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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
27401-27450 / 86044 show all | |||||||||||||||
| ckim-gatk | INDEL | D16_PLUS | HG002complexvar | homalt | 98.7952 | 99.3080 | 98.2877 | 76.3371 | 287 | 2 | 287 | 5 | 4 | 80.0000 | |
| qzeng-custom | INDEL | I1_5 | lowcmp_SimpleRepeat_triTR_11to50 | hetalt | 95.3338 | 91.6933 | 99.2754 | 35.5140 | 287 | 26 | 137 | 1 | 1 | 100.0000 | |
| ndellapenna-hhga | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | hetalt | 87.5000 | 79.0634 | 97.9522 | 47.2072 | 287 | 76 | 287 | 6 | 6 | 100.0000 | |
| mlin-fermikit | SNP | * | HG002complexvar | hetalt | 95.9866 | 92.5806 | 99.6528 | 34.0961 | 287 | 23 | 287 | 1 | 1 | 100.0000 | |
| mlin-fermikit | SNP | tv | HG002complexvar | hetalt | 95.9866 | 92.5806 | 99.6528 | 34.0961 | 287 | 23 | 287 | 1 | 1 | 100.0000 | |
| ndellapenna-hhga | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 78.8884 | 79.2818 | 78.4990 | 70.8284 | 287 | 75 | 387 | 106 | 100 | 94.3396 | |
| ltrigg-rtg2 | INDEL | I6_15 | map_siren | * | 96.2876 | 93.7705 | 98.9437 | 78.2708 | 286 | 19 | 281 | 3 | 2 | 66.6667 | |
| gduggal-bwafb | INDEL | I1_5 | map_l150_m2_e0 | het | 95.1813 | 92.5566 | 97.9592 | 89.7023 | 286 | 23 | 288 | 6 | 1 | 16.6667 | |
| raldana-dualsentieon | INDEL | I1_5 | map_l150_m1_e0 | het | 96.1457 | 95.6522 | 96.6443 | 87.6707 | 286 | 13 | 288 | 10 | 0 | 0.0000 | |
| raldana-dualsentieon | INDEL | I6_15 | map_siren | * | 95.8124 | 93.7705 | 97.9452 | 80.9150 | 286 | 19 | 286 | 6 | 3 | 50.0000 | |
| hfeng-pmm3 | INDEL | D16_PLUS | HG002complexvar | homalt | 99.1334 | 98.9619 | 99.3056 | 74.9565 | 286 | 3 | 286 | 2 | 1 | 50.0000 | |
| hfeng-pmm1 | INDEL | I1_5 | map_l150_m1_e0 | het | 97.1183 | 95.6522 | 98.6301 | 89.0019 | 286 | 13 | 288 | 4 | 0 | 0.0000 | |
| hfeng-pmm1 | INDEL | D16_PLUS | HG002complexvar | homalt | 99.1334 | 98.9619 | 99.3056 | 74.5133 | 286 | 3 | 286 | 2 | 1 | 50.0000 | |
| ckim-gatk | INDEL | D1_5 | map_l150_m0_e0 | * | 93.6362 | 98.9619 | 88.8545 | 93.9851 | 286 | 3 | 287 | 36 | 1 | 2.7778 | |
| ciseli-custom | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 42.6673 | 30.3609 | 71.7500 | 71.1191 | 286 | 656 | 287 | 113 | 96 | 84.9558 | |
| ckim-dragen | INDEL | I1_5 | map_l150_m2_e0 | het | 93.7785 | 92.5566 | 95.0331 | 91.9659 | 286 | 23 | 287 | 15 | 2 | 13.3333 | |
| gduggal-snapplat | INDEL | D1_5 | map_l125_m2_e0 | homalt | 87.4375 | 78.5714 | 98.5591 | 89.4013 | 286 | 78 | 342 | 5 | 0 | 0.0000 | |
| gduggal-bwaplat | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_51to200 | * | 62.9139 | 46.2662 | 98.2759 | 80.8707 | 285 | 331 | 285 | 5 | 5 | 100.0000 | |
| gduggal-bwavard | INDEL | * | map_l250_m1_e0 | * | 82.3699 | 93.4426 | 73.6434 | 96.1257 | 285 | 20 | 285 | 102 | 15 | 14.7059 | |
| astatham-gatk | INDEL | I1_5 | map_l150_m2_e0 | het | 95.1641 | 92.2330 | 98.2877 | 91.7561 | 285 | 24 | 287 | 5 | 0 | 0.0000 | |
| astatham-gatk | INDEL | I6_15 | map_siren | * | 95.6376 | 93.4426 | 97.9381 | 85.2956 | 285 | 20 | 285 | 6 | 4 | 66.6667 | |
| jpowers-varprowl | INDEL | I1_5 | map_l125_m0_e0 | * | 94.3709 | 91.9355 | 96.9388 | 89.0052 | 285 | 25 | 285 | 9 | 6 | 66.6667 | |
| ltrigg-rtg1 | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 85.0898 | 75.0000 | 98.3165 | 64.4737 | 285 | 95 | 292 | 5 | 5 | 100.0000 | |
| jmaeng-gatk | SNP | * | map_l250_m0_e0 | homalt | 62.1444 | 45.1510 | 99.6491 | 95.8315 | 284 | 345 | 284 | 1 | 1 | 100.0000 | |
| ltrigg-rtg1 | INDEL | I6_15 | map_siren | * | 95.4449 | 93.1148 | 97.8947 | 78.4743 | 284 | 21 | 279 | 6 | 4 | 66.6667 | |
