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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
72351-72400 / 86044 show all | |||||||||||||||
| hfeng-pmm1 | SNP | tv | map_l250_m2_e1 | * | 98.6071 | 98.3196 | 98.8962 | 88.3190 | 2867 | 49 | 2867 | 32 | 7 | 21.8750 | |
| astatham-gatk | INDEL | I1_5 | map_siren | * | 97.3853 | 95.4077 | 99.4467 | 81.4805 | 2867 | 138 | 2876 | 16 | 5 | 31.2500 | |
| gduggal-snapvard | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 93.2273 | 96.9246 | 89.8017 | 74.7396 | 2868 | 91 | 2853 | 324 | 8 | 2.4691 | |
| gduggal-snapplat | INDEL | D6_15 | HG002compoundhet | hetalt | 51.7417 | 35.1859 | 97.7226 | 44.3646 | 2868 | 5283 | 2875 | 67 | 52 | 77.6119 | |
| cchapple-custom | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 97.6989 | 96.2429 | 99.1997 | 49.1264 | 2869 | 112 | 2975 | 24 | 22 | 91.6667 | |
| eyeh-varpipe | SNP | tv | map_l250_m2_e0 | * | 98.7380 | 99.5489 | 97.9403 | 90.6578 | 2869 | 13 | 2853 | 60 | 6 | 10.0000 | |
| raldana-dualsentieon | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 95.7931 | 91.9551 | 99.9655 | 41.6230 | 2869 | 251 | 2898 | 1 | 1 | 100.0000 | |
| mlin-fermikit | SNP | tv | map_l100_m0_e0 | het | 56.5874 | 39.7258 | 98.3185 | 59.7124 | 2869 | 4353 | 2865 | 49 | 0 | 0.0000 | |
| hfeng-pmm2 | SNP | tv | map_l250_m2_e1 | * | 98.3213 | 98.4225 | 98.2204 | 89.7650 | 2870 | 46 | 2870 | 52 | 7 | 13.4615 | |
| gduggal-snapvard | SNP | tv | HG002compoundhet | homalt | 90.8698 | 84.7107 | 97.9946 | 41.8088 | 2870 | 518 | 2541 | 52 | 38 | 73.0769 | |
| jli-custom | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 97.5369 | 96.2764 | 98.8308 | 48.6037 | 2870 | 111 | 2874 | 34 | 25 | 73.5294 | |
| gduggal-snapplat | INDEL | D6_15 | * | hetalt | 51.3567 | 35.1358 | 95.3989 | 60.4943 | 2872 | 5302 | 2882 | 139 | 111 | 79.8561 | |
| hfeng-pmm3 | SNP | tv | map_l250_m2_e1 | * | 98.7629 | 98.5597 | 98.9669 | 88.4625 | 2874 | 42 | 2874 | 30 | 4 | 13.3333 | |
| mlin-fermikit | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 96.1180 | 95.8000 | 96.4382 | 69.3543 | 2874 | 126 | 2870 | 106 | 91 | 85.8491 | |
| eyeh-varpipe | INDEL | I1_5 | map_siren | * | 96.0860 | 95.6406 | 96.5357 | 78.7530 | 2874 | 131 | 3316 | 119 | 92 | 77.3109 | |
| bgallagher-sentieon | SNP | tv | map_l250_m2_e1 | * | 98.1725 | 98.5597 | 97.7884 | 89.4056 | 2874 | 42 | 2874 | 65 | 13 | 20.0000 | |
| gduggal-bwaplat | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 85.9154 | 76.4472 | 98.0606 | 64.1454 | 2879 | 887 | 2882 | 57 | 53 | 92.9825 | |
| gduggal-bwaplat | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 85.9154 | 76.4472 | 98.0606 | 64.1454 | 2879 | 887 | 2882 | 57 | 53 | 92.9825 | |
| gduggal-bwavard | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 96.3782 | 97.2964 | 95.4772 | 69.1463 | 2879 | 80 | 2871 | 136 | 12 | 8.8235 | |
| rpoplin-dv42 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 90.6827 | 89.7196 | 91.6667 | 60.0255 | 2880 | 330 | 2871 | 261 | 260 | 99.6169 | |
| ciseli-custom | SNP | tv | lowcmp_SimpleRepeat_diTR_11to50 | het | 76.8078 | 93.2966 | 65.2719 | 67.9320 | 2881 | 207 | 2917 | 1552 | 48 | 3.0928 | |
| ckim-dragen | SNP | ti | map_l250_m1_e0 | het | 96.2459 | 97.1361 | 95.3719 | 90.8281 | 2883 | 85 | 2885 | 140 | 10 | 7.1429 | |
| ndellapenna-hhga | INDEL | * | HG002complexvar | hetalt | 86.5340 | 77.9941 | 97.1740 | 71.6888 | 2885 | 814 | 2854 | 83 | 75 | 90.3614 | |
| gduggal-bwafb | SNP | ti | map_l250_m1_e0 | het | 97.3192 | 97.2372 | 97.4013 | 90.0480 | 2886 | 82 | 2886 | 77 | 22 | 28.5714 | |
