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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
9801-9850 / 86044 show all | |||||||||||||||
| hfeng-pmm3 | INDEL | D1_5 | * | het | 99.5975 | 99.3183 | 99.8783 | 55.2507 | 86977 | 597 | 86982 | 106 | 53 | 50.0000 | |
| hfeng-pmm3 | INDEL | D1_5 | HG002compoundhet | homalt | 91.1672 | 99.3127 | 84.2566 | 74.7609 | 289 | 2 | 289 | 54 | 53 | 98.1481 | |
| hfeng-pmm2 | INDEL | D16_PLUS | HG002compoundhet | het | 86.2040 | 90.6173 | 82.2006 | 57.4966 | 367 | 38 | 254 | 55 | 53 | 96.3636 | |
| hfeng-pmm2 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 97.6745 | 96.2080 | 99.1864 | 53.3595 | 7104 | 280 | 7071 | 58 | 53 | 91.3793 | |
| hfeng-pmm3 | INDEL | I16_PLUS | * | * | 97.6899 | 96.4874 | 98.9228 | 68.1825 | 6153 | 224 | 6153 | 67 | 53 | 79.1045 | |
| ckim-isaac | INDEL | I16_PLUS | * | homalt | 79.0390 | 68.3536 | 93.6842 | 50.1966 | 1067 | 494 | 1068 | 72 | 53 | 73.6111 | |
| ckim-isaac | INDEL | I16_PLUS | HG002compoundhet | homalt | 3.4483 | 33.3333 | 1.8182 | 61.5385 | 1 | 2 | 1 | 54 | 53 | 98.1481 | |
| egarrison-hhga | SNP | * | map_siren | het | 99.5365 | 99.2384 | 99.8364 | 54.0342 | 90298 | 693 | 90299 | 148 | 53 | 35.8108 | |
| egarrison-hhga | SNP | ti | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 99.3239 | 99.0379 | 99.6116 | 52.2441 | 27690 | 269 | 27695 | 108 | 53 | 49.0741 | |
| eyeh-varpipe | INDEL | C1_5 | lowcmp_SimpleRepeat_diTR_11to50 | * | 0.0000 | 0.0000 | 80.0000 | 94.8570 | 0 | 0 | 256 | 64 | 53 | 82.8125 | |
| dgrover-gatk | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 97.8320 | 96.0887 | 99.6397 | 60.4528 | 14814 | 603 | 14932 | 54 | 53 | 98.1481 | |
| dgrover-gatk | INDEL | I6_15 | * | het | 99.0704 | 98.9435 | 99.1977 | 59.7099 | 9927 | 106 | 9891 | 80 | 53 | 66.2500 | |
| dgrover-gatk | SNP | * | HG002complexvar | het | 99.9434 | 99.9156 | 99.9712 | 18.5452 | 465104 | 393 | 464974 | 134 | 53 | 39.5522 | |
| gduggal-snapfb | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 59.1477 | 49.1961 | 74.1463 | 60.0390 | 153 | 158 | 152 | 53 | 53 | 100.0000 | |
| gduggal-snapfb | SNP | tv | map_l250_m1_e0 | * | 94.8003 | 95.0510 | 94.5509 | 89.8505 | 2516 | 131 | 2516 | 145 | 53 | 36.5517 | |
| gduggal-snapplat | INDEL | * | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 90.7450 | 84.0340 | 98.6211 | 62.7612 | 23748 | 4512 | 23816 | 333 | 53 | 15.9159 | |
| gduggal-snapvard | INDEL | D1_5 | map_l150_m1_e0 | * | 86.5802 | 95.6764 | 79.0634 | 89.6914 | 686 | 31 | 861 | 228 | 53 | 23.2456 | |
| gduggal-snapvard | INDEL | D1_5 | map_l150_m2_e1 | het | 84.1666 | 98.0843 | 73.7079 | 91.1768 | 512 | 10 | 656 | 234 | 53 | 22.6496 | |
| gduggal-snapvard | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 55.8708 | 55.0239 | 56.7442 | 69.7183 | 115 | 94 | 122 | 93 | 53 | 56.9892 | |
| gduggal-snapvard | INDEL | D6_15 | map_l100_m1_e0 | het | 76.3802 | 83.3333 | 70.4981 | 82.9300 | 105 | 21 | 184 | 77 | 53 | 68.8312 | |
| gduggal-snapvard | INDEL | I6_15 | map_l125_m2_e0 | * | 60.0321 | 64.1509 | 56.4103 | 82.6087 | 34 | 19 | 88 | 68 | 53 | 77.9412 | |
| gduggal-snapvard | INDEL | I6_15 | map_l125_m2_e0 | het | 66.1017 | 86.6667 | 53.4247 | 82.5150 | 26 | 4 | 78 | 68 | 53 | 77.9412 | |
| gduggal-snapvard | INDEL | I6_15 | map_l125_m2_e1 | * | 60.1890 | 64.1509 | 56.6879 | 82.9162 | 34 | 19 | 89 | 68 | 53 | 77.9412 | |
| gduggal-snapvard | INDEL | I6_15 | map_l125_m2_e1 | het | 66.1017 | 86.6667 | 53.4247 | 82.9240 | 26 | 4 | 78 | 68 | 53 | 77.9412 | |
| gduggal-snapvard | INDEL | D16_PLUS | HG002complexvar | * | 9.5470 | 5.2952 | 48.4536 | 72.9428 | 87 | 1556 | 94 | 100 | 53 | 53.0000 | |
