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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
23001-23050 / 86044 show all | |||||||||||||||
| gduggal-bwaplat | SNP | ti | map_l150_m0_e0 | * | 58.2240 | 41.2034 | 99.2037 | 94.0967 | 3239 | 4622 | 3239 | 26 | 11 | 42.3077 | |
| jlack-gatk | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_51to200 | hetalt | 64.0121 | 47.2505 | 99.2032 | 31.2329 | 232 | 259 | 249 | 2 | 1 | 50.0000 | |
| hfeng-pmm2 | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 99.2559 | 99.3087 | 99.2032 | 69.9329 | 3735 | 26 | 3735 | 30 | 29 | 96.6667 | |
| hfeng-pmm2 | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 99.2559 | 99.3087 | 99.2032 | 69.9329 | 3735 | 26 | 3735 | 30 | 29 | 96.6667 | |
| qzeng-custom | INDEL | D1_5 | HG002complexvar | homalt | 99.0114 | 98.8205 | 99.2030 | 52.6484 | 10473 | 125 | 10456 | 84 | 62 | 73.8095 | |
| rpoplin-dv42 | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | hetalt | 94.9496 | 91.0460 | 99.2028 | 32.8775 | 1088 | 107 | 1120 | 9 | 9 | 100.0000 | |
| rpoplin-dv42 | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_51to200 | hetalt | 96.8547 | 94.6154 | 99.2026 | 23.5366 | 615 | 35 | 622 | 5 | 5 | 100.0000 | |
| gduggal-bwaplat | SNP | ti | map_siren | het | 92.8447 | 87.2527 | 99.2026 | 72.7353 | 54430 | 7952 | 54492 | 438 | 111 | 25.3425 | |
| hfeng-pmm1 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 99.4096 | 99.6175 | 99.2025 | 47.1436 | 8334 | 32 | 8334 | 67 | 66 | 98.5075 | |
| jlack-gatk | SNP | * | lowcmp_SimpleRepeat_triTR_11to50 | * | 99.5118 | 99.8232 | 99.2024 | 37.2444 | 7342 | 13 | 7338 | 59 | 5 | 8.4746 | |
| hfeng-pmm2 | SNP | ti | map_l150_m2_e0 | * | 99.3133 | 99.4247 | 99.2021 | 77.6100 | 20394 | 118 | 20390 | 164 | 20 | 12.1951 | |
| ckim-dragen | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | homalt | 99.4667 | 99.7326 | 99.2021 | 61.2371 | 373 | 1 | 373 | 3 | 2 | 66.6667 | |
| bgallagher-sentieon | SNP | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 99.0536 | 98.9058 | 99.2019 | 69.0574 | 2983 | 33 | 2983 | 24 | 5 | 20.8333 | |
| hfeng-pmm1 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 97.8839 | 96.6007 | 99.2017 | 74.1149 | 1904 | 67 | 1864 | 15 | 8 | 53.3333 | |
| hfeng-pmm1 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 97.8839 | 96.6007 | 99.2017 | 74.1149 | 1904 | 67 | 1864 | 15 | 8 | 53.3333 | |
| rpoplin-dv42 | INDEL | I16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 91.0987 | 84.2196 | 99.2016 | 58.5608 | 491 | 92 | 497 | 4 | 4 | 100.0000 | |
| hfeng-pmm3 | SNP | * | map_l150_m0_e0 | * | 99.1727 | 99.1439 | 99.2015 | 79.7142 | 11929 | 103 | 11926 | 96 | 9 | 9.3750 | |
| jli-custom | SNP | * | map_l250_m0_e0 | homalt | 98.9641 | 98.7281 | 99.2013 | 90.2386 | 621 | 8 | 621 | 5 | 5 | 100.0000 | |
| hfeng-pmm3 | SNP | * | map_l125_m0_e0 | het | 99.1347 | 99.0682 | 99.2012 | 76.1218 | 12546 | 118 | 12543 | 101 | 9 | 8.9109 | |
| jli-custom | SNP | tv | map_l125_m2_e1 | het | 99.0030 | 98.8060 | 99.2008 | 70.7055 | 10427 | 126 | 10426 | 84 | 21 | 25.0000 | |
| hfeng-pmm2 | SNP | ti | map_l150_m2_e1 | * | 99.3155 | 99.4306 | 99.2007 | 77.6747 | 20605 | 118 | 20601 | 166 | 20 | 12.0482 | |
| cchapple-custom | INDEL | * | map_siren | homalt | 98.6746 | 98.1544 | 99.2003 | 78.4454 | 2606 | 49 | 2605 | 21 | 13 | 61.9048 | |
| gduggal-bwaplat | SNP | tv | map_l125_m2_e0 | het | 78.7735 | 65.3227 | 99.2001 | 90.4805 | 6821 | 3621 | 6821 | 55 | 13 | 23.6364 | |
| eyeh-varpipe | INDEL | I1_5 | func_cds | homalt | 99.1798 | 99.1597 | 99.2000 | 23.7805 | 118 | 1 | 124 | 1 | 1 | 100.0000 | |
