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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
63501-63550 / 86044 show all | |||||||||||||||
| ckim-vqsr | INDEL | D6_15 | map_l150_m1_e0 | het | 95.0000 | 97.4359 | 92.6829 | 95.6978 | 38 | 1 | 38 | 3 | 0 | 0.0000 | |
| cchapple-custom | INDEL | D6_15 | map_l150_m1_e0 | het | 95.8628 | 97.4359 | 94.3396 | 91.6535 | 38 | 1 | 50 | 3 | 1 | 33.3333 | |
| ciseli-custom | SNP | tv | tech_badpromoters | homalt | 96.1368 | 97.4359 | 94.8718 | 56.1798 | 38 | 1 | 37 | 2 | 0 | 0.0000 | |
| ckim-dragen | INDEL | * | map_l250_m0_e0 | * | 92.1212 | 97.4359 | 87.3563 | 97.7177 | 76 | 2 | 76 | 11 | 1 | 9.0909 | |
| ckim-dragen | INDEL | * | tech_badpromoters | het | 98.7013 | 97.4359 | 100.0000 | 49.3333 | 38 | 1 | 38 | 0 | 0 | ||
| ckim-gatk | SNP | tv | tech_badpromoters | homalt | 97.4359 | 97.4359 | 97.4359 | 51.8519 | 38 | 1 | 38 | 1 | 1 | 100.0000 | |
| cchapple-custom | SNP | tv | tech_badpromoters | homalt | 97.4021 | 97.4359 | 97.3684 | 49.3333 | 38 | 1 | 37 | 1 | 1 | 100.0000 | |
| ckim-dragen | SNP | tv | tech_badpromoters | homalt | 97.4359 | 97.4359 | 97.4359 | 51.2500 | 38 | 1 | 38 | 1 | 1 | 100.0000 | |
| ckim-gatk | INDEL | * | tech_badpromoters | het | 98.7013 | 97.4359 | 100.0000 | 53.0864 | 38 | 1 | 38 | 0 | 0 | ||
| ckim-gatk | INDEL | D16_PLUS | map_siren | het | 91.8695 | 97.4359 | 86.9048 | 96.2700 | 76 | 2 | 73 | 11 | 2 | 18.1818 | |
| astatham-gatk | INDEL | * | tech_badpromoters | het | 98.7013 | 97.4359 | 100.0000 | 53.6585 | 38 | 1 | 38 | 0 | 0 | ||
| asubramanian-gatk | SNP | tv | tech_badpromoters | homalt | 97.4359 | 97.4359 | 97.4359 | 51.2500 | 38 | 1 | 38 | 1 | 1 | 100.0000 | |
| bgallagher-sentieon | INDEL | * | tech_badpromoters | het | 98.7013 | 97.4359 | 100.0000 | 52.5000 | 38 | 1 | 38 | 0 | 0 | ||
| bgallagher-sentieon | INDEL | D16_PLUS | map_siren | het | 91.8695 | 97.4359 | 86.9048 | 95.6967 | 76 | 2 | 73 | 11 | 2 | 18.1818 | |
| astatham-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 98.6028 | 97.4359 | 99.7980 | 86.4421 | 494 | 13 | 494 | 1 | 1 | 100.0000 | |
| astatham-gatk | SNP | tv | tech_badpromoters | homalt | 97.4359 | 97.4359 | 97.4359 | 51.8519 | 38 | 1 | 38 | 1 | 1 | 100.0000 | |
| asubramanian-gatk | INDEL | * | tech_badpromoters | het | 98.7013 | 97.4359 | 100.0000 | 53.6585 | 38 | 1 | 38 | 0 | 0 | ||
| bgallagher-sentieon | SNP | tv | tech_badpromoters | homalt | 97.4359 | 97.4359 | 97.4359 | 51.8519 | 38 | 1 | 38 | 1 | 1 | 100.0000 | |
| cchapple-custom | INDEL | * | tech_badpromoters | het | 98.7013 | 97.4359 | 100.0000 | 51.5789 | 38 | 1 | 46 | 0 | 0 | ||
| jli-custom | INDEL | D6_15 | map_l125_m1_e0 | * | 98.2759 | 97.4359 | 99.1304 | 88.8781 | 114 | 3 | 114 | 1 | 0 | 0.0000 | |
| hfeng-pmm3 | INDEL | * | map_l250_m0_e0 | * | 93.2515 | 97.4359 | 89.4118 | 97.2159 | 76 | 2 | 76 | 9 | 2 | 22.2222 | |
| jlack-gatk | INDEL | D6_15 | map_l150_m1_e0 | het | 90.4762 | 97.4359 | 84.4444 | 95.1665 | 38 | 1 | 38 | 7 | 0 | 0.0000 | |
| jlack-gatk | SNP | tv | tech_badpromoters | homalt | 98.7013 | 97.4359 | 100.0000 | 53.0864 | 38 | 1 | 38 | 0 | 0 | ||
| gduggal-bwavard | SNP | * | map_l100_m2_e1 | * | 96.4757 | 97.4377 | 95.5326 | 75.4346 | 72822 | 1915 | 71809 | 3358 | 246 | 7.3258 | |
| jmaeng-gatk | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 97.7912 | 97.4394 | 98.1455 | 73.7551 | 723 | 19 | 688 | 13 | 9 | 69.2308 | |
