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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
5401-5450 / 86044 show all | |||||||||||||||
| ckim-isaac | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 92.7341 | 89.2791 | 96.4674 | 63.8560 | 13907 | 1670 | 13927 | 510 | 296 | 58.0392 | |
| astatham-gatk | SNP | tv | map_l125_m2_e0 | * | 91.4434 | 84.4502 | 99.6992 | 76.7428 | 13925 | 2564 | 13923 | 42 | 14 | 33.3333 | |
| jmaeng-gatk | SNP | tv | map_siren | homalt | 89.3303 | 80.7367 | 99.9713 | 58.2484 | 13919 | 3321 | 13916 | 4 | 4 | 100.0000 | |
| gduggal-bwafb | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 94.8642 | 95.2989 | 94.4335 | 80.6105 | 13886 | 685 | 13911 | 820 | 85 | 10.3659 | |
| gduggal-bwafb | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 94.8642 | 95.2989 | 94.4335 | 80.6105 | 13886 | 685 | 13911 | 820 | 85 | 10.3659 | |
| ckim-gatk | SNP | tv | map_siren | homalt | 89.2983 | 80.6845 | 99.9712 | 58.8566 | 13910 | 3330 | 13907 | 4 | 3 | 75.0000 | |
| qzeng-custom | SNP | ti | map_l125_m2_e1 | het | 83.2669 | 73.1126 | 96.6968 | 86.6188 | 13955 | 5132 | 13905 | 475 | 387 | 81.4737 | |
| ndellapenna-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 88.1349 | 97.1942 | 80.6205 | 57.4187 | 13371 | 386 | 13903 | 3342 | 3177 | 95.0628 | |
| ndellapenna-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 88.1349 | 97.1942 | 80.6205 | 57.4187 | 13371 | 386 | 13903 | 3342 | 3177 | 95.0628 | |
| egarrison-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 87.7692 | 97.8411 | 79.5775 | 59.2240 | 13460 | 297 | 13899 | 3567 | 3388 | 94.9818 | |
| egarrison-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 87.7692 | 97.8411 | 79.5775 | 59.2240 | 13460 | 297 | 13899 | 3567 | 3388 | 94.9818 | |
| mlin-fermikit | SNP | * | map_l150_m2_e0 | * | 57.7918 | 43.6268 | 85.5779 | 66.0006 | 13896 | 17956 | 13891 | 2341 | 2055 | 87.7830 | |
| jmaeng-gatk | SNP | tv | map_l100_m2_e1 | het | 91.5298 | 87.1628 | 96.3575 | 84.5264 | 13892 | 2046 | 13888 | 525 | 14 | 2.6667 | |
| bgallagher-sentieon | SNP | ti | map_l100_m0_e0 | het | 98.9661 | 99.2777 | 98.6565 | 72.6282 | 13882 | 101 | 13879 | 189 | 28 | 14.8148 | |
| hfeng-pmm3 | SNP | ti | map_l100_m0_e0 | het | 99.3735 | 99.2634 | 99.4838 | 69.6444 | 13880 | 103 | 13877 | 72 | 7 | 9.7222 | |
| dgrover-gatk | SNP | ti | map_l100_m0_e0 | het | 99.1285 | 99.2491 | 99.0081 | 74.4536 | 13878 | 105 | 13875 | 139 | 28 | 20.1439 | |
| anovak-vg | INDEL | * | HG002compoundhet | het | 52.7411 | 50.6595 | 55.0010 | 54.9014 | 2074 | 2020 | 13874 | 11351 | 7959 | 70.1172 | |
| ckim-gatk | SNP | tv | map_l100_m2_e1 | het | 91.5697 | 87.0686 | 96.5616 | 84.2465 | 13877 | 2061 | 13873 | 494 | 16 | 3.2389 | |
| hfeng-pmm2 | SNP | ti | map_l100_m0_e0 | het | 99.0752 | 99.2276 | 98.9232 | 72.7259 | 13875 | 108 | 13872 | 151 | 12 | 7.9470 | |
| asubramanian-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 95.5812 | 92.6383 | 98.7173 | 34.2439 | 12999 | 1033 | 13853 | 180 | 164 | 91.1111 | |
| mlin-fermikit | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 95.3085 | 94.9832 | 95.6360 | 75.7457 | 13840 | 731 | 13850 | 632 | 351 | 55.5380 | |
| mlin-fermikit | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 95.3085 | 94.9832 | 95.6360 | 75.7457 | 13840 | 731 | 13850 | 632 | 351 | 55.5380 | |
| qzeng-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 93.4075 | 95.0192 | 91.8496 | 49.4485 | 10912 | 572 | 13850 | 1229 | 1043 | 84.8657 | |
