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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
38801-38850 / 86044 show all | |||||||||||||||
| eyeh-varpipe | INDEL | D1_5 | map_l150_m2_e0 | hetalt | 72.7273 | 57.1429 | 100.0000 | 96.9789 | 4 | 3 | 10 | 0 | 0 | ||
| hfeng-pmm2 | INDEL | I6_15 | map_l250_m1_e0 | * | 66.6667 | 57.1429 | 80.0000 | 98.0545 | 4 | 3 | 4 | 1 | 1 | 100.0000 | |
| hfeng-pmm1 | INDEL | I6_15 | map_l250_m1_e0 | * | 66.6667 | 57.1429 | 80.0000 | 97.7169 | 4 | 3 | 4 | 1 | 1 | 100.0000 | |
| hfeng-pmm3 | INDEL | I6_15 | map_l250_m1_e0 | * | 66.6667 | 57.1429 | 80.0000 | 97.6526 | 4 | 3 | 4 | 1 | 1 | 100.0000 | |
| jli-custom | INDEL | C1_5 | HG002complexvar | * | 0.0000 | 57.1429 | 0.0000 | 0.0000 | 4 | 3 | 0 | 0 | 0 | ||
| jli-custom | INDEL | C1_5 | HG002complexvar | het | 0.0000 | 57.1429 | 0.0000 | 0.0000 | 4 | 3 | 0 | 0 | 0 | ||
| jli-custom | INDEL | D1_5 | map_l150_m1_e0 | hetalt | 72.7273 | 57.1429 | 100.0000 | 98.3193 | 4 | 3 | 4 | 0 | 0 | ||
| jli-custom | INDEL | D1_5 | map_l150_m2_e0 | hetalt | 72.7273 | 57.1429 | 100.0000 | 98.4962 | 4 | 3 | 4 | 0 | 0 | ||
| jli-custom | INDEL | I6_15 | map_l250_m1_e0 | * | 66.6667 | 57.1429 | 80.0000 | 97.5962 | 4 | 3 | 4 | 1 | 1 | 100.0000 | |
| jmaeng-gatk | INDEL | D1_5 | map_l150_m1_e0 | hetalt | 72.7273 | 57.1429 | 100.0000 | 98.4436 | 4 | 3 | 4 | 0 | 0 | ||
| jmaeng-gatk | INDEL | D1_5 | map_l150_m2_e0 | hetalt | 72.7273 | 57.1429 | 100.0000 | 98.6254 | 4 | 3 | 4 | 0 | 0 | ||
| jmaeng-gatk | INDEL | I6_15 | map_l250_m1_e0 | * | 66.6667 | 57.1429 | 80.0000 | 98.7277 | 4 | 3 | 4 | 1 | 1 | 100.0000 | |
| jmaeng-gatk | SNP | ti | map_l100_m0_e0 | hetalt | 72.7273 | 57.1429 | 100.0000 | 90.5882 | 8 | 6 | 8 | 0 | 0 | ||
| gduggal-bwaplat | INDEL | D16_PLUS | map_l125_m2_e1 | * | 72.7273 | 57.1429 | 100.0000 | 97.4026 | 16 | 12 | 16 | 0 | 0 | ||
| gduggal-bwaplat | INDEL | D16_PLUS | map_l150_m0_e0 | * | 72.7273 | 57.1429 | 100.0000 | 98.4314 | 4 | 3 | 4 | 0 | 0 | ||
| gduggal-bwaplat | INDEL | D16_PLUS | map_l150_m0_e0 | het | 72.7273 | 57.1429 | 100.0000 | 98.0952 | 4 | 3 | 4 | 0 | 0 | ||
| gduggal-bwaplat | INDEL | D16_PLUS | map_l150_m1_e0 | het | 72.7273 | 57.1429 | 100.0000 | 97.7077 | 8 | 6 | 8 | 0 | 0 | ||
| gduggal-bwaplat | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | hetalt | 72.7273 | 57.1429 | 100.0000 | 68.2540 | 20 | 15 | 20 | 0 | 0 | ||
| gduggal-snapfb | INDEL | D1_5 | map_l150_m1_e0 | hetalt | 72.7273 | 57.1429 | 100.0000 | 97.6879 | 4 | 3 | 4 | 0 | 0 | ||
| gduggal-snapfb | INDEL | D1_5 | map_l150_m2_e0 | hetalt | 72.7273 | 57.1429 | 100.0000 | 97.8947 | 4 | 3 | 4 | 0 | 0 | ||
| gduggal-snapfb | INDEL | D6_15 | map_l250_m2_e0 | het | 69.5652 | 57.1429 | 88.8889 | 93.8356 | 8 | 6 | 8 | 1 | 1 | 100.0000 | |
| gduggal-snapfb | INDEL | D6_15 | map_l250_m2_e1 | het | 69.5652 | 57.1429 | 88.8889 | 93.9189 | 8 | 6 | 8 | 1 | 1 | 100.0000 | |
| gduggal-bwaplat | INDEL | * | map_l125_m2_e0 | hetalt | 72.7273 | 57.1429 | 100.0000 | 97.4249 | 24 | 18 | 24 | 0 | 0 | ||
| gduggal-bwafb | INDEL | D1_5 | map_l150_m1_e0 | hetalt | 72.7273 | 57.1429 | 100.0000 | 97.3684 | 4 | 3 | 4 | 0 | 0 | ||
| gduggal-bwafb | INDEL | D1_5 | map_l150_m2_e0 | hetalt | 72.7273 | 57.1429 | 100.0000 | 97.6048 | 4 | 3 | 4 | 0 | 0 | ||
