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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
83101-83150 / 86044 show all | |||||||||||||||
| hfeng-pmm1 | SNP | * | map_l100_m1_e0 | homalt | 99.8556 | 99.8408 | 99.8703 | 60.9594 | 26960 | 43 | 26960 | 35 | 17 | 48.5714 | |
| gduggal-snapvard | SNP | ti | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 91.8181 | 97.0493 | 87.1220 | 66.7143 | 27134 | 825 | 26966 | 3986 | 179 | 4.4907 | |
| hfeng-pmm2 | SNP | * | map_l100_m1_e0 | homalt | 99.8648 | 99.8704 | 99.8593 | 60.9853 | 26968 | 35 | 26968 | 38 | 19 | 50.0000 | |
| gduggal-bwaplat | SNP | * | map_l125_m1_e0 | * | 74.4387 | 59.4965 | 99.4030 | 86.9422 | 26968 | 18359 | 26975 | 162 | 46 | 28.3951 | |
| jmaeng-gatk | SNP | ti | map_l100_m2_e0 | het | 92.7126 | 88.1229 | 97.8066 | 81.8391 | 26985 | 3637 | 26978 | 605 | 56 | 9.2562 | |
| jlack-gatk | INDEL | * | HG002complexvar | homalt | 99.5756 | 99.8076 | 99.3448 | 56.8540 | 26975 | 52 | 26988 | 178 | 171 | 96.0674 | |
| hfeng-pmm1 | INDEL | * | HG002complexvar | homalt | 99.7782 | 99.8372 | 99.7192 | 55.9241 | 26983 | 44 | 26991 | 76 | 70 | 92.1053 | |
| hfeng-pmm2 | INDEL | * | HG002complexvar | homalt | 99.7542 | 99.8483 | 99.6603 | 56.1296 | 26986 | 41 | 26994 | 92 | 86 | 93.4783 | |
| hfeng-pmm3 | INDEL | * | HG002complexvar | homalt | 99.7967 | 99.8594 | 99.7340 | 55.8371 | 26989 | 38 | 26999 | 72 | 66 | 91.6667 | |
| ckim-vqsr | INDEL | * | HG002complexvar | homalt | 99.7470 | 99.8705 | 99.6237 | 57.3434 | 26992 | 35 | 27005 | 102 | 98 | 96.0784 | |
| jli-custom | INDEL | * | HG002complexvar | homalt | 99.8318 | 99.8964 | 99.7673 | 56.4104 | 26999 | 28 | 27007 | 63 | 57 | 90.4762 | |
| jmaeng-gatk | INDEL | * | HG002complexvar | homalt | 99.7212 | 99.8779 | 99.5650 | 57.3567 | 26994 | 33 | 27007 | 118 | 111 | 94.0678 | |
| raldana-dualsentieon | INDEL | * | HG002complexvar | homalt | 99.7249 | 99.9038 | 99.5467 | 56.9673 | 27001 | 26 | 27010 | 123 | 119 | 96.7480 | |
| ckim-gatk | INDEL | * | HG002complexvar | homalt | 99.7525 | 99.8890 | 99.6164 | 57.3371 | 26997 | 30 | 27010 | 104 | 99 | 95.1923 | |
| astatham-gatk | INDEL | * | HG002complexvar | homalt | 99.7747 | 99.9075 | 99.6422 | 57.3610 | 27002 | 25 | 27012 | 97 | 94 | 96.9072 | |
| ciseli-custom | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 89.4833 | 97.3914 | 82.7630 | 66.8151 | 26956 | 722 | 27013 | 5626 | 378 | 6.7188 | |
| bgallagher-sentieon | INDEL | * | HG002complexvar | homalt | 99.7010 | 99.9186 | 99.4844 | 57.3638 | 27005 | 22 | 27015 | 140 | 135 | 96.4286 | |
| dgrover-gatk | INDEL | * | HG002complexvar | homalt | 99.7765 | 99.9223 | 99.6312 | 57.3581 | 27006 | 21 | 27016 | 100 | 96 | 96.0000 | |
| eyeh-varpipe | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 91.3695 | 99.3801 | 84.5540 | 81.4321 | 28534 | 178 | 27026 | 4937 | 134 | 2.7142 | |
| eyeh-varpipe | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 91.3695 | 99.3801 | 84.5540 | 81.4321 | 28534 | 178 | 27026 | 4937 | 134 | 2.7142 | |
| gduggal-snapfb | SNP | * | map_l100_m2_e1 | homalt | 98.4483 | 97.2334 | 99.6939 | 70.5179 | 27027 | 769 | 27029 | 83 | 30 | 36.1446 | |
| ckim-gatk | SNP | ti | map_l100_m2_e0 | het | 92.8437 | 88.2960 | 97.8852 | 81.4673 | 27038 | 3584 | 27031 | 584 | 62 | 10.6164 | |
| gduggal-snapvard | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 72.2778 | 90.5780 | 60.1295 | 57.9997 | 12459 | 1296 | 27033 | 17925 | 14535 | 81.0879 | |
| gduggal-snapvard | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 72.2778 | 90.5780 | 60.1295 | 57.9997 | 12459 | 1296 | 27033 | 17925 | 14535 | 81.0879 | |
| gduggal-bwaplat | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | * | 83.5750 | 73.9861 | 96.0194 | 60.2412 | 27073 | 9519 | 27065 | 1122 | 616 | 54.9020 | |
