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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
3501-3550 / 86044 show all | |||||||||||||||
| bgallagher-sentieon | SNP | * | map_l100_m0_e0 | het | 98.8545 | 99.3162 | 98.3971 | 73.2385 | 21060 | 145 | 21056 | 343 | 49 | 14.2857 | |
| jpowers-varprowl | SNP | ti | map_l100_m0_e0 | * | 97.4083 | 96.6745 | 98.1533 | 73.0718 | 21047 | 724 | 21048 | 396 | 147 | 37.1212 | |
| hfeng-pmm3 | SNP | * | map_l100_m0_e0 | het | 99.3509 | 99.2596 | 99.4424 | 70.0348 | 21048 | 157 | 21044 | 118 | 11 | 9.3220 | |
| dgrover-gatk | SNP | * | map_l100_m0_e0 | het | 99.0469 | 99.2549 | 98.8398 | 75.0691 | 21047 | 158 | 21043 | 247 | 48 | 19.4332 | |
| hfeng-pmm2 | SNP | * | map_l100_m0_e0 | het | 99.0069 | 99.2124 | 98.8022 | 73.2241 | 21038 | 167 | 21034 | 255 | 23 | 9.0196 | |
| cchapple-custom | SNP | ti | map_l100_m0_e0 | * | 96.8619 | 96.6377 | 97.0872 | 70.6515 | 21039 | 732 | 21032 | 631 | 173 | 27.4168 | |
| gduggal-bwavard | SNP | * | HG002compoundhet | * | 84.7137 | 82.2128 | 87.3715 | 45.7405 | 21229 | 4593 | 20991 | 3034 | 2565 | 84.5419 | |
| gduggal-bwavard | SNP | ti | map_l100_m0_e0 | * | 95.3330 | 97.2027 | 93.5339 | 77.3132 | 21162 | 609 | 20989 | 1451 | 95 | 6.5472 | |
| jlack-gatk | SNP | * | map_l100_m0_e0 | het | 93.8309 | 98.9295 | 89.2321 | 81.9092 | 20978 | 227 | 20974 | 2531 | 189 | 7.4674 | |
| qzeng-custom | SNP | * | map_l150_m1_e0 | * | 80.7203 | 69.2737 | 96.6985 | 86.4603 | 21204 | 9405 | 20971 | 716 | 612 | 85.4749 | |
| hfeng-pmm1 | SNP | * | map_l100_m0_e0 | het | 99.2124 | 98.9106 | 99.5159 | 69.6159 | 20974 | 231 | 20970 | 102 | 27 | 26.4706 | |
| ckim-dragen | SNP | * | map_l100_m0_e0 | het | 97.6312 | 98.8022 | 96.4876 | 75.1408 | 20951 | 254 | 20960 | 763 | 67 | 8.7811 | |
| rpoplin-dv42 | SNP | * | map_l100_m0_e0 | het | 98.8725 | 98.8493 | 98.8958 | 68.4376 | 20961 | 244 | 20957 | 234 | 116 | 49.5726 | |
| raldana-dualsentieon | SNP | * | map_l100_m0_e0 | het | 98.7044 | 98.8116 | 98.5974 | 70.4890 | 20953 | 252 | 20949 | 298 | 3 | 1.0067 | |
| qzeng-custom | SNP | ti | map_l125_m1_e0 | * | 82.7982 | 71.8971 | 97.5960 | 82.1188 | 21091 | 8244 | 20948 | 516 | 435 | 84.3023 | |
| gduggal-snapfb | SNP | ti | map_l100_m0_e0 | * | 96.4920 | 96.2060 | 96.7797 | 70.0719 | 20945 | 826 | 20947 | 697 | 344 | 49.3544 | |
| ghariani-varprowl | SNP | * | map_l100_m0_e0 | het | 97.0530 | 98.7692 | 95.3955 | 77.5266 | 20944 | 261 | 20946 | 1011 | 206 | 20.3759 | |
| anovak-vg | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 61.2290 | 64.8241 | 58.0117 | 44.0961 | 11551 | 6268 | 20937 | 15154 | 11698 | 77.1941 | |
| gduggal-bwafb | SNP | * | map_l100_m0_e0 | het | 98.3117 | 98.5852 | 98.0398 | 73.2020 | 20905 | 300 | 20906 | 418 | 97 | 23.2057 | |
| jli-custom | SNP | * | map_l100_m0_e0 | het | 98.8927 | 98.5522 | 99.2355 | 65.8743 | 20898 | 307 | 20898 | 161 | 48 | 29.8137 | |
| egarrison-hhga | SNP | * | map_l100_m0_e0 | het | 99.1151 | 98.5051 | 99.7326 | 69.3594 | 20888 | 317 | 20889 | 56 | 24 | 42.8571 | |
| asubramanian-gatk | SNP | * | map_l100_m1_e0 | het | 63.0315 | 46.0636 | 99.7898 | 86.5707 | 20894 | 24465 | 20888 | 44 | 12 | 27.2727 | |
| gduggal-snapvard | SNP | * | HG002compoundhet | * | 79.9672 | 80.6669 | 79.2796 | 52.8107 | 20829 | 4992 | 20864 | 5453 | 2407 | 44.1408 | |
| gduggal-bwafb | INDEL | D1_5 | HG002complexvar | het | 98.1510 | 96.8794 | 99.4564 | 54.4051 | 20117 | 648 | 20856 | 114 | 44 | 38.5965 | |
| qzeng-custom | SNP | * | map_l100_m1_e0 | homalt | 87.6866 | 78.4579 | 99.3758 | 57.2534 | 21186 | 5817 | 20855 | 131 | 129 | 98.4733 | |