| ciseli-custom | SNP | ti | map_l125_m2_e1 | het | 77.9434 | 72.5730 | 84.1721 | 81.0539 | 13852 | 5235 | 13848 | 2604 | 72 | 2.7650 | |
| gduggal-bwafb | INDEL | I6_15 | * | het | 88.0827 | 80.5342 | 97.1926 | 38.4775 | 8080 | 1953 | 13848 | 400 | 379 | 94.7500 | |
| ghariani-varprowl | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 59.0686 | 94.1575 | 43.0321 | 53.7351 | 13763 | 854 | 13840 | 18322 | 18101 | 98.7938 | |
| astatham-gatk | SNP | * | HG002compoundhet | het | 98.6981 | 97.5878 | 99.8340 | 46.2177 | 13836 | 342 | 13834 | 23 | 22 | 95.6522 | |
| egarrison-hhga | SNP | * | HG002compoundhet | het | 98.5499 | 97.5455 | 99.5752 | 43.4625 | 13830 | 348 | 13830 | 59 | 31 | 52.5424 | |
| ckim-dragen | SNP | ti | map_l100_m0_e0 | het | 97.6691 | 98.8629 | 96.5038 | 74.2830 | 13824 | 159 | 13829 | 501 | 46 | 9.1816 | |
| jlack-gatk | SNP | ti | map_l100_m0_e0 | het | 94.8297 | 98.9201 | 91.0641 | 81.0915 | 13832 | 151 | 13829 | 1357 | 128 | 9.4326 | |
| hfeng-pmm1 | SNP | ti | map_l100_m0_e0 | het | 99.2035 | 98.8772 | 99.5320 | 69.1542 | 13826 | 157 | 13823 | 65 | 16 | 24.6154 | |
| rpoplin-dv42 | SNP | ti | map_l100_m0_e0 | het | 99.0327 | 98.8486 | 99.2174 | 68.2957 | 13822 | 161 | 13819 | 109 | 66 | 60.5505 | |
| ltrigg-rtg1 | SNP | * | HG002compoundhet | het | 98.6093 | 97.5384 | 99.7040 | 42.5144 | 13829 | 349 | 13809 | 41 | 9 | 21.9512 | |
| anovak-vg | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 89.3755 | 92.9518 | 86.0642 | 79.3543 | 13544 | 1027 | 13809 | 2236 | 557 | 24.9106 | |
| anovak-vg | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 89.3755 | 92.9518 | 86.0642 | 79.3543 | 13544 | 1027 | 13809 | 2236 | 557 | 24.9106 | |
| raldana-dualsentieon | SNP | ti | map_l100_m0_e0 | het | 98.6534 | 98.7699 | 98.5371 | 69.8191 | 13811 | 172 | 13808 | 205 | 2 | 0.9756 | |
| ghariani-varprowl | SNP | ti | map_l100_m0_e0 | het | 97.4217 | 98.6269 | 96.2456 | 76.6277 | 13791 | 192 | 13792 | 538 | 130 | 24.1636 | |
| gduggal-bwafb | SNP | ti | map_l100_m0_e0 | het | 98.5173 | 98.5983 | 98.4365 | 72.6281 | 13787 | 196 | 13788 | 219 | 63 | 28.7671 | |
| jli-custom | SNP | ti | map_l100_m0_e0 | het | 98.9518 | 98.5697 | 99.3369 | 65.4782 | 13783 | 200 | 13783 | 92 | 28 | 30.4348 | |
| gduggal-snapfb | SNP | ti | func_cds | * | 99.7900 | 99.9637 | 99.6169 | 26.0872 | 13782 | 5 | 13782 | 53 | 2 | 3.7736 | |
| egarrison-hhga | SNP | ti | func_cds | * | 99.9456 | 99.9637 | 99.9275 | 22.3817 | 13782 | 5 | 13782 | 10 | 0 | 0.0000 | |
| ckim-dragen | SNP | ti | func_cds | * | 99.6097 | 99.9637 | 99.2582 | 28.1352 | 13782 | 5 | 13782 | 103 | 1 | 0.9709 | |
| ndellapenna-hhga | SNP | ti | func_cds | * | 99.9384 | 99.9565 | 99.9202 | 22.0527 | 13781 | 6 | 13781 | 11 | 0 | 0.0000 | |
| hfeng-pmm2 | SNP | ti | func_cds | * | 99.9166 | 99.9710 | 99.8623 | 22.6414 | 13783 | 4 | 13781 | 19 | 0 | 0.0000 | |
| hfeng-pmm1 | SNP | ti | func_cds | * | 99.9384 | 99.9637 | 99.9130 | 21.7209 | 13782 | 5 | 13780 | 12 | 0 | 0.0000 | |
| hfeng-pmm3 | SNP | ti | func_cds | * | 99.9347 | 99.9637 | 99.9057 | 21.9632 | 13782 | 5 | 13780 | 13 | 0 | 0.0000 | |
| jli-custom | SNP | ti | func_cds | * | 99.9166 | 99.9492 | 99.8840 | 21.7559 | 13780 | 7 | 13780 | 16 | 0 | 0.0000 | |
| gduggal-bwafb | SNP | ti | func_cds | * | 99.6673 | 99.9492 | 99.3869 | 27.6810 | 13780 | 7 | 13780 | 85 | 2 | 2.3529 | |
| jlack-gatk | SNP | ti | func_cds | * | 99.4443 | 99.9565 | 98.9373 | 29.0994 | 13781 | 6 | 13779 | 148 | 1 | 0.6757 | |
| bgallagher-sentieon | SNP | ti | func_cds | * | 99.9094 | 99.9565 | 99.8623 | 22.5049 | 13781 | 6 | 13779 | 19 | 0 | 0.0000 | |