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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
59101-59150 / 86044 show all | |||||||||||||||
| ckim-isaac | SNP | tv | map_l100_m2_e1 | hetalt | 73.5294 | 58.1395 | 100.0000 | 76.6355 | 25 | 18 | 25 | 0 | 0 | ||
| ckim-vqsr | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 95.5725 | 99.1852 | 92.2138 | 66.1587 | 2191 | 18 | 2191 | 185 | 182 | 98.3784 | |
| ckim-vqsr | INDEL | * | map_l100_m2_e1 | hetalt | 92.6829 | 86.3636 | 100.0000 | 87.5536 | 114 | 18 | 116 | 0 | 0 | ||
| dgrover-gatk | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | * | 99.3002 | 99.9010 | 98.7065 | 40.6968 | 18165 | 18 | 18162 | 238 | 4 | 1.6807 | |
| dgrover-gatk | SNP | tv | map_l250_m0_e0 | het | 96.5998 | 96.8531 | 96.3478 | 94.1784 | 554 | 18 | 554 | 21 | 2 | 9.5238 | |
| egarrison-hhga | INDEL | * | map_l125_m0_e0 | het | 97.1036 | 96.9336 | 97.2743 | 89.2313 | 569 | 18 | 571 | 16 | 4 | 25.0000 | |
| ckim-isaac | INDEL | D16_PLUS | lowcmp_SimpleRepeat_triTR_11to50 | het | 78.7229 | 70.4918 | 89.1304 | 63.2000 | 43 | 18 | 41 | 5 | 2 | 40.0000 | |
| ckim-isaac | INDEL | D16_PLUS | map_l100_m2_e1 | hetalt | 57.1429 | 40.0000 | 100.0000 | 80.9524 | 12 | 18 | 12 | 0 | 0 | ||
| ckim-isaac | INDEL | D6_15 | map_l125_m1_e0 | homalt | 64.0000 | 47.0588 | 100.0000 | 75.7576 | 16 | 18 | 16 | 0 | 0 | ||
| ckim-isaac | INDEL | I16_PLUS | map_l100_m1_e0 | het | 0.0000 | 100.0000 | 0 | 18 | 0 | 0 | 0 | ||||
| ckim-isaac | INDEL | I16_PLUS | map_l100_m2_e0 | het | 0.0000 | 100.0000 | 0 | 18 | 0 | 0 | 0 | ||||
| ckim-isaac | INDEL | I16_PLUS | map_l100_m2_e1 | het | 0.0000 | 100.0000 | 0 | 18 | 0 | 0 | 0 | ||||
| egarrison-hhga | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | homalt | 98.5461 | 98.1405 | 98.9551 | 62.1889 | 950 | 18 | 947 | 10 | 7 | 70.0000 | |
| egarrison-hhga | INDEL | I1_5 | map_l100_m2_e1 | * | 98.7451 | 98.7097 | 98.7805 | 84.7650 | 1377 | 18 | 1377 | 17 | 3 | 17.6471 | |
| egarrison-hhga | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 99.4422 | 99.5809 | 99.3038 | 58.0347 | 4277 | 18 | 4279 | 30 | 5 | 16.6667 | |
| egarrison-hhga | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 90.5405 | 88.1579 | 93.0556 | 89.6552 | 134 | 18 | 134 | 10 | 5 | 50.0000 | |
| egarrison-hhga | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 95.6750 | 95.3003 | 96.0526 | 80.5028 | 365 | 18 | 365 | 15 | 12 | 80.0000 | |
| egarrison-hhga | SNP | ti | lowcmp_SimpleRepeat_triTR_11to50 | * | 99.6923 | 99.5392 | 99.8459 | 28.7987 | 3888 | 18 | 3888 | 6 | 1 | 16.6667 | |
| egarrison-hhga | SNP | tv | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 99.2342 | 98.9813 | 99.4883 | 56.1128 | 1749 | 18 | 1750 | 9 | 6 | 66.6667 | |
| egarrison-hhga | SNP | tv | lowcmp_SimpleRepeat_triTR_11to50 | * | 99.7240 | 99.4783 | 99.9709 | 35.3959 | 3432 | 18 | 3434 | 1 | 1 | 100.0000 | |
| eyeh-varpipe | INDEL | * | lowcmp_SimpleRepeat_diTR_51to200 | homalt | 36.1705 | 94.9861 | 22.3385 | 27.7457 | 341 | 18 | 363 | 1262 | 1171 | 92.7892 | |
| eyeh-varpipe | INDEL | * | map_l125_m2_e1 | hetalt | 72.5594 | 58.1395 | 96.4912 | 93.8245 | 25 | 18 | 55 | 2 | 1 | 50.0000 | |
| eyeh-varpipe | INDEL | * | map_l150_m0_e0 | * | 96.3994 | 96.4981 | 96.3009 | 96.8271 | 496 | 18 | 781 | 30 | 19 | 63.3333 | |
| ckim-vqsr | SNP | ti | map_l125_m1_e0 | hetalt | 40.0000 | 25.0000 | 100.0000 | 95.0000 | 6 | 18 | 6 | 0 | 0 | ||
