PrecisionFDA
Truth Challenge
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Explore HG002 comparison results
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| Entry | Type | Subtype | Subset | Genotype | F-score | Recall | Precision | Frac_NA | Truth TP | Truth FN | Query TP | Query FP | FP gt | % FP ma | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
7201-7250 / 86044 show all | |||||||||||||||
| eyeh-varpipe | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 53.7340 | 37.1777 | 96.8750 | 57.0119 | 2192 | 3704 | 3317 | 107 | 99 | 92.5234 | |
| jpowers-varprowl | SNP | tv | map_l100_m1_e0 | het | 96.9444 | 97.1330 | 96.7565 | 74.5209 | 14975 | 442 | 14975 | 502 | 99 | 19.7211 | |
| jmaeng-gatk | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | het | 97.5546 | 98.8657 | 96.2777 | 63.5724 | 2702 | 31 | 2690 | 104 | 99 | 95.1923 | |
| ltrigg-rtg2 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 97.3624 | 95.4205 | 99.3850 | 51.9079 | 15940 | 765 | 16321 | 101 | 99 | 98.0198 | |
| ltrigg-rtg2 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 97.3624 | 95.4205 | 99.3850 | 51.9079 | 15940 | 765 | 16321 | 101 | 99 | 98.0198 | |
| jli-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 95.1000 | 98.3080 | 92.0949 | 58.3471 | 1162 | 20 | 1165 | 100 | 99 | 99.0000 | |
| asubramanian-gatk | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 97.7550 | 98.6561 | 96.8703 | 68.6124 | 3230 | 44 | 3219 | 104 | 99 | 95.1923 | |
| anovak-vg | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 45.1042 | 39.2655 | 52.9825 | 57.7778 | 139 | 215 | 151 | 134 | 99 | 73.8806 | |
| ckim-isaac | INDEL | D6_15 | * | hetalt | 90.6237 | 83.9246 | 98.4851 | 33.2460 | 6860 | 1314 | 7281 | 112 | 99 | 88.3929 | |
| qzeng-custom | SNP | * | map_l125_m2_e1 | homalt | 83.7240 | 72.4219 | 99.2062 | 67.7495 | 12697 | 4835 | 12498 | 100 | 99 | 99.0000 | |
| ndellapenna-hhga | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 98.0065 | 98.3531 | 97.6623 | 53.6204 | 5972 | 100 | 5974 | 143 | 99 | 69.2308 | |
| gduggal-snapplat | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 32.5229 | 33.1367 | 31.9314 | 80.3989 | 1292 | 2607 | 1321 | 2816 | 99 | 3.5156 | |
| ghariani-varprowl | INDEL | I6_15 | HG002complexvar | homalt | 84.4108 | 80.1483 | 89.1522 | 51.9071 | 973 | 241 | 978 | 119 | 99 | 83.1933 | |
| gduggal-snapfb | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 54.3229 | 97.9257 | 37.5868 | 83.5805 | 4060 | 86 | 4112 | 6828 | 99 | 1.4499 | |
| gduggal-snapvard | INDEL | D1_5 | map_l125_m1_e0 | * | 87.8220 | 95.5882 | 81.2230 | 87.7784 | 1040 | 48 | 1315 | 304 | 98 | 32.2368 | |
| ghariani-varprowl | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 88.0250 | 87.1204 | 88.9485 | 79.8268 | 832 | 123 | 829 | 103 | 98 | 95.1456 | |
| ghariani-varprowl | SNP | ti | map_l125_m0_e0 | het | 96.8041 | 98.4267 | 95.2342 | 81.7798 | 8133 | 130 | 8133 | 407 | 98 | 24.0786 | |
| ghariani-varprowl | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 95.1742 | 99.7330 | 91.0140 | 84.2317 | 1494 | 4 | 1499 | 148 | 98 | 66.2162 | |
| ghariani-varprowl | SNP | tv | map_l100_m2_e0 | het | 97.2146 | 99.3218 | 95.1950 | 76.6930 | 15670 | 107 | 15671 | 791 | 98 | 12.3894 | |
| ghariani-varprowl | SNP | tv | map_l100_m2_e1 | het | 97.2241 | 99.3224 | 95.2126 | 76.7581 | 15830 | 108 | 15831 | 796 | 98 | 12.3116 | |
| gduggal-snapplat | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 78.7301 | 78.1671 | 79.3012 | 91.5881 | 7139 | 1994 | 7172 | 1872 | 98 | 5.2350 | |
| gduggal-snapplat | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 78.7301 | 78.1671 | 79.3012 | 91.5881 | 7139 | 1994 | 7172 | 1872 | 98 | 5.2350 | |
| gduggal-snapplat | INDEL | D6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 41.2069 | 31.2292 | 60.5536 | 61.3636 | 188 | 414 | 175 | 114 | 98 | 85.9649 | |
| jli-custom | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 99.4474 | 99.8648 | 99.0334 | 44.0841 | 10343 | 14 | 10348 | 101 | 98 | 97.0297 | |
