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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6751-6800 / 86044 show all | |||||||||||||||
eyeh-varpipe | SNP | tv | * | het | 98.0748 | 99.9564 | 96.2628 | 25.2886 | 591446 | 258 | 583371 | 22648 | 112 | 0.4945 | |
gduggal-bwaplat | SNP | ti | * | homalt | 99.0843 | 98.2012 | 99.9834 | 17.0820 | 788593 | 14445 | 788346 | 131 | 112 | 85.4962 | |
gduggal-snapplat | INDEL | I1_5 | HG002complexvar | hetalt | 55.6197 | 42.0046 | 82.2940 | 85.5161 | 725 | 1001 | 739 | 159 | 112 | 70.4403 | |
gduggal-snapvard | SNP | tv | map_l125_m1_e0 | het | 90.5242 | 97.5015 | 84.4788 | 81.5577 | 9873 | 253 | 9846 | 1809 | 112 | 6.1913 | |
ghariani-varprowl | SNP | tv | map_siren | het | 97.7279 | 99.4512 | 96.0633 | 68.6369 | 28452 | 157 | 28453 | 1166 | 112 | 9.6055 | |
gduggal-snapfb | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 83.9960 | 76.5257 | 93.0825 | 45.8976 | 7110 | 2181 | 2449 | 182 | 112 | 61.5385 | |
gduggal-snapfb | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 83.9960 | 76.5257 | 93.0825 | 45.8976 | 7110 | 2181 | 2449 | 182 | 112 | 61.5385 | |
hfeng-pmm1 | INDEL | D1_5 | * | * | 99.5052 | 99.1482 | 99.8648 | 57.2252 | 145495 | 1250 | 145547 | 197 | 112 | 56.8528 | |
jlack-gatk | INDEL | I6_15 | * | het | 97.9846 | 98.0664 | 97.9029 | 60.0128 | 9839 | 194 | 9804 | 210 | 112 | 53.3333 | |
hfeng-pmm2 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 97.7841 | 96.1888 | 99.4332 | 49.3970 | 21402 | 848 | 21403 | 122 | 112 | 91.8033 | |
hfeng-pmm2 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 96.4691 | 95.1249 | 97.8519 | 68.0089 | 5561 | 285 | 5512 | 121 | 112 | 92.5620 | |
hfeng-pmm2 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 96.4691 | 95.1249 | 97.8519 | 68.0089 | 5561 | 285 | 5512 | 121 | 112 | 92.5620 | |
egarrison-hhga | SNP | tv | * | * | 99.8815 | 99.8074 | 99.9558 | 20.9138 | 967822 | 1868 | 967852 | 428 | 112 | 26.1682 | |
ckim-isaac | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 79.6299 | 72.3065 | 88.6040 | 54.8263 | 953 | 365 | 933 | 120 | 112 | 93.3333 | |
ckim-isaac | INDEL | I1_5 | * | hetalt | 89.8867 | 82.5636 | 98.6351 | 45.1097 | 9243 | 1952 | 9178 | 127 | 112 | 88.1890 | |
ckim-vqsr | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 99.0685 | 99.1132 | 99.0238 | 69.1438 | 13635 | 122 | 13593 | 134 | 112 | 83.5821 | |
ckim-vqsr | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 99.0685 | 99.1132 | 99.0238 | 69.1438 | 13635 | 122 | 13593 | 134 | 112 | 83.5821 | |
ltrigg-rtg1 | SNP | ti | * | homalt | 99.9664 | 99.9474 | 99.9854 | 16.2302 | 802614 | 422 | 802519 | 117 | 112 | 95.7265 | |
jli-custom | INDEL | I1_5 | * | het | 99.6300 | 99.4800 | 99.7804 | 58.4682 | 78630 | 411 | 78600 | 173 | 112 | 64.7399 | |
jpowers-varprowl | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 81.8991 | 87.2340 | 77.1791 | 62.6848 | 492 | 72 | 487 | 144 | 112 | 77.7778 | |
rpoplin-dv42 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 94.0812 | 94.2669 | 93.8962 | 73.0279 | 1858 | 113 | 1846 | 120 | 112 | 93.3333 | |
rpoplin-dv42 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 94.0812 | 94.2669 | 93.8962 | 73.0279 | 1858 | 113 | 1846 | 120 | 112 | 93.3333 | |
ciseli-custom | SNP | * | lowcmp_SimpleRepeat_diTR_11to50 | het | 73.8977 | 92.7678 | 61.4068 | 68.2562 | 5785 | 451 | 5919 | 3720 | 112 | 3.0108 | |
ciseli-custom | SNP | * | map_l150_m2_e0 | het | 73.2869 | 67.4862 | 80.1784 | 84.7273 | 13587 | 6546 | 13571 | 3355 | 112 | 3.3383 | |
ciseli-custom | SNP | tv | map_l250_m2_e0 | homalt | 78.7009 | 75.5603 | 82.1138 | 88.5597 | 708 | 229 | 707 | 154 | 111 | 72.0779 | |
