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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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81301-81350 / 86044 show all | |||||||||||||||
| asubramanian-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 91.6951 | 91.4187 | 91.9731 | 70.0049 | 5561 | 522 | 5603 | 489 | 348 | 71.1656 | |
| jpowers-varprowl | SNP | ti | map_l125_m2_e1 | * | 97.7851 | 97.1965 | 98.3808 | 76.1142 | 29712 | 857 | 29712 | 489 | 165 | 33.7423 | |
| gduggal-snapplat | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 48.5964 | 51.3854 | 46.0946 | 95.3289 | 408 | 386 | 419 | 490 | 30 | 6.1225 | |
| ckim-dragen | SNP | ti | map_l150_m1_e0 | * | 98.2015 | 98.8636 | 97.5482 | 76.3868 | 19488 | 224 | 19495 | 490 | 66 | 13.4694 | |
| ciseli-custom | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 85.0862 | 98.1976 | 75.0636 | 85.4109 | 1471 | 27 | 1475 | 490 | 97 | 19.7959 | |
| mlin-fermikit | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 93.3394 | 94.5919 | 92.1197 | 68.0226 | 5772 | 330 | 5728 | 490 | 477 | 97.3469 | |
| anovak-vg | SNP | ti | map_l250_m0_e0 | het | 69.1155 | 80.6210 | 60.4839 | 96.0595 | 753 | 181 | 750 | 490 | 108 | 22.0408 | |
| gduggal-bwavard | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 66.5015 | 91.0448 | 52.3810 | 62.2662 | 549 | 54 | 539 | 490 | 476 | 97.1429 | |
| eyeh-varpipe | INDEL | D6_15 | HG002complexvar | homalt | 74.1328 | 83.6612 | 66.5529 | 48.6865 | 978 | 191 | 975 | 490 | 482 | 98.3673 | |
| jlack-gatk | INDEL | * | HG002complexvar | * | 99.2231 | 99.0863 | 99.3603 | 58.0205 | 76235 | 703 | 76113 | 490 | 357 | 72.8571 | |
| hfeng-pmm3 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 97.9085 | 96.6244 | 99.2272 | 64.2470 | 63145 | 2206 | 62918 | 490 | 402 | 82.0408 | |
| hfeng-pmm3 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 97.9085 | 96.6244 | 99.2272 | 64.2470 | 63145 | 2206 | 62918 | 490 | 402 | 82.0408 | |
| jlack-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 96.2893 | 95.0573 | 97.5536 | 44.7868 | 19578 | 1018 | 19579 | 491 | 468 | 95.3157 | |
| ckim-dragen | SNP | tv | map_l100_m2_e0 | het | 98.0513 | 99.1697 | 96.9579 | 75.2085 | 15646 | 131 | 15649 | 491 | 32 | 6.5173 | |
| jpowers-varprowl | INDEL | * | map_siren | het | 92.1013 | 94.6539 | 89.6827 | 84.2292 | 4267 | 241 | 4268 | 491 | 415 | 84.5214 | |
| jpowers-varprowl | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_51to200 | het | 40.8888 | 58.1818 | 31.5202 | 57.4228 | 224 | 161 | 226 | 491 | 480 | 97.7597 | |
| rpoplin-dv42 | INDEL | * | HG002complexvar | * | 98.9923 | 98.6301 | 99.3571 | 63.4999 | 75884 | 1054 | 75884 | 491 | 440 | 89.6130 | |
| raldana-dualsentieon | INDEL | I1_5 | * | * | 99.2891 | 98.9095 | 99.6717 | 56.6470 | 149021 | 1643 | 149065 | 491 | 422 | 85.9470 | |
| eyeh-varpipe | SNP | ti | map_l100_m2_e0 | * | 99.3504 | 99.7181 | 98.9854 | 68.9913 | 48823 | 138 | 47903 | 491 | 32 | 6.5173 | |
| eyeh-varpipe | SNP | ti | segdup | * | 98.6842 | 99.8874 | 97.5096 | 89.9888 | 19515 | 22 | 19225 | 491 | 13 | 2.6477 | |
| gduggal-bwaplat | SNP | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 89.7995 | 82.2060 | 98.9387 | 71.6625 | 45732 | 9899 | 45775 | 491 | 144 | 29.3279 | |
| gduggal-bwavard | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 29.8387 | 20.4965 | 54.8298 | 62.6973 | 611 | 2370 | 596 | 491 | 477 | 97.1487 | |
| eyeh-varpipe | SNP | * | map_l150_m0_e0 | * | 97.7007 | 99.5180 | 95.9486 | 82.7662 | 11974 | 58 | 11652 | 492 | 15 | 3.0488 | |
| eyeh-varpipe | SNP | tv | segdup | het | 95.3870 | 99.8298 | 91.3228 | 92.1659 | 5278 | 9 | 5178 | 492 | 4 | 0.8130 | |
