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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
73751-73800 / 86044 show all | |||||||||||||||
gduggal-bwaplat | SNP | ti | map_l100_m0_e0 | het | 76.9732 | 62.9193 | 99.1113 | 88.0688 | 8798 | 5185 | 8810 | 79 | 24 | 30.3797 | |
gduggal-bwafb | SNP | ti | map_l250_m1_e0 | * | 97.9068 | 97.5541 | 98.2622 | 89.4468 | 4467 | 112 | 4467 | 79 | 24 | 30.3797 | |
gduggal-bwafb | SNP | ti | map_l250_m2_e0 | het | 97.4935 | 97.4186 | 97.5685 | 90.4134 | 3170 | 84 | 3170 | 79 | 22 | 27.8481 | |
gduggal-bwavard | INDEL | I1_5 | map_l100_m2_e0 | * | 93.9648 | 93.7865 | 94.1438 | 86.6818 | 1283 | 85 | 1270 | 79 | 38 | 48.1013 | |
gduggal-bwavard | INDEL | I1_5 | map_l100_m2_e1 | * | 94.0042 | 93.7634 | 94.2462 | 86.7599 | 1308 | 87 | 1294 | 79 | 38 | 48.1013 | |
gduggal-bwavard | INDEL | I16_PLUS | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 35.3662 | 31.0680 | 41.0448 | 83.2080 | 64 | 142 | 55 | 79 | 42 | 53.1646 | |
eyeh-varpipe | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 87.7770 | 94.3694 | 82.0455 | 74.5958 | 419 | 25 | 361 | 79 | 28 | 35.4430 | |
jpowers-varprowl | INDEL | * | map_l150_m1_e0 | * | 92.4886 | 91.1061 | 93.9137 | 90.2023 | 1219 | 119 | 1219 | 79 | 51 | 64.5570 | |
jpowers-varprowl | INDEL | I16_PLUS | * | homalt | 77.5728 | 66.5599 | 92.9527 | 53.9441 | 1039 | 522 | 1042 | 79 | 78 | 98.7342 | |
jli-custom | INDEL | I16_PLUS | * | * | 96.2725 | 93.9627 | 98.6987 | 64.2188 | 5992 | 385 | 5992 | 79 | 51 | 64.5570 | |
jmaeng-gatk | INDEL | D6_15 | HG002complexvar | * | 97.9225 | 97.3595 | 98.4921 | 58.5358 | 5162 | 140 | 5160 | 79 | 74 | 93.6709 | |
jmaeng-gatk | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 91.5006 | 95.9083 | 87.4802 | 71.8304 | 586 | 25 | 552 | 79 | 77 | 97.4684 | |
ltrigg-rtg1 | INDEL | D1_5 | HG002complexvar | het | 99.1733 | 98.7383 | 99.6122 | 51.3027 | 20503 | 262 | 20294 | 79 | 31 | 39.2405 | |
ltrigg-rtg1 | INDEL | I1_5 | HG002complexvar | * | 99.2488 | 98.7471 | 99.7557 | 52.7857 | 32944 | 418 | 32259 | 79 | 48 | 60.7595 | |
hfeng-pmm2 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 92.9369 | 89.2961 | 96.8873 | 47.7240 | 2461 | 295 | 2459 | 79 | 77 | 97.4684 | |
hfeng-pmm1 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 96.8111 | 95.6479 | 98.0030 | 65.9757 | 3890 | 177 | 3877 | 79 | 63 | 79.7468 | |
hfeng-pmm1 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 98.1845 | 96.8509 | 99.5553 | 39.7095 | 17684 | 575 | 17685 | 79 | 67 | 84.8101 | |
hfeng-pmm1 | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 97.3392 | 96.1587 | 98.5491 | 67.9366 | 5382 | 215 | 5366 | 79 | 71 | 89.8734 | |
hfeng-pmm1 | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | * | 97.7868 | 96.4686 | 99.1416 | 42.5996 | 9124 | 334 | 9124 | 79 | 75 | 94.9367 | |
hfeng-pmm3 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 92.5922 | 88.6792 | 96.8663 | 47.5010 | 2444 | 312 | 2442 | 79 | 77 | 97.4684 | |
hfeng-pmm3 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 97.9752 | 96.7154 | 99.2683 | 46.8913 | 10718 | 364 | 10718 | 79 | 74 | 93.6709 | |
hfeng-pmm3 | SNP | ti | map_l125_m1_e0 | het | 99.4436 | 99.3211 | 99.5663 | 71.0299 | 18142 | 124 | 18138 | 79 | 8 | 10.1266 | |
hfeng-pmm3 | SNP | ti | segdup | * | 99.7137 | 99.8311 | 99.5965 | 88.9183 | 19504 | 33 | 19502 | 79 | 3 | 3.7975 | |
hfeng-pmm3 | SNP | tv | map_l100_m2_e1 | * | 99.6458 | 99.6045 | 99.6872 | 66.3290 | 25183 | 100 | 25179 | 79 | 10 | 12.6582 | |
hfeng-pmm3 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 95.5611 | 96.0968 | 95.0314 | 82.9837 | 1748 | 71 | 1511 | 79 | 62 | 78.4810 | |
