | 10 | 822 | 11 | 2 | 18.1818 | |
| bgallagher-sentieon | INDEL | I1_5 | map_l125_m2_e0 | * | 98.7770 | 98.8331 | 98.7209 | 87.0110 | 847 | 10 | 849 | 11 | 2 | 18.1818 | |
| bgallagher-sentieon | INDEL | I1_5 | map_l125_m2_e1 | * | 98.7952 | 98.8506 | 98.7400 | 87.1353 | 860 | 10 | 862 | 11 | 2 | 18.1818 | |
| astatham-gatk | INDEL | D16_PLUS | map_siren | * | 93.3991 | 94.4056 | 92.4138 | 94.9653 | 135 | 8 | 134 | 11 | 2 | 18.1818 | |
| astatham-gatk | INDEL | D1_5 | map_l150_m1_e0 | * | 96.6476 | 96.3738 | 96.9231 | 89.6121 | 691 | 26 | 693 | 22 | 4 | 18.1818 | |
| astatham-gatk | INDEL | D1_5 | map_l150_m2_e0 | * | 96.6463 | 96.1992 | 97.0976 | 90.1019 | 734 | 29 | 736 | 22 | 4 | 18.1818 | |
| astatham-gatk | INDEL | D6_15 | map_siren | het | 96.6183 | 97.1429 | 96.0993 | 87.5935 | 272 | 8 | 271 | 11 | 2 | 18.1818 | |
| asubramanian-gatk | SNP | tv | map_l100_m1_e0 | het | 60.4053 | 43.3028 | 99.8355 | 88.3520 | 6676 | 8741 | 6674 | 11 | 2 | 18.1818 | |
| bgallagher-sentieon | INDEL | D16_PLUS | map_siren | het | 91.8695 | 97.4359 | 86.9048 | 95.6967 | 76 | 2 | 73 | 11 | 2 | 18.1818 | |
| bgallagher-sentieon | INDEL | D1_5 | map_l100_m0_e0 | * | 98.2188 | 98.9571 | 97.4914 | 85.7120 | 854 | 9 | 855 | 22 | 4 | 18.1818 | |
| asubramanian-gatk | SNP | tv | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 98.8074 | 98.3509 | 99.2681 | 69.2197 | 1491 | 25 | 1492 | 11 | 2 | 18.1818 | |
| astatham-gatk | SNP | tv | map_l250_m0_e0 | het | 92.7323 | 88.1119 | 97.8641 | 94.1324 | 504 | 68 | 504 | 11 | 2 | 18.1818 | |
| qzeng-custom | INDEL | C1_5 | HG002complexvar | * | 80.7714 | 71.4286 | 92.9260 | 89.3893 | 5 | 2 | 289 | 22 | 4 | 18.1818 | |
| mlin-fermikit | SNP | tv | HG002compoundhet | het | 90.8488 | 84.0146 | 98.8934 | 54.3251 | 3926 | 747 | 3932 | 44 | 8 | 18.1818 | |
| ndellapenna-hhga | INDEL | I1_5 | map_l100_m1_e0 | * | 98.7623 | 98.3570 | 99.1711 | 82.7819 | 1317 | 22 | 1316 | 11 | 2 | 18.1818 | |
| ndellapenna-hhga | INDEL | I1_5 | map_l100_m2_e0 | * | 98.7887 | 98.3918 | 99.1888 | 84.1125 | 1346 | 22 | 1345 | 11 | 2 | 18.1818 | |
| mlin-fermikit | INDEL | D16_PLUS | map_l125_m0_e0 | homalt | 26.6667 | 100.0000 | 15.3846 | 92.8177 | 2 | 0 | 2 | 11 | 2 | 18.1818 | |
| mlin-fermikit | INDEL | D16_PLUS | map_l150_m1_e0 | * | 59.4595 | 73.3333 | 50.0000 | 93.6047 | 11 | 4 | 11 | 11 | 2 | 18.1818 | |
| qzeng-custom | INDEL | D6_15 | map_l125_m1_e0 | * | 84.5873 | 83.7607 | 85.4305 | 91.2158 | 98 | 19 | 129 | 22 | 4 | 18.1818 | |
| qzeng-custom | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 98.8890 | 98.8482 | 98.9300 | 77.8496 | 944 | 11 | 1017 | 11 | 2 | 18.1818 | |
| qzeng-custom | INDEL | I6_15 | map_l150_m1_e0 | * | 58.1704 | 48.0000 | 73.8095 | 94.1423 | 12 | 13 | 31 | 11 | 2 | 18.1818 | |
| qzeng-custom | INDEL | I6_15 | map_l150_m2_e0 | * | 58.8648 | 48.0000 | 76.0870 | 94.2284 | 12 | 13 | 35 | 11 | 2 | 18.1818 | |
| raldana-dualsentieon | INDEL | D1_5 | map_l150_m1_e0 | het | 97.6164 | 97.5104 | 97.7226 | 86.9141 | 470 | 12 | 472 | 11 | 2 | 18.1818 | |