| gduggal-bwavard | SNP | ti | map_l150_m2_e0 | homalt | 98.6236 | 97.4396 | 99.8368 | 73.2710 | 7421 | 195 | 7339 | 12 | 9 | 75.0000 | |
| astatham-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 98.5976 | 97.4414 | 99.7817 | 85.6785 | 457 | 12 | 457 | 1 | 1 | 100.0000 | |
| rpoplin-dv42 | INDEL | * | map_l150_m2_e0 | * | 97.9323 | 97.4432 | 98.4263 | 99.0377 | 1372 | 36 | 1376 | 22 | 10 | 45.4545 | |
| jlack-gatk | INDEL | * | map_l125_m0_e0 | het | 90.1770 | 97.4446 | 83.9181 | 93.0825 | 572 | 15 | 574 | 110 | 2 | 1.8182 | |
| dgrover-gatk | INDEL | * | map_l125_m0_e0 | het | 97.2014 | 97.4446 | 96.9595 | 91.3349 | 572 | 15 | 574 | 18 | 2 | 11.1111 | |
| dgrover-gatk | INDEL | D6_15 | map_siren | * | 97.7320 | 97.4460 | 98.0198 | 85.5879 | 496 | 13 | 495 | 10 | 2 | 20.0000 | |
| bgallagher-sentieon | INDEL | D6_15 | map_siren | * | 97.5395 | 97.4460 | 97.6331 | 85.2014 | 496 | 13 | 495 | 12 | 2 | 16.6667 | |
| gduggal-snapvard | SNP | tv | map_l100_m2_e1 | het | 92.6451 | 97.4464 | 88.2947 | 79.7695 | 15531 | 407 | 15471 | 2051 | 143 | 6.9722 | |
| gduggal-snapvard | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 92.3065 | 97.4471 | 87.6810 | 67.1193 | 3779 | 99 | 3694 | 519 | 13 | 2.5048 | |
| gduggal-bwavard | SNP | ti | map_l150_m1_e0 | homalt | 98.6247 | 97.4478 | 99.8303 | 71.2444 | 7140 | 187 | 7059 | 12 | 9 | 75.0000 | |
| anovak-vg | SNP | ti | segdup | het | 97.2381 | 97.4480 | 97.0290 | 93.2429 | 11723 | 307 | 11659 | 357 | 90 | 25.2101 | |
| hfeng-pmm1 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.5604 | 97.4488 | 99.6975 | 72.9214 | 8900 | 233 | 8900 | 27 | 5 | 18.5185 | |
| hfeng-pmm1 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.5604 | 97.4488 | 99.6975 | 72.9214 | 8900 | 233 | 8900 | 27 | 5 | 18.5185 | |
| ltrigg-rtg2 | INDEL | * | map_siren | het | 98.0316 | 97.4490 | 98.6212 | 76.8583 | 4393 | 115 | 4363 | 61 | 2 | 3.2787 | |
| ckim-dragen | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 97.7158 | 97.4490 | 97.9841 | 76.9231 | 2101 | 55 | 2090 | 43 | 21 | 48.8372 | |
| cchapple-custom | SNP | ti | map_l100_m2_e0 | homalt | 98.7027 | 97.4493 | 99.9888 | 57.8553 | 17842 | 467 | 17837 | 2 | 2 | 100.0000 | |
| egarrison-hhga | SNP | ti | map_l250_m2_e0 | het | 98.4630 | 97.4493 | 99.4980 | 89.1481 | 3171 | 83 | 3171 | 16 | 6 | 37.5000 | |
| astatham-gatk | SNP | * | HG002complexvar | het | 98.7010 | 97.4496 | 99.9850 | 18.8713 | 453625 | 11872 | 453498 | 68 | 28 | 41.1765 | |
| jli-custom | INDEL | D16_PLUS | * | * | 98.0920 | 97.4499 | 98.7427 | 65.2664 | 6611 | 173 | 6597 | 84 | 63 | 75.0000 | |
| jmaeng-gatk | INDEL | D16_PLUS | * | * | 97.5405 | 97.4499 | 97.6314 | 70.8962 | 6611 | 173 | 6595 | 160 | 119 | 74.3750 | |
| gduggal-snapplat | SNP | tv | HG002complexvar | homalt | 98.5607 | 97.4503 | 99.6966 | 24.7080 | 92686 | 2425 | 92657 | 282 | 135 | 47.8723 | |
| gduggal-bwavard | SNP | * | map_l100_m0_e0 | * | 94.9074 | 97.4514 | 92.4929 | 77.7735 | 32004 | 837 | 31615 | 2566 | 141 | 5.4949 | |
| cchapple-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 98.2263 | 97.4515 | 99.0136 | 67.7535 | 803 | 21 | 803 | 8 | 8 | 100.0000 | |
| cchapple-custom | SNP | tv | map_l100_m0_e0 | het | 95.4613 | 97.4522 | 93.5501 | 77.1681 | 7038 | 184 | 7049 | 486 | 83 | 17.0782 | |
| ckim-dragen | SNP | * | tech_badpromoters | * | 98.0769 | 97.4522 | 98.7097 | 43.8406 | 153 | 4 | 153 | 2 | 2 | 100.0000 | |