| gduggal-bwavard | INDEL | D6_15 | map_l150_m0_e0 | homalt | 72.7273 | 57.1429 | 100.0000 | 95.2381 | 4 | 3 | 4 | 0 | 0 | ||
| gduggal-bwavard | INDEL | I6_15 | map_l150_m1_e0 | homalt | 66.6667 | 57.1429 | 80.0000 | 87.5000 | 4 | 3 | 4 | 1 | 0 | 0.0000 | |
| gduggal-bwavard | INDEL | I6_15 | map_l150_m2_e0 | homalt | 66.6667 | 57.1429 | 80.0000 | 90.0000 | 4 | 3 | 4 | 1 | 0 | 0.0000 | |
| gduggal-bwaplat | SNP | * | map_l100_m2_e0 | hetalt | 72.7273 | 57.1429 | 100.0000 | 91.3669 | 24 | 18 | 24 | 0 | 0 | ||
| gduggal-bwaplat | SNP | tv | map_l100_m2_e0 | hetalt | 72.7273 | 57.1429 | 100.0000 | 91.3669 | 24 | 18 | 24 | 0 | 0 | ||
| mlin-fermikit | INDEL | D16_PLUS | map_l150_m0_e0 | * | 40.0000 | 57.1429 | 30.7692 | 93.1937 | 4 | 3 | 4 | 9 | 2 | 22.2222 | |
| mlin-fermikit | INDEL | D16_PLUS | map_l150_m0_e0 | het | 53.3333 | 57.1429 | 50.0000 | 91.0112 | 4 | 3 | 4 | 4 | 0 | 0.0000 | |
| raldana-dualsentieon | INDEL | I6_15 | map_l250_m1_e0 | * | 72.7273 | 57.1429 | 100.0000 | 97.5155 | 4 | 3 | 4 | 0 | 0 | ||
| qzeng-custom | INDEL | D1_5 | map_l150_m1_e0 | hetalt | 57.1429 | 100.0000 | 4 | 3 | 0 | 0 | 0 | ||||
| qzeng-custom | INDEL | D1_5 | map_l150_m2_e0 | hetalt | 57.1429 | 100.0000 | 4 | 3 | 0 | 0 | 0 | ||||
| qzeng-custom | INDEL | D6_15 | map_l250_m2_e0 | het | 64.2336 | 57.1429 | 73.3333 | 98.2935 | 8 | 6 | 11 | 4 | 2 | 50.0000 | |
| qzeng-custom | INDEL | D6_15 | map_l250_m2_e1 | het | 64.2336 | 57.1429 | 73.3333 | 98.3221 | 8 | 6 | 11 | 4 | 2 | 50.0000 | |
| anovak-vg | INDEL | D16_PLUS | map_l150_m0_e0 | * | 72.7273 | 57.1429 | 100.0000 | 96.6102 | 4 | 3 | 4 | 0 | 0 | ||
| anovak-vg | INDEL | D16_PLUS | map_l150_m0_e0 | het | 72.7273 | 57.1429 | 100.0000 | 95.1807 | 4 | 3 | 4 | 0 | 0 | ||
| anovak-vg | INDEL | D16_PLUS | map_l150_m1_e0 | het | 69.5652 | 57.1429 | 88.8889 | 92.3729 | 8 | 6 | 8 | 1 | 1 | 100.0000 | |
| anovak-vg | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_gt200bp_gt95identity_merged | het | 66.6667 | 57.1429 | 80.0000 | 99.3990 | 4 | 3 | 4 | 1 | 1 | 100.0000 | |
| asubramanian-gatk | INDEL | I6_15 | map_l150_m1_e0 | homalt | 72.7273 | 57.1429 | 100.0000 | 97.3510 | 4 | 3 | 4 | 0 | 0 | ||
| asubramanian-gatk | INDEL | I6_15 | map_l150_m2_e0 | homalt | 72.7273 | 57.1429 | 100.0000 | 97.6879 | 4 | 3 | 4 | 0 | 0 | ||
| asubramanian-gatk | INDEL | I6_15 | map_l250_m1_e0 | * | 67.7966 | 57.1429 | 83.3333 | 98.1928 | 4 | 3 | 5 | 1 | 1 | 100.0000 | |
| mlin-fermikit | SNP | ti | map_l125_m1_e0 | homalt | 66.1427 | 57.1480 | 78.4977 | 52.8912 | 6312 | 4733 | 6312 | 1729 | 1647 | 95.2574 | |
| jmaeng-gatk | SNP | * | map_l150_m2_e0 | homalt | 72.7253 | 57.1502 | 99.9701 | 80.8789 | 6686 | 5013 | 6686 | 2 | 2 | 100.0000 | |
| mlin-fermikit | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 72.4268 | 57.1879 | 98.7375 | 38.9205 | 1452 | 1087 | 1486 | 19 | 19 | 100.0000 | |
| anovak-vg | INDEL | I1_5 | HG002complexvar | * | 58.0984 | 57.1891 | 59.0370 | 52.0780 | 19080 | 14283 | 19360 | 13433 | 12541 | 93.3596 | |
| qzeng-custom | SNP | ti | map_l150_m0_e0 | homalt | 72.5105 | 57.1894 | 99.0446 | 79.2025 | 1579 | 1182 | 1555 | 15 | 15 | 100.0000 | |
| gduggal-snapfb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 53.0813 | 57.1912 | 49.5224 | 53.3105 | 676 | 506 | 674 | 687 | 585 | 85.1528 | |