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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
37201-37250 / 86044 show all | |||||||||||||||
| jlack-gatk | SNP | tv | tech_badpromoters | het | 94.2857 | 100.0000 | 89.1892 | 52.5641 | 33 | 0 | 33 | 4 | 0 | 0.0000 | |
| jli-custom | INDEL | * | tech_badpromoters | homalt | 100.0000 | 100.0000 | 100.0000 | 56.5789 | 33 | 0 | 33 | 0 | 0 | ||
| jlack-gatk | INDEL | * | tech_badpromoters | homalt | 100.0000 | 100.0000 | 100.0000 | 56.5789 | 33 | 0 | 33 | 0 | 0 | ||
| jlack-gatk | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | hetalt | 91.6667 | 84.6154 | 100.0000 | 58.7500 | 33 | 6 | 33 | 0 | 0 | ||
| hfeng-pmm1 | INDEL | * | tech_badpromoters | homalt | 100.0000 | 100.0000 | 100.0000 | 56.5789 | 33 | 0 | 33 | 0 | 0 | ||
| hfeng-pmm1 | INDEL | D16_PLUS | lowcmp_SimpleRepeat_homopolymer_gt10 | het | 85.7143 | 75.0000 | 100.0000 | 96.6292 | 33 | 11 | 33 | 0 | 0 | ||
| hfeng-pmm1 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | hetalt | 91.6667 | 84.6154 | 100.0000 | 60.7143 | 33 | 6 | 33 | 0 | 0 | ||
| hfeng-pmm1 | INDEL | D6_15 | map_l125_m1_e0 | homalt | 98.5075 | 97.0588 | 100.0000 | 86.4754 | 33 | 1 | 33 | 0 | 0 | ||
| hfeng-pmm2 | INDEL | D1_5 | map_l250_m0_e0 | het | 90.4110 | 100.0000 | 82.5000 | 97.1711 | 33 | 0 | 33 | 7 | 0 | 0.0000 | |
| hfeng-pmm2 | INDEL | D6_15 | map_l125_m1_e0 | homalt | 98.5075 | 97.0588 | 100.0000 | 87.4046 | 33 | 1 | 33 | 0 | 0 | ||
| hfeng-pmm3 | INDEL | D1_5 | map_l250_m0_e0 | het | 95.6522 | 100.0000 | 91.6667 | 96.7003 | 33 | 0 | 33 | 3 | 0 | 0.0000 | |
| hfeng-pmm3 | INDEL | D6_15 | map_l125_m1_e0 | homalt | 98.5075 | 97.0588 | 100.0000 | 86.4754 | 33 | 1 | 33 | 0 | 0 | ||
| hfeng-pmm2 | SNP | ti | lowcmp_SimpleRepeat_quadTR_51to200 | homalt | 97.0588 | 94.2857 | 100.0000 | 94.0325 | 33 | 2 | 33 | 0 | 0 | ||
| hfeng-pmm3 | INDEL | * | tech_badpromoters | homalt | 100.0000 | 100.0000 | 100.0000 | 57.1429 | 33 | 0 | 33 | 0 | 0 | ||
| hfeng-pmm1 | SNP | ti | lowcmp_SimpleRepeat_quadTR_51to200 | homalt | 97.0588 | 94.2857 | 100.0000 | 93.2099 | 33 | 2 | 33 | 0 | 0 | ||
| hfeng-pmm2 | INDEL | * | tech_badpromoters | homalt | 100.0000 | 100.0000 | 100.0000 | 54.7945 | 33 | 0 | 33 | 0 | 0 | ||
| eyeh-varpipe | SNP | tv | tech_badpromoters | het | 63.4615 | 100.0000 | 46.4789 | 76.6447 | 33 | 0 | 33 | 38 | 0 | 0.0000 | |
| gduggal-bwafb | INDEL | * | map_l125_m1_e0 | hetalt | 90.4110 | 82.5000 | 100.0000 | 95.1952 | 33 | 7 | 16 | 0 | 0 | ||
| gduggal-bwafb | INDEL | * | tech_badpromoters | homalt | 98.5075 | 100.0000 | 97.0588 | 53.4247 | 33 | 0 | 33 | 1 | 1 | 100.0000 | |
| gduggal-bwavard | INDEL | D1_5 | map_l250_m0_e0 | het | 69.4737 | 100.0000 | 53.2258 | 97.1702 | 33 | 0 | 33 | 29 | 2 | 6.8966 | |
| gduggal-bwavard | INDEL | I6_15 | segdup | homalt | 82.5000 | 70.2128 | 100.0000 | 88.7681 | 33 | 14 | 31 | 0 | 0 | ||
| gduggal-bwaplat | INDEL | D6_15 | map_l100_m1_e0 | hetalt | 65.3465 | 48.5294 | 100.0000 | 89.8773 | 33 | 35 | 33 | 0 | 0 | ||
| gduggal-bwaplat | INDEL | D6_15 | map_l100_m2_e0 | hetalt | 65.3465 | 48.5294 | 100.0000 | 90.4348 | 33 | 35 | 33 | 0 | 0 | ||
| gduggal-bwafb | INDEL | D1_5 | map_l100_m2_e0 | hetalt | 79.9308 | 68.7500 | 95.4545 | 93.6047 | 33 | 15 | 21 | 1 | 1 | 100.0000 | |
| gduggal-bwafb | INDEL | D1_5 | map_l100_m2_e1 | hetalt | 77.1285 | 64.7059 | 95.4545 | 93.7143 | 33 | 18 | 21 | 1 | 1 | 100.0000 | |
