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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
14401-14450 / 86044 show all | |||||||||||||||
| hfeng-pmm3 | SNP | ti | map_l100_m0_e0 | het | 99.3735 | 99.2634 | 99.4838 | 69.6444 | 13880 | 103 | 13877 | 72 | 7 | 9.7222 | |
| gduggal-snapfb | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 89.1402 | 99.2630 | 80.8911 | 72.6164 | 27474 | 204 | 27579 | 6515 | 214 | 3.2847 | |
| ckim-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 99.2068 | 99.2630 | 99.1506 | 88.9811 | 1751 | 13 | 1751 | 15 | 13 | 86.6667 | |
| rpoplin-dv42 | SNP | * | map_l100_m1_e0 | * | 99.3983 | 99.2625 | 99.5346 | 63.1596 | 71869 | 534 | 71858 | 336 | 196 | 58.3333 | |
| eyeh-varpipe | SNP | ti | map_l250_m2_e0 | het | 98.6087 | 99.2624 | 97.9636 | 91.2085 | 3230 | 24 | 3175 | 66 | 4 | 6.0606 | |
| gduggal-bwafb | SNP | tv | segdup | het | 98.1577 | 99.2623 | 97.0773 | 93.8623 | 5248 | 39 | 5248 | 158 | 6 | 3.7975 | |
| ltrigg-rtg1 | SNP | * | lowcmp_SimpleRepeat_diTR_11to50 | het | 99.3904 | 99.2623 | 99.5188 | 66.4857 | 6190 | 46 | 6205 | 30 | 5 | 16.6667 | |
| astatham-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 99.5662 | 99.2623 | 99.8720 | 56.6274 | 3902 | 29 | 3902 | 5 | 0 | 0.0000 | |
| jpowers-varprowl | SNP | ti | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 99.3721 | 99.2620 | 99.4824 | 48.6065 | 4035 | 30 | 4036 | 21 | 4 | 19.0476 | |
| mlin-fermikit | SNP | * | func_cds | * | 99.4453 | 99.2617 | 99.6295 | 19.0809 | 18016 | 134 | 18016 | 67 | 48 | 71.6418 | |
| ckim-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 98.9346 | 99.2616 | 98.6098 | 64.3360 | 8334 | 62 | 8299 | 117 | 105 | 89.7436 | |
| gduggal-bwafb | SNP | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 98.5852 | 99.2612 | 97.9184 | 64.7490 | 55220 | 411 | 55320 | 1176 | 260 | 22.1088 | |
| asubramanian-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 98.2431 | 99.2607 | 97.2461 | 57.3108 | 5639 | 42 | 5650 | 160 | 149 | 93.1250 | |
| ckim-dragen | SNP | ti | map_l125_m2_e0 | homalt | 99.5541 | 99.2604 | 99.8495 | 63.2256 | 11274 | 84 | 11279 | 17 | 16 | 94.1176 | |
| ckim-dragen | SNP | ti | map_l100_m2_e1 | het | 98.1227 | 99.2603 | 97.0108 | 73.2091 | 30731 | 229 | 30734 | 947 | 88 | 9.2925 | |
| gduggal-bwafb | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 98.2904 | 99.2602 | 97.3394 | 75.4562 | 21737 | 162 | 21732 | 594 | 582 | 97.9798 | |
| ckim-dragen | SNP | tv | map_l250_m2_e1 | homalt | 99.1552 | 99.2600 | 99.0506 | 84.6353 | 939 | 7 | 939 | 9 | 7 | 77.7778 | |
| hfeng-pmm2 | INDEL | I1_5 | HG002complexvar | * | 99.5522 | 99.2597 | 99.8464 | 56.6743 | 33116 | 247 | 33159 | 51 | 38 | 74.5098 | |
| hfeng-pmm3 | SNP | * | map_l100_m0_e0 | het | 99.3509 | 99.2596 | 99.4424 | 70.0348 | 21048 | 157 | 21044 | 118 | 11 | 9.3220 | |
| jlack-gatk | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 98.5212 | 99.2593 | 97.7941 | 64.3045 | 268 | 2 | 266 | 6 | 3 | 50.0000 | |
| jli-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 99.6283 | 99.2593 | 100.0000 | 59.6970 | 268 | 2 | 266 | 0 | 0 | ||
| hfeng-pmm3 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 99.6283 | 99.2593 | 100.0000 | 60.5341 | 268 | 2 | 266 | 0 | 0 | ||
| jlack-gatk | INDEL | I1_5 | map_l100_m2_e1 | homalt | 99.1674 | 99.2593 | 99.0758 | 82.1511 | 536 | 4 | 536 | 5 | 3 | 60.0000 | |
| ckim-dragen | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 99.2565 | 99.2593 | 99.2537 | 65.0131 | 268 | 2 | 266 | 2 | 0 | 0.0000 | |
