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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
85801-85850 / 86044 show all | |||||||||||||||
| eyeh-varpipe | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 75.9304 | 73.7693 | 78.2218 | 69.0738 | 48209 | 17142 | 62008 | 17264 | 16584 | 96.0612 | |
| eyeh-varpipe | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 75.9304 | 73.7693 | 78.2218 | 69.0738 | 48209 | 17142 | 62008 | 17264 | 16584 | 96.0612 | |
| astatham-gatk | SNP | * | map_siren | * | 93.7139 | 88.2540 | 99.8939 | 58.6796 | 129052 | 17176 | 129029 | 137 | 67 | 48.9051 | |
| ghariani-varprowl | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 47.3491 | 46.0834 | 48.6863 | 59.5527 | 14743 | 17249 | 14732 | 15527 | 15257 | 98.2611 | |
| gduggal-bwavard | SNP | * | * | het | 99.2301 | 99.0784 | 99.3822 | 26.2938 | 1856334 | 17267 | 1845056 | 11469 | 3208 | 27.9711 | |
| gduggal-snapvard | INDEL | * | HG002compoundhet | * | 47.5012 | 42.0784 | 54.5285 | 56.5286 | 12605 | 17351 | 24630 | 20539 | 16069 | 78.2365 | |
| ckim-isaac | SNP | tv | * | het | 98.4858 | 97.0571 | 99.9572 | 19.2906 | 574291 | 17413 | 574576 | 246 | 32 | 13.0081 | |
| mlin-fermikit | SNP | ti | map_siren | het | 83.4382 | 72.0464 | 99.1091 | 46.3223 | 44944 | 17438 | 44944 | 404 | 15 | 3.7129 | |
| ckim-vqsr | SNP | ti | map_l100_m1_e0 | * | 77.5493 | 63.5768 | 99.3932 | 81.5266 | 30473 | 17458 | 30468 | 186 | 13 | 6.9893 | |
| ciseli-custom | SNP | * | map_siren | * | 89.7321 | 87.9989 | 91.5349 | 59.0239 | 128679 | 17549 | 128115 | 11848 | 2967 | 25.0422 | |
| ckim-isaac | SNP | * | map_siren | homalt | 81.0505 | 68.1522 | 99.9707 | 46.5592 | 37590 | 17566 | 37591 | 11 | 11 | 100.0000 | |
| gduggal-snapplat | INDEL | I6_15 | * | * | 41.4207 | 29.2310 | 71.0492 | 57.1777 | 7256 | 17567 | 7117 | 2900 | 649 | 22.3793 | |
| ckim-vqsr | SNP | ti | map_l100_m2_e0 | * | 77.9188 | 64.0796 | 99.3822 | 82.5443 | 31374 | 17587 | 31369 | 195 | 15 | 7.6923 | |
| ckim-vqsr | SNP | * | * | het | 99.4736 | 99.0611 | 99.8894 | 26.9578 | 1855996 | 17591 | 1855876 | 2054 | 101 | 4.9172 | |
| mlin-fermikit | INDEL | * | * | * | 95.5997 | 94.8918 | 96.3183 | 54.9677 | 326942 | 17600 | 326572 | 12483 | 12097 | 96.9078 | |
| mlin-fermikit | SNP | * | map_l150_m1_e0 | * | 56.5558 | 42.3405 | 85.1406 | 61.3631 | 12960 | 17649 | 12955 | 2261 | 1991 | 88.0584 | |
| ckim-vqsr | SNP | ti | map_l100_m2_e1 | * | 78.0470 | 64.2498 | 99.3903 | 82.5096 | 31794 | 17691 | 31789 | 195 | 15 | 7.6923 | |
| gduggal-snapplat | SNP | tv | * | * | 98.6169 | 98.1754 | 99.0623 | 31.7051 | 952005 | 17693 | 952368 | 9015 | 1026 | 11.3810 | |
| jpowers-varprowl | INDEL | D1_5 | * | * | 89.7951 | 87.9294 | 91.7417 | 58.6226 | 129032 | 17713 | 128909 | 11604 | 11168 | 96.2427 | |
| mlin-fermikit | SNP | * | map_l100_m0_e0 | * | 59.6148 | 45.9548 | 84.8308 | 53.4081 | 15092 | 17749 | 15088 | 2698 | 2419 | 89.6590 | |
| gduggal-snapfb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 77.3261 | 72.6018 | 82.7081 | 62.1191 | 47446 | 17905 | 52604 | 10998 | 5193 | 47.2177 | |
| gduggal-snapfb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 77.3261 | 72.6018 | 82.7081 | 62.1191 | 47446 | 17905 | 52604 | 10998 | 5193 | 47.2177 | |
| mlin-fermikit | SNP | * | map_l150_m2_e0 | * | 57.7918 | 43.6268 | 85.5779 | 66.0006 | 13896 | 17956 | 13891 | 2341 | 2055 | 87.7830 | |
| ckim-vqsr | SNP | * | HG002complexvar | * | 98.7826 | 97.6098 | 99.9840 | 19.7255 | 736350 | 18031 | 736201 | 118 | 58 | 49.1525 | |
| ciseli-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 53.8310 | 52.3323 | 55.4180 | 55.7723 | 19835 | 18067 | 20150 | 16210 | 13033 | 80.4010 | |