| gduggal-bwafb | INDEL | I16_PLUS | map_siren | * | 54.1375 | 38.3721 | 91.8919 | 72.3881 | 33 | 53 | 34 | 3 | 3 | 100.0000 | |
| gduggal-bwafb | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | hetalt | 65.6064 | 54.0984 | 83.3333 | 66.0377 | 33 | 28 | 15 | 3 | 3 | 100.0000 | |
| gduggal-bwafb | SNP | tv | tech_badpromoters | het | 94.2857 | 100.0000 | 89.1892 | 66.6667 | 33 | 0 | 33 | 4 | 0 | 0.0000 | |
| gduggal-bwaplat | INDEL | D16_PLUS | lowcmp_SimpleRepeat_triTR_11to50 | homalt | 84.6154 | 73.3333 | 100.0000 | 54.7945 | 33 | 12 | 33 | 0 | 0 | ||
| ltrigg-rtg2 | SNP | tv | tech_badpromoters | het | 97.0588 | 100.0000 | 94.2857 | 65.6863 | 33 | 0 | 33 | 2 | 0 | 0.0000 | |
| mlin-fermikit | INDEL | * | tech_badpromoters | homalt | 97.0588 | 100.0000 | 94.2857 | 54.5455 | 33 | 0 | 33 | 2 | 2 | 100.0000 | |
| ltrigg-rtg2 | INDEL | D6_15 | map_l125_m1_e0 | homalt | 98.5075 | 97.0588 | 100.0000 | 81.3253 | 33 | 1 | 31 | 0 | 0 | ||
| ltrigg-rtg2 | INDEL | I16_PLUS | lowcmp_SimpleRepeat_triTR_11to50 | * | 92.9577 | 89.1892 | 97.0588 | 68.8073 | 33 | 4 | 33 | 1 | 1 | 100.0000 | |
| ndellapenna-hhga | INDEL | I16_PLUS | lowcmp_SimpleRepeat_triTR_11to50 | * | 92.9577 | 89.1892 | 97.0588 | 77.0270 | 33 | 4 | 33 | 1 | 1 | 100.0000 | |
| ndellapenna-hhga | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | homalt | 91.6667 | 91.6667 | 91.6667 | 72.7273 | 33 | 3 | 33 | 3 | 3 | 100.0000 | |
| ndellapenna-hhga | SNP | tv | lowcmp_SimpleRepeat_quadTR_51to200 | * | 86.8064 | 78.5714 | 96.9697 | 88.5813 | 33 | 9 | 32 | 1 | 0 | 0.0000 | |
| qzeng-custom | INDEL | * | map_l125_m2_e0 | hetalt | 88.0000 | 78.5714 | 100.0000 | 93.2000 | 33 | 9 | 17 | 0 | 0 | ||
| qzeng-custom | INDEL | * | map_l125_m2_e1 | hetalt | 86.8421 | 76.7442 | 100.0000 | 93.2806 | 33 | 10 | 17 | 0 | 0 | ||
| qzeng-custom | INDEL | I6_15 | lowcmp_SimpleRepeat_diTR_51to200 | * | 44.0143 | 35.8696 | 56.9444 | 58.6207 | 33 | 59 | 41 | 31 | 27 | 87.0968 | |
| raldana-dualsentieon | INDEL | * | tech_badpromoters | homalt | 100.0000 | 100.0000 | 100.0000 | 57.1429 | 33 | 0 | 33 | 0 | 0 | ||
| qzeng-custom | INDEL | D6_15 | lowcmp_SimpleRepeat_homopolymer_gt10 | het | 68.3576 | 78.5714 | 60.4938 | 98.6745 | 33 | 9 | 49 | 32 | 0 | 0.0000 | |
| mlin-fermikit | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | homalt | 95.6930 | 94.2857 | 97.1429 | 83.7209 | 33 | 2 | 34 | 1 | 1 | 100.0000 | |
| mlin-fermikit | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | homalt | 91.6667 | 91.6667 | 91.6667 | 70.0000 | 33 | 3 | 33 | 3 | 3 | 100.0000 | |
| mlin-fermikit | INDEL | I6_15 | map_l125_m1_e0 | * | 71.1252 | 62.2642 | 82.9268 | 83.4677 | 33 | 20 | 34 | 7 | 6 | 85.7143 | |
| mlin-fermikit | INDEL | I6_15 | map_l125_m2_e0 | * | 71.1252 | 62.2642 | 82.9268 | 86.1017 | 33 | 20 | 34 | 7 | 6 | 85.7143 | |
| mlin-fermikit | INDEL | I6_15 | map_l125_m2_e1 | * | 71.1252 | 62.2642 | 82.9268 | 86.6013 | 33 | 20 | 34 | 7 | 6 | 85.7143 | |
| ndellapenna-hhga | INDEL | D6_15 | map_l125_m1_e0 | homalt | 97.0588 | 97.0588 | 97.0588 | 88.0282 | 33 | 1 | 33 | 1 | 1 | 100.0000 | |
| jmaeng-gatk | INDEL | D16_PLUS | map_siren | homalt | 92.9577 | 97.0588 | 89.1892 | 94.0419 | 33 | 1 | 33 | 4 | 0 | 0.0000 | |
| jmaeng-gatk | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | hetalt | 91.6667 | 84.6154 | 100.0000 | 59.7561 | 33 | 6 | 33 | 0 | 0 | ||
| jmaeng-gatk | INDEL | D6_15 | map_l125_m1_e0 | homalt | 98.5075 | 97.0588 | 100.0000 | 89.4569 | 33 | 1 | 33 | 0 | 0 | ||