| gduggal-bwafb | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | hetalt | 94.0050 | 89.8734 | 98.5348 | 73.8506 | 284 | 32 | 269 | 4 | 4 | 100.0000 | |
| rpoplin-dv42 | INDEL | D16_PLUS | HG002complexvar | homalt | 98.6111 | 98.2699 | 98.9547 | 72.7704 | 284 | 5 | 284 | 3 | 2 | 66.6667 | |
| egarrison-hhga | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 84.4254 | 74.7368 | 97.0000 | 58.7912 | 284 | 96 | 291 | 9 | 8 | 88.8889 | |
| mlin-fermikit | INDEL | * | map_l150_m1_e0 | homalt | 67.2189 | 61.4719 | 74.1514 | 83.0230 | 284 | 178 | 284 | 99 | 88 | 88.8889 | |
| ndellapenna-hhga | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 84.5480 | 74.7368 | 97.3244 | 58.8721 | 284 | 96 | 291 | 8 | 7 | 87.5000 | |
| asubramanian-gatk | SNP | tv | HG002complexvar | hetalt | 94.3522 | 91.6129 | 97.2603 | 39.0397 | 284 | 26 | 284 | 8 | 0 | 0.0000 | |
| asubramanian-gatk | SNP | * | HG002complexvar | hetalt | 93.8843 | 91.6129 | 96.2712 | 41.3519 | 284 | 26 | 284 | 11 | 0 | 0.0000 | |
| hfeng-pmm2 | INDEL | D16_PLUS | HG002complexvar | homalt | 98.1002 | 98.2699 | 97.9310 | 75.1286 | 284 | 5 | 284 | 6 | 5 | 83.3333 | |
| cchapple-custom | INDEL | I1_5 | map_l150_m1_e0 | het | 94.8942 | 94.9833 | 94.8052 | 89.4916 | 284 | 15 | 292 | 16 | 2 | 12.5000 | |
| ciseli-custom | INDEL | I1_5 | map_l100_m0_e0 | * | 58.4054 | 52.3020 | 66.1215 | 87.8959 | 284 | 259 | 283 | 145 | 118 | 81.3793 | |
| ciseli-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 62.0432 | 53.7002 | 73.4554 | 68.7187 | 283 | 244 | 321 | 116 | 109 | 93.9655 | |
| ciseli-custom | INDEL | I6_15 | lowcmp_SimpleRepeat_diTR_11to50 | * | 19.2271 | 11.7330 | 53.2189 | 75.6912 | 283 | 2129 | 248 | 218 | 182 | 83.4862 | |
| dgrover-gatk | INDEL | D1_5 | map_l150_m0_e0 | * | 97.4236 | 97.9239 | 96.9283 | 92.3837 | 283 | 6 | 284 | 9 | 1 | 11.1111 | |
| ckim-vqsr | INDEL | D1_5 | map_l150_m0_e0 | * | 95.6081 | 97.9239 | 93.3993 | 94.3364 | 283 | 6 | 283 | 20 | 1 | 5.0000 | |
| rpoplin-dv42 | INDEL | D1_5 | map_l150_m0_e0 | * | 97.9275 | 97.9239 | 97.9310 | 91.1206 | 283 | 6 | 284 | 6 | 1 | 16.6667 | |
| rpoplin-dv42 | INDEL | I16_PLUS | HG002complexvar | hetalt | 91.5858 | 84.4776 | 100.0000 | 64.2417 | 283 | 52 | 290 | 0 | 0 | ||
| ltrigg-rtg2 | INDEL | * | map_l250_m1_e0 | * | 95.7733 | 92.7869 | 98.9583 | 92.4330 | 283 | 22 | 285 | 3 | 0 | 0.0000 | |
| jli-custom | INDEL | D1_5 | map_l150_m0_e0 | * | 97.5862 | 97.9239 | 97.2509 | 90.5458 | 283 | 6 | 283 | 8 | 1 | 12.5000 | |
| jmaeng-gatk | INDEL | D1_5 | map_l150_m0_e0 | * | 94.0364 | 97.9239 | 90.4459 | 94.1809 | 283 | 6 | 284 | 30 | 1 | 3.3333 | |
| gduggal-bwaplat | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_51to200 | hetalt | 48.6672 | 32.4541 | 97.2509 | 55.2995 | 283 | 589 | 283 | 8 | 8 | 100.0000 | |
| gduggal-bwaplat | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 59.5931 | 46.9320 | 81.6092 | 83.6389 | 283 | 320 | 284 | 64 | 1 | 1.5625 | |
| eyeh-varpipe | INDEL | D1_5 | map_l150_m0_e0 | * | 97.0408 | 97.9239 | 96.1735 | 91.2206 | 283 | 6 | 377 | 15 | 8 | 53.3333 | |
| ghariani-varprowl | INDEL | * | map_l250_m1_e0 | * | 87.2111 | 92.7869 | 82.2674 | 98.0750 | 283 | 22 | 283 | 61 | 12 | 19.6721 | |
| gduggal-snapplat | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 71.3745 | 60.3412 | 87.3457 | 93.7848 | 283 | 186 | 283 | 41 | 21 | 51.2195 | |
| jlack-gatk | INDEL | D16_PLUS | HG002complexvar | homalt | 98.0936 | 97.9239 | 98.2639 | 75.8186 | 283 | 6 | 283 | 5 | 4 | 80.0000 | |