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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1601-1650 / 86044 show all | |||||||||||||||
| ckim-vqsr | SNP | * | map_l100_m1_e0 | * | 76.6064 | 62.3814 | 99.2353 | 82.7403 | 45166 | 27237 | 45158 | 348 | 14 | 4.0230 | |
| egarrison-hhga | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 99.0424 | 98.7834 | 99.3028 | 71.2490 | 45146 | 556 | 45149 | 317 | 104 | 32.8076 | |
| egarrison-hhga | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 99.0424 | 98.7834 | 99.3028 | 71.2490 | 45146 | 556 | 45149 | 317 | 104 | 32.8076 | |
| bgallagher-sentieon | SNP | * | map_l100_m1_e0 | het | 99.2217 | 99.5084 | 98.9366 | 68.7750 | 45136 | 223 | 45125 | 485 | 63 | 12.9897 | |
| ltrigg-rtg2 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.3394 | 98.7572 | 97.9251 | 69.6626 | 45134 | 568 | 45544 | 965 | 45 | 4.6632 | |
| ltrigg-rtg2 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.3394 | 98.7572 | 97.9251 | 69.6626 | 45134 | 568 | 45544 | 965 | 45 | 4.6632 | |
| jpowers-varprowl | SNP | tv | map_siren | * | 98.2043 | 98.2321 | 98.1765 | 64.5026 | 45118 | 812 | 45118 | 838 | 186 | 22.1957 | |
| dgrover-gatk | SNP | * | map_l100_m1_e0 | het | 99.3755 | 99.4665 | 99.2846 | 70.4056 | 45117 | 242 | 45106 | 325 | 62 | 19.0769 | |
| gduggal-snapvard | SNP | * | map_l125_m2_e0 | * | 93.7014 | 96.5392 | 91.0256 | 79.3194 | 45106 | 1617 | 44517 | 4389 | 336 | 7.6555 | |
| hfeng-pmm3 | SNP | * | map_l100_m1_e0 | het | 99.5486 | 99.4400 | 99.6575 | 64.8095 | 45105 | 254 | 45094 | 155 | 14 | 9.0323 | |
| hfeng-pmm3 | SNP | * | map_l125_m1_e0 | * | 99.5551 | 99.4838 | 99.6266 | 69.4654 | 45093 | 234 | 45087 | 169 | 26 | 15.3846 | |
| hfeng-pmm2 | SNP | * | map_l125_m1_e0 | * | 99.3629 | 99.4529 | 99.2732 | 71.9477 | 45079 | 248 | 45073 | 330 | 39 | 11.8182 | |
| hfeng-pmm2 | SNP | * | map_l100_m1_e0 | het | 99.3136 | 99.3717 | 99.2555 | 68.4046 | 45074 | 285 | 45063 | 338 | 28 | 8.2840 | |
| hfeng-pmm3 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 99.1804 | 98.6259 | 99.7411 | 70.8758 | 45074 | 628 | 45075 | 117 | 14 | 11.9658 | |
| hfeng-pmm3 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 99.1804 | 98.6259 | 99.7411 | 70.8758 | 45074 | 628 | 45075 | 117 | 14 | 11.9658 | |
| bgallagher-sentieon | SNP | * | map_l125_m1_e0 | * | 99.2644 | 99.4418 | 99.0876 | 71.3529 | 45074 | 253 | 45068 | 415 | 70 | 16.8675 | |
| ghariani-varprowl | INDEL | * | HG002complexvar | het | 93.2466 | 97.4941 | 89.3538 | 59.7893 | 45053 | 1158 | 45020 | 5364 | 4472 | 83.3706 | |
| jpowers-varprowl | SNP | * | map_l100_m2_e0 | het | 97.3254 | 97.0883 | 97.5636 | 74.0402 | 45048 | 1351 | 45050 | 1125 | 264 | 23.4667 | |
| ghariani-varprowl | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 90.5713 | 98.5668 | 83.7756 | 81.6259 | 45047 | 655 | 45212 | 8756 | 515 | 5.8817 | |
| ghariani-varprowl | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 90.5713 | 98.5668 | 83.7756 | 81.6259 | 45047 | 655 | 45212 | 8756 | 515 | 5.8817 | |
| ndellapenna-hhga | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.8172 | 98.5296 | 99.1064 | 71.0184 | 45030 | 672 | 45029 | 406 | 140 | 34.4828 | |
| ndellapenna-hhga | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.8172 | 98.5296 | 99.1064 | 71.0184 | 45030 | 672 | 45029 | 406 | 140 | 34.4828 | |
| hfeng-pmm1 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 99.1653 | 98.5252 | 99.8138 | 69.6830 | 45028 | 674 | 45028 | 84 | 10 | 11.9048 | |
| hfeng-pmm1 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 99.1653 | 98.5252 | 99.8138 | 69.6830 | 45028 | 674 | 45028 | 84 | 10 | 11.9048 | |
