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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
61951-62000 / 86044 show all | |||||||||||||||
| egarrison-hhga | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 98.4476 | 97.8775 | 99.0244 | 81.2649 | 4058 | 88 | 4060 | 40 | 19 | 47.5000 | |
| gduggal-snapfb | INDEL | * | HG002compoundhet | het | 71.1390 | 60.5520 | 86.2126 | 38.8614 | 2479 | 1615 | 23405 | 3743 | 1778 | 47.5020 | |
| gduggal-snapplat | INDEL | D1_5 | HG002compoundhet | het | 31.7181 | 49.3634 | 23.3658 | 68.0565 | 853 | 875 | 1126 | 3693 | 1755 | 47.5223 | |
| gduggal-snapfb | INDEL | * | * | * | 92.2602 | 90.5733 | 94.0112 | 57.2799 | 312063 | 32479 | 322983 | 20575 | 9778 | 47.5237 | |
| qzeng-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 89.5573 | 95.0633 | 84.6541 | 45.2951 | 3678 | 191 | 10586 | 1919 | 912 | 47.5248 | |
| gduggal-snapfb | SNP | ti | map_l125_m1_e0 | het | 96.3921 | 97.2572 | 95.5423 | 70.8639 | 17765 | 501 | 17768 | 829 | 394 | 47.5271 | |
| anovak-vg | SNP | tv | lowcmp_SimpleRepeat_triTR_11to50 | * | 97.2061 | 97.3623 | 97.0504 | 40.0412 | 3359 | 91 | 3389 | 103 | 49 | 47.5728 | |
| gduggal-snapfb | SNP | ti | map_l125_m1_e0 | * | 96.8890 | 96.7104 | 97.0682 | 71.9792 | 28370 | 965 | 28374 | 857 | 408 | 47.6079 | |
| gduggal-snapfb | SNP | ti | map_l125_m0_e0 | homalt | 96.3354 | 93.3645 | 99.5017 | 80.4209 | 4193 | 298 | 4193 | 21 | 10 | 47.6190 | |
| gduggal-snapvard | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 89.9292 | 85.2071 | 95.2055 | 89.4101 | 432 | 75 | 417 | 21 | 10 | 47.6190 | |
| ghariani-varprowl | SNP | * | map_l125_m0_e0 | homalt | 98.5153 | 97.3778 | 99.6797 | 71.5507 | 6536 | 176 | 6536 | 21 | 10 | 47.6190 | |
| hfeng-pmm1 | INDEL | D16_PLUS | HG002complexvar | * | 96.9275 | 95.2526 | 98.6624 | 64.9632 | 1565 | 78 | 1549 | 21 | 10 | 47.6190 | |
| gduggal-snapplat | SNP | * | map_l250_m1_e0 | het | 87.0994 | 83.6172 | 90.8842 | 94.6651 | 3976 | 779 | 3978 | 399 | 190 | 47.6190 | |
| astatham-gatk | SNP | * | map_l150_m2_e0 | * | 91.4701 | 84.5033 | 99.6888 | 80.0769 | 26916 | 4936 | 26910 | 84 | 40 | 47.6190 | |
| astatham-gatk | SNP | * | map_l150_m2_e1 | * | 91.4615 | 84.4862 | 99.6922 | 80.1245 | 27213 | 4997 | 27207 | 84 | 40 | 47.6190 | |
| egarrison-hhga | SNP | ti | map_l150_m2_e1 | * | 99.3895 | 98.9866 | 99.7957 | 75.2728 | 20513 | 210 | 20513 | 42 | 20 | 47.6190 | |
| egarrison-hhga | SNP | tv | HG002compoundhet | het | 98.2001 | 96.8971 | 99.5386 | 52.4849 | 4528 | 145 | 4530 | 21 | 10 | 47.6190 | |
| ltrigg-rtg2 | INDEL | D6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 96.6005 | 95.5255 | 97.6999 | 63.9558 | 918 | 43 | 892 | 21 | 10 | 47.6190 | |
| ltrigg-rtg1 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 96.8306 | 94.1224 | 99.6991 | 48.9729 | 6950 | 434 | 6959 | 21 | 10 | 47.6190 | |
| ltrigg-rtg1 | INDEL | D6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 96.5497 | 95.4214 | 97.7049 | 66.6424 | 917 | 44 | 894 | 21 | 10 | 47.6190 | |
| qzeng-custom | INDEL | D1_5 | lowcmp_SimpleRepeat_triTR_11to50 | het | 99.0268 | 98.8184 | 99.2361 | 41.7338 | 2258 | 27 | 2728 | 21 | 10 | 47.6190 | |
| ndellapenna-hhga | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | het | 99.2051 | 98.7842 | 99.6296 | 37.6999 | 11294 | 139 | 11296 | 42 | 20 | 47.6190 | |
| ndellapenna-hhga | SNP | ti | lowcmp_SimpleRepeat_diTR_11to50 | het | 97.9224 | 96.5693 | 99.3139 | 68.5406 | 3040 | 108 | 3040 | 21 | 10 | 47.6190 | |
| ndellapenna-hhga | SNP | ti | map_l125_m1_e0 | het | 98.8592 | 97.9689 | 99.7658 | 69.2090 | 17895 | 371 | 17895 | 42 | 20 | 47.6190 | |
