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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
71051-71100 / 86044 show all | |||||||||||||||
| gduggal-bwavard | SNP | ti | lowcmp_SimpleRepeat_quadTR_11to50 | het | 96.8600 | 98.1613 | 95.5927 | 59.3604 | 6620 | 124 | 6572 | 303 | 63 | 20.7921 | |
| gduggal-bwavard | SNP | tv | lowcmp_SimpleRepeat_triTR_11to50 | * | 97.5587 | 96.4058 | 98.7395 | 42.1025 | 3326 | 124 | 3290 | 42 | 14 | 33.3333 | |
| hfeng-pmm2 | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 93.9147 | 88.7681 | 99.6948 | 86.0725 | 980 | 124 | 980 | 3 | 0 | 0.0000 | |
| hfeng-pmm3 | INDEL | D16_PLUS | * | hetalt | 96.6173 | 93.5851 | 99.8525 | 38.5313 | 1809 | 124 | 2031 | 3 | 3 | 100.0000 | |
| hfeng-pmm3 | INDEL | D16_PLUS | HG002compoundhet | hetalt | 96.6774 | 93.5685 | 100.0000 | 26.2024 | 1804 | 124 | 1918 | 0 | 0 | ||
| hfeng-pmm3 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 96.6136 | 93.5785 | 99.8523 | 38.4918 | 1807 | 124 | 2028 | 3 | 3 | 100.0000 | |
| hfeng-pmm3 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 96.6136 | 93.5785 | 99.8523 | 38.4918 | 1807 | 124 | 2028 | 3 | 3 | 100.0000 | |
| jlack-gatk | SNP | tv | map_siren | homalt | 99.5956 | 99.2807 | 99.9124 | 53.4780 | 17116 | 124 | 17113 | 15 | 10 | 66.6667 | |
| jli-custom | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | * | 96.7744 | 95.3296 | 98.2636 | 65.4439 | 2531 | 124 | 2490 | 44 | 33 | 75.0000 | |
| hfeng-pmm1 | SNP | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 98.5556 | 97.3971 | 99.7420 | 65.4794 | 4640 | 124 | 4640 | 12 | 1 | 8.3333 | |
| hfeng-pmm3 | SNP | ti | map_l100_m0_e0 | * | 99.5150 | 99.4304 | 99.5997 | 67.5390 | 21647 | 124 | 21644 | 87 | 13 | 14.9425 | |
| hfeng-pmm3 | SNP | ti | map_l125_m1_e0 | het | 99.4436 | 99.3211 | 99.5663 | 71.0299 | 18142 | 124 | 18138 | 79 | 8 | 10.1266 | |
| hfeng-pmm2 | INDEL | I6_15 | lowcmp_SimpleRepeat_diTR_11to50 | * | 97.0727 | 94.8590 | 99.3921 | 62.0781 | 2288 | 124 | 2289 | 14 | 8 | 57.1429 | |
| ltrigg-rtg1 | SNP | tv | map_l250_m1_e0 | het | 96.2660 | 93.0610 | 99.6997 | 76.8718 | 1663 | 124 | 1660 | 5 | 2 | 40.0000 | |
| jli-custom | SNP | ti | map_l250_m1_e0 | * | 98.2684 | 97.2920 | 99.2647 | 86.0135 | 4455 | 124 | 4455 | 33 | 18 | 54.5455 | |
| jpowers-varprowl | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 51.4864 | 39.5122 | 73.8739 | 83.1563 | 81 | 124 | 82 | 29 | 28 | 96.5517 | |
| jpowers-varprowl | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 51.4864 | 39.5122 | 73.8739 | 83.1563 | 81 | 124 | 82 | 29 | 28 | 96.5517 | |
| jpowers-varprowl | INDEL | * | map_l100_m2_e0 | hetalt | 0.0000 | 0.8000 | 0.0000 | 0.0000 | 1 | 124 | 0 | 0 | 0 | ||
| ghariani-varprowl | INDEL | * | map_l100_m2_e0 | hetalt | 0.0000 | 0.8000 | 0.0000 | 0.0000 | 1 | 124 | 0 | 0 | 0 | ||
| gduggal-snapvard | INDEL | D1_5 | map_siren | homalt | 93.2963 | 89.3836 | 97.5673 | 70.4493 | 1044 | 124 | 1123 | 28 | 26 | 92.8571 | |
| gduggal-snapvard | INDEL | * | map_l100_m1_e0 | het | 84.8981 | 94.4519 | 77.0994 | 87.8634 | 2111 | 124 | 2993 | 889 | 409 | 46.0067 | |
| ghariani-varprowl | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | het | 95.5503 | 98.9154 | 92.4066 | 58.6255 | 11309 | 124 | 11354 | 933 | 13 | 1.3934 | |
| mlin-fermikit | INDEL | D6_15 | lowcmp_SimpleRepeat_triTR_11to50 | hetalt | 87.7870 | 78.7671 | 99.1398 | 19.4107 | 460 | 124 | 461 | 4 | 4 | 100.0000 | |
| ndellapenna-hhga | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 84.8521 | 85.8447 | 83.8821 | 72.0175 | 752 | 124 | 968 | 186 | 175 | 94.0860 | |
| qzeng-custom | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 92.1119 | 93.7088 | 90.5685 | 58.7145 | 1847 | 124 | 5608 | 584 | 448 | 76.7123 | |
