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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
84551-84600 / 86044 show all | |||||||||||||||
| jmaeng-gatk | SNP | * | map_l125_m2_e0 | het | 88.4835 | 81.5574 | 96.6953 | 87.4762 | 23911 | 5407 | 23905 | 817 | 51 | 6.2424 | |
| jmaeng-gatk | SNP | * | map_l125_m2_e1 | het | 88.5956 | 81.7375 | 96.7099 | 87.4772 | 24227 | 5413 | 24221 | 824 | 52 | 6.3107 | |
| ghariani-varprowl | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 0.0000 | 0.4046 | 0.0000 | 0.0000 | 22 | 5416 | 0 | 0 | 0 | ||
| jpowers-varprowl | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 0.0000 | 0.3862 | 0.0000 | 0.0000 | 21 | 5417 | 0 | 0 | 0 | ||
| ckim-isaac | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 90.8083 | 87.4974 | 94.3796 | 47.9598 | 37917 | 5418 | 37363 | 2225 | 1830 | 82.2472 | |
| gduggal-snapplat | INDEL | I6_15 | * | hetalt | 52.6793 | 36.6390 | 93.7008 | 46.4917 | 3133 | 5418 | 3094 | 208 | 167 | 80.2885 | |
| gduggal-bwavard | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 0.0000 | 0.2574 | 0.0000 | 0.0000 | 14 | 5424 | 0 | 0 | 0 | ||
| gduggal-bwaplat | SNP | tv | map_l150_m1_e0 | * | 66.7357 | 50.1924 | 99.5456 | 91.4813 | 5477 | 5435 | 5477 | 25 | 5 | 20.0000 | |
| ckim-isaac | SNP | tv | map_l100_m2_e1 | het | 79.3382 | 65.8928 | 99.6774 | 69.5352 | 10502 | 5436 | 10505 | 34 | 8 | 23.5294 | |
| anovak-vg | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 0.0000 | 24.0312 | 0.0000 | 0.0000 | 1724 | 5450 | 0 | 0 | 0 | ||
| jmaeng-gatk | SNP | tv | map_siren | * | 92.8750 | 88.1232 | 98.1685 | 71.3358 | 40475 | 5455 | 40467 | 755 | 31 | 4.1060 | |
| jpowers-varprowl | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 30.6992 | 20.9726 | 57.2507 | 58.7917 | 1449 | 5460 | 1441 | 1076 | 1033 | 96.0037 | |
| ckim-gatk | SNP | tv | map_siren | * | 92.9580 | 88.1058 | 98.3758 | 71.0821 | 40467 | 5463 | 40459 | 668 | 31 | 4.6407 | |
| qzeng-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 91.5884 | 91.6329 | 91.5440 | 60.2311 | 59883 | 5468 | 83381 | 7702 | 4718 | 61.2568 | |
| qzeng-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 91.5884 | 91.6329 | 91.5440 | 60.2311 | 59883 | 5468 | 83381 | 7702 | 4718 | 61.2568 | |
| ghariani-varprowl | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 46.4146 | 34.9744 | 68.9769 | 73.6604 | 2941 | 5468 | 2926 | 1316 | 1208 | 91.7933 | |
| gduggal-bwaplat | SNP | tv | map_l150_m2_e0 | * | 67.9659 | 51.5984 | 99.5413 | 91.9142 | 5859 | 5496 | 5859 | 27 | 5 | 18.5185 | |
| anovak-vg | SNP | ti | map_l100_m1_e0 | * | 84.3963 | 88.5106 | 80.6475 | 68.7475 | 42424 | 5507 | 42052 | 10091 | 2274 | 22.5349 | |
| gduggal-snapvard | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 64.3466 | 65.7191 | 63.0303 | 66.4559 | 10565 | 5511 | 13341 | 7825 | 6132 | 78.3642 | |
| gduggal-snapvard | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 64.3466 | 65.7191 | 63.0303 | 66.4559 | 10565 | 5511 | 13341 | 7825 | 6132 | 78.3642 | |
| gduggal-bwafb | INDEL | * | HG002compoundhet | * | 86.4141 | 81.5955 | 91.8376 | 53.1940 | 24446 | 5514 | 37872 | 3366 | 3207 | 95.2763 | |
| ckim-vqsr | SNP | ti | map_l150_m1_e0 | homalt | 39.6323 | 24.7168 | 99.9448 | 90.0193 | 1811 | 5516 | 1811 | 1 | 1 | 100.0000 | |
| gduggal-bwaplat | SNP | tv | map_l150_m2_e1 | * | 68.1907 | 51.8692 | 99.4997 | 91.8775 | 5966 | 5536 | 5966 | 30 | 5 | 16.6667 | |
| mlin-fermikit | SNP | * | map_l150_m1_e0 | homalt | 59.9718 | 50.8826 | 73.0143 | 56.6613 | 5736 | 5537 | 5736 | 2120 | 1986 | 93.6792 | |