| gduggal-bwaplat | INDEL | * | HG002compoundhet | * | 80.3779 | 69.5961 | 95.1127 | 70.6361 | 20851 | 9109 | 20843 | 1071 | 677 | 63.2120 | |
| ciseli-custom | SNP | * | map_l125_m2_e0 | het | 76.6942 | 71.0212 | 83.3520 | 81.2570 | 20822 | 8496 | 20798 | 4154 | 134 | 3.2258 | |
| astatham-gatk | SNP | tv | map_l100_m1_e0 | * | 91.7374 | 84.8986 | 99.7745 | 70.4613 | 20801 | 3700 | 20797 | 47 | 16 | 34.0426 | |
| jmaeng-gatk | SNP | * | map_l150_m1_e0 | * | 80.0329 | 67.8918 | 97.4620 | 88.1625 | 20781 | 9828 | 20775 | 541 | 41 | 7.5786 | |
| qzeng-custom | SNP | * | map_l125_m1_e0 | het | 83.6399 | 73.7567 | 96.5816 | 86.1149 | 20941 | 7451 | 20766 | 735 | 611 | 83.1293 | |
| ckim-gatk | SNP | * | map_l150_m1_e0 | * | 80.0337 | 67.8232 | 97.6062 | 88.0251 | 20760 | 9849 | 20754 | 509 | 42 | 8.2515 | |
| qzeng-custom | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 91.7828 | 89.8112 | 93.8428 | 47.3895 | 19983 | 2267 | 20728 | 1360 | 1094 | 80.4412 | |
| ndellapenna-hhga | SNP | * | map_l100_m0_e0 | het | 98.6808 | 97.7128 | 99.6681 | 67.9602 | 20720 | 485 | 20721 | 69 | 32 | 46.3768 | |
| bgallagher-sentieon | INDEL | D1_5 | HG002complexvar | het | 99.8096 | 99.7111 | 99.9084 | 56.0707 | 20705 | 60 | 20713 | 19 | 12 | 63.1579 | |
| dgrover-gatk | INDEL | D1_5 | HG002complexvar | het | 99.8048 | 99.6966 | 99.9132 | 56.2931 | 20702 | 63 | 20710 | 18 | 11 | 61.1111 | |
| ckim-gatk | INDEL | D1_5 | HG002complexvar | het | 99.7759 | 99.7111 | 99.8409 | 56.3066 | 20705 | 60 | 20710 | 33 | 15 | 45.4545 | |
| jlack-gatk | INDEL | D1_5 | HG002complexvar | het | 99.5570 | 99.5377 | 99.5763 | 55.9428 | 20669 | 96 | 20681 | 88 | 29 | 32.9545 | |
| jmaeng-gatk | INDEL | D1_5 | HG002complexvar | het | 99.6962 | 99.5666 | 99.8262 | 56.4161 | 20675 | 90 | 20679 | 36 | 18 | 50.0000 | |
| ckim-isaac | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 97.0619 | 94.5157 | 99.7491 | 65.9214 | 20698 | 1201 | 20677 | 52 | 34 | 65.3846 | |
| qzeng-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 94.6261 | 95.9485 | 93.3397 | 58.3275 | 17430 | 736 | 20671 | 1475 | 1218 | 82.5763 | |
| qzeng-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 94.6261 | 95.9485 | 93.3397 | 58.3275 | 17430 | 736 | 20671 | 1475 | 1218 | 82.5763 | |
| jli-custom | INDEL | D1_5 | HG002complexvar | het | 99.7322 | 99.5618 | 99.9033 | 54.7904 | 20674 | 91 | 20667 | 20 | 6 | 30.0000 | |
| astatham-gatk | INDEL | D1_5 | HG002complexvar | het | 99.6863 | 99.4751 | 99.8985 | 56.1634 | 20656 | 109 | 20662 | 21 | 12 | 57.1429 | |
| ckim-vqsr | INDEL | D1_5 | HG002complexvar | het | 99.6767 | 99.4799 | 99.8743 | 56.3731 | 20657 | 108 | 20661 | 26 | 12 | 46.1538 | |
| gduggal-snapvard | SNP | ti | map_l100_m0_e0 | * | 92.9211 | 95.6915 | 90.3065 | 76.7821 | 20833 | 938 | 20654 | 2217 | 198 | 8.9310 | |
| rpoplin-dv42 | INDEL | D1_5 | HG002complexvar | het | 99.5249 | 99.3402 | 99.7103 | 55.5097 | 20628 | 137 | 20652 | 60 | 48 | 80.0000 | |
| gduggal-snapfb | INDEL | D1_5 | HG002complexvar | het | 94.7486 | 94.6159 | 94.8816 | 54.6441 | 19647 | 1118 | 20632 | 1113 | 329 | 29.5597 | |
| ckim-dragen | INDEL | D1_5 | HG002complexvar | het | 99.7370 | 99.6292 | 99.8451 | 55.8027 | 20688 | 77 | 20632 | 32 | 11 | 34.3750 | |
| ltrigg-rtg1 | SNP | * | map_l100_m0_e0 | het | 98.4261 | 97.1705 | 99.7145 | 55.4883 | 20605 | 600 | 20610 | 59 | 8 | 13.5593 | |
| hfeng-pmm3 | SNP | ti | map_l150_m2_e1 | * | 99.5026 | 99.4402 | 99.5651 | 75.5918 | 20607 | 116 | 20603 | 90 | 14 | 15.5556 | |