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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
451-500 / 86044 show all | |||||||||||||||
| mlin-fermikit | SNP | * | map_l100_m0_e0 | het | 57.3538 | 40.4669 | 98.4278 | 57.0061 | 8581 | 12624 | 8577 | 137 | 4 | 2.9197 | |
| asubramanian-gatk | SNP | * | map_l125_m1_e0 | homalt | 40.5846 | 25.4599 | 99.9768 | 87.4504 | 4304 | 12601 | 4304 | 1 | 0 | 0.0000 | |
| jpowers-varprowl | SNP | * | * | het | 99.3161 | 99.3290 | 99.3033 | 25.1238 | 1861010 | 12572 | 1861335 | 13059 | 459 | 3.5148 | |
| gduggal-bwavard | SNP | * | HG002complexvar | het | 98.2730 | 97.3044 | 99.2610 | 20.1947 | 452952 | 12548 | 441659 | 3288 | 2162 | 65.7543 | |
| anovak-vg | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 63.3637 | 60.1216 | 66.9753 | 55.5677 | 18883 | 12525 | 19891 | 9808 | 7269 | 74.1130 | |
| anovak-vg | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 63.3637 | 60.1216 | 66.9753 | 55.5677 | 18883 | 12525 | 19891 | 9808 | 7269 | 74.1130 | |
| eyeh-varpipe | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 69.6812 | 67.0967 | 72.4727 | 44.4064 | 25431 | 12471 | 36677 | 13931 | 13653 | 98.0045 | |
| anovak-vg | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 0.0000 | 25.3457 | 0.0000 | 0.0000 | 4234 | 12471 | 0 | 0 | 0 | ||
| anovak-vg | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 0.0000 | 25.3457 | 0.0000 | 0.0000 | 4234 | 12471 | 0 | 0 | 0 | ||
| gduggal-snapvard | SNP | * | * | homalt | 99.4378 | 98.9468 | 99.9337 | 17.0443 | 1167733 | 12429 | 1158113 | 768 | 475 | 61.8490 | |
| mlin-fermikit | SNP | * | map_l150_m2_e1 | het | 55.7873 | 38.9825 | 98.0593 | 70.1751 | 7938 | 12425 | 7933 | 157 | 5 | 3.1847 | |
| qzeng-custom | SNP | * | map_l125_m2_e1 | * | 83.9768 | 73.7003 | 97.5835 | 83.0865 | 34788 | 12414 | 34406 | 852 | 714 | 83.8028 | |
| asubramanian-gatk | SNP | ti | map_l125_m2_e1 | het | 51.8016 | 34.9872 | 99.7311 | 92.1950 | 6678 | 12409 | 6676 | 18 | 6 | 33.3333 | |
| gduggal-bwaplat | SNP | * | map_siren | het | 92.3406 | 86.3635 | 99.2066 | 74.9301 | 78583 | 12408 | 78653 | 629 | 157 | 24.9603 | |
| qzeng-custom | SNP | * | map_l125_m2_e0 | * | 83.8659 | 73.5398 | 97.5657 | 83.0916 | 34360 | 12363 | 33987 | 848 | 710 | 83.7264 | |
| mlin-fermikit | SNP | * | map_l150_m2_e0 | het | 55.5672 | 38.7672 | 98.0639 | 69.9736 | 7805 | 12328 | 7800 | 154 | 5 | 3.2468 | |
| qzeng-custom | SNP | * | map_siren | het | 92.1648 | 86.4602 | 98.6753 | 68.8551 | 78671 | 12320 | 77914 | 1046 | 710 | 67.8776 | |
| asubramanian-gatk | SNP | ti | map_l125_m2_e0 | het | 51.5556 | 34.7637 | 99.7264 | 92.2284 | 6562 | 12314 | 6560 | 18 | 6 | 33.3333 | |
| jpowers-varprowl | INDEL | I6_15 | * | * | 57.4140 | 50.4492 | 66.6100 | 47.5997 | 12523 | 12300 | 12542 | 6287 | 6247 | 99.3638 | |
| gduggal-snapplat | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | * | 47.9906 | 38.1180 | 64.7645 | 71.6412 | 7571 | 12291 | 10067 | 5477 | 926 | 16.9071 | |
| qzeng-custom | SNP | * | map_l125_m1_e0 | * | 83.4865 | 72.9742 | 97.5374 | 82.2302 | 33077 | 12250 | 32716 | 826 | 701 | 84.8668 | |
| gduggal-snapvard | INDEL | * | HG002complexvar | * | 84.5803 | 84.0929 | 85.0735 | 55.5785 | 64696 | 12238 | 73113 | 12828 | 8678 | 67.6489 | |
| gduggal-bwaplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 73.3800 | 60.1280 | 94.1249 | 85.4676 | 18327 | 12153 | 18328 | 1144 | 321 | 28.0594 | |
| gduggal-bwaplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 73.3800 | 60.1280 | 94.1249 | 85.4676 | 18327 | 12153 | 18328 | 1144 | 321 | 28.0594 | |
