PrecisionFDA
Truth Challenge
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Explore HG002 comparison results
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Entry | Type | Subtype | Subset | Genotype | F-score | Recall | Precision | Frac_NA | Truth TP | Truth FN | Query TP | Query FP | FP gt | % FP ma | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
74901-74950 / 86044 show all | |||||||||||||||
ndellapenna-hhga | INDEL | I1_5 | map_l150_m0_e0 | homalt | 99.2593 | 100.0000 | 98.5294 | 88.5714 | 67 | 0 | 67 | 1 | 1 | 100.0000 | |
rpoplin-dv42 | INDEL | I1_5 | map_l150_m0_e0 | homalt | 99.2593 | 100.0000 | 98.5294 | 88.9610 | 67 | 0 | 67 | 1 | 1 | 100.0000 | |
bgallagher-sentieon | INDEL | I1_5 | map_l150_m2_e0 | homalt | 99.2593 | 100.0000 | 98.5294 | 88.1257 | 201 | 0 | 201 | 3 | 2 | 66.6667 | |
astatham-gatk | INDEL | I1_5 | map_l150_m2_e0 | homalt | 99.2593 | 100.0000 | 98.5294 | 88.3095 | 201 | 0 | 201 | 3 | 2 | 66.6667 | |
gduggal-bwafb | INDEL | I1_5 | map_l150_m0_e0 | homalt | 99.2593 | 100.0000 | 98.5294 | 90.3272 | 67 | 0 | 67 | 1 | 1 | 100.0000 | |
ckim-gatk | SNP | tv | HG002compoundhet | het | 99.2595 | 98.9728 | 99.5478 | 55.8932 | 4625 | 48 | 4623 | 21 | 13 | 61.9048 | |
hfeng-pmm1 | INDEL | D16_PLUS | * | homalt | 99.2597 | 99.0544 | 99.4659 | 65.7799 | 1676 | 16 | 1676 | 9 | 4 | 44.4444 | |
ltrigg-rtg1 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 99.2598 | 99.1413 | 99.3785 | 84.5990 | 1501 | 13 | 1439 | 9 | 0 | 0.0000 | |
egarrison-hhga | SNP | ti | map_l125_m2_e0 | het | 99.2599 | 98.7550 | 99.7699 | 71.8619 | 18641 | 235 | 18641 | 43 | 16 | 37.2093 | |
egarrison-hhga | SNP | ti | map_l125_m2_e1 | het | 99.2602 | 98.7583 | 99.7671 | 71.8965 | 18850 | 237 | 18850 | 44 | 16 | 36.3636 | |
ltrigg-rtg2 | INDEL | I1_5 | map_l150_m2_e1 | homalt | 99.2605 | 99.0196 | 99.5025 | 85.2747 | 202 | 2 | 200 | 1 | 0 | 0.0000 | |
raldana-dualsentieon | INDEL | D1_5 | map_l100_m2_e0 | homalt | 99.2605 | 98.8543 | 99.6700 | 82.3014 | 604 | 7 | 604 | 2 | 2 | 100.0000 | |
rpoplin-dv42 | INDEL | I1_5 | map_l100_m2_e1 | homalt | 99.2606 | 99.4444 | 99.0775 | 82.2062 | 537 | 3 | 537 | 5 | 3 | 60.0000 | |
jmaeng-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 99.2612 | 99.0548 | 99.4685 | 84.3994 | 2620 | 25 | 2620 | 14 | 6 | 42.8571 | |
gduggal-snapvard | SNP | tv | func_cds | homalt | 99.2613 | 98.5915 | 99.9402 | 26.1484 | 1680 | 24 | 1671 | 1 | 1 | 100.0000 | |
hfeng-pmm2 | SNP | tv | map_l100_m1_e0 | het | 99.2617 | 99.4357 | 99.0884 | 69.5075 | 15330 | 87 | 15326 | 141 | 12 | 8.5106 | |
ltrigg-rtg2 | INDEL | I1_5 | map_l125_m2_e0 | homalt | 99.2619 | 98.8270 | 99.7006 | 80.6936 | 337 | 4 | 333 | 1 | 0 | 0.0000 | |
ltrigg-rtg2 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | homalt | 99.2620 | 98.5348 | 100.0000 | 70.7344 | 538 | 8 | 530 | 0 | 0 | ||
hfeng-pmm3 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 99.2623 | 98.7000 | 99.8311 | 74.5091 | 2961 | 39 | 2955 | 5 | 1 | 20.0000 | |
ltrigg-rtg2 | SNP | * | lowcmp_SimpleRepeat_diTR_11to50 | het | 99.2624 | 99.1501 | 99.3749 | 64.2935 | 6183 | 53 | 6200 | 39 | 5 | 12.8205 | |
ndellapenna-hhga | SNP | ti | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 99.2625 | 98.9379 | 99.5892 | 62.6573 | 1211 | 13 | 1212 | 5 | 5 | 100.0000 | |
ckim-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 99.2626 | 99.2439 | 99.2814 | 84.2685 | 2625 | 20 | 2625 | 19 | 7 | 36.8421 | |
ckim-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 99.2628 | 99.1167 | 99.4094 | 87.9803 | 2693 | 24 | 2693 | 16 | 14 | 87.5000 | |
ltrigg-rtg1 | INDEL | I1_5 | map_l150_m2_e1 | homalt | 99.2629 | 100.0000 | 98.5366 | 88.2723 | 204 | 0 | 202 | 3 | 1 | 33.3333 | |
