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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
13401-13450 / 86044 show all | |||||||||||||||
rpoplin-dv42 | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 99.7078 | 99.4172 | 100.0000 | 48.8609 | 853 | 5 | 853 | 0 | 0 | ||
eyeh-varpipe | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 99.4679 | 99.4172 | 99.5187 | 47.0701 | 853 | 5 | 827 | 4 | 1 | 25.0000 | |
gduggal-bwafb | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 99.6495 | 99.4172 | 99.8828 | 51.6714 | 853 | 5 | 852 | 1 | 0 | 0.0000 | |
ckim-dragen | SNP | tv | map_l150_m1_e0 | homalt | 99.5559 | 99.4171 | 99.6950 | 66.7792 | 3923 | 23 | 3923 | 12 | 10 | 83.3333 | |
egarrison-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 98.9819 | 99.4169 | 98.5507 | 55.3109 | 341 | 2 | 340 | 5 | 3 | 60.0000 | |
asubramanian-gatk | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 99.5620 | 99.4169 | 99.7076 | 57.3034 | 341 | 2 | 341 | 1 | 0 | 0.0000 | |
jmaeng-gatk | INDEL | I1_5 | map_l125_m2_e1 | homalt | 99.2722 | 99.4169 | 99.1279 | 84.8990 | 341 | 2 | 341 | 3 | 2 | 66.6667 | |
rpoplin-dv42 | INDEL | I1_5 | map_l125_m2_e1 | homalt | 99.4169 | 99.4169 | 99.4169 | 84.8965 | 341 | 2 | 341 | 2 | 1 | 50.0000 | |
raldana-dualsentieon | INDEL | * | HG002compoundhet | homalt | 57.9932 | 99.4169 | 40.9364 | 81.2893 | 682 | 4 | 682 | 984 | 980 | 99.5935 | |
ndellapenna-hhga | INDEL | I1_5 | map_l125_m2_e1 | homalt | 99.2722 | 99.4169 | 99.1279 | 85.2297 | 341 | 2 | 341 | 3 | 1 | 33.3333 | |
hfeng-pmm3 | INDEL | * | HG002compoundhet | homalt | 74.6579 | 99.4169 | 59.7721 | 77.4506 | 682 | 4 | 682 | 459 | 454 | 98.9107 | |
hfeng-pmm2 | INDEL | * | HG002compoundhet | homalt | 70.6370 | 99.4169 | 54.7791 | 80.4614 | 682 | 4 | 682 | 563 | 558 | 99.1119 | |
jmaeng-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 99.5131 | 99.4163 | 99.6101 | 78.2596 | 1533 | 9 | 1533 | 6 | 5 | 83.3333 | |
ltrigg-rtg1 | SNP | tv | map_l250_m1_e0 | homalt | 99.6487 | 99.4159 | 99.8826 | 86.0259 | 851 | 5 | 851 | 1 | 1 | 100.0000 | |
ltrigg-rtg2 | SNP | tv | map_l250_m1_e0 | homalt | 99.7071 | 99.4159 | 100.0000 | 83.9646 | 851 | 5 | 851 | 0 | 0 | ||
raldana-dualsentieon | SNP | tv | map_l250_m1_e0 | homalt | 99.4740 | 99.4159 | 99.5322 | 84.0366 | 851 | 5 | 851 | 4 | 2 | 50.0000 | |
bgallagher-sentieon | INDEL | D1_5 | map_l250_m1_e0 | * | 97.4212 | 99.4152 | 95.5056 | 95.3670 | 170 | 1 | 170 | 8 | 1 | 12.5000 | |
gduggal-bwafb | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 95.6084 | 99.4152 | 92.0824 | 70.5431 | 850 | 5 | 849 | 73 | 4 | 5.4795 | |
ltrigg-rtg1 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 96.9927 | 99.4152 | 94.6855 | 62.3980 | 850 | 5 | 873 | 49 | 1 | 2.0408 | |
hfeng-pmm2 | INDEL | D1_5 | map_l250_m1_e0 | * | 96.8661 | 99.4152 | 94.4444 | 95.1987 | 170 | 1 | 170 | 10 | 1 | 10.0000 | |
raldana-dualsentieon | SNP | tv | map_l125_m0_e0 | homalt | 99.6165 | 99.4147 | 99.8192 | 66.9456 | 2208 | 13 | 2208 | 4 | 2 | 50.0000 | |
egarrison-hhga | SNP | tv | map_l125_m0_e0 | homalt | 99.6615 | 99.4147 | 99.9095 | 69.6595 | 2208 | 13 | 2208 | 2 | 2 | 100.0000 | |
ckim-gatk | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | het | 97.9553 | 99.4146 | 96.5382 | 63.5394 | 2717 | 16 | 2705 | 97 | 91 | 93.8144 | |
jpowers-varprowl | SNP | * | map_siren | homalt | 99.5443 | 99.4144 | 99.6746 | 55.8957 | 54833 | 323 | 54834 | 179 | 129 | 72.0670 | |
ltrigg-rtg2 | SNP | tv | segdup | het | 98.5667 | 99.4137 | 97.7340 | 87.6779 | 5256 | 31 | 5262 | 122 | 2 | 1.6393 | |