hfeng-pmm3 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 95.5611 | 96.0968 | 95.0314 | 82.9837 | 1748 | 71 | 1511 | 79 | 62 | 78.4810 | |
ndellapenna-hhga | SNP | * | map_l125_m1_e0 | het | 98.8381 | 97.9748 | 99.7168 | 68.7996 | 27817 | 575 | 27817 | 79 | 36 | 45.5696 | |
ndellapenna-hhga | SNP | * | map_l150_m2_e0 | * | 99.0356 | 98.3329 | 99.7484 | 73.8523 | 31321 | 531 | 31321 | 79 | 40 | 50.6329 | |
ndellapenna-hhga | SNP | ti | map_l100_m2_e1 | * | 99.3624 | 98.8906 | 99.8388 | 63.3822 | 48936 | 549 | 48938 | 79 | 40 | 50.6329 | |
qzeng-custom | SNP | tv | map_siren | homalt | 92.1926 | 85.9107 | 99.4656 | 52.8075 | 14811 | 2429 | 14705 | 79 | 75 | 94.9367 | |
mlin-fermikit | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 98.6157 | 98.5123 | 98.7194 | 55.0135 | 6092 | 92 | 6090 | 79 | 51 | 64.5570 | |
qzeng-custom | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 98.9865 | 98.4716 | 99.5069 | 53.0976 | 1353 | 21 | 15941 | 79 | 10 | 12.6582 | |
bgallagher-sentieon | SNP | ti | map_l250_m2_e0 | het | 98.3066 | 99.0166 | 97.6068 | 90.7462 | 3222 | 32 | 3222 | 79 | 16 | 20.2532 | |
asubramanian-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 95.9616 | 93.1237 | 98.9779 | 28.5807 | 7611 | 562 | 7650 | 79 | 73 | 92.4051 | |
anovak-vg | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 96.9502 | 97.0480 | 96.8526 | 49.3747 | 2367 | 72 | 2431 | 79 | 39 | 49.3671 | |
anovak-vg | SNP | ti | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 97.7147 | 97.4166 | 98.0146 | 32.9344 | 3884 | 103 | 3900 | 79 | 74 | 93.6709 | |
asubramanian-gatk | SNP | ti | segdup | * | 98.1992 | 96.8521 | 99.5842 | 91.3917 | 18922 | 615 | 18920 | 79 | 8 | 10.1266 | |
asubramanian-gatk | INDEL | C16_PLUS | * | * | 0.0000 | 0.0000 | 87.7138 | 0 | 0 | 0 | 79 | 0 | 0.0000 | ||
anovak-vg | INDEL | D1_5 | segdup | * | 91.5860 | 90.4805 | 92.7189 | 94.7590 | 998 | 105 | 1006 | 79 | 52 | 65.8228 | |
cchapple-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 98.8536 | 98.8377 | 98.8695 | 82.8620 | 6803 | 80 | 6909 | 79 | 25 | 31.6456 | |
ckim-dragen | INDEL | D16_PLUS | HG002compoundhet | homalt | 16.8421 | 100.0000 | 9.1954 | 61.3333 | 8 | 0 | 8 | 79 | 79 | 100.0000 | |
ciseli-custom | INDEL | C6_15 | HG002compoundhet | * | 0.0000 | 0.0000 | 4.8193 | 89.6894 | 0 | 0 | 4 | 79 | 28 | 35.4430 | |
ciseli-custom | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_51to200 | * | 17.0866 | 13.7546 | 22.5490 | 86.7704 | 37 | 232 | 23 | 79 | 9 | 11.3924 | |
ckim-dragen | SNP | tv | map_l250_m2_e1 | het | 96.2700 | 96.5394 | 96.0020 | 91.4117 | 1897 | 68 | 1897 | 79 | 5 | 6.3291 | |
egarrison-hhga | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 97.2212 | 95.8530 | 98.6289 | 40.6591 | 5686 | 246 | 5683 | 79 | 58 | 73.4177 | |
egarrison-hhga | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 97.2567 | 96.6498 | 97.8712 | 70.9851 | 3635 | 126 | 3632 | 79 | 58 | 73.4177 | |
egarrison-hhga | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 91.8070 | 92.9697 | 90.6730 | 69.1101 | 767 | 58 | 768 | 79 | 66 | 83.5443 | |
egarrison-hhga | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 91.8070 | 92.9697 | 90.6730 | 69.1101 | 767 | 58 | 768 | 79 | 66 | 83.5443 | |
egarrison-hhga | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 98.4855 | 98.1673 | 98.8057 | 79.9095 | 6535 | 122 | 6536 | 79 | 33 | 41.7722 | |
ckim-isaac | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 92.5582 | 86.9571 | 98.9306 | 27.1355 | 7107 | 1066 | 7308 | 79 | 75 | 94.9367 |