PrecisionFDA
Truth Challenge
Engage and improve DNA test results with our community challenges
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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
68851-68900 / 86044 show all | |||||||||||||||
| bgallagher-sentieon | SNP | tv | map_l250_m2_e1 | * | 98.1725 | 98.5597 | 97.7884 | 89.4056 | 2874 | 42 | 2874 | 65 | 13 | 20.0000 | |
| ckim-dragen | INDEL | I6_15 | HG002complexvar | * | 98.1726 | 97.5167 | 98.8375 | 57.3399 | 4673 | 119 | 4676 | 55 | 54 | 98.1818 | |
| eyeh-varpipe | SNP | * | map_l125_m2_e0 | het | 98.1728 | 99.6214 | 96.7658 | 76.7357 | 29207 | 111 | 28304 | 946 | 28 | 2.9598 | |
| ckim-gatk | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 98.1731 | 97.9516 | 98.3956 | 52.7295 | 10855 | 227 | 10855 | 177 | 173 | 97.7401 | |
| hfeng-pmm3 | INDEL | I6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 98.1732 | 96.4119 | 100.0000 | 43.7500 | 618 | 23 | 621 | 0 | 0 | ||
| mlin-fermikit | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 98.1732 | 97.8142 | 98.5348 | 74.0741 | 537 | 12 | 538 | 8 | 7 | 87.5000 | |
| dgrover-gatk | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 98.1733 | 99.8938 | 96.5110 | 60.0492 | 3762 | 4 | 3762 | 136 | 134 | 98.5294 | |
| dgrover-gatk | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 98.1733 | 99.8938 | 96.5110 | 60.0492 | 3762 | 4 | 3762 | 136 | 134 | 98.5294 | |
| cchapple-custom | INDEL | I6_15 | HG002complexvar | het | 98.1734 | 97.1975 | 99.1692 | 56.5725 | 2289 | 66 | 3581 | 30 | 25 | 83.3333 | |
| bgallagher-sentieon | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 98.1735 | 98.8506 | 97.5057 | 69.0309 | 430 | 5 | 430 | 11 | 5 | 45.4545 | |
| asubramanian-gatk | SNP | ti | HG002complexvar | homalt | 98.1740 | 96.4210 | 99.9920 | 18.6413 | 186539 | 6924 | 186529 | 15 | 15 | 100.0000 | |
| hfeng-pmm3 | INDEL | I6_15 | HG002complexvar | * | 98.1740 | 97.0367 | 99.3383 | 57.2224 | 4650 | 142 | 4654 | 31 | 31 | 100.0000 | |
| asubramanian-gatk | SNP | ti | segdup | het | 98.1746 | 97.0158 | 99.3614 | 92.7228 | 11671 | 359 | 11669 | 75 | 4 | 5.3333 | |
| hfeng-pmm1 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 98.1747 | 97.0673 | 99.3076 | 46.3948 | 10757 | 325 | 10757 | 75 | 72 | 96.0000 | |
| hfeng-pmm1 | INDEL | I1_5 | HG002complexvar | hetalt | 98.1752 | 96.5238 | 99.8841 | 71.0548 | 1666 | 60 | 1724 | 2 | 2 | 100.0000 | |
| ndellapenna-hhga | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 98.1764 | 97.4871 | 98.8756 | 71.7313 | 1319 | 34 | 1319 | 15 | 8 | 53.3333 | |
| ckim-dragen | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | * | 98.1771 | 97.9914 | 98.3635 | 52.4340 | 35857 | 735 | 35764 | 595 | 553 | 92.9412 | |
| jli-custom | INDEL | * | map_l150_m2_e0 | het | 98.1776 | 98.0132 | 98.3425 | 89.4239 | 888 | 18 | 890 | 15 | 4 | 26.6667 | |
| asubramanian-gatk | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.1776 | 97.0330 | 99.3494 | 70.2755 | 30219 | 924 | 30236 | 198 | 22 | 11.1111 | |
| asubramanian-gatk | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.1776 | 97.0330 | 99.3494 | 70.2755 | 30219 | 924 | 30236 | 198 | 22 | 11.1111 | |
| ndellapenna-hhga | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 98.1778 | 97.6714 | 98.6894 | 75.0164 | 755 | 18 | 753 | 10 | 4 | 40.0000 | |
| bgallagher-sentieon | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 98.1780 | 97.2561 | 99.1176 | 38.1818 | 319 | 9 | 337 | 3 | 3 | 100.0000 | |
| ltrigg-rtg1 | SNP | ti | map_l150_m0_e0 | * | 98.1783 | 96.6671 | 99.7375 | 70.0220 | 7599 | 262 | 7598 | 20 | 11 | 55.0000 | |