| gduggal-bwavard | INDEL | D6_15 | map_l100_m2_e1 | het | 77.2912 | 99.2593 | 63.2850 | 90.3316 | 134 | 1 | 131 | 76 | 63 | 82.8947 | |
| bgallagher-sentieon | INDEL | D16_PLUS | HG002compoundhet | het | 87.9457 | 99.2593 | 78.9474 | 58.5057 | 402 | 3 | 285 | 76 | 73 | 96.0526 | |
| jmaeng-gatk | INDEL | D16_PLUS | HG002compoundhet | het | 87.0277 | 99.2593 | 77.4799 | 58.6932 | 402 | 3 | 289 | 84 | 83 | 98.8095 | |
| raldana-dualsentieon | INDEL | I1_5 | map_l100_m2_e1 | homalt | 99.3513 | 99.2593 | 99.4434 | 80.9339 | 536 | 4 | 536 | 3 | 2 | 66.6667 | |
| ndellapenna-hhga | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 98.7142 | 99.2593 | 98.1752 | 59.8829 | 268 | 2 | 269 | 5 | 4 | 80.0000 | |
| gduggal-snapfb | INDEL | I1_5 | map_l100_m2_e1 | homalt | 98.7109 | 99.2593 | 98.1685 | 87.1891 | 536 | 4 | 536 | 10 | 4 | 40.0000 | |
| hfeng-pmm1 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 99.2565 | 99.2593 | 99.2537 | 60.8759 | 268 | 2 | 266 | 2 | 0 | 0.0000 | |
| egarrison-hhga | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 99.0758 | 99.2593 | 98.8930 | 58.8771 | 268 | 2 | 268 | 3 | 3 | 100.0000 | |
| egarrison-hhga | INDEL | I1_5 | map_l100_m2_e1 | homalt | 99.1674 | 99.2593 | 99.0758 | 83.1779 | 536 | 4 | 536 | 5 | 2 | 40.0000 | |
| dgrover-gatk | INDEL | D16_PLUS | HG002compoundhet | het | 89.2587 | 99.2593 | 81.0888 | 59.0856 | 402 | 3 | 283 | 66 | 63 | 95.4545 | |
| ckim-vqsr | INDEL | D16_PLUS | HG002compoundhet | het | 88.8043 | 99.2593 | 80.3419 | 59.7015 | 402 | 3 | 282 | 69 | 67 | 97.1014 | |
| dgrover-gatk | SNP | tv | map_l125_m2_e1 | homalt | 99.5624 | 99.2591 | 99.8675 | 67.1759 | 6029 | 45 | 6029 | 8 | 5 | 62.5000 | |
| astatham-gatk | SNP | tv | map_l100_m1_e0 | homalt | 99.5729 | 99.2591 | 99.8887 | 59.2933 | 8976 | 67 | 8976 | 10 | 6 | 60.0000 | |
| cchapple-custom | SNP | ti | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 99.2140 | 99.2589 | 99.1691 | 72.0797 | 2009 | 15 | 2029 | 17 | 3 | 17.6471 | |
| ltrigg-rtg1 | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 99.5211 | 99.2589 | 99.7847 | 51.9691 | 6027 | 45 | 6024 | 13 | 8 | 61.5385 | |
| bgallagher-sentieon | INDEL | I1_5 | * | * | 99.4227 | 99.2586 | 99.5873 | 58.2134 | 149547 | 1117 | 149597 | 620 | 500 | 80.6452 | |
| cchapple-custom | INDEL | I6_15 | HG002complexvar | homalt | 98.1176 | 99.2586 | 97.0025 | 48.4991 | 1205 | 9 | 1165 | 36 | 35 | 97.2222 | |
| ciseli-custom | SNP | ti | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 95.3321 | 99.2576 | 91.7054 | 59.1877 | 10027 | 75 | 10072 | 911 | 306 | 33.5895 | |
| ndellapenna-hhga | INDEL | I1_5 | map_siren | homalt | 99.2574 | 99.2574 | 99.2574 | 77.6960 | 1203 | 9 | 1203 | 9 | 5 | 55.5556 | |
| ckim-gatk | SNP | ti | * | homalt | 99.6240 | 99.2571 | 99.9936 | 16.1503 | 797072 | 5966 | 797063 | 51 | 33 | 64.7059 | |
| jlack-gatk | SNP | * | map_l100_m1_e0 | het | 95.6776 | 99.2570 | 92.3473 | 78.4943 | 45022 | 337 | 45011 | 3730 | 265 | 7.1046 | |
| hfeng-pmm3 | INDEL | I1_5 | segdup | het | 99.5342 | 99.2565 | 99.8134 | 94.7961 | 534 | 4 | 535 | 1 | 0 | 0.0000 | |
| hfeng-pmm3 | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 99.5425 | 99.2565 | 99.8300 | 53.1529 | 2937 | 22 | 2937 | 5 | 0 | 0.0000 | |
| jli-custom | INDEL | I1_5 | segdup | het | 99.3483 | 99.2565 | 99.4403 | 94.7265 | 534 | 4 | 533 | 3 | 0 | 0.0000 | |
| ckim-dragen | INDEL | * | HG002complexvar | * | 99.3944 | 99.2565 | 99.5327 | 58.0987 | 76366 | 572 | 76037 | 357 | 301 | 84.3137 | |
| ckim-dragen | INDEL | I1_5 | segdup | het | 95.3418 | 99.2565 | 91.7241 | 96.0707 | 534 | 4 | 532 | 48 | 1 | 2.0833 | |