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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
13101-13150 / 86044 show all | |||||||||||||||
| hfeng-pmm1 | SNP | ti | HG002complexvar | * | 99.8935 | 99.8000 | 99.9872 | 17.3497 | 507419 | 1017 | 507360 | 65 | 31 | 47.6923 | |
| dgrover-gatk | SNP | * | HG002complexvar | homalt | 99.9653 | 99.9435 | 99.9872 | 19.8551 | 288411 | 163 | 288386 | 37 | 35 | 94.5946 | |
| cchapple-custom | SNP | * | HG002complexvar | homalt | 99.8273 | 99.6680 | 99.9871 | 18.5601 | 287616 | 958 | 286343 | 37 | 32 | 86.4865 | |
| cchapple-custom | SNP | * | map_siren | homalt | 99.1241 | 98.2758 | 99.9871 | 48.6990 | 54205 | 951 | 54173 | 7 | 7 | 100.0000 | |
| ckim-gatk | SNP | * | HG002complexvar | homalt | 99.2945 | 98.6114 | 99.9870 | 20.0389 | 284567 | 4007 | 284543 | 37 | 31 | 83.7838 | |
| hfeng-pmm2 | INDEL | D6_15 | HG002compoundhet | hetalt | 96.9666 | 94.1234 | 99.9870 | 24.8188 | 7672 | 479 | 7675 | 1 | 0 | 0.0000 | |
| ltrigg-rtg2 | SNP | tv | * | homalt | 99.9678 | 99.9486 | 99.9870 | 19.3650 | 376927 | 194 | 376951 | 49 | 41 | 83.6735 | |
| hfeng-pmm1 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 96.8385 | 93.8823 | 99.9870 | 28.1495 | 7673 | 500 | 7710 | 1 | 0 | 0.0000 | |
| hfeng-pmm1 | INDEL | D6_15 | HG002compoundhet | hetalt | 97.0967 | 94.3688 | 99.9870 | 24.8266 | 7692 | 459 | 7696 | 1 | 0 | 0.0000 | |
| raldana-dualsentieon | INDEL | D6_15 | * | hetalt | 96.4666 | 93.1857 | 99.9870 | 32.1144 | 7617 | 557 | 7666 | 1 | 1 | 100.0000 | |
| raldana-dualsentieon | INDEL | I6_15 | * | hetalt | 94.4979 | 89.5802 | 99.9870 | 36.2816 | 7660 | 891 | 7700 | 1 | 1 | 100.0000 | |
| hfeng-pmm3 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 96.4989 | 93.2461 | 99.9869 | 27.4123 | 7621 | 552 | 7657 | 1 | 0 | 0.0000 | |
| hfeng-pmm3 | INDEL | D6_15 | HG002compoundhet | hetalt | 96.8362 | 93.8781 | 99.9869 | 24.0528 | 7652 | 499 | 7656 | 1 | 0 | 0.0000 | |
| hfeng-pmm1 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 96.8663 | 93.9345 | 99.9869 | 25.8659 | 7604 | 491 | 7640 | 1 | 0 | 0.0000 | |
| raldana-dualsentieon | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 96.4144 | 93.0885 | 99.9868 | 28.9050 | 7502 | 557 | 7550 | 1 | 1 | 100.0000 | |
| raldana-dualsentieon | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 96.4144 | 93.0885 | 99.9868 | 28.9050 | 7502 | 557 | 7550 | 1 | 1 | 100.0000 | |
| hfeng-pmm3 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 96.5302 | 93.3045 | 99.9868 | 25.2315 | 7553 | 542 | 7588 | 1 | 0 | 0.0000 | |
| hfeng-pmm3 | SNP | ti | HG002complexvar | * | 99.9019 | 99.8171 | 99.9868 | 17.4486 | 507506 | 930 | 507446 | 67 | 25 | 37.3134 | |
| jlack-gatk | SNP | tv | * | homalt | 99.9678 | 99.9488 | 99.9867 | 20.1040 | 376930 | 193 | 376912 | 50 | 30 | 60.0000 | |
| cchapple-custom | SNP | ti | map_l100_m0_e0 | homalt | 98.0662 | 96.2182 | 99.9866 | 56.4787 | 7480 | 294 | 7479 | 1 | 1 | 100.0000 | |
| cchapple-custom | SNP | ti | map_siren | homalt | 99.1409 | 98.3094 | 99.9866 | 47.3567 | 37275 | 641 | 37258 | 5 | 5 | 100.0000 | |
| astatham-gatk | SNP | ti | HG002complexvar | * | 99.2181 | 98.4614 | 99.9866 | 17.7102 | 500613 | 7823 | 500548 | 67 | 41 | 61.1940 | |
| cchapple-custom | SNP | ti | map_l150_m2_e1 | homalt | 98.1938 | 96.4643 | 99.9865 | 68.8251 | 7421 | 272 | 7418 | 1 | 1 | 100.0000 | |
| cchapple-custom | SNP | ti | map_l150_m2_e0 | homalt | 98.1821 | 96.4417 | 99.9864 | 68.7543 | 7345 | 271 | 7343 | 1 | 1 | 100.0000 | |
| ckim-gatk | SNP | ti | HG002complexvar | homalt | 99.3341 | 98.6902 | 99.9864 | 18.4846 | 190929 | 2534 | 190919 | 26 | 23 | 88.4615 | |
