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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
81901-81950 / 86044 show all | |||||||||||||||
| ltrigg-rtg2 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 98.8703 | 98.0010 | 99.7551 | 37.4155 | 17894 | 365 | 17924 | 44 | 41 | 93.1818 | |
| ndellapenna-hhga | SNP | ti | map_l125_m1_e0 | het | 98.8592 | 97.9689 | 99.7658 | 69.2090 | 17895 | 371 | 17895 | 42 | 20 | 47.6190 | |
| jli-custom | SNP | ti | map_l100_m1_e0 | homalt | 99.7965 | 99.6548 | 99.9386 | 56.4067 | 17898 | 62 | 17898 | 11 | 11 | 100.0000 | |
| bgallagher-sentieon | SNP | ti | map_l100_m1_e0 | homalt | 99.7937 | 99.6659 | 99.9218 | 56.9365 | 17900 | 60 | 17900 | 14 | 12 | 85.7143 | |
| ndellapenna-hhga | SNP | ti | map_l100_m1_e0 | homalt | 99.7965 | 99.6659 | 99.9274 | 59.1233 | 17900 | 60 | 17900 | 13 | 13 | 100.0000 | |
| ltrigg-rtg2 | SNP | ti | map_l100_m1_e0 | homalt | 99.8049 | 99.6715 | 99.9386 | 57.1476 | 17901 | 59 | 17900 | 11 | 11 | 100.0000 | |
| raldana-dualsentieon | SNP | ti | map_l100_m1_e0 | homalt | 99.8161 | 99.7049 | 99.9275 | 56.2318 | 17907 | 53 | 17907 | 13 | 12 | 92.3077 | |
| ltrigg-rtg1 | SNP | ti | map_l100_m1_e0 | homalt | 99.8050 | 99.7216 | 99.8885 | 59.4316 | 17910 | 50 | 17910 | 20 | 20 | 100.0000 | |
| astatham-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 98.4990 | 98.1160 | 98.8851 | 46.7540 | 17915 | 344 | 17916 | 202 | 197 | 97.5248 | |
| egarrison-hhga | SNP | ti | map_l100_m1_e0 | homalt | 99.8579 | 99.7829 | 99.9331 | 60.2302 | 17921 | 39 | 17921 | 12 | 12 | 100.0000 | |
| egarrison-hhga | INDEL | I1_5 | HG002complexvar | het | 98.9830 | 98.5431 | 99.4269 | 55.1160 | 17924 | 265 | 17869 | 103 | 26 | 25.2427 | |
| dgrover-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 98.5379 | 98.1817 | 98.8967 | 47.5296 | 17927 | 332 | 17928 | 200 | 196 | 98.0000 | |
| hfeng-pmm1 | SNP | ti | map_l100_m1_e0 | homalt | 99.8580 | 99.8385 | 99.8775 | 60.1505 | 17931 | 29 | 17931 | 22 | 12 | 54.5455 | |
| hfeng-pmm3 | SNP | ti | map_l100_m1_e0 | homalt | 99.8636 | 99.8497 | 99.8775 | 60.0521 | 17933 | 27 | 17933 | 22 | 12 | 54.5455 | |
| ckim-isaac | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | * | 93.4046 | 90.2930 | 96.7382 | 47.0617 | 17934 | 1928 | 17795 | 600 | 351 | 58.5000 | |
| gduggal-snapplat | SNP | ti | map_l125_m2_e1 | het | 94.1854 | 93.9645 | 94.4074 | 84.4472 | 17935 | 1152 | 17961 | 1064 | 575 | 54.0414 | |
| eyeh-varpipe | SNP | ti | map_l100_m1_e0 | homalt | 99.8788 | 99.8719 | 99.8856 | 62.1452 | 17937 | 23 | 17464 | 20 | 12 | 60.0000 | |
| hfeng-pmm2 | SNP | ti | map_l100_m1_e0 | homalt | 99.8719 | 99.8775 | 99.8664 | 60.1447 | 17938 | 22 | 17938 | 24 | 14 | 58.3333 | |
| ckim-isaac | SNP | * | func_cds | * | 99.4183 | 98.8760 | 99.9666 | 20.1352 | 17946 | 204 | 17946 | 6 | 2 | 33.3333 | |
| asubramanian-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 97.3939 | 98.8110 | 96.0169 | 66.9230 | 17950 | 216 | 18586 | 771 | 551 | 71.4656 | |
| asubramanian-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 97.3939 | 98.8110 | 96.0169 | 66.9230 | 17950 | 216 | 18586 | 771 | 551 | 71.4656 | |
| jli-custom | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 98.8579 | 98.3570 | 99.3639 | 41.8770 | 17959 | 300 | 17963 | 115 | 109 | 94.7826 | |
| gduggal-bwavard | SNP | * | func_cds | * | 99.3111 | 98.9862 | 99.6380 | 30.1556 | 17966 | 184 | 17892 | 65 | 23 | 35.3846 | |
| ltrigg-rtg1 | INDEL | I1_5 | HG002complexvar | het | 99.2372 | 98.7905 | 99.6881 | 51.9353 | 17969 | 220 | 17257 | 54 | 28 | 51.8519 | |
| cchapple-custom | INDEL | I1_5 | HG002complexvar | het | 99.2036 | 98.7960 | 99.6147 | 56.4110 | 17970 | 219 | 19130 | 74 | 62 | 83.7838 | |
