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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
70951-71000 / 86044 show all | |||||||||||||||
qzeng-custom | INDEL | I1_5 | HG002complexvar | het | 98.6121 | 98.1362 | 99.0926 | 55.1360 | 17850 | 339 | 18675 | 171 | 70 | 40.9357 | |
bgallagher-sentieon | INDEL | I1_5 | map_l100_m2_e0 | het | 98.6122 | 98.3607 | 98.8651 | 85.4415 | 780 | 13 | 784 | 9 | 0 | 0.0000 | |
jlack-gatk | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 98.6126 | 98.8520 | 98.3745 | 60.9084 | 1636 | 19 | 1634 | 27 | 12 | 44.4444 | |
jmaeng-gatk | SNP | * | * | hetalt | 98.6127 | 97.9334 | 99.3015 | 55.2138 | 853 | 18 | 853 | 6 | 5 | 83.3333 | |
jmaeng-gatk | SNP | tv | * | hetalt | 98.6127 | 97.9334 | 99.3015 | 55.2138 | 853 | 18 | 853 | 6 | 5 | 83.3333 | |
ghariani-varprowl | SNP | ti | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 98.6127 | 99.7743 | 97.4780 | 44.0701 | 3978 | 9 | 3981 | 103 | 61 | 59.2233 | |
gduggal-bwafb | SNP | ti | map_l125_m2_e1 | het | 98.6133 | 98.7321 | 98.4947 | 75.9784 | 18845 | 242 | 18845 | 288 | 78 | 27.0833 | |
hfeng-pmm1 | INDEL | I1_5 | map_l125_m2_e1 | * | 98.6137 | 98.0460 | 99.1879 | 86.1881 | 853 | 17 | 855 | 7 | 2 | 28.5714 | |
astatham-gatk | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.6137 | 98.0720 | 99.1614 | 75.6166 | 1933 | 38 | 1892 | 16 | 8 | 50.0000 | |
astatham-gatk | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.6137 | 98.0720 | 99.1614 | 75.6166 | 1933 | 38 | 1892 | 16 | 8 | 50.0000 | |
gduggal-bwavard | SNP | * | map_l100_m2_e0 | homalt | 98.6138 | 97.3767 | 99.8826 | 62.7969 | 26801 | 722 | 26381 | 31 | 25 | 80.6452 | |
rpoplin-dv42 | INDEL | I1_5 | map_l100_m1_e0 | * | 98.6138 | 98.2076 | 99.0233 | 82.7345 | 1315 | 24 | 1318 | 13 | 6 | 46.1538 | |
ndellapenna-hhga | INDEL | I1_5 | map_l150_m1_e0 | * | 98.6139 | 98.4190 | 98.8095 | 88.8938 | 498 | 8 | 498 | 6 | 1 | 16.6667 | |
ltrigg-rtg1 | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 98.6147 | 97.5887 | 99.6624 | 46.5729 | 1457 | 36 | 1476 | 5 | 5 | 100.0000 | |
gduggal-bwavard | SNP | ti | map_l125_m1_e0 | homalt | 98.6148 | 97.3744 | 99.8872 | 66.1535 | 10755 | 290 | 10628 | 12 | 9 | 75.0000 | |
ckim-dragen | INDEL | I16_PLUS | HG002complexvar | * | 98.6149 | 97.9374 | 99.3018 | 67.0164 | 1282 | 27 | 1280 | 9 | 8 | 88.8889 | |
gduggal-bwavard | SNP | * | map_l100_m1_e0 | homalt | 98.6152 | 97.3744 | 99.8881 | 60.4751 | 26294 | 709 | 25878 | 29 | 23 | 79.3103 | |
ckim-gatk | INDEL | I16_PLUS | HG002complexvar | * | 98.6154 | 97.9374 | 99.3029 | 66.7953 | 1282 | 27 | 1282 | 9 | 9 | 100.0000 | |
gduggal-bwafb | SNP | * | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 98.6157 | 97.9161 | 99.3253 | 64.1874 | 3383 | 72 | 3386 | 23 | 21 | 91.3043 | |
gduggal-snapfb | INDEL | D1_5 | segdup | homalt | 98.6157 | 98.8858 | 98.3471 | 95.1952 | 355 | 4 | 357 | 6 | 2 | 33.3333 | |
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 | |
hfeng-pmm3 | INDEL | I1_5 | map_l100_m0_e0 | het | 98.6161 | 98.1595 | 99.0769 | 84.9885 | 320 | 6 | 322 | 3 | 0 | 0.0000 | |
jmaeng-gatk | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 98.6163 | 97.7687 | 99.4788 | 68.1894 | 3812 | 87 | 3817 | 20 | 13 | 65.0000 | |
jli-custom | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | * | 98.6166 | 98.0433 | 99.1967 | 49.3156 | 35876 | 716 | 35813 | 290 | 255 | 87.9310 | |
hfeng-pmm1 | INDEL | I6_15 | HG002complexvar | homalt | 98.6168 | 99.8353 | 97.4277 | 55.0578 | 1212 | 2 | 1212 | 32 | 32 | 100.0000 | |
