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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
28551-28600 / 86044 show all | |||||||||||||||
| asubramanian-gatk | SNP | ti | map_l100_m2_e0 | hetalt | 53.6585 | 36.6667 | 100.0000 | 89.6226 | 11 | 19 | 11 | 0 | 0 | ||
| jmaeng-gatk | INDEL | * | map_l150_m2_e0 | homalt | 98.6416 | 98.1289 | 99.1597 | 89.6206 | 472 | 9 | 472 | 4 | 3 | 75.0000 | |
| gduggal-snapfb | INDEL | * | map_l125_m2_e0 | homalt | 97.0861 | 96.0682 | 98.1258 | 89.6192 | 733 | 30 | 733 | 14 | 9 | 64.2857 | |
| ltrigg-rtg1 | INDEL | D1_5 | map_l250_m2_e1 | het | 93.4498 | 87.7049 | 100.0000 | 89.6190 | 107 | 15 | 109 | 0 | 0 | ||
| ghariani-varprowl | INDEL | D1_5 | map_l100_m0_e0 | het | 89.8148 | 98.4772 | 82.5532 | 89.6186 | 582 | 9 | 582 | 123 | 22 | 17.8862 | |
| egarrison-hhga | SNP | * | segdup | het | 99.4921 | 99.5438 | 99.4404 | 89.6178 | 17238 | 79 | 17238 | 97 | 4 | 4.1237 | |
| ghariani-varprowl | SNP | tv | map_l250_m2_e0 | homalt | 97.8308 | 96.2647 | 99.4487 | 89.6177 | 902 | 35 | 902 | 5 | 1 | 20.0000 | |
| hfeng-pmm2 | INDEL | D1_5 | map_l150_m2_e0 | het | 97.5224 | 99.2218 | 95.8801 | 89.6170 | 510 | 4 | 512 | 22 | 2 | 9.0909 | |
| eyeh-varpipe | INDEL | D6_15 | map_l150_m1_e0 | het | 95.4545 | 100.0000 | 91.3043 | 89.6163 | 39 | 0 | 42 | 4 | 4 | 100.0000 | |
| astatham-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 97.5501 | 95.9474 | 99.2072 | 89.6154 | 876 | 37 | 876 | 7 | 6 | 85.7143 | |
| gduggal-bwavard | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 81.2556 | 88.9456 | 74.7895 | 89.6153 | 1569 | 195 | 1510 | 509 | 141 | 27.7014 | |
| gduggal-snapvard | SNP | tv | lowcmp_SimpleRepeat_quadTR_51to200 | * | 51.3219 | 83.3333 | 37.0787 | 89.6149 | 35 | 7 | 33 | 56 | 0 | 0.0000 | |
| gduggal-snapplat | INDEL | * | map_siren | * | 79.6077 | 71.8219 | 89.2868 | 89.6136 | 5322 | 2088 | 5709 | 685 | 78 | 11.3869 | |
| dgrover-gatk | INDEL | I1_5 | map_l100_m2_e1 | hetalt | 97.7273 | 95.5556 | 100.0000 | 89.6135 | 43 | 2 | 43 | 0 | 0 | ||
| anovak-vg | INDEL | D1_5 | map_l150_m1_e0 | * | 81.6618 | 83.6820 | 79.7368 | 89.6132 | 600 | 117 | 606 | 154 | 60 | 38.9610 | |
| bgallagher-sentieon | SNP | ti | map_l250_m2_e1 | * | 98.6646 | 98.9756 | 98.3555 | 89.6132 | 5024 | 52 | 5024 | 84 | 19 | 22.6190 | |
| cchapple-custom | INDEL | I1_5 | map_l150_m2_e1 | * | 96.3108 | 96.0452 | 96.5779 | 89.6130 | 510 | 21 | 508 | 18 | 3 | 16.6667 | |
| astatham-gatk | INDEL | D1_5 | map_l150_m1_e0 | * | 96.6476 | 96.3738 | 96.9231 | 89.6121 | 691 | 26 | 693 | 22 | 4 | 18.1818 | |
| jli-custom | INDEL | I1_5 | map_l150_m2_e1 | het | 98.5702 | 97.7918 | 99.3610 | 89.6117 | 310 | 7 | 311 | 2 | 0 | 0.0000 | |
| egarrison-hhga | INDEL | * | map_l100_m2_e0 | hetalt | 82.9138 | 72.0000 | 97.7273 | 89.6104 | 90 | 35 | 86 | 2 | 1 | 50.0000 | |
| gduggal-bwafb | INDEL | D1_5 | map_l150_m1_e0 | homalt | 98.6784 | 98.2456 | 99.1150 | 89.6092 | 224 | 4 | 224 | 2 | 2 | 100.0000 | |
| gduggal-snapfb | INDEL | I1_5 | map_l125_m2_e1 | homalt | 98.6912 | 99.1254 | 98.2609 | 89.6084 | 340 | 3 | 339 | 6 | 3 | 50.0000 | |
| cchapple-custom | SNP | * | map_l250_m1_e0 | * | 96.0890 | 95.7906 | 96.3892 | 89.6069 | 6918 | 304 | 6914 | 259 | 62 | 23.9382 | |
| cchapple-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 94.7350 | 92.2280 | 97.3822 | 89.6054 | 356 | 30 | 372 | 10 | 1 | 10.0000 | |