| eyeh-varpipe | SNP | * | map_l125_m2_e1 | het | 98.1785 | 99.6221 | 96.7760 | 76.7928 | 29528 | 112 | 28607 | 953 | 28 | 2.9381 | |
| ndellapenna-hhga | SNP | ti | map_l150_m0_e0 | het | 98.1786 | 96.7628 | 99.6364 | 79.7339 | 4932 | 165 | 4932 | 18 | 7 | 38.8889 | |
| rpoplin-dv42 | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 98.1787 | 97.7376 | 98.6239 | 91.0177 | 216 | 5 | 215 | 3 | 2 | 66.6667 | |
| raldana-dualsentieon | INDEL | I6_15 | HG002complexvar | homalt | 98.1789 | 99.9176 | 96.4996 | 55.2987 | 1213 | 1 | 1213 | 44 | 44 | 100.0000 | |
| ckim-vqsr | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 98.1793 | 97.2561 | 99.1202 | 37.6600 | 319 | 9 | 338 | 3 | 3 | 100.0000 | |
| ckim-gatk | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 98.1793 | 97.2561 | 99.1202 | 37.6600 | 319 | 9 | 338 | 3 | 3 | 100.0000 | |
| hfeng-pmm2 | SNP | ti | lowcmp_SimpleRepeat_diTR_11to50 | * | 98.1795 | 96.4441 | 99.9786 | 67.5115 | 4665 | 172 | 4665 | 1 | 0 | 0.0000 | |
| raldana-dualsentieon | SNP | * | map_l250_m2_e0 | * | 98.1797 | 98.1611 | 98.1984 | 88.2926 | 7740 | 145 | 7740 | 142 | 6 | 4.2254 | |
| ltrigg-rtg2 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 98.1797 | 98.9154 | 97.4549 | 72.8477 | 912 | 10 | 919 | 24 | 3 | 12.5000 | |
| cchapple-custom | INDEL | I6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 98.1802 | 96.7672 | 99.6350 | 61.0934 | 449 | 15 | 1092 | 4 | 4 | 100.0000 | |
| ndellapenna-hhga | SNP | * | map_l250_m2_e0 | * | 98.1811 | 96.8675 | 99.5309 | 87.5400 | 7638 | 247 | 7638 | 36 | 19 | 52.7778 | |
| raldana-dualsentieon | SNP | tv | map_l250_m0_e0 | homalt | 98.1818 | 97.9275 | 98.4375 | 91.2528 | 189 | 4 | 189 | 3 | 1 | 33.3333 | |
| rpoplin-dv42 | INDEL | D6_15 | map_l150_m2_e0 | homalt | 98.1818 | 96.4286 | 100.0000 | 90.5263 | 27 | 1 | 27 | 0 | 0 | ||
| rpoplin-dv42 | INDEL | I6_15 | segdup | het | 98.1818 | 97.5904 | 98.7805 | 92.4632 | 81 | 2 | 81 | 1 | 1 | 100.0000 | |
| rpoplin-dv42 | SNP | * | map_siren | hetalt | 98.1818 | 100.0000 | 96.4286 | 79.8561 | 81 | 0 | 81 | 3 | 3 | 100.0000 | |
| rpoplin-dv42 | SNP | tv | map_siren | hetalt | 98.1818 | 100.0000 | 96.4286 | 79.8561 | 81 | 0 | 81 | 3 | 3 | 100.0000 | |
| ltrigg-rtg2 | INDEL | D6_15 | map_l150_m2_e0 | homalt | 98.1818 | 96.4286 | 100.0000 | 82.5503 | 27 | 1 | 26 | 0 | 0 | ||
| ltrigg-rtg2 | INDEL | I1_5 | map_siren | hetalt | 98.1818 | 96.4286 | 100.0000 | 92.1300 | 108 | 4 | 109 | 0 | 0 | ||
| ltrigg-rtg1 | INDEL | D6_15 | map_l150_m2_e0 | homalt | 98.1818 | 96.4286 | 100.0000 | 86.5285 | 27 | 1 | 26 | 0 | 0 | ||
| jmaeng-gatk | INDEL | D6_15 | map_l150_m2_e0 | * | 98.1818 | 98.7805 | 97.5904 | 94.2640 | 81 | 1 | 81 | 2 | 0 | 0.0000 | |
| jmaeng-gatk | INDEL | D6_15 | map_l150_m2_e0 | homalt | 98.1818 | 96.4286 | 100.0000 | 90.0000 | 27 | 1 | 27 | 0 | 0 | ||
| ckim-vqsr | INDEL | D6_15 | map_l150_m2_e0 | homalt | 98.1818 | 96.4286 | 100.0000 | 90.2527 | 27 | 1 | 27 | 0 | 0 | ||
| dgrover-gatk | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | hetalt | 98.1818 | 96.4286 | 100.0000 | 75.2860 | 108 | 4 | 108 | 0 | 0 | ||
| dgrover-gatk | SNP | tv | map_l250_m0_e0 | homalt | 98.1818 | 97.9275 | 98.4375 | 92.5983 | 189 | 4 | 189 | 3 | 2 | 66.6667 | |
| ckim-vqsr | INDEL | I6_15 | segdup | het | 98.1818 | 97.5904 | 98.7805 | 95.4267 | 81 | 2 | 81 | 1 | 0 | 0.0000 | |
| eyeh-varpipe | INDEL | * | map_l250_m0_e0 | homalt | 98.1818 | 100.0000 | 96.4286 | 97.2305 | 25 | 0 | 54 | 2 | 2 | 100.0000 | |
| bgallagher-sentieon | INDEL | D6_15 | map_l150_m2_e0 | * | 98.1818 | 98.7805 | 97.5904 | 92.7320 | 81 | 1 | 81 | 2 | 0 | 0.0000 | |