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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
78251-78300 / 86044 show all | |||||||||||||||
| eyeh-varpipe | SNP | tv | lowcmp_SimpleRepeat_diTR_11to50 | * | 97.0524 | 98.8880 | 95.2837 | 61.3406 | 4802 | 54 | 4182 | 207 | 43 | 20.7729 | |
| raldana-dualsentieon | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 97.7010 | 96.5880 | 98.8399 | 43.3164 | 17636 | 623 | 17637 | 207 | 204 | 98.5507 | |
| gduggal-snapfb | INDEL | I1_5 | lowcmp_SimpleRepeat_triTR_11to50 | * | 86.8494 | 93.7143 | 80.9217 | 61.7014 | 984 | 66 | 878 | 207 | 45 | 21.7391 | |
| gduggal-snapvard | INDEL | * | map_l250_m2_e1 | * | 77.7498 | 91.2913 | 67.7067 | 95.6730 | 304 | 29 | 434 | 207 | 49 | 23.6715 | |
| cchapple-custom | INDEL | I1_5 | HG002compoundhet | homalt | 69.4826 | 98.7842 | 53.5874 | 88.0589 | 325 | 4 | 239 | 207 | 207 | 100.0000 | |
| ciseli-custom | INDEL | D1_5 | map_siren | homalt | 86.4005 | 89.6404 | 83.3866 | 80.5952 | 1047 | 121 | 1044 | 208 | 167 | 80.2885 | |
| eyeh-varpipe | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 89.0264 | 97.4704 | 81.9288 | 85.3506 | 1233 | 32 | 943 | 208 | 28 | 13.4615 | |
| gduggal-bwafb | INDEL | D16_PLUS | HG002compoundhet | * | 82.3584 | 75.6514 | 90.3704 | 28.6893 | 1771 | 570 | 1952 | 208 | 208 | 100.0000 | |
| gduggal-bwaplat | SNP | * | HG002complexvar | homalt | 98.2316 | 96.5943 | 99.9253 | 21.0137 | 278746 | 9828 | 278424 | 208 | 186 | 89.4231 | |
| gduggal-bwavard | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 97.1768 | 97.7361 | 96.6239 | 63.2047 | 6044 | 140 | 5953 | 208 | 24 | 11.5385 | |
| gduggal-bwaplat | INDEL | D1_5 | * | homalt | 94.9240 | 90.7227 | 99.5332 | 62.2451 | 44387 | 4539 | 44353 | 208 | 178 | 85.5769 | |
| gduggal-bwaplat | INDEL | D1_5 | HG002complexvar | het | 91.4572 | 85.1047 | 98.8344 | 59.4901 | 17672 | 3093 | 17637 | 208 | 101 | 48.5577 | |
| jmaeng-gatk | SNP | * | map_l150_m0_e0 | * | 72.2268 | 57.5050 | 97.0803 | 92.6384 | 6919 | 5113 | 6916 | 208 | 23 | 11.0577 | |
| dgrover-gatk | SNP | ti | map_l100_m2_e1 | * | 99.5279 | 99.4766 | 99.5792 | 67.5880 | 49226 | 259 | 49219 | 208 | 50 | 24.0385 | |
| egarrison-hhga | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 93.4915 | 90.6675 | 96.4971 | 60.4318 | 5732 | 590 | 5730 | 208 | 164 | 78.8462 | |
| egarrison-hhga | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 93.4915 | 90.6675 | 96.4971 | 60.4318 | 5732 | 590 | 5730 | 208 | 164 | 78.8462 | |
| eyeh-varpipe | INDEL | * | lowcmp_SimpleRepeat_homopolymer_6to10 | homalt | 99.0261 | 98.9819 | 99.0704 | 52.1206 | 11181 | 115 | 22167 | 208 | 201 | 96.6346 | |
| ckim-vqsr | SNP | * | map_l100_m0_e0 | * | 70.1414 | 54.3558 | 98.8482 | 87.4638 | 17851 | 14990 | 17850 | 208 | 2 | 0.9615 | |
| ckim-vqsr | SNP | * | map_l100_m0_e0 | het | 80.5244 | 68.0594 | 98.5791 | 88.0545 | 14432 | 6773 | 14431 | 208 | 2 | 0.9615 | |
| mlin-fermikit | INDEL | * | map_l125_m2_e0 | * | 69.1050 | 57.7869 | 85.9364 | 82.6204 | 1269 | 927 | 1271 | 208 | 160 | 76.9231 | |
| jlack-gatk | SNP | tv | HG002complexvar | het | 99.8776 | 99.8932 | 99.8620 | 22.3009 | 150570 | 161 | 150494 | 208 | 64 | 30.7692 | |
| gduggal-snapplat | INDEL | I6_15 | * | hetalt | 52.6793 | 36.6390 | 93.7008 | 46.4917 | 3133 | 5418 | 3094 | 208 | 167 | 80.2885 | |
| ghariani-varprowl | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 50.2079 | 86.2903 | 35.4037 | 86.0546 | 107 | 17 | 114 | 208 | 3 | 1.4423 | |
| asubramanian-gatk | INDEL | * | HG002compoundhet | hetalt | 95.7396 | 92.5814 | 99.1208 | 52.6709 | 23312 | 1868 | 23449 | 208 | 188 | 90.3846 | |
| raldana-dualsentieon | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.4907 | 97.7292 | 99.2642 | 69.7423 | 28060 | 652 | 28060 | 208 | 16 | 7.6923 | |