ciseli-custom | SNP | tv | map_l250_m2_e1 | homalt | 78.9120 | 75.7928 | 82.2989 | 88.6021 | 717 | 229 | 716 | 154 | 111 | 72.0779 | |
ciseli-custom | INDEL | * | map_l125_m0_e0 | * | 65.7143 | 59.9773 | 72.6648 | 92.6716 | 529 | 353 | 529 | 199 | 111 | 55.7789 | |
ciseli-custom | INDEL | I1_5 | map_l150_m1_e0 | * | 55.6515 | 48.6166 | 65.0667 | 91.6126 | 246 | 260 | 244 | 131 | 111 | 84.7328 | |
ciseli-custom | INDEL | I1_5 | map_l150_m2_e0 | * | 55.9084 | 48.7476 | 65.5352 | 92.4128 | 253 | 266 | 251 | 132 | 111 | 84.0909 | |
ckim-gatk | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 98.6238 | 99.4640 | 97.7977 | 72.6194 | 5567 | 30 | 5551 | 125 | 111 | 88.8000 | |
egarrison-hhga | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 94.4732 | 91.9834 | 97.1014 | 61.6929 | 4888 | 426 | 4891 | 146 | 111 | 76.0274 | |
dgrover-gatk | INDEL | D1_5 | HG002compoundhet | het | 96.0763 | 98.4375 | 93.8258 | 79.0071 | 1701 | 27 | 1702 | 112 | 111 | 99.1071 | |
dgrover-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 98.8574 | 99.1901 | 98.5270 | 64.5573 | 8328 | 68 | 8294 | 124 | 111 | 89.5161 | |
gduggal-snapplat | INDEL | D6_15 | * | hetalt | 51.3567 | 35.1358 | 95.3989 | 60.4943 | 2872 | 5302 | 2882 | 139 | 111 | 79.8561 | |
gduggal-snapvard | INDEL | C1_5 | HG002compoundhet | * | 0.0000 | 0.0000 | 30.1095 | 80.7008 | 0 | 1 | 330 | 766 | 111 | 14.4909 | |
ghariani-varprowl | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 55.8140 | 72.1805 | 45.4976 | 78.8365 | 96 | 37 | 96 | 115 | 111 | 96.5217 | |
gduggal-snapvard | INDEL | I1_5 | map_l100_m2_e0 | * | 90.7740 | 93.4211 | 88.2728 | 86.1304 | 1278 | 90 | 1799 | 239 | 111 | 46.4435 | |
gduggal-snapvard | INDEL | I1_5 | map_l100_m2_e1 | het | 89.6492 | 98.3951 | 82.3311 | 88.9834 | 797 | 13 | 1109 | 238 | 111 | 46.6387 | |
ghariani-varprowl | INDEL | D1_5 | map_siren | het | 93.3499 | 99.2534 | 88.1092 | 86.6204 | 2260 | 17 | 2260 | 305 | 111 | 36.3934 | |
mlin-fermikit | INDEL | I1_5 | map_siren | * | 83.5106 | 74.6755 | 94.7168 | 75.2199 | 2244 | 761 | 2241 | 125 | 111 | 88.8000 | |
mlin-fermikit | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_51to200 | het | 48.0237 | 81.0651 | 34.1176 | 68.8073 | 137 | 32 | 58 | 112 | 111 | 99.1071 | |
gduggal-bwaplat | SNP | ti | map_siren | het | 92.8447 | 87.2527 | 99.2026 | 72.7353 | 54430 | 7952 | 54492 | 438 | 111 | 25.3425 | |
gduggal-bwafb | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 78.5045 | 69.6510 | 89.9365 | 50.9342 | 918 | 400 | 992 | 111 | 111 | 100.0000 | |
gduggal-bwafb | SNP | ti | * | homalt | 99.9234 | 99.8676 | 99.9793 | 17.0184 | 801976 | 1063 | 801993 | 166 | 111 | 66.8675 | |
eyeh-varpipe | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 93.7133 | 98.5372 | 89.3396 | 84.5796 | 10643 | 158 | 9822 | 1172 | 111 | 9.4710 | |
gduggal-bwafb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 82.7375 | 72.6354 | 96.1036 | 54.2365 | 1582 | 596 | 3675 | 149 | 111 | 74.4966 | |
hfeng-pmm1 | INDEL | D6_15 | * | het | 98.2571 | 97.6449 | 98.8769 | 58.2726 | 11319 | 273 | 11269 | 128 | 111 | 86.7188 | |
astatham-gatk | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 98.5692 | 99.3032 | 97.8460 | 72.1465 | 5558 | 39 | 5542 | 122 | 111 | 90.9836 | |
bgallagher-sentieon | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 96.7603 | 96.7298 | 96.7909 | 69.6486 | 3934 | 133 | 3921 | 130 | 111 | 85.3846 | |
asubramanian-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.3287 | 97.7902 | 98.8731 | 68.6335 | 13453 | 304 | 13424 | 153 | 111 | 72.5490 |