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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
8801-8850 / 86044 show all | |||||||||||||||
dgrover-gatk | SNP | tv | map_l100_m0_e0 | het | 98.8895 | 99.2661 | 98.5157 | 76.1747 | 7169 | 53 | 7168 | 108 | 20 | 18.5185 | |
hfeng-pmm3 | SNP | tv | map_l100_m0_e0 | het | 99.3072 | 99.2523 | 99.3623 | 70.7621 | 7168 | 54 | 7167 | 46 | 4 | 8.6957 | |
rpoplin-dv42 | SNP | tv | map_l150_m2_e0 | het | 98.7872 | 98.8555 | 98.7190 | 75.1931 | 7169 | 83 | 7167 | 93 | 49 | 52.6882 | |
gduggal-bwaplat | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 86.7364 | 78.3970 | 97.0612 | 92.7953 | 7160 | 1973 | 7167 | 217 | 34 | 15.6682 | |
gduggal-bwaplat | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 86.7364 | 78.3970 | 97.0612 | 92.7953 | 7160 | 1973 | 7167 | 217 | 34 | 15.6682 | |
anovak-vg | SNP | ti | map_l125_m0_e0 | het | 76.2921 | 87.1596 | 67.8342 | 82.4188 | 7202 | 1061 | 7166 | 3398 | 912 | 26.8393 | |
ciseli-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 59.8797 | 85.7519 | 46.0008 | 48.3317 | 7174 | 1192 | 7166 | 8412 | 7803 | 92.7603 | |
raldana-dualsentieon | SNP | tv | map_l150_m2_e0 | het | 98.6373 | 98.8279 | 98.4474 | 78.1985 | 7167 | 85 | 7165 | 113 | 1 | 0.8850 | |
ckim-vqsr | SNP | tv | map_l125_m2_e0 | het | 80.8052 | 68.6171 | 98.2581 | 89.8954 | 7165 | 3277 | 7164 | 127 | 1 | 0.7874 | |
gduggal-snapfb | SNP | tv | map_l150_m2_e1 | het | 95.8395 | 97.4959 | 94.2384 | 77.2735 | 7164 | 184 | 7164 | 438 | 174 | 39.7260 | |
asubramanian-gatk | SNP | ti | HG002compoundhet | homalt | 98.3931 | 96.8894 | 99.9442 | 30.6032 | 7164 | 230 | 7164 | 4 | 3 | 75.0000 | |
ckim-gatk | SNP | * | map_l100_m0_e0 | homalt | 76.2549 | 61.6437 | 99.9442 | 71.4939 | 7163 | 4457 | 7163 | 4 | 2 | 50.0000 | |
ckim-isaac | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 90.1687 | 84.9804 | 96.0316 | 53.5294 | 7146 | 1263 | 7163 | 296 | 207 | 69.9324 | |
hfeng-pmm2 | SNP | tv | map_l100_m0_e0 | het | 98.8749 | 99.1831 | 98.5687 | 74.1359 | 7163 | 59 | 7162 | 104 | 11 | 10.5769 | |
hfeng-pmm1 | SNP | tv | map_l150_m2_e0 | het | 99.1075 | 98.7728 | 99.4445 | 75.8631 | 7163 | 89 | 7161 | 40 | 10 | 25.0000 | |
eyeh-varpipe | SNP | tv | map_l150_m2_e0 | het | 96.2702 | 99.7104 | 93.0595 | 80.3258 | 7231 | 21 | 7160 | 534 | 11 | 2.0599 | |
cchapple-custom | SNP | tv | map_l150_m2_e1 | het | 95.2289 | 97.2237 | 93.3142 | 82.3755 | 7144 | 204 | 7160 | 513 | 83 | 16.1793 | |
rpoplin-dv42 | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 99.2372 | 98.7305 | 99.7490 | 37.0877 | 7155 | 92 | 7154 | 18 | 18 | 100.0000 | |
ghariani-varprowl | SNP | tv | map_l100_m0_e0 | het | 96.3501 | 99.0446 | 93.7983 | 79.0409 | 7153 | 69 | 7154 | 473 | 76 | 16.0677 | |
gduggal-snapvard | SNP | tv | lowcmp_SimpleRepeat_quadTR_11to50 | * | 93.8195 | 97.1685 | 90.6935 | 51.4915 | 7241 | 211 | 7153 | 734 | 47 | 6.4033 | |
ckim-dragen | SNP | tv | map_l150_m2_e0 | het | 97.5182 | 98.6211 | 96.4396 | 82.0747 | 7152 | 100 | 7151 | 264 | 17 | 6.4394 | |
ckim-isaac | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 90.5907 | 83.7697 | 98.6209 | 32.2653 | 6751 | 1308 | 7151 | 100 | 87 | 87.0000 | |
ckim-isaac | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 90.5907 | 83.7697 | 98.6209 | 32.2653 | 6751 | 1308 | 7151 | 100 | 87 | 87.0000 | |
ciseli-custom | SNP | tv | map_l125_m2_e0 | het | 74.6164 | 68.4639 | 81.9839 | 81.7497 | 7149 | 3293 | 7149 | 1571 | 62 | 3.9465 | |