| cchapple-custom | INDEL | D1_5 | map_l150_m0_e0 | homalt | 96.3707 | 94.1176 | 98.7342 | 89.6053 | 80 | 5 | 78 | 1 | 1 | 100.0000 | |
| ckim-dragen | INDEL | D1_5 | map_l125_m0_e0 | het | 95.6942 | 96.8116 | 94.6023 | 89.6043 | 334 | 11 | 333 | 19 | 1 | 5.2632 | |
| ckim-vqsr | SNP | tv | map_l125_m2_e0 | * | 69.7523 | 53.9693 | 98.5819 | 89.6043 | 8899 | 7590 | 8898 | 128 | 1 | 0.7813 | |
| qzeng-custom | INDEL | C1_5 | HG002complexvar | het | 80.8034 | 71.4286 | 93.0108 | 89.6031 | 5 | 2 | 173 | 13 | 1 | 7.6923 | |
| jmaeng-gatk | INDEL | I1_5 | map_l100_m1_e0 | het | 96.8346 | 98.0695 | 95.6305 | 89.6028 | 762 | 15 | 766 | 35 | 1 | 2.8571 | |
| anovak-vg | SNP | ti | lowcmp_SimpleRepeat_quadTR_51to200 | homalt | 73.8636 | 71.4286 | 76.4706 | 89.6024 | 25 | 10 | 26 | 8 | 5 | 62.5000 | |
| ciseli-custom | INDEL | I6_15 | segdup | * | 43.2432 | 32.0000 | 66.6667 | 89.6021 | 56 | 119 | 54 | 27 | 25 | 92.5926 | |
| qzeng-custom | SNP | ti | map_l150_m1_e0 | het | 79.9066 | 68.7551 | 95.3758 | 89.6012 | 8505 | 3865 | 8477 | 411 | 348 | 84.6715 | |
| jmaeng-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 98.9011 | 98.5761 | 99.2282 | 89.6010 | 900 | 13 | 900 | 7 | 6 | 85.7143 | |
| ckim-vqsr | SNP | tv | map_l125_m2_e1 | * | 69.8938 | 54.1334 | 98.6002 | 89.6003 | 9017 | 7640 | 9016 | 128 | 1 | 0.7813 | |
| gduggal-snapfb | SNP | ti | lowcmp_SimpleRepeat_diTR_51to200 | homalt | 14.2857 | 100.0000 | 7.6923 | 89.6000 | 6 | 0 | 6 | 72 | 0 | 0.0000 | |
| ltrigg-rtg2 | INDEL | D6_15 | segdup | homalt | 98.9899 | 98.0000 | 100.0000 | 89.5966 | 49 | 1 | 49 | 0 | 0 | ||
| gduggal-snapfb | INDEL | D1_5 | map_l125_m2_e1 | homalt | 98.3846 | 98.1183 | 98.6523 | 89.5962 | 365 | 7 | 366 | 5 | 3 | 60.0000 | |
| ckim-vqsr | SNP | tv | lowcmp_SimpleRepeat_quadTR_51to200 | * | 96.3855 | 95.2381 | 97.5610 | 89.5939 | 40 | 2 | 40 | 1 | 0 | 0.0000 | |
| ckim-gatk | SNP | tv | lowcmp_SimpleRepeat_quadTR_51to200 | * | 96.3855 | 95.2381 | 97.5610 | 89.5939 | 40 | 2 | 40 | 1 | 0 | 0.0000 | |
| hfeng-pmm3 | INDEL | I1_5 | map_l150_m2_e1 | het | 97.7828 | 97.1609 | 98.4127 | 89.5937 | 308 | 9 | 310 | 5 | 0 | 0.0000 | |
| mlin-fermikit | INDEL | D1_5 | map_l100_m2_e0 | hetalt | 62.8571 | 45.8333 | 100.0000 | 89.5928 | 22 | 26 | 23 | 0 | 0 | ||
| ltrigg-rtg1 | INDEL | D16_PLUS | map_l125_m1_e0 | * | 90.1158 | 85.1852 | 95.6522 | 89.5928 | 23 | 4 | 22 | 1 | 0 | 0.0000 | |
| ltrigg-rtg2 | INDEL | C16_PLUS | HG002complexvar | * | 0.0000 | 0.0000 | 94.2029 | 89.5928 | 0 | 0 | 65 | 4 | 3 | 75.0000 | |
| raldana-dualsentieon | SNP | ti | map_l250_m2_e1 | het | 97.5433 | 98.0903 | 97.0024 | 89.5913 | 3236 | 63 | 3236 | 100 | 2 | 2.0000 | |
| ndellapenna-hhga | INDEL | D6_15 | map_l150_m2_e0 | homalt | 96.4286 | 96.4286 | 96.4286 | 89.5911 | 27 | 1 | 27 | 1 | 1 | 100.0000 | |
| qzeng-custom | INDEL | I16_PLUS | map_l125_m2_e0 | * | 66.6667 | 66.6667 | 66.6667 | 89.5899 | 10 | 5 | 22 | 11 | 0 | 0.0000 | |
| ckim-vqsr | INDEL | D6_15 | map_l125_m1_e0 | homalt | 98.5075 | 97.0588 | 100.0000 | 89.5899 | 33 | 1 | 33 | 0 | 0 | ||
| bgallagher-sentieon | SNP | ti | segdup | * | 99.5103 | 99.8567 | 99.1663 | 89.5899 | 19509 | 28 | 19507 | 164 | 6 | 3.6585 | |
| ckim-gatk | INDEL | D6_15 | map_l125_m1_e0 | homalt | 98.5075 | 97.0588 | 100.0000 | 89.5899 | 33 | 1 | 33 | 0 | 0 | ||
| asubramanian-gatk | INDEL | * | map_l100_m1_e0 | het | 89.5146 | 84.5190 | 95.1378 | 89.5888 | 1889 | 346 | 1898 | 97 | 13 | 13.4021 | |