ndellapenna-hhga | INDEL | I1_5 | map_l125_m2_e0 | homalt | 99.2679 | 99.4135 | 99.1228 | 84.9406 | 339 | 2 | 339 | 3 | 1 | 33.3333 | |
rpoplin-dv42 | INDEL | I1_5 | map_l125_m2_e0 | homalt | 99.4135 | 99.4135 | 99.4135 | 84.6119 | 339 | 2 | 339 | 2 | 1 | 50.0000 | |
jmaeng-gatk | INDEL | I1_5 | map_l125_m2_e0 | homalt | 99.2679 | 99.4135 | 99.1228 | 84.7048 | 339 | 2 | 339 | 3 | 2 | 66.6667 | |
jmaeng-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 99.6471 | 99.4131 | 99.8821 | 84.7756 | 847 | 5 | 847 | 1 | 1 | 100.0000 | |
jpowers-varprowl | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 84.3287 | 99.4131 | 73.2189 | 85.2401 | 847 | 5 | 853 | 312 | 168 | 53.8462 | |
bgallagher-sentieon | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 99.2083 | 99.4128 | 99.0047 | 74.3003 | 1693 | 10 | 1691 | 17 | 5 | 29.4118 | |
ckim-dragen | SNP | tv | map_siren | het | 98.4766 | 99.4128 | 97.5580 | 65.5354 | 28441 | 168 | 28444 | 712 | 52 | 7.3034 | |
ckim-gatk | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 99.2958 | 99.4125 | 99.1794 | 88.4605 | 846 | 5 | 846 | 7 | 6 | 85.7143 | |
ckim-vqsr | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 99.2958 | 99.4125 | 99.1794 | 88.4605 | 846 | 5 | 846 | 7 | 6 | 85.7143 | |
jlack-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 99.6416 | 99.4125 | 99.8717 | 75.1815 | 3892 | 23 | 3892 | 5 | 5 | 100.0000 | |
jlack-gatk | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 98.6014 | 99.4125 | 97.8035 | 88.8214 | 846 | 5 | 846 | 19 | 8 | 42.1053 | |
hfeng-pmm3 | SNP | * | map_l100_m0_e0 | * | 99.4850 | 99.4123 | 99.5578 | 68.0774 | 32648 | 193 | 32644 | 145 | 21 | 14.4828 | |
jli-custom | SNP | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 99.2976 | 99.4123 | 99.1832 | 67.8581 | 4736 | 28 | 4736 | 39 | 8 | 20.5128 | |
ckim-dragen | SNP | * | map_l100_m2_e0 | homalt | 99.6377 | 99.4114 | 99.8650 | 58.3933 | 27361 | 162 | 27366 | 37 | 33 | 89.1892 | |
hfeng-pmm2 | INDEL | D1_5 | lowcmp_SimpleRepeat_triTR_11to50 | * | 99.6680 | 99.4113 | 99.9261 | 41.1569 | 4053 | 24 | 4056 | 3 | 0 | 0.0000 | |
ckim-dragen | INDEL | D1_5 | * | * | 99.4199 | 99.4105 | 99.4294 | 60.9956 | 145880 | 865 | 145840 | 837 | 396 | 47.3118 | |
ndellapenna-hhga | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 99.4691 | 99.4104 | 99.5279 | 48.5945 | 2529 | 15 | 2530 | 12 | 1 | 8.3333 | |
ckim-dragen | SNP | * | map_l100_m2_e1 | homalt | 99.6376 | 99.4100 | 99.8663 | 58.3837 | 27632 | 164 | 27637 | 37 | 33 | 89.1892 | |
ltrigg-rtg1 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 99.6218 | 99.4099 | 99.8345 | 72.5123 | 5391 | 32 | 5430 | 9 | 0 | 0.0000 | |
ltrigg-rtg1 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 99.6218 | 99.4099 | 99.8345 | 72.5123 | 5391 | 32 | 5430 | 9 | 0 | 0.0000 | |
dgrover-gatk | INDEL | D16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 98.0391 | 99.4096 | 96.7059 | 82.8744 | 1347 | 8 | 1233 | 42 | 28 | 66.6667 | |
ckim-vqsr | INDEL | D16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 98.1537 | 99.4096 | 96.9291 | 83.2983 | 1347 | 8 | 1231 | 39 | 30 | 76.9231 | |
hfeng-pmm1 | SNP | tv | map_siren | het | 99.6130 | 99.4093 | 99.8175 | 56.2607 | 28440 | 169 | 28435 | 52 | 14 | 26.9231 | |
rpoplin-dv42 | SNP | tv | map_siren | het | 99.4388 | 99.4093 | 99.4683 | 57.2644 | 28440 | 169 | 28436 | 152 | 65 | 42.7632 | |
mlin-fermikit | SNP | * | lowcmp_SimpleRepeat_homopolymer_6to10 | homalt | 98.6888 | 99.4087 | 97.9793 | 56.5956 | 6052 | 36 | 6061 | 125 | 121 | 96.8000 |