| gduggal-bwafb | INDEL | I1_5 | lowcmp_SimpleRepeat_triTR_11to50 | homalt | 95.9381 | 92.8839 | 99.2000 | 63.6099 | 248 | 19 | 248 | 2 | 2 | 100.0000 | |
| ltrigg-rtg1 | INDEL | D1_5 | map_l125_m2_e1 | homalt | 99.3310 | 99.4624 | 99.2000 | 83.9812 | 370 | 2 | 372 | 3 | 2 | 66.6667 | |
| ltrigg-rtg1 | INDEL | D1_5 | map_l150_m2_e1 | homalt | 99.3980 | 99.5968 | 99.2000 | 86.4352 | 247 | 1 | 248 | 2 | 2 | 100.0000 | |
| ltrigg-rtg2 | INDEL | * | map_l100_m0_e0 | homalt | 98.5147 | 97.8389 | 99.2000 | 76.5368 | 498 | 11 | 496 | 4 | 2 | 50.0000 | |
| cchapple-custom | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 98.1453 | 97.1129 | 99.2000 | 58.1707 | 740 | 22 | 744 | 6 | 4 | 66.6667 | |
| cchapple-custom | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 97.6989 | 96.2429 | 99.1997 | 49.1264 | 2869 | 112 | 2975 | 24 | 22 | 91.6667 | |
| ltrigg-rtg1 | INDEL | * | map_l100_m1_e0 | het | 96.7206 | 94.3624 | 99.1996 | 75.5384 | 2109 | 126 | 2107 | 17 | 2 | 11.7647 | |
| jli-custom | SNP | * | map_l150_m2_e1 | het | 98.8617 | 98.5267 | 99.1989 | 74.7124 | 20063 | 300 | 20060 | 162 | 49 | 30.2469 | |
| egarrison-hhga | INDEL | I1_5 | map_siren | * | 99.0333 | 98.8686 | 99.1987 | 80.5885 | 2971 | 34 | 2971 | 24 | 6 | 25.0000 | |
| ltrigg-rtg2 | SNP | * | func_cds | het | 99.5132 | 99.8298 | 99.1986 | 22.7101 | 11142 | 19 | 11141 | 90 | 1 | 1.1111 | |
| rpoplin-dv42 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | hetalt | 91.9839 | 85.7475 | 99.1986 | 31.0197 | 1107 | 184 | 1114 | 9 | 9 | 100.0000 | |
| jlack-gatk | SNP | * | * | het | 99.5639 | 99.9321 | 99.1985 | 27.0831 | 1872315 | 1272 | 1872190 | 15127 | 441 | 2.9153 | |
| ghariani-varprowl | SNP | ti | * | * | 99.5372 | 99.8784 | 99.1982 | 22.5770 | 2082957 | 2536 | 2083186 | 16837 | 1291 | 7.6676 | |
| jmaeng-gatk | INDEL | * | * | * | 99.1098 | 99.0216 | 99.1981 | 60.9184 | 341171 | 3371 | 341038 | 2757 | 1621 | 58.7958 | |
| hfeng-pmm1 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 98.2781 | 97.3753 | 99.1979 | 63.8123 | 742 | 20 | 742 | 6 | 1 | 16.6667 | |
| dgrover-gatk | SNP | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 99.5314 | 99.8673 | 99.1977 | 62.4958 | 35372 | 47 | 35361 | 286 | 20 | 6.9930 | |
| dgrover-gatk | INDEL | I6_15 | * | het | 99.0704 | 98.9435 | 99.1977 | 59.7099 | 9927 | 106 | 9891 | 80 | 53 | 66.2500 | |
| ltrigg-rtg2 | INDEL | D16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 97.6427 | 96.1360 | 99.1974 | 40.4967 | 1244 | 50 | 1236 | 10 | 10 | 100.0000 | |
| ckim-isaac | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | homalt | 90.9907 | 84.0382 | 99.1974 | 59.7025 | 616 | 117 | 618 | 5 | 2 | 40.0000 | |
| raldana-dualsentieon | SNP | * | map_l250_m0_e0 | homalt | 98.7220 | 98.2512 | 99.1974 | 90.2732 | 618 | 11 | 618 | 5 | 2 | 40.0000 | |
| ltrigg-rtg2 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 98.5540 | 97.9189 | 99.1972 | 85.2279 | 894 | 19 | 865 | 7 | 0 | 0.0000 | |
| ckim-isaac | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 96.5210 | 93.9856 | 99.1970 | 53.9957 | 2344 | 150 | 2347 | 19 | 2 | 10.5263 | |
| ckim-vqsr | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_51to200 | * | 95.3668 | 91.8216 | 99.1968 | 76.6417 | 247 | 22 | 247 | 2 | 1 | 50.0000 | |
| ltrigg-rtg1 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | hetalt | 95.6106 | 92.2747 | 99.1968 | 83.5535 | 215 | 18 | 247 | 2 | 2 | 100.0000 | |
| ltrigg-rtg2 | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | het | 98.5858 | 97.9822 | 99.1968 | 53.1729 | 15442 | 318 | 15438 | 125 | 48 | 38.4000 | |
| hfeng-pmm1 | INDEL | D1_5 | map_l150_m2_e0 | * | 98.0117 | 96.8545 | 99.1968 | 86.8347 | 739 | 24 | 741 | 6 | 1 | 16.6667 | |