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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
61801-61850 / 86044 show all | |||||||||||||||
gduggal-snapvard | SNP | tv | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 97.1847 | 95.8015 | 98.6083 | 75.1972 | 502 | 22 | 496 | 7 | 4 | 57.1429 | |
ckim-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 99.4059 | 99.0138 | 99.8012 | 86.2267 | 502 | 5 | 502 | 1 | 1 | 100.0000 | |
ckim-dragen | INDEL | D1_5 | map_l150_m2_e0 | het | 96.3484 | 97.6654 | 95.0664 | 90.7186 | 502 | 12 | 501 | 26 | 2 | 7.6923 | |
ckim-dragen | INDEL | I1_5 | map_l150_m2_e1 | * | 95.4459 | 94.7269 | 96.1759 | 90.8774 | 503 | 28 | 503 | 20 | 5 | 25.0000 | |
ciseli-custom | INDEL | I1_5 | segdup | het | 90.6052 | 93.4944 | 87.8893 | 95.0934 | 503 | 35 | 508 | 70 | 50 | 71.4286 | |
ckim-dragen | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 98.7242 | 99.2110 | 98.2422 | 85.7580 | 503 | 4 | 503 | 9 | 2 | 22.2222 | |
egarrison-hhga | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | hetalt | 77.2448 | 63.4300 | 98.7526 | 34.5578 | 503 | 290 | 475 | 6 | 4 | 66.6667 | |
gduggal-bwafb | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_51to200 | hetalt | 86.4554 | 77.3846 | 97.9351 | 23.6486 | 503 | 147 | 332 | 7 | 7 | 100.0000 | |
ltrigg-rtg2 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 97.3846 | 95.4459 | 99.4036 | 72.5886 | 503 | 24 | 500 | 3 | 3 | 100.0000 | |
qzeng-custom | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 98.9116 | 99.2110 | 98.6139 | 86.9408 | 503 | 4 | 498 | 7 | 6 | 85.7143 | |
jli-custom | INDEL | * | map_l100_m0_e0 | homalt | 98.6275 | 98.8212 | 98.4344 | 83.3605 | 503 | 6 | 503 | 8 | 5 | 62.5000 | |
raldana-dualsentieon | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 94.1097 | 95.4459 | 92.8105 | 80.6084 | 503 | 24 | 426 | 33 | 33 | 100.0000 | |
rpoplin-dv42 | INDEL | D1_5 | map_l150_m2_e0 | het | 98.0541 | 97.8599 | 98.2490 | 88.2809 | 503 | 11 | 505 | 9 | 2 | 22.2222 | |
rpoplin-dv42 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 99.6047 | 99.4083 | 99.8020 | 85.1950 | 504 | 3 | 504 | 1 | 0 | 0.0000 | |
mlin-fermikit | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_51to200 | * | 47.8252 | 42.6757 | 54.3879 | 44.5978 | 504 | 677 | 502 | 421 | 421 | 100.0000 | |
ckim-vqsr | INDEL | * | map_l100_m0_e0 | homalt | 98.8235 | 99.0177 | 98.6301 | 85.4747 | 504 | 5 | 504 | 7 | 4 | 57.1429 | |
ltrigg-rtg1 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 97.4827 | 95.6357 | 99.4024 | 72.8208 | 504 | 23 | 499 | 3 | 3 | 100.0000 | |
ltrigg-rtg1 | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_51to200 | * | 82.9686 | 72.3099 | 97.3129 | 50.8954 | 504 | 193 | 507 | 14 | 13 | 92.8571 | |
ltrigg-rtg1 | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 85.6972 | 75.6757 | 98.7780 | 69.6726 | 504 | 162 | 485 | 6 | 1 | 16.6667 | |
ltrigg-rtg1 | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 85.6972 | 75.6757 | 98.7780 | 69.6726 | 504 | 162 | 485 | 6 | 1 | 16.6667 | |
ltrigg-rtg1 | INDEL | I1_5 | map_l150_m2_e1 | * | 96.9175 | 94.9153 | 99.0060 | 86.8531 | 504 | 27 | 498 | 5 | 1 | 20.0000 | |
ckim-gatk | INDEL | * | map_l100_m0_e0 | homalt | 98.7267 | 99.0177 | 98.4375 | 85.4504 | 504 | 5 | 504 | 8 | 5 | 62.5000 | |
ciseli-custom | INDEL | D6_15 | HG002compoundhet | * | 6.6832 | 5.5814 | 8.3271 | 39.0416 | 504 | 8526 | 554 | 6099 | 5283 | 86.6208 | |
gduggal-bwaplat | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 64.9523 | 50.2994 | 91.6515 | 76.9456 | 504 | 498 | 505 | 46 | 8 | 17.3913 | |
