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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
84751-84800 / 86044 show all | |||||||||||||||
| gduggal-snapfb | INDEL | I6_15 | * | * | 76.3979 | 68.7024 | 86.0349 | 35.3787 | 17054 | 7769 | 17786 | 2887 | 2798 | 96.9172 | |
| gduggal-bwavard | SNP | * | map_l125_m1_e0 | het | 94.0558 | 97.9149 | 90.4894 | 82.0185 | 27800 | 592 | 27478 | 2888 | 162 | 5.6094 | |
| ciseli-custom | SNP | tv | map_l100_m1_e0 | * | 82.8010 | 79.0049 | 86.9802 | 71.6783 | 19357 | 5144 | 19347 | 2896 | 701 | 24.2058 | |
| gduggal-snapvard | SNP | ti | map_l100_m1_e0 | het | 93.5196 | 96.3997 | 90.8067 | 76.8858 | 28864 | 1078 | 28615 | 2897 | 247 | 8.5261 | |
| gduggal-snapplat | INDEL | I6_15 | * | * | 41.4207 | 29.2310 | 71.0492 | 57.1777 | 7256 | 17567 | 7117 | 2900 | 649 | 22.3793 | |
| ciseli-custom | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 62.2772 | 53.6141 | 74.2796 | 69.6025 | 8619 | 7457 | 8378 | 2901 | 2024 | 69.7690 | |
| ciseli-custom | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 62.2772 | 53.6141 | 74.2796 | 69.6025 | 8619 | 7457 | 8378 | 2901 | 2024 | 69.7690 | |
| qzeng-custom | SNP | tv | * | het | 99.3391 | 99.1721 | 99.5067 | 29.7409 | 586805 | 4899 | 585578 | 2903 | 302 | 10.4030 | |
| gduggal-bwavard | SNP | * | map_l125_m2_e0 | het | 94.1644 | 97.8921 | 90.7102 | 83.1354 | 28700 | 618 | 28366 | 2905 | 164 | 5.6454 | |
| gduggal-snapvard | SNP | ti | map_l100_m2_e0 | het | 93.6224 | 96.4339 | 90.9701 | 78.1195 | 29530 | 1092 | 29276 | 2906 | 248 | 8.5341 | |
| gduggal-bwavard | SNP | * | map_l125_m1_e0 | * | 95.6870 | 97.6989 | 93.7563 | 78.5243 | 44284 | 1043 | 43712 | 2911 | 180 | 6.1834 | |
| gduggal-bwavard | SNP | * | map_l125_m2_e1 | het | 94.2043 | 97.9082 | 90.7704 | 83.1773 | 29020 | 620 | 28678 | 2916 | 165 | 5.6584 | |
| ciseli-custom | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 71.6485 | 93.5583 | 58.0534 | 81.2561 | 3965 | 273 | 4044 | 2922 | 58 | 1.9849 | |
| egarrison-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 83.3079 | 82.7701 | 83.8526 | 37.1677 | 15113 | 3146 | 15179 | 2923 | 2748 | 94.0130 | |
| gduggal-snapvard | SNP | ti | map_l100_m2_e1 | het | 93.6568 | 96.4632 | 91.0091 | 78.1383 | 29865 | 1095 | 29608 | 2925 | 251 | 8.5812 | |
| asubramanian-gatk | INDEL | * | * | * | 98.8418 | 98.5404 | 99.1451 | 71.3671 | 339513 | 5029 | 339442 | 2927 | 1779 | 60.7790 | |
| gduggal-bwavard | SNP | * | map_l125_m2_e0 | * | 95.7523 | 97.6821 | 93.8973 | 79.8955 | 45640 | 1083 | 45051 | 2928 | 182 | 6.2159 | |
| gduggal-snapfb | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 80.5780 | 99.1753 | 67.8540 | 65.4237 | 6133 | 51 | 6191 | 2933 | 43 | 1.4661 | |
| gduggal-snapvard | SNP | ti | map_l100_m1_e0 | * | 95.0911 | 96.2467 | 93.9630 | 72.8656 | 46132 | 1799 | 45682 | 2935 | 278 | 9.4719 | |
| gduggal-bwavard | SNP | * | map_l125_m2_e1 | * | 95.7732 | 97.6865 | 93.9333 | 79.9451 | 46110 | 1092 | 45506 | 2939 | 183 | 6.2266 | |
| gduggal-snapvard | SNP | * | map_l125_m0_e0 | het | 87.4804 | 96.0281 | 80.3301 | 84.3236 | 12161 | 503 | 12023 | 2944 | 184 | 6.2500 | |
| ciseli-custom | SNP | tv | map_l100_m2_e0 | * | 83.0120 | 79.3073 | 87.0798 | 73.4407 | 19853 | 5180 | 19842 | 2944 | 713 | 24.2188 | |
| ciseli-custom | SNP | ti | map_l150_m2_e0 | * | 79.2695 | 75.0926 | 83.9385 | 81.3448 | 15403 | 5109 | 15396 | 2946 | 753 | 25.5601 | |
| gduggal-snapvard | SNP | ti | map_l100_m2_e0 | * | 95.1595 | 96.2807 | 94.0641 | 74.3570 | 47140 | 1821 | 46684 | 2946 | 281 | 9.5384 | |
| gduggal-snapfb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 81.2103 | 79.4781 | 83.0196 | 65.6096 | 14438 | 3728 | 14423 | 2950 | 2467 | 83.6271 | |
