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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
21801-21850 / 86044 show all | |||||||||||||||
| gduggal-snapplat | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 50.0000 | 39.1304 | 69.2308 | 97.4017 | 27 | 42 | 27 | 12 | 6 | 50.0000 | |
| gduggal-snapplat | SNP | ti | lowcmp_SimpleRepeat_quadTR_51to200 | * | 23.2323 | 22.7723 | 23.7113 | 98.6305 | 23 | 78 | 23 | 74 | 6 | 8.1081 | |
| gduggal-snapplat | SNP | ti | map_l125_m1_e0 | hetalt | 84.6154 | 91.6667 | 78.5714 | 78.4615 | 22 | 2 | 22 | 6 | 6 | 100.0000 | |
| gduggal-snapplat | SNP | ti | map_l125_m2_e0 | hetalt | 84.6154 | 91.6667 | 78.5714 | 81.9355 | 22 | 2 | 22 | 6 | 6 | 100.0000 | |
| gduggal-snapplat | SNP | ti | map_l125_m2_e1 | hetalt | 84.6154 | 91.6667 | 78.5714 | 81.9355 | 22 | 2 | 22 | 6 | 6 | 100.0000 | |
| gduggal-snapplat | SNP | ti | segdup | homalt | 99.4715 | 99.0673 | 99.8790 | 87.9842 | 7435 | 70 | 7429 | 9 | 6 | 66.6667 | |
| gduggal-snapplat | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 78.2077 | 80.0368 | 76.4603 | 79.5968 | 1740 | 434 | 1741 | 536 | 6 | 1.1194 | |
| gduggal-snapplat | SNP | tv | segdup | het | 98.3319 | 98.0329 | 98.6327 | 95.7233 | 5183 | 104 | 5194 | 72 | 6 | 8.3333 | |
| gduggal-snapvard | INDEL | * | map_l150_m1_e0 | homalt | 92.4102 | 87.0130 | 98.5213 | 84.2778 | 402 | 60 | 533 | 8 | 6 | 75.0000 | |
| gduggal-snapvard | INDEL | * | map_l150_m2_e0 | homalt | 92.6163 | 87.3181 | 98.5989 | 84.8461 | 420 | 61 | 563 | 8 | 6 | 75.0000 | |
| gduggal-snapvard | INDEL | * | map_l150_m2_e1 | homalt | 92.4410 | 86.9919 | 98.6183 | 84.9532 | 428 | 64 | 571 | 8 | 6 | 75.0000 | |
| gduggal-snapvard | INDEL | C16_PLUS | * | * | 0.0000 | 0.0000 | 22.5352 | 85.7143 | 0 | 0 | 16 | 55 | 6 | 10.9091 | |
| gduggal-snapvard | INDEL | C16_PLUS | HG002complexvar | * | 0.0000 | 0.0000 | 35.5556 | 72.5610 | 0 | 0 | 16 | 29 | 6 | 20.6897 | |
| gduggal-snapvard | INDEL | C1_5 | map_l125_m2_e0 | * | 0.0000 | 0.0000 | 44.5455 | 96.0686 | 0 | 0 | 49 | 61 | 6 | 9.8361 | |
| gduggal-snapvard | INDEL | C1_5 | map_l125_m2_e0 | het | 0.0000 | 0.0000 | 37.7551 | 96.0098 | 0 | 0 | 37 | 61 | 6 | 9.8361 | |
| gduggal-snapvard | INDEL | C1_5 | map_l125_m2_e1 | * | 0.0000 | 0.0000 | 44.5455 | 96.1417 | 0 | 0 | 49 | 61 | 6 | 9.8361 | |
| gduggal-snapvard | INDEL | C1_5 | map_l125_m2_e1 | het | 0.0000 | 0.0000 | 37.7551 | 96.0863 | 0 | 0 | 37 | 61 | 6 | 9.8361 | |
| gduggal-snapvard | INDEL | C6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 0.0000 | 0.0000 | 17.5000 | 82.5708 | 0 | 0 | 14 | 66 | 6 | 9.0909 | |
| gduggal-snapvard | INDEL | C6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 0.0000 | 0.0000 | 16.4557 | 81.6279 | 0 | 0 | 13 | 66 | 6 | 9.0909 | |
| gduggal-snapvard | INDEL | D16_PLUS | map_siren | * | 9.6970 | 5.5944 | 36.3636 | 92.6174 | 8 | 135 | 8 | 14 | 6 | 42.8571 | |
| gduggal-snapvard | INDEL | D16_PLUS | map_siren | het | 14.1414 | 8.9744 | 33.3333 | 92.6056 | 7 | 71 | 7 | 14 | 6 | 42.8571 | |
| gduggal-snapfb | INDEL | I6_15 | map_l100_m1_e0 | * | 81.3037 | 72.8070 | 92.0455 | 76.5957 | 83 | 31 | 81 | 7 | 6 | 85.7143 | |
| gduggal-snapfb | INDEL | I6_15 | map_l100_m2_e0 | * | 81.0925 | 72.4138 | 92.1348 | 78.6058 | 84 | 32 | 82 | 7 | 6 | 85.7143 | |
| gduggal-snapfb | INDEL | I6_15 | map_l100_m2_e1 | * | 81.0925 | 72.4138 | 92.1348 | 79.2056 | 84 | 32 | 82 | 7 | 6 | 85.7143 | |
| gduggal-snapfb | INDEL | I6_15 | map_siren | hetalt | 66.0377 | 62.5000 | 70.0000 | 76.1905 | 45 | 27 | 14 | 6 | 6 | 100.0000 | |