| qzeng-custom | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 92.1119 | 93.7088 | 90.5685 | 58.7145 | 1847 | 124 | 5608 | 584 | 448 | 76.7123 | |
| ndellapenna-hhga | SNP | ti | map_l250_m1_e0 | het | 97.6313 | 95.8221 | 99.5101 | 88.0937 | 2844 | 124 | 2844 | 14 | 6 | 42.8571 | |
| ndellapenna-hhga | SNP | tv | map_l125_m0_e0 | het | 98.2879 | 97.1825 | 99.4189 | 73.8528 | 4277 | 124 | 4277 | 25 | 11 | 44.0000 | |
| qzeng-custom | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 0.0000 | 84.1837 | 0.0000 | 0.0000 | 660 | 124 | 0 | 0 | 0 | ||
| ckim-dragen | INDEL | I1_5 | * | homalt | 99.5565 | 99.7948 | 99.3194 | 55.1956 | 60304 | 124 | 60271 | 413 | 409 | 99.0315 | |
| ckim-dragen | SNP | tv | map_l150_m1_e0 | * | 98.2065 | 98.8636 | 97.5581 | 77.3404 | 10788 | 124 | 10787 | 270 | 27 | 10.0000 | |
| ckim-dragen | SNP | tv | map_l150_m2_e0 | * | 98.2503 | 98.9080 | 97.6013 | 79.0121 | 11231 | 124 | 11230 | 276 | 27 | 9.7826 | |
| cchapple-custom | INDEL | I1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | hetalt | 0.0000 | 86.1761 | 0.0000 | 0.0000 | 773 | 124 | 0 | 0 | 0 | ||
| ciseli-custom | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 48.6704 | 84.3829 | 34.1974 | 80.6855 | 670 | 124 | 686 | 1320 | 25 | 1.8939 | |
| ckim-dragen | INDEL | D16_PLUS | HG002compoundhet | hetalt | 96.4348 | 93.5685 | 99.4824 | 26.5399 | 1804 | 124 | 1922 | 10 | 10 | 100.0000 | |
| ciseli-custom | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 11.3208 | 6.7669 | 34.6154 | 89.9614 | 9 | 124 | 9 | 17 | 13 | 76.4706 | |
| ciseli-custom | INDEL | I16_PLUS | lowcmp_SimpleRepeat_diTR_11to50 | het | 32.8326 | 22.5000 | 60.7143 | 91.1532 | 36 | 124 | 34 | 22 | 12 | 54.5455 | |
| raldana-dualsentieon | SNP | * | map_l250_m2_e1 | het | 97.5147 | 97.6444 | 97.3854 | 89.4825 | 5140 | 124 | 5140 | 138 | 3 | 2.1739 | |
| rpoplin-dv42 | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 96.3271 | 94.3866 | 98.3491 | 65.6458 | 2085 | 124 | 2085 | 35 | 29 | 82.8571 | |
| rpoplin-dv42 | INDEL | D16_PLUS | HG002complexvar | * | 93.9813 | 92.4528 | 95.5612 | 63.5376 | 1519 | 124 | 1507 | 70 | 64 | 91.4286 | |
| anovak-vg | INDEL | D1_5 | map_siren | homalt | 92.1020 | 89.3836 | 94.9909 | 79.6667 | 1044 | 124 | 1043 | 55 | 46 | 83.6364 | |
| bgallagher-sentieon | INDEL | I6_15 | lowcmp_SimpleRepeat_diTR_11to50 | * | 96.9904 | 94.8590 | 99.2198 | 62.4389 | 2288 | 124 | 2289 | 18 | 13 | 72.2222 | |
| asubramanian-gatk | INDEL | D1_5 | map_l125_m1_e0 | * | 91.7244 | 88.6029 | 95.0739 | 89.7371 | 964 | 124 | 965 | 50 | 5 | 10.0000 | |
| asubramanian-gatk | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 98.5568 | 97.9679 | 99.1528 | 76.0152 | 5978 | 124 | 7490 | 64 | 52 | 81.2500 | |
| anovak-vg | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 23.2825 | 16.1074 | 41.9847 | 51.3011 | 24 | 125 | 55 | 76 | 63 | 82.8947 | |
| astatham-gatk | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 95.4126 | 96.9059 | 93.9646 | 79.4691 | 3915 | 125 | 3612 | 232 | 195 | 84.0517 | |
| astatham-gatk | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 97.3915 | 95.8068 | 99.0295 | 51.2175 | 2856 | 125 | 2857 | 28 | 23 | 82.1429 | |
| astatham-gatk | SNP | * | lowcmp_SimpleRepeat_diTR_11to50 | het | 98.9155 | 97.9955 | 99.8529 | 70.5060 | 6111 | 125 | 6111 | 9 | 8 | 88.8889 | |
| ghariani-varprowl | INDEL | * | lowcmp_SimpleRepeat_triTR_51to200 | hetalt | 0.0000 | 0.0000 | 0.0000 | 0 | 125 | 0 | 0 | 0 | |||
| ghariani-varprowl | INDEL | * | map_l125_m2_e1 | * | 91.8033 | 94.3820 | 89.3617 | 94.1271 | 2100 | 125 | 2100 | 250 | 82 | 32.8000 | |