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Explore HG002 comparison results
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Entry | Type | Subtype | Subset | Genotype | F-score | Recall | Precision | Frac_NA | Truth TP | Truth FN | Query TP | Query FP | FP gt | % FP ma | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
23051-23100 / 86044 show all | |||||||||||||||
mlin-fermikit | INDEL | I16_PLUS | map_siren | * | 77.8754 | 73.2558 | 83.1169 | 87.6603 | 63 | 23 | 64 | 13 | 9 | 69.2308 | |
mlin-fermikit | INDEL | I1_5 | map_l150_m0_e0 | * | 50.5929 | 36.3636 | 83.1169 | 85.4717 | 64 | 112 | 64 | 13 | 11 | 84.6154 | |
mlin-fermikit | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 91.2698 | 88.4298 | 94.2982 | 65.0842 | 214 | 28 | 215 | 13 | 13 | 100.0000 | |
mlin-fermikit | INDEL | I6_15 | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 87.3343 | 83.8710 | 91.0959 | 81.8408 | 130 | 25 | 133 | 13 | 13 | 100.0000 | |
mlin-fermikit | SNP | * | lowcmp_SimpleRepeat_quadTR_51to200 | het | 74.3169 | 66.6667 | 83.9506 | 94.3906 | 68 | 34 | 68 | 13 | 3 | 23.0769 | |
mlin-fermikit | SNP | tv | lowcmp_SimpleRepeat_quadTR_51to200 | * | 67.4699 | 66.6667 | 68.2927 | 90.5747 | 28 | 14 | 28 | 13 | 12 | 92.3077 | |
mlin-fermikit | SNP | tv | map_l250_m1_e0 | het | 40.2130 | 25.3497 | 97.2103 | 81.1869 | 453 | 1334 | 453 | 13 | 0 | 0.0000 | |
mlin-fermikit | SNP | tv | map_l250_m2_e0 | het | 41.9263 | 26.7010 | 97.5518 | 84.3317 | 518 | 1422 | 518 | 13 | 0 | 0.0000 | |
mlin-fermikit | SNP | tv | map_l250_m2_e1 | het | 42.3276 | 27.0229 | 97.6103 | 84.4394 | 531 | 1434 | 531 | 13 | 0 | 0.0000 | |
ndellapenna-hhga | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_51to200 | homalt | 91.5094 | 95.0980 | 88.1818 | 60.7143 | 97 | 5 | 97 | 13 | 8 | 61.5385 | |
ndellapenna-hhga | INDEL | D16_PLUS | map_l100_m2_e0 | * | 83.1183 | 81.1111 | 85.2273 | 88.2353 | 73 | 17 | 75 | 13 | 6 | 46.1538 | |
ndellapenna-hhga | INDEL | D16_PLUS | map_l100_m2_e1 | * | 83.7401 | 81.4433 | 86.1702 | 87.8866 | 79 | 18 | 81 | 13 | 6 | 46.1538 | |
ndellapenna-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 97.9481 | 97.8691 | 98.0273 | 75.4654 | 643 | 14 | 646 | 13 | 6 | 46.1538 | |
ndellapenna-hhga | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_51to200 | homalt | 80.8511 | 80.2817 | 81.4286 | 43.5484 | 57 | 14 | 57 | 13 | 11 | 84.6154 | |
ndellapenna-hhga | INDEL | D1_5 | map_l150_m2_e1 | * | 97.8696 | 97.4293 | 98.3139 | 88.2398 | 758 | 20 | 758 | 13 | 6 | 46.1538 | |
ndellapenna-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 91.2758 | 92.1260 | 90.4412 | 74.2424 | 117 | 10 | 123 | 13 | 5 | 38.4615 | |
ndellapenna-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 98.2552 | 98.0301 | 98.4813 | 61.4241 | 846 | 17 | 843 | 13 | 9 | 69.2308 | |
ndellapenna-hhga | INDEL | I16_PLUS | HG002compoundhet | hetalt | 90.0250 | 82.3698 | 99.2490 | 40.2898 | 1724 | 369 | 1718 | 13 | 9 | 69.2308 | |
ndellapenna-hhga | INDEL | I16_PLUS | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 83.7170 | 82.1053 | 85.3933 | 87.5698 | 78 | 17 | 76 | 13 | 5 | 38.4615 | |
ltrigg-rtg2 | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 97.7893 | 96.6821 | 98.9221 | 82.4044 | 1253 | 43 | 1193 | 13 | 1 | 7.6923 | |
ltrigg-rtg2 | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 97.9578 | 97.5323 | 98.3871 | 83.8380 | 830 | 21 | 793 | 13 | 1 | 7.6923 | |
ltrigg-rtg2 | SNP | ti | map_l100_m2_e0 | homalt | 99.8031 | 99.6778 | 99.9288 | 59.8461 | 18250 | 59 | 18249 | 13 | 13 | 100.0000 | |
ltrigg-rtg2 | SNP | ti | map_l100_m2_e1 | homalt | 99.8051 | 99.6810 | 99.9295 | 59.8306 | 18435 | 59 | 18434 | 13 | 13 | 100.0000 | |