| egarrison-hhga | SNP | ti | map_l250_m1_e0 | het | 98.3472 | 97.2372 | 99.4829 | 88.9494 | 2886 | 82 | 2886 | 15 | 5 | 33.3333 | |
| ckim-isaac | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 83.6123 | 74.0570 | 95.9987 | 49.9006 | 2886 | 1011 | 2903 | 121 | 83 | 68.5950 | |
| ciseli-custom | INDEL | I6_15 | * | homalt | 49.3008 | 46.2895 | 52.7313 | 38.8345 | 2888 | 3351 | 2867 | 2570 | 2475 | 96.3035 | |
| hfeng-pmm2 | INDEL | D6_15 | HG002complexvar | het | 95.8142 | 92.5641 | 99.3009 | 57.1386 | 2888 | 232 | 2841 | 20 | 16 | 80.0000 | |
| eyeh-varpipe | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 55.8126 | 45.6817 | 71.7174 | 42.4460 | 2888 | 3434 | 6598 | 2602 | 2576 | 99.0008 | |
| eyeh-varpipe | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 55.8126 | 45.6817 | 71.7174 | 42.4460 | 2888 | 3434 | 6598 | 2602 | 2576 | 99.0008 | |
| anovak-vg | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 0.0000 | 27.5800 | 0.0000 | 0.0000 | 2889 | 7586 | 0 | 0 | 0 | ||
| raldana-dualsentieon | INDEL | D6_15 | HG002complexvar | het | 95.7688 | 92.6603 | 99.0931 | 57.6076 | 2891 | 229 | 2841 | 26 | 24 | 92.3077 | |
| hfeng-pmm3 | INDEL | D6_15 | HG002complexvar | het | 95.8678 | 92.7244 | 99.2318 | 57.2218 | 2893 | 227 | 2842 | 22 | 17 | 77.2727 | |
| gduggal-bwavard | SNP | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 91.9826 | 95.9549 | 88.3261 | 82.4603 | 2894 | 122 | 2860 | 378 | 43 | 11.3757 | |
| ndellapenna-hhga | INDEL | D6_15 | HG002complexvar | het | 92.6198 | 92.8205 | 92.4200 | 56.3998 | 2896 | 224 | 2975 | 244 | 197 | 80.7377 | |
| hfeng-pmm1 | INDEL | D6_15 | HG002complexvar | het | 95.9519 | 92.8205 | 99.3019 | 57.0271 | 2896 | 224 | 2845 | 20 | 17 | 85.0000 | |
| hfeng-pmm2 | SNP | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 97.6573 | 96.0544 | 99.3146 | 65.3032 | 2897 | 119 | 2898 | 20 | 0 | 0.0000 | |
| gduggal-bwavard | SNP | ti | map_l250_m1_e0 | het | 87.4417 | 97.6415 | 79.1712 | 92.9128 | 2898 | 70 | 2885 | 759 | 20 | 2.6351 | |
| ciseli-custom | INDEL | D1_5 | map_siren | * | 83.6317 | 82.1196 | 85.2005 | 84.5008 | 2898 | 631 | 2890 | 502 | 233 | 46.4143 | |
| ghariani-varprowl | SNP | ti | map_l250_m1_e0 | het | 94.9386 | 97.6415 | 92.3813 | 91.9764 | 2898 | 70 | 2898 | 239 | 49 | 20.5021 | |
| ckim-vqsr | SNP | ti | map_l150_m0_e0 | het | 72.0358 | 56.8570 | 98.2706 | 94.0511 | 2898 | 2199 | 2898 | 51 | 0 | 0.0000 | |
| mlin-fermikit | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 98.1375 | 97.9385 | 98.3373 | 54.7451 | 2898 | 61 | 2898 | 49 | 23 | 46.9388 | |
| gduggal-snapfb | INDEL | I1_5 | map_siren | * | 95.6890 | 96.4725 | 94.9180 | 82.9590 | 2899 | 106 | 2895 | 155 | 39 | 25.1613 | |
| asubramanian-gatk | SNP | ti | map_l125_m1_e0 | homalt | 41.5806 | 26.2472 | 100.0000 | 86.8829 | 2899 | 8146 | 2899 | 0 | 0 | ||
| ckim-isaac | INDEL | D16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 86.8178 | 81.4097 | 92.9955 | 56.2615 | 2899 | 662 | 2881 | 217 | 142 | 65.4378 | |
| gduggal-bwafb | INDEL | D16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 86.1916 | 81.4378 | 91.5347 | 58.1069 | 2900 | 661 | 3006 | 278 | 275 | 98.9209 | |
| gduggal-bwaplat | SNP | tv | map_l125_m2_e1 | homalt | 64.6312 | 47.7445 | 100.0000 | 81.7242 | 2900 | 3174 | 2900 | 0 | 0 | ||
| gduggal-bwafb | INDEL | I1_5 | map_siren | * | 97.6773 | 96.5391 | 98.8428 | 79.9276 | 2901 | 104 | 2904 | 34 | 18 | 52.9412 | |
| qzeng-custom | SNP | tv | map_l150_m2_e1 | homalt | 82.0801 | 70.1984 | 98.8034 | 73.9699 | 2902 | 1232 | 2890 | 35 | 35 | 100.0000 | |
| eyeh-varpipe | SNP | tv | map_l250_m2_e1 | * | 98.7186 | 99.5542 | 97.8969 | 90.7430 | 2903 | 13 | 2886 | 62 | 6 | 9.6774 | |