gduggal-snapplat | SNP | tv | * | * | 98.6169 | 98.1754 | 99.0623 | 31.7051 | 952005 | 17693 | 952368 | 9015 | 1026 | 11.3810 | |
ckim-dragen | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 98.6173 | 97.7724 | 99.4771 | 72.6068 | 15230 | 347 | 15218 | 80 | 60 | 75.0000 | |
gduggal-bwavard | SNP | ti | map_l125_m2_e0 | homalt | 98.6173 | 97.3763 | 99.8904 | 68.4929 | 11060 | 298 | 10932 | 12 | 9 | 75.0000 | |
ckim-vqsr | INDEL | * | map_l250_m1_e0 | homalt | 98.6175 | 98.1651 | 99.0741 | 95.2880 | 107 | 2 | 107 | 1 | 1 | 100.0000 | |
ndellapenna-hhga | INDEL | I1_5 | map_l100_m0_e0 | * | 98.6175 | 98.5267 | 98.7085 | 84.4298 | 535 | 8 | 535 | 7 | 2 | 28.5714 | |
mlin-fermikit | SNP | * | segdup | homalt | 98.6182 | 98.6689 | 98.5676 | 86.0366 | 10600 | 143 | 10597 | 154 | 135 | 87.6623 | |
ltrigg-rtg1 | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 98.6187 | 98.4724 | 98.7654 | 85.1838 | 838 | 13 | 800 | 10 | 1 | 10.0000 | |
ndellapenna-hhga | SNP | * | map_l150_m1_e0 | het | 98.6191 | 97.6082 | 99.6512 | 73.3059 | 18854 | 462 | 18854 | 66 | 30 | 45.4545 | |
dgrover-gatk | SNP | ti | map_l250_m2_e1 | * | 98.6193 | 98.5028 | 98.7362 | 90.4249 | 5000 | 76 | 5000 | 64 | 18 | 28.1250 | |
dgrover-gatk | INDEL | D1_5 | map_l125_m2_e1 | * | 98.6196 | 98.7035 | 98.5357 | 88.1988 | 1142 | 15 | 1144 | 17 | 4 | 23.5294 | |
hfeng-pmm3 | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 98.6199 | 97.4770 | 99.7898 | 71.4168 | 15184 | 393 | 15192 | 32 | 22 | 68.7500 | |
gduggal-bwaplat | SNP | tv | * | homalt | 98.6202 | 97.3009 | 99.9757 | 22.0523 | 366944 | 10179 | 366871 | 89 | 82 | 92.1348 | |
dgrover-gatk | SNP | ti | map_l250_m2_e0 | * | 98.6206 | 98.5024 | 98.7390 | 90.3671 | 4933 | 75 | 4933 | 63 | 18 | 28.5714 | |
jmaeng-gatk | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 98.6207 | 99.7211 | 97.5443 | 61.5021 | 715 | 2 | 715 | 18 | 17 | 94.4444 | |
ltrigg-rtg1 | SNP | ti | map_l125_m0_e0 | * | 98.6208 | 97.4926 | 99.7755 | 64.1831 | 12442 | 320 | 12442 | 28 | 12 | 42.8571 | |
ltrigg-rtg2 | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 98.6210 | 97.6408 | 99.6211 | 50.6118 | 6746 | 163 | 6836 | 26 | 12 | 46.1538 | |
jmaeng-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.6217 | 99.0631 | 98.1843 | 79.0142 | 28443 | 269 | 28443 | 526 | 29 | 5.5133 | |
jmaeng-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.6217 | 99.0631 | 98.1843 | 79.0142 | 28443 | 269 | 28443 | 526 | 29 | 5.5133 | |
raldana-dualsentieon | INDEL | * | map_l100_m0_e0 | homalt | 98.6220 | 98.4283 | 98.8166 | 82.4931 | 501 | 8 | 501 | 6 | 3 | 50.0000 | |
ltrigg-rtg2 | SNP | tv | map_l100_m0_e0 | * | 98.6223 | 97.5189 | 99.7508 | 54.0500 | 10809 | 275 | 10808 | 27 | 2 | 7.4074 | |
dgrover-gatk | INDEL | I1_5 | map_l100_m0_e0 | * | 98.6228 | 98.7109 | 98.5348 | 85.9278 | 536 | 7 | 538 | 8 | 3 | 37.5000 | |
jpowers-varprowl | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | homalt | 98.6230 | 99.8728 | 97.4042 | 72.7150 | 785 | 1 | 788 | 21 | 13 | 61.9048 | |
hfeng-pmm3 | INDEL | * | map_l125_m1_e0 | * | 98.6235 | 98.5287 | 98.7186 | 85.1274 | 2076 | 31 | 2080 | 27 | 6 | 22.2222 | |
gduggal-bwavard | SNP | ti | map_l150_m2_e0 | homalt | 98.6236 | 97.4396 | 99.8368 | 73.2710 | 7421 | 195 | 7339 | 12 | 9 | 75.0000 | |
jli-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 98.6237 | 98.6866 | 98.5609 | 63.0877 | 3231 | 43 | 3219 | 47 | 44 | 93.6170 |