| jlack-gatk | SNP | * | map_l100_m1_e0 | het | 95.6776 | 99.2570 | 92.3473 | 78.4943 | 45022 | 337 | 45011 | 3730 | 265 | 7.1046 | |
| dgrover-gatk | SNP | * | map_l125_m1_e0 | * | 99.3215 | 99.3139 | 99.3291 | 72.7346 | 45016 | 311 | 45010 | 304 | 68 | 22.3684 | |
| ckim-dragen | SNP | * | map_l100_m1_e0 | het | 98.1047 | 99.2152 | 97.0189 | 72.1356 | 45003 | 356 | 45009 | 1383 | 119 | 8.6045 | |
| raldana-dualsentieon | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.9892 | 98.4640 | 99.5201 | 68.3963 | 45000 | 702 | 45000 | 217 | 24 | 11.0599 | |
| raldana-dualsentieon | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.9892 | 98.4640 | 99.5201 | 68.3963 | 45000 | 702 | 45000 | 217 | 24 | 11.0599 | |
| egarrison-hhga | INDEL | * | HG002complexvar | het | 97.6548 | 97.3665 | 97.9448 | 54.4695 | 44995 | 1217 | 44989 | 944 | 675 | 71.5042 | |
| raldana-dualsentieon | SNP | * | map_l100_m1_e0 | het | 99.0827 | 99.1953 | 98.9703 | 66.7199 | 44994 | 365 | 44983 | 468 | 7 | 1.4957 | |
| hfeng-pmm2 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 99.0097 | 98.4465 | 99.5795 | 70.5535 | 44992 | 710 | 44993 | 190 | 10 | 5.2632 | |
| hfeng-pmm2 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 99.0097 | 98.4465 | 99.5795 | 70.5535 | 44992 | 710 | 44993 | 190 | 10 | 5.2632 | |
| gduggal-bwavard | INDEL | * | HG002complexvar | het | 91.7227 | 97.3578 | 86.7042 | 60.1106 | 44991 | 1221 | 44670 | 6850 | 5497 | 80.2482 | |
| ckim-vqsr | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.9367 | 98.4377 | 99.4408 | 75.9589 | 44988 | 714 | 44988 | 253 | 34 | 13.4387 | |
| ckim-vqsr | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.9367 | 98.4377 | 99.4408 | 75.9589 | 44988 | 714 | 44988 | 253 | 34 | 13.4387 | |
| hfeng-pmm1 | SNP | * | map_l125_m1_e0 | * | 99.4583 | 99.2389 | 99.6786 | 68.9911 | 44982 | 345 | 44976 | 145 | 41 | 28.2759 | |
| ghariani-varprowl | SNP | * | map_l100_m1_e0 | het | 97.8610 | 99.1424 | 96.6122 | 73.4449 | 44970 | 389 | 44973 | 1577 | 254 | 16.1065 | |
| rpoplin-dv42 | SNP | * | map_l100_m1_e0 | het | 99.2638 | 99.1402 | 99.3876 | 64.2170 | 44969 | 390 | 44957 | 277 | 141 | 50.9025 | |
| raldana-dualsentieon | SNP | * | map_l125_m1_e0 | * | 99.1433 | 99.2014 | 99.0854 | 69.5094 | 44965 | 362 | 44959 | 415 | 15 | 3.6145 | |
| jli-custom | SNP | * | map_l100_m1_e0 | het | 99.2812 | 99.1159 | 99.4470 | 63.0672 | 44958 | 401 | 44955 | 250 | 62 | 24.8000 | |
| hfeng-pmm1 | SNP | * | map_l100_m1_e0 | het | 99.4173 | 99.1159 | 99.7205 | 63.9471 | 44958 | 401 | 44947 | 126 | 32 | 25.3968 | |
| mlin-fermikit | SNP | ti | map_siren | het | 83.4382 | 72.0464 | 99.1091 | 46.3223 | 44944 | 17438 | 44944 | 404 | 15 | 3.7129 | |
| ckim-dragen | SNP | * | map_l125_m1_e0 | * | 98.3997 | 99.0866 | 97.7222 | 72.8507 | 44913 | 414 | 44919 | 1047 | 117 | 11.1748 | |
| jli-custom | SNP | * | map_l125_m1_e0 | * | 99.3178 | 99.0844 | 99.5522 | 66.7512 | 44912 | 415 | 44909 | 202 | 67 | 33.1683 | |
| gduggal-bwafb | SNP | * | map_l100_m1_e0 | het | 98.6881 | 99.0035 | 98.3746 | 69.4458 | 44907 | 452 | 44909 | 742 | 142 | 19.1375 | |
| egarrison-hhga | SNP | * | map_l125_m1_e0 | * | 99.4419 | 99.0690 | 99.8177 | 68.7095 | 44905 | 422 | 44905 | 82 | 41 | 50.0000 | |
| qzeng-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 97.6793 | 98.2539 | 97.1113 | 81.2381 | 44904 | 798 | 44812 | 1333 | 148 | 11.1028 | |
| qzeng-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 97.6793 | 98.2539 | 97.1113 | 81.2381 | 44904 | 798 | 44812 | 1333 | 148 | 11.1028 | |
| gduggal-snapvard | SNP | * | map_l100_m2_e0 | het | 93.3360 | 96.7693 | 90.1379 | 78.6381 | 44900 | 1499 | 44319 | 4849 | 371 | 7.6511 | |