| gduggal-snapfb | SNP | * | lowcmp_SimpleRepeat_quadTR_51to200 | homalt | 56.9106 | 85.3659 | 42.6829 | 94.4180 | 35 | 6 | 35 | 47 | 6 | 12.7660 | |
| gduggal-snapfb | SNP | ti | HG002compoundhet | hetalt | 97.8831 | 99.8273 | 96.0133 | 26.9417 | 578 | 1 | 578 | 24 | 6 | 25.0000 | |
| gduggal-snapfb | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 97.1716 | 99.7669 | 94.7078 | 58.2028 | 856 | 2 | 859 | 48 | 6 | 12.5000 | |
| gduggal-snapfb | SNP | ti | lowcmp_SimpleRepeat_homopolymer_6to10 | homalt | 99.5691 | 99.7274 | 99.4112 | 46.0147 | 2195 | 6 | 2195 | 13 | 6 | 46.1538 | |
| gduggal-snapfb | SNP | ti | lowcmp_SimpleRepeat_quadTR_51to200 | homalt | 62.6263 | 88.5714 | 48.4375 | 94.7840 | 31 | 4 | 31 | 33 | 6 | 18.1818 | |
| gduggal-snapfb | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 78.0360 | 99.3263 | 64.2617 | 73.0595 | 1327 | 9 | 1336 | 743 | 6 | 0.8075 | |
| gduggal-snapfb | SNP | tv | map_l100_m0_e0 | homalt | 97.1883 | 95.2678 | 99.1879 | 78.6252 | 3664 | 182 | 3664 | 30 | 6 | 20.0000 | |
| gduggal-snapfb | SNP | tv | map_l125_m0_e0 | homalt | 96.2107 | 93.7416 | 98.8135 | 84.7573 | 2082 | 139 | 2082 | 25 | 6 | 24.0000 | |
| gduggal-snapfb | SNP | tv | map_l150_m1_e0 | homalt | 97.1916 | 95.1597 | 99.3122 | 81.5059 | 3755 | 191 | 3754 | 26 | 6 | 23.0769 | |
| gduggal-snapfb | SNP | tv | map_l150_m2_e0 | homalt | 97.2621 | 95.2731 | 99.3359 | 82.3744 | 3890 | 193 | 3889 | 26 | 6 | 23.0769 | |
| gduggal-snapfb | SNP | tv | map_l150_m2_e1 | homalt | 97.2966 | 95.3314 | 99.3444 | 82.3553 | 3941 | 193 | 3940 | 26 | 6 | 23.0769 | |
| gduggal-snapplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | hetalt | 39.0387 | 28.0303 | 64.2857 | 93.0175 | 37 | 95 | 36 | 20 | 6 | 30.0000 | |
| jli-custom | INDEL | D16_PLUS | HG002complexvar | het | 97.1408 | 95.7543 | 98.5680 | 65.7400 | 1060 | 47 | 826 | 12 | 6 | 50.0000 | |
| jli-custom | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | * | 98.6345 | 97.9145 | 99.3651 | 67.4587 | 939 | 20 | 939 | 6 | 6 | 100.0000 | |
| jli-custom | INDEL | D1_5 | HG002complexvar | het | 99.7322 | 99.5618 | 99.9033 | 54.7904 | 20674 | 91 | 20667 | 20 | 6 | 30.0000 | |
| jli-custom | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 98.6785 | 97.8849 | 99.4850 | 27.4595 | 1157 | 25 | 1159 | 6 | 6 | 100.0000 | |
| jli-custom | INDEL | I16_PLUS | HG002compoundhet | het | 74.1746 | 87.2340 | 64.5161 | 91.9481 | 41 | 6 | 20 | 11 | 6 | 54.5455 | |
| jli-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 99.8378 | 99.7231 | 99.9528 | 67.2930 | 16928 | 47 | 16928 | 8 | 6 | 75.0000 | |
| jli-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 99.8378 | 99.7231 | 99.9528 | 67.2930 | 16928 | 47 | 16928 | 8 | 6 | 75.0000 | |
| jli-custom | SNP | * | map_l250_m1_e0 | homalt | 99.3477 | 98.9444 | 99.7544 | 84.2418 | 2437 | 26 | 2437 | 6 | 6 | 100.0000 | |
| jli-custom | SNP | * | map_l250_m2_e0 | homalt | 99.3833 | 98.9948 | 99.7749 | 85.5202 | 2659 | 27 | 2659 | 6 | 6 | 100.0000 | |
| jli-custom | SNP | * | map_l250_m2_e1 | homalt | 99.3906 | 99.0066 | 99.7775 | 85.5799 | 2691 | 27 | 2691 | 6 | 6 | 100.0000 | |
| jli-custom | SNP | ti | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 99.3229 | 99.3534 | 99.2923 | 66.7825 | 3227 | 21 | 3227 | 23 | 6 | 26.0870 | |
| jli-custom | SNP | ti | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 99.6032 | 99.8263 | 99.3810 | 56.4884 | 17820 | 31 | 17821 | 111 | 6 | 5.4054 | |
| jli-custom | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 98.8825 | 98.9969 | 98.7683 | 87.0977 | 1283 | 13 | 1283 | 16 | 6 | 37.5000 | |