| gduggal-snapvard | INDEL | I1_5 | * | * | 88.2138 | 87.9937 | 88.4349 | 55.6066 | 132574 | 18089 | 133297 | 17432 | 13523 | 77.5757 | |
| mlin-fermikit | SNP | * | map_l150_m2_e1 | * | 57.9744 | 43.8280 | 85.6051 | 66.1929 | 14117 | 18093 | 14112 | 2373 | 2083 | 87.7792 | |
| anovak-vg | INDEL | * | HG002complexvar | het | 72.0208 | 60.7851 | 88.3522 | 57.0408 | 28090 | 18122 | 30129 | 3972 | 2361 | 59.4411 | |
| mlin-fermikit | SNP | tv | * | * | 98.7665 | 98.1308 | 99.4104 | 19.3147 | 951572 | 18126 | 951506 | 5643 | 4116 | 72.9399 | |
| gduggal-bwaplat | SNP | * | map_l125_m1_e0 | * | 74.4387 | 59.4965 | 99.4030 | 86.9422 | 26968 | 18359 | 26975 | 162 | 46 | 28.3951 | |
| gduggal-snapvard | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 54.3999 | 51.2849 | 57.9178 | 44.7526 | 19438 | 18464 | 33023 | 23994 | 20921 | 87.1926 | |
| gduggal-bwavard | INDEL | I1_5 | * | * | 89.8158 | 87.7423 | 91.9898 | 54.5219 | 132196 | 18468 | 131206 | 11425 | 10755 | 94.1357 | |
| gduggal-bwaplat | SNP | * | map_l125_m2_e0 | * | 75.1671 | 60.4306 | 99.4087 | 87.7400 | 28235 | 18488 | 28242 | 168 | 47 | 27.9762 | |
| gduggal-bwaplat | SNP | * | map_l125_m2_e1 | * | 75.3654 | 60.6881 | 99.4067 | 87.7186 | 28646 | 18556 | 28653 | 171 | 47 | 27.4854 | |
| anovak-vg | INDEL | * | HG002compoundhet | hetalt | 0.0000 | 25.9095 | 0.0000 | 0.0000 | 6524 | 18656 | 0 | 0 | 0 | ||
| anovak-vg | INDEL | * | * | hetalt | 0.0000 | 25.9341 | 0.0000 | 0.0000 | 6545 | 18692 | 0 | 0 | 0 | ||
| ciseli-custom | INDEL | I6_15 | * | * | 35.4599 | 24.6948 | 62.8636 | 46.3768 | 6130 | 18693 | 6094 | 3600 | 3400 | 94.4444 | |
| jpowers-varprowl | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 43.8182 | 41.5354 | 46.3666 | 49.7641 | 13288 | 18704 | 13278 | 15359 | 15221 | 99.1015 | |
| mlin-fermikit | SNP | ti | map_l100_m1_e0 | * | 73.0893 | 60.7644 | 91.6861 | 50.6018 | 29125 | 18806 | 29125 | 2641 | 2337 | 88.4892 | |
| gduggal-snapplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 44.0360 | 38.0774 | 52.2053 | 83.4017 | 11606 | 18874 | 14180 | 12982 | 2052 | 15.8065 | |
| gduggal-snapplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 44.0360 | 38.0774 | 52.2053 | 83.4017 | 11606 | 18874 | 14180 | 12982 | 2052 | 15.8065 | |
| mlin-fermikit | SNP | ti | map_l100_m2_e0 | * | 73.5756 | 61.3876 | 91.8021 | 54.4848 | 30056 | 18905 | 30056 | 2684 | 2362 | 88.0030 | |
| mlin-fermikit | SNP | ti | map_l100_m2_e1 | * | 73.7873 | 61.6490 | 91.8775 | 54.5530 | 30507 | 18978 | 30507 | 2697 | 2372 | 87.9496 | |
| gduggal-snapplat | INDEL | * | HG002compoundhet | * | 42.2745 | 36.5854 | 50.0587 | 72.5688 | 10961 | 18999 | 11522 | 11495 | 5404 | 47.0117 | |
| asubramanian-gatk | SNP | * | map_l125_m1_e0 | het | 49.6482 | 33.0516 | 99.7236 | 92.3828 | 9384 | 19008 | 9381 | 26 | 6 | 23.0769 | |
| ckim-isaac | SNP | * | map_l125_m1_e0 | * | 73.2800 | 57.9125 | 99.7492 | 70.8000 | 26250 | 19077 | 26252 | 66 | 16 | 24.2424 | |
| gduggal-snapplat | SNP | * | HG002complexvar | * | 97.9967 | 97.4708 | 98.5284 | 22.9400 | 735305 | 19080 | 736073 | 10994 | 1866 | 16.9729 | |
| ciseli-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 56.8514 | 55.5879 | 58.1738 | 61.2449 | 24089 | 19246 | 24394 | 17539 | 13551 | 77.2621 | |
| gduggal-snapvard | SNP | * | * | het | 98.8907 | 98.9717 | 98.8098 | 27.4520 | 1854334 | 19266 | 1842523 | 22194 | 3216 | 14.4904 | |
| asubramanian-gatk | SNP | * | map_l125_m2_e0 | het | 50.9572 | 34.2281 | 99.6721 | 92.5837 | 10035 | 19283 | 10032 | 33 | 8 | 24.2424 | |