| ciseli-custom | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | * | 44.0541 | 41.4041 | 47.0666 | 44.8610 | 3916 | 5542 | 3939 | 4430 | 3649 | 82.3702 | |
| asubramanian-gatk | SNP | * | map_l125_m0_e0 | homalt | 29.6663 | 17.4166 | 100.0000 | 92.5404 | 1169 | 5543 | 1169 | 0 | 0 | ||
| ckim-isaac | SNP | tv | map_l150_m2_e0 | * | 67.6247 | 51.1845 | 99.6230 | 78.7586 | 5812 | 5543 | 5813 | 22 | 7 | 31.8182 | |
| ckim-isaac | SNP | ti | map_l125_m0_e0 | * | 72.1772 | 56.5507 | 99.7374 | 74.7461 | 7217 | 5545 | 7217 | 19 | 4 | 21.0526 | |
| mlin-fermikit | SNP | ti | map_l125_m0_e0 | het | 49.2645 | 32.8331 | 98.6182 | 61.3058 | 2713 | 5550 | 2712 | 38 | 3 | 7.8947 | |
| gduggal-snapplat | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 54.8241 | 40.1571 | 86.3699 | 66.0570 | 3731 | 5560 | 3783 | 597 | 508 | 85.0921 | |
| gduggal-snapplat | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 54.8241 | 40.1571 | 86.3699 | 66.0570 | 3731 | 5560 | 3783 | 597 | 508 | 85.0921 | |
| gduggal-snapplat | SNP | * | HG002complexvar | homalt | 98.9173 | 98.0729 | 99.7763 | 21.2516 | 283014 | 5561 | 282787 | 634 | 338 | 53.3123 | |
| mlin-fermikit | SNP | tv | HG002complexvar | het | 98.0988 | 96.3081 | 99.9573 | 20.3091 | 145169 | 5565 | 145103 | 62 | 9 | 14.5161 | |
| gduggal-bwaplat | SNP | ti | map_l125_m1_e0 | homalt | 66.2065 | 49.4975 | 99.9451 | 78.1716 | 5467 | 5578 | 5460 | 3 | 3 | 100.0000 | |
| gduggal-bwavard | INDEL | I1_5 | * | homalt | 95.1435 | 90.7626 | 99.9687 | 33.2973 | 54846 | 5582 | 54343 | 17 | 11 | 64.7059 | |
| anovak-vg | SNP | ti | map_l100_m2_e0 | * | 84.5385 | 88.5991 | 80.8339 | 70.4808 | 43379 | 5582 | 43002 | 10196 | 2298 | 22.5383 | |
| gduggal-snapfb | INDEL | * | HG002complexvar | het | 90.2528 | 87.9122 | 92.7215 | 54.1807 | 40626 | 5586 | 43300 | 3399 | 1261 | 37.0991 | |
| gduggal-snapplat | SNP | tv | HG002complexvar | het | 96.9038 | 96.2928 | 97.5225 | 28.0304 | 145146 | 5588 | 145527 | 3697 | 526 | 14.2278 | |
| gduggal-bwavard | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 44.8658 | 33.4523 | 68.1013 | 69.9638 | 2813 | 5596 | 2769 | 1297 | 1197 | 92.2899 | |
| anovak-vg | SNP | ti | map_siren | het | 85.3428 | 91.0279 | 80.3260 | 62.0963 | 56785 | 5597 | 56323 | 13795 | 3334 | 24.1682 | |
| gduggal-snapplat | INDEL | I6_15 | HG002compoundhet | * | 49.4889 | 36.1782 | 78.2955 | 43.1184 | 3175 | 5601 | 3142 | 871 | 568 | 65.2124 | |
| gduggal-bwaplat | INDEL | I6_15 | * | * | 86.3949 | 77.4322 | 97.7041 | 60.0483 | 19221 | 5602 | 19235 | 452 | 296 | 65.4867 | |
| ckim-isaac | SNP | tv | map_l150_m2_e1 | * | 67.7075 | 51.2780 | 99.6284 | 78.7389 | 5898 | 5604 | 5899 | 22 | 7 | 31.8182 | |
| gduggal-bwaplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 80.9828 | 69.1181 | 97.7650 | 72.5426 | 12556 | 5610 | 12554 | 287 | 244 | 85.0174 | |
| gduggal-bwaplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 80.9828 | 69.1181 | 97.7650 | 72.5426 | 12556 | 5610 | 12554 | 287 | 244 | 85.0174 | |
| mlin-fermikit | SNP | * | map_l150_m2_e0 | homalt | 60.9384 | 52.0130 | 73.5614 | 61.0344 | 6085 | 5614 | 6085 | 2187 | 2050 | 93.7357 | |
| ckim-vqsr | SNP | tv | map_l150_m1_e0 | * | 64.9686 | 48.5062 | 98.3460 | 91.7373 | 5293 | 5619 | 5292 | 89 | 0 | 0.0000 | |
| anovak-vg | SNP | ti | map_l100_m2_e1 | * | 84.6108 | 88.6390 | 80.9329 | 70.4744 | 43863 | 5622 | 43482 | 10244 | 2310 | 22.5498 | |
| gduggal-bwaplat | SNP | ti | map_l125_m2_e0 | homalt | 67.0606 | 50.4578 | 99.9476 | 79.7932 | 5731 | 5627 | 5724 | 3 | 3 | 100.0000 | |
| anovak-vg | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 79.2304 | 81.6976 | 76.9079 | 69.6191 | 25131 | 5630 | 27693 | 8315 | 7083 | 85.1834 | |