| cchapple-custom | INDEL | C6_15 | HG002complexvar | het | 95.9847 | 100.0000 | 92.2794 | 83.1056 | 4 | 0 | 251 | 21 | 10 | 47.6190 | |
| cchapple-custom | INDEL | D16_PLUS | map_siren | * | 85.4653 | 85.3147 | 85.6164 | 91.3558 | 122 | 21 | 125 | 21 | 10 | 47.6190 | |
| ckim-isaac | INDEL | * | map_l100_m1_e0 | * | 81.4370 | 69.4925 | 98.3399 | 83.2871 | 2492 | 1094 | 2488 | 42 | 20 | 47.6190 | |
| jlack-gatk | INDEL | I16_PLUS | lowcmp_SimpleRepeat_diTR_11to50 | * | 93.2955 | 91.2500 | 95.4348 | 82.0942 | 438 | 42 | 439 | 21 | 10 | 47.6190 | |
| anovak-vg | SNP | tv | lowcmp_SimpleRepeat_quadTR_11to50 | * | 96.7152 | 97.3162 | 96.1216 | 41.6514 | 7252 | 200 | 7336 | 296 | 141 | 47.6351 | |
| anovak-vg | SNP | ti | lowcmp_SimpleRepeat_diTR_11to50 | * | 90.7748 | 94.4594 | 87.3670 | 66.7807 | 4569 | 268 | 5007 | 724 | 345 | 47.6519 | |
| ndellapenna-hhga | SNP | * | map_l100_m1_e0 | * | 99.3352 | 98.8536 | 99.8215 | 61.7229 | 71573 | 830 | 71575 | 128 | 61 | 47.6562 | |
| qzeng-custom | INDEL | D1_5 | HG002complexvar | het | 98.6823 | 98.3530 | 99.0138 | 55.4973 | 20423 | 342 | 21686 | 216 | 103 | 47.6852 | |
| hfeng-pmm1 | SNP | ti | HG002complexvar | * | 99.8935 | 99.8000 | 99.9872 | 17.3497 | 507419 | 1017 | 507360 | 65 | 31 | 47.6923 | |
| ciseli-custom | INDEL | D1_5 | map_l150_m2_e1 | * | 74.1635 | 68.7661 | 80.4805 | 92.8937 | 535 | 243 | 536 | 130 | 62 | 47.6923 | |
| jpowers-varprowl | INDEL | D1_5 | map_l100_m0_e0 | het | 94.2548 | 95.7699 | 92.7869 | 86.8336 | 566 | 25 | 566 | 44 | 21 | 47.7273 | |
| asubramanian-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 97.1594 | 97.2539 | 97.0650 | 73.4982 | 29643 | 837 | 30823 | 932 | 445 | 47.7468 | |
| asubramanian-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 97.1594 | 97.2539 | 97.0650 | 73.4982 | 29643 | 837 | 30823 | 932 | 445 | 47.7468 | |
| gduggal-snapplat | SNP | ti | map_siren | het | 96.8090 | 96.4253 | 97.1959 | 70.5211 | 60152 | 2230 | 60242 | 1738 | 830 | 47.7560 | |
| egarrison-hhga | SNP | * | map_l150_m1_e0 | * | 99.3388 | 98.9023 | 99.7792 | 73.2772 | 30273 | 336 | 30273 | 67 | 32 | 47.7612 | |
| ltrigg-rtg1 | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 94.1956 | 90.5120 | 98.1916 | 59.9330 | 3606 | 378 | 3638 | 67 | 32 | 47.7612 | |
| gduggal-snapplat | SNP | * | map_l250_m2_e1 | het | 87.7421 | 84.4985 | 91.2446 | 94.9087 | 4448 | 816 | 4450 | 427 | 204 | 47.7752 | |
| gduggal-snapfb | SNP | * | map_l125_m0_e0 | het | 95.0102 | 96.1466 | 93.9004 | 73.7575 | 12176 | 488 | 12177 | 791 | 378 | 47.7876 | |
| gduggal-snapfb | INDEL | D1_5 | map_siren | homalt | 98.1197 | 98.2021 | 98.0375 | 84.5627 | 1147 | 21 | 1149 | 23 | 11 | 47.8261 | |
| gduggal-snapvard | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 0.0000 | 0.0000 | 37.8378 | 72.5926 | 0 | 108 | 14 | 23 | 11 | 47.8261 | |
| gduggal-snapvard | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 0.0000 | 0.0000 | 36.1111 | 72.9323 | 0 | 66 | 13 | 23 | 11 | 47.8261 | |
| jpowers-varprowl | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 75.7282 | 95.1220 | 62.9032 | 93.1188 | 39 | 2 | 39 | 23 | 11 | 47.8261 | |
| ciseli-custom | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 81.1856 | 91.0405 | 73.2558 | 68.6589 | 315 | 31 | 315 | 115 | 55 | 47.8261 | |
| ciseli-custom | INDEL | * | map_l250_m2_e0 | het | 58.1040 | 54.2857 | 62.5000 | 97.7123 | 114 | 96 | 115 | 69 | 33 | 47.8261 | |
| ndellapenna-hhga | SNP | tv | map_l125_m2_e1 | * | 99.1365 | 98.5592 | 99.7206 | 69.3660 | 16417 | 240 | 16417 | 46 | 22 | 47.8261 | |
| ndellapenna-hhga | INDEL | D6_15 | map_l100_m1_e0 | * | 90.3034 | 89.5349 | 91.0853 | 85.3075 | 231 | 27 | 235 | 23 | 11 | 47.8261 | |