| gduggal-snapvard | INDEL | D16_PLUS | HG002complexvar | het | 12.2286 | 7.0461 | 46.2366 | 72.6872 | 78 | 1029 | 86 | 100 | 53 | 53.0000 | |
| gduggal-snapplat | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 47.2065 | 34.2838 | 75.7645 | 57.3941 | 1022 | 1959 | 991 | 317 | 53 | 16.7192 | |
| gduggal-snapplat | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 88.5191 | 81.9668 | 96.2101 | 86.7350 | 3209 | 706 | 3224 | 127 | 53 | 41.7323 | |
| ghariani-varprowl | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | homalt | 83.7845 | 74.5493 | 95.6314 | 66.3759 | 1406 | 480 | 1401 | 64 | 53 | 82.8125 | |
| jmaeng-gatk | INDEL | I6_15 | HG002compoundhet | het | 84.9309 | 97.1154 | 75.4630 | 84.4268 | 202 | 6 | 163 | 53 | 53 | 100.0000 | |
| jpowers-varprowl | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 43.0380 | 36.1702 | 53.1250 | 73.1092 | 68 | 120 | 68 | 60 | 53 | 88.3333 | |
| jpowers-varprowl | INDEL | I6_15 | map_siren | * | 66.5799 | 58.6885 | 76.9231 | 81.1897 | 179 | 126 | 180 | 54 | 53 | 98.1481 | |
| jpowers-varprowl | SNP | tv | map_l150_m0_e0 | het | 93.9990 | 95.0405 | 92.9800 | 87.0071 | 2702 | 141 | 2702 | 204 | 53 | 25.9804 | |
| jli-custom | INDEL | D16_PLUS | HG002compoundhet | * | 96.5889 | 95.5575 | 97.6430 | 32.3191 | 2237 | 104 | 2237 | 54 | 53 | 98.1481 | |
| jli-custom | INDEL | D6_15 | HG002complexvar | * | 98.1282 | 97.3972 | 98.8702 | 56.5015 | 5164 | 138 | 5163 | 59 | 53 | 89.8305 | |
| jli-custom | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 98.7999 | 98.6779 | 98.9222 | 68.1958 | 5523 | 74 | 5507 | 60 | 53 | 88.3333 | |
| jmaeng-gatk | INDEL | * | HG002compoundhet | hetalt | 95.3319 | 91.2708 | 99.7711 | 50.5352 | 22982 | 2198 | 23098 | 53 | 53 | 100.0000 | |
| ltrigg-rtg1 | INDEL | I16_PLUS | * | homalt | 94.3162 | 92.3767 | 96.3390 | 45.5318 | 1442 | 119 | 1421 | 54 | 53 | 98.1481 | |
| ltrigg-rtg1 | INDEL | D1_5 | * | het | 99.2847 | 98.8627 | 99.7103 | 52.7629 | 86578 | 996 | 86378 | 251 | 52 | 20.7171 | |
| ltrigg-rtg1 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 97.4336 | 95.2855 | 99.6808 | 39.8879 | 19625 | 971 | 19673 | 63 | 52 | 82.5397 | |
| ltrigg-rtg1 | INDEL | I16_PLUS | HG002compoundhet | homalt | 10.1695 | 100.0000 | 5.3571 | 68.1818 | 3 | 0 | 3 | 53 | 52 | 98.1132 | |
| ltrigg-rtg1 | INDEL | I1_5 | HG002compoundhet | * | 96.6675 | 94.0758 | 99.4060 | 64.7187 | 11624 | 732 | 11547 | 69 | 52 | 75.3623 | |
| ltrigg-rtg1 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 98.8202 | 97.9852 | 99.6695 | 59.8782 | 17800 | 366 | 17792 | 59 | 52 | 88.1356 | |
| ltrigg-rtg1 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 98.8202 | 97.9852 | 99.6695 | 59.8782 | 17800 | 366 | 17792 | 59 | 52 | 88.1356 | |
| jmaeng-gatk | SNP | tv | * | het | 99.5410 | 99.5807 | 99.5013 | 31.3482 | 589215 | 2481 | 589142 | 2953 | 52 | 1.7609 | |
| jpowers-varprowl | INDEL | * | map_l150_m2_e0 | * | 92.6847 | 91.3352 | 94.0746 | 90.7989 | 1286 | 122 | 1286 | 81 | 52 | 64.1975 | |
| jmaeng-gatk | SNP | * | map_l125_m2_e1 | het | 88.5956 | 81.7375 | 96.7099 | 87.4772 | 24227 | 5413 | 24221 | 824 | 52 | 6.3107 | |
| jmaeng-gatk | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 96.2177 | 93.0272 | 99.6348 | 58.3838 | 14342 | 1075 | 14459 | 53 | 52 | 98.1132 | |
| jli-custom | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 98.9711 | 98.6779 | 99.2660 | 59.5335 | 8285 | 111 | 8250 | 61 | 52 | 85.2459 | |
| ltrigg-rtg1 | INDEL | I6_15 | * | homalt | 98.7666 | 98.4933 | 99.0414 | 43.6510 | 6145 | 94 | 6096 | 59 | 52 | 88.1356 | |