PrecisionFDA
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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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
24101-24150 / 86044 show all | |||||||||||||||
| asubramanian-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 98.8815 | 98.4877 | 99.2784 | 83.9265 | 2605 | 40 | 2614 | 19 | 9 | 47.3684 | |
| astatham-gatk | INDEL | I1_5 | HG002complexvar | het | 99.6251 | 99.3568 | 99.8949 | 58.0548 | 18072 | 117 | 18051 | 19 | 9 | 47.3684 | |
| astatham-gatk | SNP | ti | map_l150_m1_e0 | het | 85.9873 | 75.6508 | 99.5954 | 82.9552 | 9358 | 3012 | 9354 | 38 | 18 | 47.3684 | |
| asubramanian-gatk | INDEL | D16_PLUS | HG002complexvar | het | 97.1610 | 96.5673 | 97.7621 | 69.4274 | 1069 | 38 | 830 | 19 | 9 | 47.3684 | |
| anovak-vg | INDEL | D1_5 | map_l250_m0_e0 | * | 66.7485 | 69.5652 | 64.1509 | 98.1232 | 32 | 14 | 34 | 19 | 9 | 47.3684 | |
| jli-custom | SNP | * | HG002compoundhet | * | 99.7328 | 99.7599 | 99.7058 | 41.1267 | 25760 | 62 | 25757 | 76 | 36 | 47.3684 | |
| ciseli-custom | INDEL | D6_15 | map_l125_m0_e0 | * | 48.2759 | 44.6809 | 52.5000 | 95.1574 | 21 | 26 | 21 | 19 | 9 | 47.3684 | |
| ciseli-custom | SNP | * | HG002complexvar | hetalt | 70.4724 | 57.7419 | 90.4040 | 39.8176 | 179 | 131 | 179 | 19 | 9 | 47.3684 | |
| cchapple-custom | INDEL | C1_5 | map_l100_m2_e0 | * | 0.0000 | 0.0000 | 65.4545 | 95.2132 | 0 | 0 | 36 | 19 | 9 | 47.3684 | |
| cchapple-custom | INDEL | C1_5 | map_l100_m2_e0 | het | 0.0000 | 0.0000 | 57.7778 | 95.0166 | 0 | 0 | 26 | 19 | 9 | 47.3684 | |
| cchapple-custom | INDEL | C1_5 | map_l100_m2_e1 | * | 0.0000 | 0.0000 | 66.0714 | 95.2421 | 0 | 0 | 37 | 19 | 9 | 47.3684 | |
| cchapple-custom | INDEL | C1_5 | map_l100_m2_e1 | het | 0.0000 | 0.0000 | 58.6957 | 95.0324 | 0 | 0 | 27 | 19 | 9 | 47.3684 | |
| cchapple-custom | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_51to200 | * | 96.7357 | 95.1299 | 98.3966 | 42.6150 | 1172 | 60 | 1166 | 19 | 9 | 47.3684 | |
| ciseli-custom | SNP | tv | HG002complexvar | hetalt | 70.4724 | 57.7419 | 90.4040 | 39.8176 | 179 | 131 | 179 | 19 | 9 | 47.3684 | |
| cchapple-custom | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 97.3086 | 96.6046 | 98.0229 | 87.6589 | 882 | 31 | 942 | 19 | 9 | 47.3684 | |
| ciseli-custom | INDEL | * | map_l150_m0_e0 | het | 64.8517 | 61.2903 | 68.8525 | 95.2903 | 209 | 132 | 210 | 95 | 45 | 47.3684 | |
| ckim-dragen | SNP | ti | HG002compoundhet | * | 99.7941 | 99.8055 | 99.7828 | 35.8899 | 17444 | 34 | 17457 | 38 | 18 | 47.3684 | |
| hfeng-pmm1 | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 97.2475 | 95.8170 | 98.7214 | 83.8109 | 1466 | 64 | 1467 | 19 | 9 | 47.3684 | |
| hfeng-pmm1 | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 97.2475 | 95.8170 | 98.7214 | 83.8109 | 1466 | 64 | 1467 | 19 | 9 | 47.3684 | |
| hfeng-pmm2 | SNP | ti | map_l125_m1_e0 | homalt | 99.8234 | 99.8189 | 99.8280 | 66.1185 | 11025 | 20 | 11025 | 19 | 9 | 47.3684 | |
| hfeng-pmm2 | SNP | ti | map_l125_m2_e0 | homalt | 99.8283 | 99.8239 | 99.8327 | 68.6045 | 11338 | 20 | 11338 | 19 | 9 | 47.3684 | |
| hfeng-pmm2 | SNP | ti | map_l125_m2_e1 | homalt | 99.8298 | 99.8254 | 99.8342 | 68.6316 | 11438 | 20 | 11438 | 19 | 9 | 47.3684 | |
| jlack-gatk | SNP | ti | lowcmp_SimpleRepeat_diTR_11to50 | het | 99.4922 | 99.5870 | 99.3976 | 71.7079 | 3135 | 13 | 3135 | 19 | 9 | 47.3684 | |
| ndellapenna-hhga | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 96.2543 | 95.9220 | 96.5889 | 67.3888 | 541 | 23 | 538 | 19 | 9 | 47.3684 | |
| qzeng-custom | INDEL | D6_15 | lowcmp_SimpleRepeat_triTR_51to200 | * | 79.6385 | 80.2817 | 79.0055 | 39.4649 | 114 | 28 | 143 | 38 | 18 | 47.3684 | |