bgallagher-sentieon | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 99.2629 | 99.2900 | 99.2358 | 50.5266 | 1818 | 13 | 1818 | 14 | 0 | 0.0000 | |
bgallagher-sentieon | SNP | ti | map_l100_m2_e0 | het | 99.2634 | 99.4775 | 99.0503 | 69.3746 | 30462 | 160 | 30455 | 292 | 38 | 13.0137 | |
ckim-dragen | INDEL | * | * | homalt | 99.2636 | 99.8234 | 98.7101 | 59.5235 | 124951 | 221 | 124887 | 1632 | 1607 | 98.4681 | |
asubramanian-gatk | INDEL | D1_5 | * | * | 99.2637 | 98.9281 | 99.6016 | 61.0980 | 145172 | 1573 | 145253 | 581 | 383 | 65.9208 | |
rpoplin-dv42 | SNP | * | map_l100_m1_e0 | het | 99.2638 | 99.1402 | 99.3876 | 64.2170 | 44969 | 390 | 44957 | 277 | 141 | 50.9025 | |
egarrison-hhga | SNP | * | HG002compoundhet | homalt | 99.2639 | 99.4064 | 99.1218 | 35.3785 | 10718 | 64 | 10722 | 95 | 82 | 86.3158 | |
ltrigg-rtg1 | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 99.2639 | 98.7961 | 99.7361 | 66.9655 | 2626 | 32 | 2646 | 7 | 4 | 57.1429 | |
egarrison-hhga | INDEL | D1_5 | map_l100_m2_e0 | homalt | 99.2641 | 99.3453 | 99.1830 | 83.4862 | 607 | 4 | 607 | 5 | 4 | 80.0000 | |
hfeng-pmm1 | SNP | * | map_l125_m2_e0 | het | 99.2641 | 98.9290 | 99.6016 | 71.5339 | 29004 | 314 | 28998 | 116 | 29 | 25.0000 | |
raldana-dualsentieon | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 99.2643 | 98.8474 | 99.6847 | 73.5302 | 5060 | 59 | 5058 | 16 | 12 | 75.0000 | |
bgallagher-sentieon | SNP | * | map_l125_m1_e0 | * | 99.2644 | 99.4418 | 99.0876 | 71.3529 | 45074 | 253 | 45068 | 415 | 70 | 16.8675 | |
jli-custom | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 99.2647 | 99.7712 | 98.7633 | 53.6568 | 5668 | 13 | 5670 | 71 | 69 | 97.1831 | |
bgallagher-sentieon | SNP | * | segdup | het | 99.2648 | 99.8268 | 98.7091 | 91.1291 | 17287 | 30 | 17281 | 226 | 2 | 0.8850 | |
jli-custom | SNP | tv | map_l125_m2_e0 | * | 99.2648 | 99.0782 | 99.4521 | 69.0688 | 16337 | 152 | 16336 | 90 | 26 | 28.8889 | |
jmaeng-gatk | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 99.2650 | 98.9969 | 99.5345 | 87.4939 | 1283 | 13 | 1283 | 6 | 4 | 66.6667 | |
ndellapenna-hhga | SNP | * | map_l250_m1_e0 | homalt | 99.2653 | 98.7414 | 99.7948 | 85.6165 | 2432 | 31 | 2432 | 5 | 5 | 100.0000 | |
qzeng-custom | SNP | * | segdup | homalt | 99.2653 | 99.1250 | 99.4061 | 87.8458 | 10649 | 94 | 10544 | 63 | 57 | 90.4762 | |
bgallagher-sentieon | INDEL | D1_5 | map_siren | * | 99.2660 | 99.4899 | 99.0431 | 81.6382 | 3511 | 18 | 3519 | 34 | 6 | 17.6471 | |
ltrigg-rtg1 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 99.2661 | 99.8221 | 98.7161 | 56.1302 | 6173 | 11 | 6305 | 82 | 1 | 1.2195 | |
dgrover-gatk | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 99.2662 | 99.3541 | 99.1784 | 74.9780 | 1692 | 11 | 1690 | 14 | 3 | 21.4286 | |
jmaeng-gatk | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 99.2664 | 99.8896 | 98.6509 | 37.0615 | 7239 | 8 | 7239 | 99 | 98 | 98.9899 | |
hfeng-pmm3 | INDEL | * | map_l100_m1_e0 | homalt | 99.2665 | 99.2665 | 99.2665 | 80.9205 | 1218 | 9 | 1218 | 9 | 4 | 44.4444 | |
ckim-vqsr | INDEL | I1_5 | map_l150_m2_e1 | homalt | 99.2665 | 99.5098 | 99.0244 | 88.9488 | 203 | 1 | 203 | 2 | 1 | 50.0000 | |
rpoplin-dv42 | INDEL | I1_5 | map_l150_m2_e1 | homalt | 99.2665 | 99.5098 | 99.0244 | 88.6364 | 203 | 1 | 203 | 2 | 1 | 50.0000 | |
jlack-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 99.2666 | 99.8474 | 98.6925 | 59.1977 | 3925 | 6 | 3925 | 52 | 1 | 1.9231 | |
mlin-fermikit | SNP | tv | func_cds | * | 99.2667 | 99.1078 | 99.4262 | 22.7208 | 4332 | 39 | 4332 | 25 | 14 | 56.0000 |