| gduggal-snapfb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 81.2103 | 79.4781 | 83.0196 | 65.6096 | 14438 | 3728 | 14423 | 2950 | 2467 | 83.6271 | |
| eyeh-varpipe | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | * | 84.4279 | 81.5933 | 87.4666 | 33.3286 | 20023 | 4517 | 20601 | 2952 | 2912 | 98.6450 | |
| jmaeng-gatk | SNP | tv | * | het | 99.5410 | 99.5807 | 99.5013 | 31.3482 | 589215 | 2481 | 589142 | 2953 | 52 | 1.7609 | |
| eyeh-varpipe | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 94.9804 | 93.5841 | 96.4190 | 67.2497 | 45174 | 3097 | 79672 | 2959 | 2749 | 92.9030 | |
| ndellapenna-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 83.0202 | 97.6165 | 72.2212 | 39.7852 | 7208 | 176 | 7693 | 2959 | 2890 | 97.6681 | |
| gduggal-bwaplat | SNP | tv | * | * | 98.5599 | 97.4574 | 99.6876 | 31.4101 | 945035 | 24655 | 945254 | 2962 | 440 | 14.8548 | |
| gduggal-snapvard | SNP | ti | map_l100_m2_e1 | * | 95.1804 | 96.2979 | 94.0886 | 74.3752 | 47653 | 1832 | 47192 | 2965 | 284 | 9.5784 | |
| gduggal-snapfb | SNP | ti | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 57.6740 | 98.5178 | 40.7711 | 77.3433 | 1994 | 30 | 2041 | 2965 | 42 | 1.4165 | |
| anovak-vg | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 88.5672 | 91.1998 | 86.0824 | 76.7383 | 17856 | 1723 | 18339 | 2965 | 857 | 28.9039 | |
| anovak-vg | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 88.5672 | 91.1998 | 86.0824 | 76.7383 | 17856 | 1723 | 18339 | 2965 | 857 | 28.9039 | |
| ciseli-custom | SNP | tv | map_l100_m2_e1 | * | 83.0739 | 79.3893 | 87.1172 | 73.4544 | 20072 | 5211 | 20057 | 2966 | 720 | 24.2751 | |
| gduggal-snapvard | SNP | * | map_l125_m0_e0 | * | 90.5380 | 95.5326 | 86.0396 | 81.8589 | 18519 | 866 | 18286 | 2967 | 202 | 6.8082 | |
| ciseli-custom | INDEL | D1_5 | HG002complexvar | homalt | 84.8845 | 94.7915 | 76.8524 | 57.1696 | 10046 | 552 | 9864 | 2971 | 1988 | 66.9135 | |
| gduggal-snapplat | SNP | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 87.5770 | 82.0514 | 93.9006 | 76.3684 | 45646 | 9985 | 45754 | 2972 | 322 | 10.8345 | |
| eyeh-varpipe | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 76.3850 | 99.7475 | 61.8895 | 40.6948 | 4741 | 12 | 4828 | 2973 | 2967 | 99.7982 | |
| ckim-isaac | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 89.4545 | 89.1929 | 89.7177 | 61.8267 | 27186 | 3294 | 25967 | 2976 | 2168 | 72.8495 | |
| ckim-isaac | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 89.4545 | 89.1929 | 89.7177 | 61.8267 | 27186 | 3294 | 25967 | 2976 | 2168 | 72.8495 | |
| ciseli-custom | SNP | ti | map_l150_m2_e1 | * | 79.2822 | 75.1146 | 83.9394 | 81.3843 | 15566 | 5157 | 15559 | 2977 | 763 | 25.6298 | |
| ciseli-custom | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 78.1562 | 80.3015 | 76.1225 | 51.8771 | 9535 | 2339 | 9494 | 2978 | 1387 | 46.5749 | |
| eyeh-varpipe | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 67.6237 | 92.1660 | 53.4032 | 48.7367 | 3353 | 285 | 3413 | 2978 | 2941 | 98.7576 | |
| anovak-vg | SNP | tv | HG002complexvar | het | 97.4369 | 96.9012 | 97.9786 | 22.5474 | 146063 | 4671 | 144347 | 2978 | 2196 | 73.7408 | |
| ckim-isaac | INDEL | * | HG002complexvar | * | 91.9300 | 88.4153 | 95.7357 | 48.5598 | 68025 | 8913 | 67037 | 2986 | 1352 | 45.2780 | |
| ndellapenna-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 84.3874 | 97.5345 | 74.3636 | 48.4035 | 8189 | 207 | 8676 | 2991 | 2903 | 97.0578 | |
| jmaeng-gatk | SNP | tv | * | * | 99.5370 | 99.3842 | 99.6902 | 27.5023 | 963719 | 5971 | 963632 | 2995 | 80 | 2.6711 | |
| gduggal-snapfb | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 41.4402 | 94.0217 | 26.5770 | 81.1312 | 1038 | 66 | 1087 | 3003 | 81 | 2.6973 | |