| qzeng-custom | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 96.2008 | 97.1098 | 95.3086 | 72.1458 | 336 | 10 | 386 | 19 | 9 | 47.3684 | |
| ltrigg-rtg1 | SNP | ti | HG002complexvar | * | 99.8532 | 99.7400 | 99.9667 | 17.5108 | 507114 | 1322 | 507034 | 169 | 80 | 47.3373 | |
| bgallagher-sentieon | SNP | ti | HG002complexvar | * | 99.9558 | 99.9337 | 99.9780 | 17.4939 | 508099 | 337 | 508035 | 112 | 53 | 47.3214 | |
| gduggal-snapvard | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 95.1902 | 91.5599 | 99.1202 | 67.5348 | 10577 | 975 | 10478 | 93 | 44 | 47.3118 | |
| gduggal-snapvard | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 95.1902 | 91.5599 | 99.1202 | 67.5348 | 10577 | 975 | 10478 | 93 | 44 | 47.3118 | |
| ckim-dragen | INDEL | D1_5 | * | * | 99.4199 | 99.4105 | 99.4294 | 60.9956 | 145880 | 865 | 145840 | 837 | 396 | 47.3118 | |
| ckim-dragen | SNP | tv | HG002complexvar | het | 99.9058 | 99.9098 | 99.9019 | 22.2740 | 150595 | 136 | 150740 | 148 | 70 | 47.2973 | |
| ciseli-custom | INDEL | D1_5 | map_l150_m2_e0 | * | 74.1130 | 68.8073 | 80.3053 | 92.8974 | 525 | 238 | 526 | 129 | 61 | 47.2868 | |
| astatham-gatk | SNP | * | map_l100_m1_e0 | * | 91.9136 | 85.1664 | 99.8219 | 69.0267 | 61663 | 10740 | 61652 | 110 | 52 | 47.2727 | |
| astatham-gatk | SNP | * | map_l100_m2_e0 | * | 91.9897 | 85.2942 | 99.8259 | 70.5601 | 63087 | 10877 | 63076 | 110 | 52 | 47.2727 | |
| ltrigg-rtg1 | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | * | 95.6549 | 93.5593 | 97.8465 | 65.3460 | 2484 | 171 | 2499 | 55 | 26 | 47.2727 | |
| ghariani-varprowl | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 88.0685 | 85.1768 | 91.1634 | 69.1509 | 2264 | 394 | 2249 | 218 | 103 | 47.2477 | |
| ghariani-varprowl | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 77.6739 | 95.6522 | 65.3846 | 90.8852 | 66 | 3 | 68 | 36 | 17 | 47.2222 | |
| ciseli-custom | SNP | ti | lowcmp_SimpleRepeat_homopolymer_6to10 | homalt | 98.1931 | 99.5911 | 96.8338 | 44.7388 | 2192 | 9 | 2202 | 72 | 34 | 47.2222 | |
| ckim-isaac | INDEL | D1_5 | HG002complexvar | het | 94.5641 | 92.7330 | 96.4689 | 45.1790 | 19256 | 1509 | 18687 | 684 | 323 | 47.2222 | |
| egarrison-hhga | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | het | 99.3197 | 98.9592 | 99.6829 | 37.2866 | 11314 | 119 | 11317 | 36 | 17 | 47.2222 | |
| egarrison-hhga | SNP | tv | map_l125_m2_e0 | * | 99.4065 | 99.0357 | 99.7800 | 70.1050 | 16330 | 159 | 16330 | 36 | 17 | 47.2222 | |
| egarrison-hhga | SNP | tv | map_l125_m2_e1 | * | 99.4064 | 99.0334 | 99.7822 | 70.1626 | 16496 | 161 | 16496 | 36 | 17 | 47.2222 | |
| ndellapenna-hhga | SNP | tv | map_l150_m1_e0 | * | 98.9384 | 98.2221 | 99.6652 | 71.6791 | 10718 | 194 | 10718 | 36 | 17 | 47.2222 | |
| ndellapenna-hhga | INDEL | D1_5 | map_l100_m1_e0 | * | 97.6365 | 97.2403 | 98.0360 | 81.9551 | 1797 | 51 | 1797 | 36 | 17 | 47.2222 | |
| ndellapenna-hhga | INDEL | D1_5 | map_l100_m2_e0 | * | 97.6927 | 97.2846 | 98.1043 | 82.7144 | 1863 | 52 | 1863 | 36 | 17 | 47.2222 | |
| ndellapenna-hhga | SNP | ti | map_l150_m2_e0 | het | 98.7101 | 97.7253 | 99.7148 | 75.0553 | 12588 | 293 | 12588 | 36 | 17 | 47.2222 | |
| gduggal-snapfb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 77.3261 | 72.6018 | 82.7081 | 62.1191 | 47446 | 17905 | 52604 | 10998 | 5193 | 47.2177 | |
| gduggal-snapfb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 77.3261 | 72.6018 | 82.7081 | 62.1191 | 47446 | 17905 | 52604 | 10998 | 5193 | 47.2177 | |
| gduggal-snapfb | SNP | * | map_l150_m1_e0 | het | 95.7011 | 96.8575 | 94.5719 | 74.7840 | 18709 | 607 | 18712 | 1074 | 507 | 47.2067 | |