mlin-fermikit | INDEL | D16_PLUS | lowcmp_SimpleRepeat_homopolymer_gt10 | * | 70.4000 | 64.7059 | 77.1930 | 96.8784 | 44 | 24 | 44 | 13 | 13 | 100.0000 | |
mlin-fermikit | INDEL | D16_PLUS | lowcmp_SimpleRepeat_triTR_51to200 | * | 67.4157 | 65.2174 | 69.7674 | 63.8655 | 30 | 16 | 30 | 13 | 13 | 100.0000 | |
mlin-fermikit | INDEL | D16_PLUS | map_l150_m2_e0 | * | 60.4651 | 76.4706 | 50.0000 | 94.0774 | 13 | 4 | 13 | 13 | 2 | 15.3846 | |
mlin-fermikit | INDEL | D16_PLUS | map_l150_m2_e1 | * | 59.0909 | 72.2222 | 50.0000 | 94.2094 | 13 | 5 | 13 | 13 | 2 | 15.3846 | |
mlin-fermikit | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 97.8552 | 97.7169 | 97.9938 | 73.0000 | 642 | 15 | 635 | 13 | 12 | 92.3077 | |
mlin-fermikit | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 77.3563 | 63.1748 | 99.7477 | 25.6850 | 5114 | 2981 | 5140 | 13 | 13 | 100.0000 | |
mlin-fermikit | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 77.4004 | 63.2326 | 99.7503 | 28.0442 | 5168 | 3005 | 5193 | 13 | 13 | 100.0000 | |
mlin-fermikit | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 82.8097 | 70.7958 | 99.7345 | 26.8052 | 4875 | 2011 | 4883 | 13 | 13 | 100.0000 | |
ltrigg-rtg2 | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_51to200 | * | 86.9605 | 78.3357 | 97.7193 | 42.0142 | 546 | 151 | 557 | 13 | 12 | 92.3077 | |
ltrigg-rtg2 | INDEL | D1_5 | map_l100_m1_e0 | * | 98.1106 | 96.9697 | 99.2786 | 76.3393 | 1792 | 56 | 1789 | 13 | 1 | 7.6923 | |
ltrigg-rtg2 | INDEL | D1_5 | map_l100_m2_e0 | het | 97.9878 | 97.0541 | 98.9396 | 75.7755 | 1219 | 37 | 1213 | 13 | 1 | 7.6923 | |
ltrigg-rtg2 | INDEL | I1_5 | HG002complexvar | homalt | 99.5439 | 99.1894 | 99.9010 | 45.4107 | 13338 | 109 | 13119 | 13 | 8 | 61.5385 | |
ltrigg-rtg2 | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 93.1288 | 90.9722 | 95.3901 | 71.8563 | 262 | 26 | 269 | 13 | 1 | 7.6923 | |
ltrigg-rtg2 | INDEL | I1_5 | map_l100_m2_e0 | * | 98.0425 | 97.0760 | 99.0284 | 79.6316 | 1328 | 40 | 1325 | 13 | 2 | 15.3846 | |
ltrigg-rtg2 | INDEL | I6_15 | HG002compoundhet | hetalt | 97.3702 | 95.0217 | 99.8378 | 29.8617 | 8112 | 425 | 8001 | 13 | 12 | 92.3077 | |
ltrigg-rtg2 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 97.9550 | 96.3415 | 99.6234 | 50.0434 | 3397 | 129 | 3439 | 13 | 12 | 92.3077 | |
ltrigg-rtg2 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 97.9550 | 96.3415 | 99.6234 | 50.0434 | 3397 | 129 | 3439 | 13 | 12 | 92.3077 | |
qzeng-custom | INDEL | C1_5 | HG002complexvar | het | 80.8034 | 71.4286 | 93.0108 | 89.6031 | 5 | 2 | 173 | 13 | 1 | 7.6923 | |
qzeng-custom | INDEL | D16_PLUS | map_l125_m0_e0 | het | 60.6061 | 100.0000 | 43.4783 | 97.1357 | 9 | 0 | 10 | 13 | 0 | 0.0000 | |
qzeng-custom | INDEL | D1_5 | map_l150_m0_e0 | * | 82.7722 | 73.3564 | 94.9612 | 95.8904 | 212 | 77 | 245 | 13 | 12 | 92.3077 | |
qzeng-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 98.0405 | 98.5626 | 97.5238 | 64.3342 | 480 | 7 | 512 | 13 | 4 | 30.7692 | |
qzeng-custom | INDEL | D6_15 | map_l150_m2_e0 | * | 84.5874 | 82.9268 | 86.3158 | 93.7949 | 68 | 14 | 82 | 13 | 6 | 46.1538 | |
qzeng-custom | INDEL | D6_15 | map_l150_m2_e1 | * | 84.3557 | 82.3529 | 86.4583 | 93.8184 | 70 | 15 | 83 | 13 | 6 | 46.1538 | |
qzeng-custom | INDEL | I16_PLUS | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 59.6849 | 56.0000 | 63.8889 | 83.7838 | 14 | 11 | 23 | 13 | 5 | 38.4615 | |
qzeng-custom | INDEL | I16_PLUS | lowcmp_SimpleRepeat_triTR_11to50 | homalt | 75.4717 | 100.0000 | 60.6061 | 66.3265 | 8 | 0 | 20 | 13 | 6 | 46.1538 | |
qzeng-custom | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_51to200 | het | 77.9185 | 72.5490 | 84.1463 | 86.5132 | 37 | 14 | 69 | 13 | 7 | 53.8462 | |
qzeng-custom | INDEL | I1_5 | map_l150_m2_e0 | * | 76.0546 | 62.4277 | 97.2917 | 93.6809 | 324 | 195 | 467 | 13 | 8 | 61.5385 |