| asubramanian-gatk | SNP | ti | map_l125_m1_e0 | het | 50.2744 | 33.6034 | 99.7724 | 92.0217 | 6138 | 12128 | 6136 | 14 | 5 | 35.7143 | |
| astatham-gatk | SNP | * | HG002complexvar | * | 99.1835 | 98.3938 | 99.9860 | 19.2643 | 742264 | 12117 | 742112 | 104 | 62 | 59.6154 | |
| ghariani-varprowl | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 49.3962 | 45.5461 | 53.9573 | 55.1768 | 10134 | 12116 | 10117 | 8633 | 8451 | 97.8918 | |
| gduggal-bwavard | SNP | ti | * | het | 99.2556 | 99.0550 | 99.4571 | 24.6552 | 1269783 | 12114 | 1265789 | 6910 | 2002 | 28.9725 | |
| ckim-vqsr | SNP | * | map_l125_m2_e1 | homalt | 47.2295 | 30.9206 | 99.9447 | 86.7543 | 5421 | 12111 | 5421 | 3 | 2 | 66.6667 | |
| mlin-fermikit | SNP | * | map_l150_m1_e0 | het | 54.1179 | 37.3680 | 98.0827 | 65.3701 | 7218 | 12098 | 7213 | 141 | 5 | 3.5461 | |
| ckim-isaac | SNP | ti | map_l125_m2_e1 | * | 75.3035 | 60.4665 | 99.7895 | 72.3331 | 18484 | 12085 | 18484 | 39 | 8 | 20.5128 | |
| ckim-vqsr | SNP | * | map_l125_m2_e0 | homalt | 47.0112 | 30.7338 | 99.9439 | 86.8214 | 5340 | 12035 | 5340 | 3 | 2 | 66.6667 | |
| mlin-fermikit | SNP | * | map_l125_m0_e0 | * | 52.1003 | 37.9727 | 82.9686 | 58.9613 | 7361 | 12024 | 7356 | 1510 | 1338 | 88.6093 | |
| gduggal-bwavard | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 50.5742 | 45.9865 | 56.1787 | 51.4566 | 10232 | 12018 | 10138 | 7908 | 7671 | 97.0030 | |
| gduggal-bwaplat | INDEL | * | HG002complexvar | * | 90.8863 | 84.3874 | 98.4697 | 61.0933 | 64926 | 12012 | 64799 | 1007 | 684 | 67.9245 | |
| ckim-isaac | SNP | tv | HG002complexvar | het | 95.8287 | 92.0463 | 99.9352 | 18.9218 | 138745 | 11989 | 138887 | 90 | 17 | 18.8889 | |
| ckim-isaac | SNP | ti | map_l125_m2_e0 | * | 75.2532 | 60.4006 | 99.7925 | 72.3144 | 18276 | 11982 | 18276 | 38 | 7 | 18.4211 | |
| ghariani-varprowl | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 45.8395 | 42.0033 | 50.4468 | 47.0151 | 8651 | 11945 | 8637 | 8484 | 8329 | 98.1730 | |
| ckim-gatk | SNP | * | map_l125_m2_e1 | * | 84.7700 | 74.7850 | 97.8324 | 85.1204 | 35300 | 11902 | 35294 | 782 | 60 | 7.6726 | |
| ckim-vqsr | SNP | * | map_l125_m1_e0 | homalt | 45.7370 | 29.6539 | 99.9402 | 85.9137 | 5013 | 11892 | 5013 | 3 | 2 | 66.6667 | |
| jmaeng-gatk | SNP | * | map_l125_m2_e1 | * | 84.7588 | 74.8379 | 97.7121 | 85.2730 | 35325 | 11877 | 35319 | 827 | 55 | 6.6505 | |
| gduggal-bwavard | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 46.9955 | 42.3432 | 52.7964 | 40.4686 | 8721 | 11875 | 8666 | 7748 | 7585 | 97.8962 | |
| ckim-gatk | SNP | * | map_l125_m2_e0 | * | 84.6410 | 74.5907 | 97.8215 | 85.1222 | 34851 | 11872 | 34845 | 776 | 59 | 7.6031 | |
| astatham-gatk | SNP | * | HG002complexvar | het | 98.7010 | 97.4496 | 99.9850 | 18.8713 | 453625 | 11872 | 453498 | 68 | 28 | 41.1765 | |
| jmaeng-gatk | SNP | * | map_l125_m2_e0 | * | 84.6294 | 74.6420 | 97.7024 | 85.2765 | 34875 | 11848 | 34869 | 820 | 54 | 6.5854 | |
| ckim-gatk | SNP | * | map_l125_m1_e0 | * | 84.2159 | 73.9471 | 97.7967 | 84.1626 | 33518 | 11809 | 33512 | 755 | 58 | 7.6821 | |
| gduggal-bwaplat | INDEL | * | * | homalt | 94.8233 | 90.5786 | 99.4855 | 59.5744 | 113379 | 11793 | 113311 | 586 | 499 | 85.1536 | |
| jmaeng-gatk | SNP | * | map_l125_m1_e0 | * | 84.2085 | 74.0000 | 97.6843 | 84.3364 | 33542 | 11785 | 33536 | 795 | 54 | 6.7925 | |
| ckim-isaac | SNP | ti | map_l125_m1_e0 | * | 74.8103 | 59.8330 | 99.7896 | 70.2803 | 17552 | 11783 | 17552 | 37 | 7 | 18.9189 | |
| mlin-fermikit | SNP | * | * | homalt | 98.9666 | 99.0041 | 98.9290 | 17.0911 | 1168409 | 11753 | 1168425 | 12649 | 12153 | 96.0787 | |