| jlack-gatk | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 92.4826 | 97.3404 | 88.0866 | 60.7649 | 732 | 20 | 732 | 99 | 98 | 98.9899 | |
| eyeh-varpipe | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | het | 70.1872 | 69.5761 | 70.8092 | 55.2972 | 279 | 122 | 245 | 101 | 98 | 97.0297 | |
| eyeh-varpipe | INDEL | D1_5 | HG002complexvar | het | 98.4401 | 97.6258 | 99.2681 | 46.7116 | 20272 | 493 | 18853 | 139 | 98 | 70.5036 | |
| eyeh-varpipe | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 91.1773 | 86.7440 | 96.0881 | 48.8639 | 2840 | 434 | 2530 | 103 | 98 | 95.1456 | |
| gduggal-bwafb | INDEL | I16_PLUS | HG002compoundhet | homalt | 3.8462 | 66.6667 | 1.9802 | 47.1204 | 2 | 1 | 2 | 99 | 98 | 98.9899 | |
| gduggal-bwavard | SNP | * | map_l125_m0_e0 | * | 93.5292 | 97.4826 | 89.8840 | 82.4074 | 18897 | 488 | 18668 | 2101 | 98 | 4.6645 | |
| gduggal-bwaplat | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | * | 77.9097 | 64.7065 | 97.8826 | 70.2472 | 12852 | 7010 | 12851 | 278 | 98 | 35.2518 | |
| ciseli-custom | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 86.4138 | 96.3627 | 78.3270 | 66.2442 | 16929 | 639 | 17004 | 4705 | 98 | 2.0829 | |
| ckim-isaac | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 91.0211 | 84.5394 | 98.5791 | 36.6641 | 8049 | 1472 | 8048 | 116 | 98 | 84.4828 | |
| ciseli-custom | INDEL | D1_5 | map_l100_m1_e0 | homalt | 83.5566 | 85.6419 | 81.5705 | 83.0803 | 507 | 85 | 509 | 115 | 98 | 85.2174 | |
| cchapple-custom | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 99.1720 | 99.7378 | 98.6126 | 26.3903 | 7228 | 19 | 7179 | 101 | 98 | 97.0297 | |
| cchapple-custom | INDEL | D6_15 | HG002complexvar | * | 96.6422 | 95.3791 | 97.9391 | 52.4803 | 5057 | 245 | 5085 | 107 | 98 | 91.5888 | |
| ltrigg-rtg2 | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 94.5468 | 91.3928 | 97.9261 | 61.6841 | 9206 | 867 | 9255 | 196 | 98 | 50.0000 | |
| jmaeng-gatk | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 99.2664 | 99.8896 | 98.6509 | 37.0615 | 7239 | 8 | 7239 | 99 | 98 | 98.9899 | |
| jli-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 98.6957 | 98.3216 | 99.0726 | 47.6211 | 10896 | 186 | 10896 | 102 | 98 | 96.0784 | |
| jpowers-varprowl | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 86.8788 | 84.7120 | 89.1593 | 77.2464 | 809 | 146 | 806 | 98 | 98 | 100.0000 | |
| ndellapenna-hhga | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 76.5549 | 62.5570 | 98.6231 | 39.2209 | 8778 | 5254 | 8094 | 113 | 98 | 86.7257 | |
| ndellapenna-hhga | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 89.6468 | 92.1537 | 87.2727 | 64.8656 | 1151 | 98 | 1152 | 168 | 98 | 58.3333 | |
| ndellapenna-hhga | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 89.6468 | 92.1537 | 87.2727 | 64.8656 | 1151 | 98 | 1152 | 168 | 98 | 58.3333 | |
| mlin-fermikit | SNP | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 96.1773 | 99.3135 | 93.2331 | 71.4592 | 1736 | 12 | 1736 | 126 | 98 | 77.7778 | |
| ltrigg-rtg2 | SNP | ti | * | homalt | 99.9701 | 99.9529 | 99.9873 | 15.8538 | 802658 | 378 | 802554 | 102 | 98 | 96.0784 | |
| ltrigg-rtg2 | SNP | ti | HG002complexvar | * | 99.8779 | 99.7988 | 99.9570 | 17.4272 | 507413 | 1023 | 507316 | 218 | 98 | 44.9541 | |
| mlin-fermikit | INDEL | D1_5 | lowcmp_SimpleRepeat_triTR_11to50 | het | 96.3317 | 97.1116 | 95.5642 | 35.5358 | 2219 | 66 | 2219 | 103 | 98 | 95.1456 | |
| anovak-vg | INDEL | I1_5 | map_l125_m0_e0 | * | 57.2924 | 58.7097 | 55.9420 | 90.7507 | 182 | 128 | 193 | 152 | 98 | 64.4737 | |
| bgallagher-sentieon | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 98.9858 | 99.4610 | 98.5152 | 56.4669 | 6643 | 36 | 6635 | 100 | 98 | 98.0000 | |
| bgallagher-sentieon | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | het | 99.2229 | 99.4523 | 98.9946 | 49.9952 | 10350 | 57 | 10339 | 105 | 98 | 93.3333 | |