| jlack-gatk | INDEL | * | HG002compoundhet | * | 91.0082 | 90.7410 | 91.2769 | 62.3551 | 27186 | 2774 | 27070 | 2587 | 2465 | 95.2841 | |
| gduggal-snapplat | SNP | ti | map_l125_m1_e0 | * | 94.1774 | 92.2277 | 96.2113 | 79.7747 | 27055 | 2280 | 27070 | 1066 | 586 | 54.9719 | |
| gduggal-snapvard | SNP | * | segdup | * | 98.2794 | 97.3955 | 99.1795 | 93.1728 | 27336 | 731 | 27076 | 224 | 72 | 32.1429 | |
| anovak-vg | SNP | * | map_l150_m2_e0 | * | 79.6445 | 85.9852 | 74.1747 | 80.0306 | 27388 | 4464 | 27076 | 9427 | 2180 | 23.1251 | |
| jpowers-varprowl | INDEL | * | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 96.4342 | 95.8599 | 97.0154 | 57.1729 | 27090 | 1170 | 27077 | 833 | 772 | 92.6771 | |
| eyeh-varpipe | SNP | ti | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 97.8170 | 99.3884 | 96.2946 | 56.5927 | 27788 | 171 | 27079 | 1042 | 134 | 12.8599 | |
| cchapple-custom | SNP | * | map_l100_m2_e1 | homalt | 98.7359 | 97.5104 | 99.9926 | 58.6714 | 27104 | 692 | 27093 | 2 | 2 | 100.0000 | |
| ckim-isaac | SNP | * | segdup | * | 98.2480 | 96.6046 | 99.9484 | 87.4705 | 27114 | 953 | 27116 | 14 | 7 | 50.0000 | |
| mlin-fermikit | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 98.1160 | 97.8900 | 98.3429 | 64.4756 | 27094 | 584 | 27122 | 457 | 344 | 75.2735 | |
| gduggal-bwavard | SNP | ti | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 97.4880 | 97.6215 | 97.3548 | 60.2420 | 27294 | 665 | 27125 | 737 | 204 | 27.6798 | |
| gduggal-bwaplat | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 92.4986 | 87.0629 | 98.6582 | 85.3332 | 27114 | 4029 | 27131 | 369 | 118 | 31.9783 | |
| gduggal-bwaplat | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 92.4986 | 87.0629 | 98.6582 | 85.3332 | 27114 | 4029 | 27131 | 369 | 118 | 31.9783 | |
| gduggal-bwavard | SNP | * | segdup | * | 98.3638 | 97.5737 | 99.1668 | 93.3246 | 27386 | 681 | 27135 | 228 | 70 | 30.7018 | |
| ndellapenna-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 86.9809 | 86.1182 | 87.8610 | 55.6334 | 27048 | 4360 | 27135 | 3749 | 3406 | 90.8509 | |
| ndellapenna-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 86.9809 | 86.1182 | 87.8610 | 55.6334 | 27048 | 4360 | 27135 | 3749 | 3406 | 90.8509 | |
| mlin-fermikit | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 86.0733 | 85.0400 | 87.1320 | 47.7048 | 27206 | 4786 | 27139 | 4008 | 3953 | 98.6277 | |
| asubramanian-gatk | SNP | * | segdup | * | 98.1237 | 96.8005 | 99.4836 | 92.0357 | 27169 | 898 | 27163 | 141 | 14 | 9.9291 | |
| gduggal-snapvard | SNP | * | map_l125_m1_e0 | het | 91.2586 | 96.8794 | 86.2542 | 81.2481 | 27506 | 886 | 27183 | 4332 | 306 | 7.0637 | |
| egarrison-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 86.8726 | 86.3602 | 87.3912 | 57.0498 | 27124 | 4284 | 27204 | 3925 | 3577 | 91.1338 | |
| egarrison-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 86.8726 | 86.3602 | 87.3912 | 57.0498 | 27124 | 4284 | 27204 | 3925 | 3577 | 91.1338 | |
| astatham-gatk | SNP | * | map_l150_m2_e1 | * | 91.4615 | 84.4862 | 99.6922 | 80.1245 | 27213 | 4997 | 27207 | 84 | 40 | 47.6190 | |
| gduggal-bwafb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 93.1643 | 88.4244 | 98.4410 | 44.1529 | 12925 | 1692 | 27215 | 431 | 341 | 79.1183 | |
| ciseli-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 76.7889 | 93.7761 | 65.0122 | 76.1162 | 26925 | 1787 | 27218 | 14648 | 266 | 1.8160 | |
| ciseli-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 76.7889 | 93.7761 | 65.0122 | 76.1162 | 26925 | 1787 | 27218 | 14648 | 266 | 1.8160 | |
| anovak-vg | SNP | * | segdup | * | 97.8173 | 97.8231 | 97.8116 | 92.2860 | 27456 | 611 | 27219 | 609 | 236 | 38.7521 | |