hfeng-pmm3 | INDEL | * | map_l100_m0_e0 | homalt | 98.7267 | 99.0177 | 98.4375 | 81.9591 | 504 | 5 | 504 | 8 | 4 | 50.0000 | |
hfeng-pmm2 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 95.4738 | 95.6357 | 95.3125 | 79.8742 | 504 | 23 | 427 | 21 | 20 | 95.2381 | |
gduggal-snapvard | INDEL | I1_5 | map_l150_m2_e1 | * | 89.7320 | 94.9153 | 85.0856 | 90.9633 | 504 | 27 | 696 | 122 | 45 | 36.8852 | |
gduggal-snapvard | INDEL | I6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 41.1383 | 38.1818 | 44.5910 | 44.9927 | 504 | 816 | 845 | 1050 | 781 | 74.3810 | |
ghariani-varprowl | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 88.8489 | 99.4083 | 80.3175 | 86.3311 | 504 | 3 | 506 | 124 | 83 | 66.9355 | |
hfeng-pmm1 | INDEL | * | map_l100_m0_e0 | homalt | 98.5337 | 99.0177 | 98.0545 | 82.5704 | 504 | 5 | 504 | 10 | 4 | 40.0000 | |
gduggal-snapplat | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 28.6628 | 18.2874 | 66.2500 | 62.2444 | 504 | 2252 | 477 | 243 | 131 | 53.9095 | |
astatham-gatk | SNP | tv | map_l250_m0_e0 | het | 92.7323 | 88.1119 | 97.8641 | 94.1324 | 504 | 68 | 504 | 11 | 2 | 18.1818 | |
anovak-vg | INDEL | D1_5 | map_l100_m1_e0 | homalt | 89.7866 | 85.3041 | 94.7664 | 81.8274 | 505 | 87 | 507 | 28 | 27 | 96.4286 | |
asubramanian-gatk | INDEL | I1_5 | map_l100_m2_e1 | homalt | 96.4668 | 93.5185 | 99.6071 | 83.0446 | 505 | 35 | 507 | 2 | 2 | 100.0000 | |
bgallagher-sentieon | INDEL | * | map_l100_m0_e0 | homalt | 98.5366 | 99.2141 | 97.8682 | 84.8680 | 505 | 4 | 505 | 11 | 5 | 45.4545 | |
bgallagher-sentieon | INDEL | * | map_l150_m0_e0 | * | 97.3095 | 98.2490 | 96.3878 | 92.6248 | 505 | 9 | 507 | 19 | 4 | 21.0526 | |
bgallagher-sentieon | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_51to200 | * | 78.7119 | 72.4534 | 86.1538 | 53.4606 | 505 | 192 | 504 | 81 | 80 | 98.7654 | |
astatham-gatk | INDEL | * | map_l100_m0_e0 | homalt | 98.7292 | 99.2141 | 98.2490 | 85.0971 | 505 | 4 | 505 | 9 | 5 | 55.5556 | |
ciseli-custom | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | homalt | 85.5522 | 92.4908 | 79.5820 | 75.9660 | 505 | 41 | 495 | 127 | 74 | 58.2677 | |
ckim-dragen | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_51to200 | * | 78.9679 | 72.4534 | 86.7698 | 52.5285 | 505 | 192 | 505 | 77 | 76 | 98.7013 | |
jpowers-varprowl | INDEL | I6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 47.5294 | 38.2286 | 62.8109 | 62.6047 | 505 | 816 | 505 | 299 | 296 | 98.9967 | |
jpowers-varprowl | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 86.9634 | 99.6055 | 77.1689 | 87.2477 | 505 | 2 | 507 | 150 | 85 | 56.6667 | |
ltrigg-rtg1 | INDEL | * | map_l100_m0_e0 | homalt | 99.0173 | 99.2141 | 98.8212 | 82.1404 | 505 | 4 | 503 | 6 | 3 | 50.0000 | |
gduggal-snapvard | INDEL | D1_5 | map_l150_m2_e0 | het | 84.3060 | 98.2490 | 73.8286 | 91.1437 | 505 | 9 | 646 | 229 | 52 | 22.7074 | |
eyeh-varpipe | INDEL | I1_5 | map_l150_m2_e0 | * | 97.6695 | 97.3025 | 98.0392 | 88.0317 | 505 | 14 | 800 | 16 | 10 | 62.5000 | |
hfeng-pmm3 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 95.2485 | 95.8254 | 94.6785 | 79.7485 | 505 | 22 | 427 | 24 | 23 | 95.8333 | |
hfeng-pmm1 | INDEL | I1_5 | map_l150_m2_e0 | * | 97.9658 | 97.3025 | 98.6381 | 89.4909 | 505 | 14 | 507 | 7 | 2 | 28.5714 | |
hfeng-pmm2 | INDEL | * | map_l100_m0_e0 | homalt | 98.6328 | 99.2141 | 98.0583 | 83.0759 | 505 | 4 | 505 | 10 | 5 | 50.0000 | |
hfeng-pmm2 | INDEL | * | map_l150_m0_e0 | * | 97.3151 | 98.4436 | 96.2121 | 92.3077 | 506 | 8 | 508 | 20 | 4 | 20.0000 | |
hfeng-pmm1 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 95.3481 | 96.0152 | 94.6903 | 79.5197 | 506 | 21 | 428 | 24 | 23 | 95.8333 |