| ckim-vqsr | SNP | ti | map_l125_m2_e0 | hetalt | 40.0000 | 25.0000 | 100.0000 | 95.9732 | 6 | 18 | 6 | 0 | 0 | ||
| ckim-vqsr | SNP | ti | map_l125_m2_e1 | hetalt | 40.0000 | 25.0000 | 100.0000 | 95.9732 | 6 | 18 | 6 | 0 | 0 | ||
| dgrover-gatk | INDEL | * | map_l150_m1_e0 | het | 97.6722 | 97.8947 | 97.4508 | 91.3510 | 837 | 18 | 841 | 22 | 3 | 13.6364 | |
| dgrover-gatk | INDEL | * | map_l150_m2_e0 | het | 97.8027 | 98.0132 | 97.5930 | 91.8342 | 888 | 18 | 892 | 22 | 3 | 13.6364 | |
| dgrover-gatk | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | het | 98.0250 | 99.3414 | 96.7430 | 63.3526 | 2715 | 18 | 2703 | 91 | 87 | 95.6044 | |
| hfeng-pmm2 | INDEL | D1_5 | map_l100_m2_e0 | * | 98.7266 | 99.0601 | 98.3954 | 83.7702 | 1897 | 18 | 1901 | 31 | 4 | 12.9032 | |
| hfeng-pmm2 | INDEL | D1_5 | map_l100_m2_e1 | * | 98.7423 | 99.0717 | 98.4151 | 83.8640 | 1921 | 18 | 1925 | 31 | 4 | 12.9032 | |
| hfeng-pmm2 | INDEL | I16_PLUS | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 93.7656 | 91.2621 | 96.4103 | 87.8429 | 188 | 18 | 188 | 7 | 2 | 28.5714 | |
| hfeng-pmm3 | SNP | tv | segdup | * | 99.7247 | 99.7890 | 99.6604 | 90.6553 | 8514 | 18 | 8510 | 29 | 5 | 17.2414 | |
| jlack-gatk | INDEL | * | map_l100_m2_e1 | hetalt | 92.3109 | 86.3636 | 99.1379 | 88.0903 | 114 | 18 | 115 | 1 | 0 | 0.0000 | |
| jlack-gatk | INDEL | * | map_l150_m2_e1 | het | 91.3160 | 98.0519 | 85.4460 | 93.5089 | 906 | 18 | 910 | 155 | 6 | 3.8710 | |
| jlack-gatk | INDEL | D16_PLUS | * | homalt | 98.8194 | 98.9362 | 98.7028 | 69.0115 | 1674 | 18 | 1674 | 22 | 15 | 68.1818 | |
| jlack-gatk | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 98.4013 | 98.5588 | 98.2442 | 73.3744 | 1231 | 18 | 1231 | 22 | 15 | 68.1818 | |
| jlack-gatk | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 98.4013 | 98.5588 | 98.2442 | 73.3744 | 1231 | 18 | 1231 | 22 | 15 | 68.1818 | |
| jlack-gatk | INDEL | D6_15 | map_siren | * | 94.4231 | 96.4637 | 92.4670 | 85.5628 | 491 | 18 | 491 | 40 | 5 | 12.5000 | |
| hfeng-pmm1 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 93.8416 | 89.8876 | 98.1595 | 71.7504 | 160 | 18 | 160 | 3 | 2 | 66.6667 | |
| hfeng-pmm1 | INDEL | I6_15 | map_siren | * | 96.4706 | 94.0984 | 98.9655 | 83.1395 | 287 | 18 | 287 | 3 | 3 | 100.0000 | |
| hfeng-pmm1 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 99.7696 | 99.5402 | 100.0000 | 80.2993 | 3897 | 18 | 3897 | 0 | 0 | ||
| hfeng-pmm1 | SNP | ti | map_l150_m1_e0 | homalt | 99.7748 | 99.7543 | 99.7952 | 71.0227 | 7309 | 18 | 7309 | 15 | 6 | 40.0000 | |
| hfeng-pmm1 | SNP | ti | map_l150_m2_e0 | homalt | 99.7833 | 99.7637 | 99.8030 | 73.2106 | 7598 | 18 | 7598 | 15 | 6 | 40.0000 | |
| hfeng-pmm1 | SNP | ti | map_l150_m2_e1 | homalt | 99.7855 | 99.7660 | 99.8049 | 73.2531 | 7675 | 18 | 7675 | 15 | 6 | 40.0000 | |
| hfeng-pmm2 | INDEL | * | map_l100_m0_e0 | het | 97.3349 | 98.2370 | 96.4491 | 87.4337 | 1003 | 18 | 1005 | 37 | 3 | 8.1081 | |
| hfeng-pmm2 | INDEL | * | map_siren | hetalt | 96.2185 | 92.7126 | 100.0000 | 87.6338 | 229 | 18 | 231 | 0 | 0 | ||
| hfeng-pmm3 | INDEL | I16_PLUS | HG002complexvar | het | 98.6280 | 97.2932 | 100.0000 | 62.8860 | 647 | 18 | 625 | 0 | 0 | ||
| hfeng-pmm3 | INDEL | I16_PLUS | HG002complexvar | hetalt | 96.8227 | 94.6269 | 99.1228 | 69.7613 | 317 | 18 | 339 | 3 | 3 | 100.0000 | |
| hfeng-pmm3 | INDEL | I16_PLUS | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 94.2356 | 91.2621 | 97.4093 | 87.4594 | 188 | 18 | 188 | 5 | 2 | 40.0000 | |