| raldana-dualsentieon | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.4907 | 97.7292 | 99.2642 | 69.7423 | 28060 | 652 | 28060 | 208 | 16 | 7.6923 | |
| ltrigg-rtg2 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.0316 | 97.6012 | 98.4657 | 62.5780 | 13427 | 330 | 13413 | 209 | 47 | 22.4880 | |
| ltrigg-rtg2 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.0316 | 97.6012 | 98.4657 | 62.5780 | 13427 | 330 | 13413 | 209 | 47 | 22.4880 | |
| mlin-fermikit | INDEL | D1_5 | map_siren | * | 85.3013 | 78.7759 | 93.0054 | 76.3252 | 2780 | 749 | 2779 | 209 | 185 | 88.5167 | |
| gduggal-bwafb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 84.1057 | 79.3599 | 89.4551 | 69.7220 | 1711 | 445 | 1773 | 209 | 166 | 79.4258 | |
| eyeh-varpipe | INDEL | D16_PLUS | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 46.1659 | 40.4511 | 53.7611 | 64.5212 | 269 | 396 | 243 | 209 | 202 | 96.6507 | |
| gduggal-bwavard | INDEL | * | map_l150_m2_e0 | het | 88.9752 | 98.5651 | 81.0860 | 93.2486 | 893 | 13 | 896 | 209 | 44 | 21.0526 | |
| gduggal-bwavard | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 37.3529 | 30.5677 | 48.0100 | 79.3529 | 210 | 477 | 193 | 209 | 153 | 73.2057 | |
| ckim-isaac | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 92.9113 | 89.3360 | 96.7846 | 77.0025 | 6149 | 734 | 6291 | 209 | 19 | 9.0909 | |
| anovak-vg | INDEL | D1_5 | map_l125_m2_e0 | het | 82.1558 | 88.4817 | 76.6741 | 87.9456 | 676 | 88 | 687 | 209 | 69 | 33.0144 | |
| asubramanian-gatk | SNP | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 98.9233 | 98.8811 | 98.9655 | 57.0313 | 19973 | 226 | 19994 | 209 | 5 | 2.3923 | |
| bgallagher-sentieon | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 98.6936 | 99.8565 | 97.5576 | 63.3125 | 8348 | 12 | 8348 | 209 | 208 | 99.5215 | |
| bgallagher-sentieon | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 98.6936 | 99.8565 | 97.5576 | 63.3125 | 8348 | 12 | 8348 | 209 | 208 | 99.5215 | |
| jli-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 94.5494 | 92.7996 | 96.3665 | 60.4456 | 5645 | 438 | 5543 | 209 | 197 | 94.2584 | |
| jlack-gatk | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | het | 95.3982 | 98.2071 | 92.7456 | 62.2313 | 2684 | 49 | 2672 | 209 | 198 | 94.7368 | |
| gduggal-snapfb | SNP | tv | segdup | * | 98.5144 | 99.4491 | 97.5971 | 92.7173 | 8485 | 47 | 8489 | 209 | 12 | 5.7416 | |
| gduggal-snapfb | SNP | ti | segdup | het | 98.8224 | 99.3766 | 98.2744 | 91.5559 | 11955 | 75 | 11960 | 210 | 13 | 6.1905 | |
| gduggal-snapvard | INDEL | I6_15 | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 47.5592 | 44.5161 | 51.0490 | 71.9424 | 69 | 86 | 219 | 210 | 175 | 83.3333 | |
| gduggal-bwaplat | SNP | ti | map_l100_m2_e0 | het | 87.1494 | 77.7546 | 99.1265 | 83.6970 | 23810 | 6812 | 23832 | 210 | 63 | 30.0000 | |
| eyeh-varpipe | SNP | tv | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 88.9665 | 98.0847 | 81.3995 | 77.6081 | 973 | 19 | 919 | 210 | 7 | 3.3333 | |
| gduggal-bwafb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 92.5150 | 94.1534 | 90.9326 | 70.9811 | 2013 | 125 | 2106 | 210 | 201 | 95.7143 | |
| raldana-dualsentieon | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 97.6195 | 96.5975 | 98.6634 | 57.7294 | 15501 | 546 | 15502 | 210 | 201 | 95.7143 | |
| raldana-dualsentieon | INDEL | I1_5 | * | het | 99.5073 | 99.2827 | 99.7331 | 57.9285 | 78474 | 567 | 78457 | 210 | 142 | 67.6190 | |
| rpoplin-dv42 | SNP | ti | map_siren | * | 99.6562 | 99.5227 | 99.7902 | 53.3616 | 99876 | 479 | 99868 | 210 | 138 | 65.7143 | |
| cchapple-custom | SNP | tv | HG002complexvar | het | 99.7615 | 99.6630 | 99.8602 | 21.5432 | 150223 | 508 | 149954 | 210 | 146 | 69.5238 | |