| hfeng-pmm1 | SNP | tv | HG002complexvar | homalt | 99.9763 | 99.9664 | 99.9863 | 22.9407 | 95079 | 32 | 95072 | 13 | 11 | 84.6154 | |
| dgrover-gatk | SNP | tv | HG002complexvar | homalt | 99.9637 | 99.9411 | 99.9863 | 22.7977 | 95055 | 56 | 95040 | 13 | 11 | 84.6154 | |
| ltrigg-rtg2 | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 99.5298 | 99.0776 | 99.9861 | 69.5819 | 21697 | 202 | 21585 | 3 | 3 | 100.0000 | |
| astatham-gatk | SNP | ti | HG002complexvar | het | 98.7599 | 97.5636 | 99.9860 | 17.3084 | 307097 | 7669 | 307042 | 43 | 17 | 39.5349 | |
| astatham-gatk | SNP | * | HG002complexvar | * | 99.1835 | 98.3938 | 99.9860 | 19.2643 | 742264 | 12117 | 742112 | 104 | 62 | 59.6154 | |
| hfeng-pmm1 | SNP | ti | HG002complexvar | het | 99.8377 | 99.6899 | 99.9860 | 16.6225 | 313790 | 976 | 313739 | 44 | 10 | 22.7273 | |
| hfeng-pmm1 | SNP | * | HG002complexvar | * | 99.8780 | 99.7704 | 99.9859 | 18.8078 | 752649 | 1732 | 752504 | 106 | 51 | 48.1132 | |
| hfeng-pmm3 | SNP | * | HG002complexvar | * | 99.8875 | 99.7894 | 99.9859 | 18.8968 | 752792 | 1589 | 752645 | 106 | 40 | 37.7358 | |
| ckim-dragen | SNP | * | HG002complexvar | homalt | 99.9551 | 99.9245 | 99.9858 | 19.8995 | 288356 | 218 | 288565 | 41 | 41 | 100.0000 | |
| cchapple-custom | SNP | ti | map_l150_m1_e0 | homalt | 98.1515 | 96.3832 | 99.9858 | 66.0349 | 7062 | 265 | 7060 | 1 | 1 | 100.0000 | |
| hfeng-pmm1 | SNP | tv | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 99.7572 | 99.5298 | 99.9857 | 59.8113 | 6986 | 33 | 6983 | 1 | 0 | 0.0000 | |
| hfeng-pmm3 | SNP | tv | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 99.7572 | 99.5298 | 99.9857 | 59.9128 | 6986 | 33 | 6983 | 1 | 0 | 0.0000 | |
| hfeng-pmm2 | SNP | tv | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 99.7071 | 99.4301 | 99.9857 | 60.0126 | 6979 | 40 | 6976 | 1 | 0 | 0.0000 | |
| gduggal-snapplat | SNP | * | func_cds | homalt | 99.7054 | 99.4269 | 99.9856 | 21.7587 | 6939 | 40 | 6939 | 1 | 1 | 100.0000 | |
| ltrigg-rtg1 | SNP | ti | * | homalt | 99.9664 | 99.9474 | 99.9854 | 16.2302 | 802614 | 422 | 802519 | 117 | 112 | 95.7265 | |
| rpoplin-dv42 | SNP | ti | * | homalt | 99.9800 | 99.9747 | 99.9853 | 16.8487 | 802835 | 203 | 802832 | 118 | 106 | 89.8305 | |
| raldana-dualsentieon | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 99.9852 | 99.9852 | 99.9852 | 34.3808 | 6744 | 1 | 6744 | 1 | 1 | 100.0000 | |
| cchapple-custom | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 99.9481 | 99.9110 | 99.9851 | 30.4766 | 6739 | 6 | 6724 | 1 | 1 | 100.0000 | |
| jmaeng-gatk | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 99.8292 | 99.6738 | 99.9851 | 35.1779 | 6723 | 22 | 6723 | 1 | 1 | 100.0000 | |
| astatham-gatk | SNP | * | HG002complexvar | het | 98.7010 | 97.4496 | 99.9850 | 18.8713 | 453625 | 11872 | 453498 | 68 | 28 | 41.1765 | |
| cchapple-custom | SNP | ti | HG002complexvar | homalt | 99.8348 | 99.6852 | 99.9849 | 17.4009 | 192854 | 609 | 192184 | 29 | 25 | 86.2069 | |
| ckim-vqsr | SNP | ti | HG002complexvar | * | 98.8535 | 97.7474 | 99.9849 | 18.1351 | 496983 | 11453 | 496925 | 75 | 38 | 50.6667 | |
| hfeng-pmm1 | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 97.6291 | 95.3819 | 99.9848 | 25.9951 | 6568 | 318 | 6581 | 1 | 0 | 0.0000 | |
| hfeng-pmm1 | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 98.2527 | 96.5796 | 99.9848 | 34.0696 | 6579 | 233 | 6596 | 1 | 0 | 0.0000 | |
| jmaeng-gatk | SNP | ti | HG002complexvar | homalt | 99.3419 | 98.7072 | 99.9848 | 18.4737 | 190962 | 2501 | 190952 | 29 | 26 | 89.6552 | |