| raldana-dualsentieon | INDEL | D1_5 | map_l150_m2_e0 | het | 97.7646 | 97.6654 | 97.8641 | 87.4604 | 502 | 12 | 504 | 11 | 2 | 18.1818 | |
| raldana-dualsentieon | INDEL | D1_5 | map_l150_m2_e1 | het | 97.7008 | 97.5096 | 97.8927 | 87.5328 | 509 | 13 | 511 | 11 | 2 | 18.1818 | |
| rpoplin-dv42 | INDEL | D1_5 | map_l100_m0_e0 | het | 97.7076 | 97.2927 | 98.1261 | 84.3425 | 575 | 16 | 576 | 11 | 2 | 18.1818 | |
| jli-custom | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 99.0767 | 99.3951 | 98.7603 | 83.0758 | 2629 | 16 | 2629 | 33 | 6 | 18.1818 | |
| ltrigg-rtg2 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 99.1130 | 99.2516 | 98.9748 | 72.3987 | 2122 | 16 | 2124 | 22 | 4 | 18.1818 | |
| ltrigg-rtg2 | INDEL | C1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 0.0000 | 0.0000 | 92.2807 | 95.7828 | 0 | 1 | 263 | 22 | 4 | 18.1818 | |
| ltrigg-rtg2 | INDEL | C1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 0.0000 | 0.0000 | 92.2807 | 95.7828 | 0 | 1 | 263 | 22 | 4 | 18.1818 | |
| ltrigg-rtg1 | SNP | tv | lowcmp_SimpleRepeat_triTR_11to50 | het | 99.6037 | 99.7194 | 99.4884 | 35.8783 | 2132 | 6 | 2139 | 11 | 2 | 18.1818 | |
| jpowers-varprowl | SNP | * | tech_badpromoters | * | 95.3271 | 97.4522 | 93.2927 | 57.8406 | 153 | 4 | 153 | 11 | 2 | 18.1818 | |
| ltrigg-rtg1 | INDEL | * | lowcmp_SimpleRepeat_triTR_11to50 | het | 99.1048 | 98.5238 | 99.6927 | 45.3838 | 3604 | 54 | 3568 | 11 | 2 | 18.1818 | |
| dgrover-gatk | SNP | tv | map_l150_m1_e0 | het | 98.7950 | 99.1650 | 98.4277 | 80.3450 | 6888 | 58 | 6886 | 110 | 20 | 18.1818 | |
| dgrover-gatk | SNP | tv | map_l250_m1_e0 | het | 97.6809 | 97.8176 | 97.5446 | 90.8347 | 1748 | 39 | 1748 | 44 | 8 | 18.1818 | |
| ckim-vqsr | INDEL | D6_15 | map_siren | * | 97.3325 | 96.8566 | 97.8131 | 86.8634 | 493 | 16 | 492 | 11 | 2 | 18.1818 | |
| ckim-vqsr | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 99.2066 | 99.0169 | 99.3969 | 52.5864 | 1813 | 18 | 1813 | 11 | 2 | 18.1818 | |
| dgrover-gatk | INDEL | * | map_l250_m0_e0 | * | 90.1235 | 93.5897 | 86.9048 | 97.9749 | 73 | 5 | 73 | 11 | 2 | 18.1818 | |
| dgrover-gatk | INDEL | D16_PLUS | map_siren | het | 91.2085 | 96.1538 | 86.7470 | 95.9234 | 75 | 3 | 72 | 11 | 2 | 18.1818 | |
| ciseli-custom | INDEL | D6_15 | map_l125_m0_e0 | het | 46.1538 | 41.3793 | 52.1739 | 96.1474 | 12 | 17 | 12 | 11 | 2 | 18.1818 | |
| ckim-gatk | INDEL | I1_5 | map_l150_m0_e0 | * | 95.8387 | 97.7273 | 94.0217 | 94.6543 | 172 | 4 | 173 | 11 | 2 | 18.1818 | |
| ckim-gatk | INDEL | D16_PLUS | map_siren | het | 91.8695 | 97.4359 | 86.9048 | 96.2700 | 76 | 2 | 73 | 11 | 2 | 18.1818 | |
| ckim-dragen | INDEL | D1_5 | map_l250_m1_e0 | * | 95.0825 | 96.4912 | 93.7143 | 95.4967 | 165 | 6 | 164 | 11 | 2 | 18.1818 | |
| ckim-dragen | INDEL | D1_5 | map_l250_m2_e0 | * | 95.4265 | 96.7391 | 94.1489 | 95.7629 | 178 | 6 | 177 | 11 | 2 | 18.1818 | |
| ckim-dragen | INDEL | D1_5 | map_l250_m2_e1 | * | 95.4509 | 96.7568 | 94.1799 | 95.8498 | 179 | 6 | 178 | 11 | 2 | 18.1818 | |
| qzeng-custom | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 97.5943 | 98.9387 | 96.2859 | 86.8966 | 4102 | 44 | 4122 | 159 | 29 | 18.2390 | |