ltrigg-rtg1 | INDEL | * | map_siren | * | 97.9785 | 96.9096 | 99.0713 | 78.1949 | 7181 | 229 | 7147 | 67 | 16 | 23.8806 | |
hfeng-pmm1 | SNP | tv | map_l100_m0_e0 | het | 99.2295 | 98.9754 | 99.4850 | 70.4702 | 7148 | 74 | 7147 | 37 | 11 | 29.7297 | |
gduggal-bwafb | INDEL | * | map_siren | * | 96.8227 | 95.3306 | 98.3622 | 80.8381 | 7064 | 346 | 7147 | 119 | 50 | 42.0168 | |
gduggal-snapvard | INDEL | * | lowcmp_SimpleRepeat_triTR_11to50 | * | 73.1367 | 73.8749 | 72.4131 | 44.0488 | 4974 | 1759 | 7145 | 2722 | 2236 | 82.1455 | |
jlack-gatk | SNP | tv | map_l100_m0_e0 | het | 91.9563 | 98.9477 | 85.8877 | 83.2329 | 7146 | 76 | 7145 | 1174 | 61 | 5.1959 | |
ghariani-varprowl | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 62.6517 | 96.2893 | 46.4314 | 47.0193 | 7110 | 274 | 7143 | 8241 | 8121 | 98.5439 | |
raldana-dualsentieon | SNP | tv | map_l100_m0_e0 | het | 98.8033 | 98.8923 | 98.7144 | 71.7057 | 7142 | 80 | 7141 | 93 | 1 | 1.0753 | |
astatham-gatk | INDEL | * | map_siren | * | 97.4708 | 96.1673 | 98.8100 | 83.5327 | 7126 | 284 | 7141 | 86 | 20 | 23.2558 | |
eyeh-varpipe | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 91.3228 | 88.0846 | 94.8081 | 46.5735 | 2166 | 293 | 7140 | 391 | 343 | 87.7238 | |
jli-custom | SNP | tv | map_l150_m2_e0 | het | 98.7416 | 98.4694 | 99.0154 | 74.3882 | 7141 | 111 | 7140 | 71 | 19 | 26.7606 | |
hfeng-pmm3 | SNP | * | map_l250_m1_e0 | * | 98.9535 | 98.8507 | 99.0565 | 88.1658 | 7139 | 83 | 7139 | 68 | 9 | 13.2353 | |
gduggal-bwafb | SNP | tv | map_l150_m2_e0 | het | 97.9956 | 98.4280 | 97.5670 | 79.8007 | 7138 | 114 | 7138 | 178 | 33 | 18.5393 | |
rpoplin-dv42 | SNP | tv | map_l100_m0_e0 | het | 98.5640 | 98.8507 | 98.2789 | 68.7061 | 7139 | 83 | 7138 | 125 | 50 | 40.0000 | |
egarrison-hhga | SNP | tv | map_l150_m2_e0 | het | 99.0356 | 98.4142 | 99.6649 | 74.5802 | 7137 | 115 | 7137 | 24 | 9 | 37.5000 | |
eyeh-varpipe | SNP | tv | map_l100_m0_e0 | het | 94.2875 | 99.6677 | 89.4585 | 75.0937 | 7198 | 24 | 7137 | 841 | 11 | 1.3080 | |
eyeh-varpipe | SNP | ti | map_l150_m1_e0 | homalt | 99.8623 | 99.8226 | 99.9020 | 73.1001 | 7314 | 13 | 7136 | 7 | 5 | 71.4286 | |
ltrigg-rtg1 | SNP | tv | map_l150_m2_e1 | het | 98.3805 | 97.1421 | 99.6509 | 65.0308 | 7138 | 210 | 7136 | 25 | 4 | 16.0000 | |
hfeng-pmm2 | SNP | * | map_l250_m1_e0 | * | 98.5497 | 98.7953 | 98.3053 | 89.3707 | 7135 | 87 | 7135 | 123 | 15 | 12.1951 | |
bgallagher-sentieon | SNP | * | map_l250_m1_e0 | * | 98.3858 | 98.7400 | 98.0341 | 88.9251 | 7131 | 91 | 7131 | 143 | 31 | 21.6783 | |
ckim-dragen | SNP | tv | map_l100_m0_e0 | het | 97.5576 | 98.6846 | 96.4561 | 76.6502 | 7127 | 95 | 7131 | 262 | 21 | 8.0153 | |
qzeng-custom | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 85.8273 | 81.4433 | 90.7101 | 41.4412 | 2844 | 648 | 7128 | 730 | 664 | 90.9589 | |
gduggal-snapvard | SNP | tv | map_l150_m2_e1 | het | 88.7208 | 97.3054 | 81.5281 | 85.1064 | 7150 | 198 | 7128 | 1615 | 97 | 6.0062 | |
gduggal-snapvard | SNP | tv | HG002compoundhet | * | 76.6128 | 76.8912 | 76.3364 | 58.1709 | 6861 | 2062 | 7126 | 2209 | 1084 | 49.0720 | |
hfeng-pmm1 | SNP | * | map_l250_m1_e0 | * | 98.8139 | 98.6292 | 98.9993 | 88.0247 | 7123 | 99 | 7123 | 72 | 16 | 22.2222 | |
gduggal-bwafb | SNP | tv | map_l100_m0_e0 | het | 97.9160 | 98.5600 | 97.2803 | 74.2359 | 7118 | 104 | 7118 | 199 | 34 | 17.0854 | |
gduggal-snapplat | INDEL | I6_15 | * | * | 41.4207 | 29.2310 | 71.0492 | 57.1777 | 7256 | 17567 | 7117 | 2900 | 649 | 22.3793 |