| gduggal-snapvard | SNP | * | func_cds | * | 99.3360 | 99.0138 | 99.6603 | 29.3432 | 17971 | 179 | 17895 | 61 | 23 | 37.7049 | |
| gduggal-snapfb | SNP | ti | map_l100_m2_e1 | homalt | 98.4714 | 97.1829 | 99.7946 | 68.9893 | 17973 | 521 | 17974 | 37 | 21 | 56.7568 | |
| gduggal-bwavard | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 92.2695 | 91.8075 | 92.7362 | 81.6429 | 17975 | 1604 | 17848 | 1398 | 224 | 16.0229 | |
| gduggal-bwavard | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 92.2695 | 91.8075 | 92.7362 | 81.6429 | 17975 | 1604 | 17848 | 1398 | 224 | 16.0229 | |
| gduggal-bwavard | SNP | ti | map_l100_m2_e1 | homalt | 98.5250 | 97.1937 | 99.8932 | 62.3163 | 17975 | 519 | 17773 | 19 | 15 | 78.9474 | |
| asubramanian-gatk | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | * | 98.4506 | 98.8726 | 98.0323 | 41.8823 | 17978 | 205 | 17985 | 361 | 4 | 1.1080 | |
| jpowers-varprowl | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | * | 97.9586 | 98.9331 | 97.0031 | 50.6413 | 17989 | 194 | 18029 | 557 | 149 | 26.7504 | |
| raldana-dualsentieon | INDEL | I1_5 | HG002complexvar | het | 99.3867 | 98.9004 | 99.8777 | 56.7573 | 17989 | 200 | 17970 | 22 | 13 | 59.0909 | |
| gduggal-snapfb | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | * | 90.7849 | 98.9826 | 83.8412 | 55.2905 | 17998 | 185 | 18103 | 3489 | 157 | 4.4999 | |
| ndellapenna-hhga | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | * | 99.2994 | 98.9826 | 99.6182 | 37.5156 | 17998 | 185 | 18004 | 69 | 46 | 66.6667 | |
| mlin-fermikit | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 94.8405 | 91.9659 | 97.9006 | 68.3752 | 18006 | 1573 | 18000 | 386 | 15 | 3.8860 | |
| mlin-fermikit | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 94.8405 | 91.9659 | 97.9006 | 68.3752 | 18006 | 1573 | 18000 | 386 | 15 | 3.8860 | |
| gduggal-bwaplat | SNP | * | func_cds | * | 99.4779 | 99.2121 | 99.7452 | 34.2475 | 18007 | 143 | 18007 | 46 | 4 | 8.6957 | |
| mlin-fermikit | SNP | * | func_cds | * | 99.4453 | 99.2617 | 99.6295 | 19.0809 | 18016 | 134 | 18016 | 67 | 48 | 71.6418 | |
| gduggal-bwafb | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | * | 98.5802 | 99.1091 | 98.0569 | 48.2748 | 18021 | 162 | 18066 | 358 | 80 | 22.3464 | |
| gduggal-bwafb | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | * | 93.9385 | 90.7361 | 97.3752 | 52.7808 | 18022 | 1840 | 18957 | 511 | 394 | 77.1037 | |
| hfeng-pmm2 | INDEL | I1_5 | HG002complexvar | het | 99.4756 | 99.0819 | 99.8724 | 57.6818 | 18022 | 167 | 18002 | 23 | 11 | 47.8261 | |
| cchapple-custom | SNP | ti | map_l100_m2_e1 | homalt | 98.7103 | 97.4640 | 99.9889 | 57.8502 | 18025 | 469 | 18020 | 2 | 2 | 100.0000 | |
| egarrison-hhga | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | * | 99.4319 | 99.1366 | 99.7290 | 37.0539 | 18026 | 157 | 18031 | 49 | 28 | 57.1429 | |
| gduggal-bwafb | SNP | ti | map_l125_m1_e0 | het | 98.5889 | 98.6861 | 98.4920 | 74.2606 | 18026 | 240 | 18026 | 276 | 77 | 27.8986 | |
| gduggal-snapplat | SNP | * | func_cds | * | 99.4703 | 99.3223 | 99.6187 | 31.7106 | 18027 | 123 | 18027 | 69 | 5 | 7.2464 | |
| hfeng-pmm2 | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | * | 99.4758 | 99.1531 | 99.8007 | 37.5709 | 18029 | 154 | 18026 | 36 | 2 | 5.5556 | |
| hfeng-pmm1 | INDEL | I1_5 | HG002complexvar | het | 99.4978 | 99.1313 | 99.8669 | 57.6162 | 18031 | 158 | 18012 | 24 | 10 | 41.6667 | |
| astatham-gatk | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | * | 99.5556 | 99.1696 | 99.9446 | 40.0259 | 18032 | 151 | 18029 | 10 | 2 | 20.0000 | |
| egarrison-hhga | SNP | ti | map_l125_m1_e0 | het | 99.2515 | 98.7299 | 99.7787 | 70.5410 | 18034 | 232 | 18034 | 40 | 16 | 40.0000 | |