| ckim-dragen | SNP | tv | map_l100_m2_e1 | het | 98.0614 | 99.1655 | 96.9816 | 75.2723 | 15805 | 133 | 15808 | 492 | 32 | 6.5041 | |
| hfeng-pmm3 | INDEL | * | * | homalt | 99.7023 | 99.7971 | 99.6077 | 55.0410 | 124918 | 254 | 124928 | 492 | 475 | 96.5447 | |
| jlack-gatk | SNP | ti | map_l250_m2_e0 | * | 94.3425 | 98.0631 | 90.8939 | 92.7804 | 4911 | 97 | 4911 | 492 | 44 | 8.9431 | |
| jlack-gatk | SNP | ti | map_l250_m2_e1 | het | 92.2399 | 98.3631 | 86.8344 | 94.0808 | 3245 | 54 | 3245 | 492 | 42 | 8.5366 | |
| ghariani-varprowl | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 97.6620 | 99.4893 | 95.9007 | 73.2635 | 11493 | 59 | 11510 | 492 | 263 | 53.4553 | |
| ghariani-varprowl | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 97.6620 | 99.4893 | 95.9007 | 73.2635 | 11493 | 59 | 11510 | 492 | 263 | 53.4553 | |
| ghariani-varprowl | SNP | tv | map_l150_m1_e0 | * | 96.9968 | 98.4146 | 95.6193 | 80.2097 | 10739 | 173 | 10739 | 492 | 89 | 18.0894 | |
| rpoplin-dv42 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 89.7118 | 87.9829 | 91.5099 | 73.1427 | 5352 | 731 | 5303 | 492 | 469 | 95.3252 | |
| anovak-vg | SNP | * | segdup | het | 97.2290 | 97.3206 | 97.1375 | 93.7111 | 16853 | 464 | 16696 | 492 | 128 | 26.0163 | |
| astatham-gatk | INDEL | I1_5 | * | * | 99.4616 | 99.2520 | 99.6722 | 58.6147 | 149537 | 1127 | 149586 | 492 | 402 | 81.7073 | |
| ciseli-custom | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 87.0437 | 97.4877 | 78.6210 | 66.4142 | 1785 | 46 | 1813 | 493 | 9 | 1.8256 | |
| ckim-gatk | SNP | tv | map_l100_m2_e0 | het | 91.4895 | 86.9494 | 96.5299 | 84.2447 | 13718 | 2059 | 13714 | 493 | 16 | 3.2454 | |
| cchapple-custom | SNP | tv | map_l150_m1_e0 | * | 96.2415 | 96.9483 | 95.5449 | 77.7956 | 10579 | 333 | 10573 | 493 | 81 | 16.4300 | |
| cchapple-custom | SNP | tv | map_l150_m1_e0 | het | 95.1002 | 97.0775 | 93.2019 | 81.0524 | 6743 | 203 | 6759 | 493 | 81 | 16.4300 | |
| mlin-fermikit | INDEL | I16_PLUS | HG002compoundhet | * | 58.0506 | 50.3033 | 68.6187 | 53.6851 | 1078 | 1065 | 1078 | 493 | 492 | 99.7972 | |
| mlin-fermikit | SNP | ti | map_l150_m0_e0 | homalt | 53.2251 | 42.7381 | 70.5320 | 59.3142 | 1180 | 1581 | 1180 | 493 | 459 | 93.1034 | |
| ghariani-varprowl | SNP | * | map_l250_m2_e0 | het | 94.4212 | 97.9207 | 91.1633 | 92.2470 | 5086 | 108 | 5086 | 493 | 83 | 16.8357 | |
| gduggal-snapplat | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 56.5111 | 56.6123 | 56.4103 | 93.4064 | 625 | 479 | 638 | 493 | 43 | 8.7221 | |
| ghariani-varprowl | SNP | tv | map_l100_m0_e0 | * | 97.0755 | 98.5204 | 95.6724 | 76.1776 | 10920 | 164 | 10921 | 494 | 87 | 17.6113 | |
| gduggal-snapvard | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 89.8366 | 96.6865 | 83.8931 | 79.2152 | 2597 | 89 | 2573 | 494 | 7 | 1.4170 | |
| anovak-vg | SNP | ti | map_l250_m0_e0 | * | 72.4774 | 77.4453 | 68.1085 | 95.7045 | 1061 | 309 | 1055 | 494 | 111 | 22.4696 | |
| astatham-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.6446 | 98.9272 | 98.3637 | 73.5579 | 30153 | 327 | 29696 | 494 | 401 | 81.1741 | |
| astatham-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.6446 | 98.9272 | 98.3637 | 73.5579 | 30153 | 327 | 29696 | 494 | 401 | 81.1741 | |
| ndellapenna-hhga | INDEL | D16_PLUS | * | * | 85.7572 | 80.4393 | 91.8280 | 64.0820 | 5457 | 1327 | 5551 | 494 | 372 | 75.3036 | |
| ckim-gatk | INDEL | D1_5 | * | het | 99.6268 | 99.8162 | 99.4381 | 60.7761 | 87413 | 161 | 87419 | 494 | 126 | 25.5061 | |
| ckim-gatk | SNP | tv | map_l100_m2_e1 | het | 91.5697 | 87.0686 | 96.5616 | 84.2465 | 13877 | 2061 | 13873 | 494 | 16 | 3.2389 | |