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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
50101-50150 / 86044 show all | |||||||||||||||
| bgallagher-sentieon | INDEL | I1_5 | map_l100_m1_e0 | * | 98.9183 | 98.8798 | 98.9568 | 83.1237 | 1324 | 15 | 1328 | 14 | 4 | 28.5714 | |
| ciseli-custom | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | homalt | 35.4839 | 31.4286 | 40.7407 | 83.1250 | 11 | 24 | 11 | 16 | 15 | 93.7500 | |
| ckim-isaac | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 82.7602 | 77.8800 | 88.2929 | 83.1252 | 2116 | 601 | 2255 | 299 | 150 | 50.1672 | |
| ltrigg-rtg1 | INDEL | I16_PLUS | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 67.7419 | 56.0000 | 85.7143 | 83.1325 | 14 | 11 | 12 | 2 | 2 | 100.0000 | |
| jli-custom | INDEL | D1_5 | map_l100_m2_e1 | * | 98.6576 | 98.5044 | 98.8114 | 83.1328 | 1910 | 29 | 1912 | 23 | 8 | 34.7826 | |
| gduggal-bwavard | SNP | * | map_l150_m2_e1 | * | 95.0047 | 97.7678 | 92.3934 | 83.1339 | 31491 | 719 | 31083 | 2559 | 143 | 5.5881 | |
| anovak-vg | SNP | tv | map_l125_m0_e0 | het | 76.8817 | 88.8434 | 67.7587 | 83.1340 | 3910 | 491 | 3909 | 1860 | 528 | 28.3871 | |
| gduggal-bwavard | SNP | * | map_l125_m2_e0 | het | 94.1644 | 97.8921 | 90.7102 | 83.1354 | 28700 | 618 | 28366 | 2905 | 164 | 5.6454 | |
| gduggal-bwaplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 78.4458 | 66.0000 | 96.6764 | 83.1355 | 1980 | 1020 | 1978 | 68 | 17 | 25.0000 | |
| qzeng-custom | INDEL | I16_PLUS | map_l100_m2_e1 | * | 52.5373 | 61.5385 | 45.8333 | 83.1382 | 16 | 10 | 33 | 39 | 0 | 0.0000 | |
| ndellapenna-hhga | INDEL | * | map_l100_m2_e1 | homalt | 98.4736 | 98.2045 | 98.7441 | 83.1392 | 1258 | 23 | 1258 | 16 | 11 | 68.7500 | |
| hfeng-pmm1 | INDEL | I6_15 | map_siren | * | 96.4706 | 94.0984 | 98.9655 | 83.1395 | 287 | 18 | 287 | 3 | 3 | 100.0000 | |
| jpowers-varprowl | INDEL | I1_5 | map_l100_m1_e0 | * | 93.9404 | 91.4862 | 96.5300 | 83.1405 | 1225 | 114 | 1224 | 44 | 31 | 70.4545 | |
| hfeng-pmm3 | INDEL | I1_5 | map_l125_m0_e0 | homalt | 98.7013 | 100.0000 | 97.4359 | 83.1412 | 114 | 0 | 114 | 3 | 2 | 66.6667 | |
| jpowers-varprowl | INDEL | I6_15 | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 66.1090 | 79.0323 | 56.8182 | 83.1418 | 49 | 13 | 50 | 38 | 38 | 100.0000 | |
| bgallagher-sentieon | SNP | * | map_l150_m0_e0 | het | 98.2803 | 98.9924 | 97.5782 | 83.1442 | 7860 | 80 | 7857 | 195 | 22 | 11.2821 | |
| ckim-dragen | SNP | ti | map_l150_m2_e0 | hetalt | 100.0000 | 100.0000 | 100.0000 | 83.1461 | 15 | 0 | 15 | 0 | 0 | ||
| ckim-dragen | SNP | ti | map_l150_m2_e1 | hetalt | 100.0000 | 100.0000 | 100.0000 | 83.1461 | 15 | 0 | 15 | 0 | 0 | ||
| ltrigg-rtg1 | INDEL | D1_5 | map_l125_m1_e0 | homalt | 99.4261 | 99.4269 | 99.4253 | 83.1477 | 347 | 2 | 346 | 2 | 2 | 100.0000 | |
| hfeng-pmm1 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 95.1724 | 96.1517 | 94.2128 | 83.1481 | 1749 | 70 | 1514 | 93 | 61 | 65.5914 | |
| hfeng-pmm1 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 95.1724 | 96.1517 | 94.2128 | 83.1481 | 1749 | 70 | 1514 | 93 | 61 | 65.5914 | |
| jmaeng-gatk | SNP | ti | map_l100_m0_e0 | * | 83.3904 | 72.5047 | 98.1224 | 83.1489 | 15785 | 5986 | 15782 | 302 | 37 | 12.2517 | |
| mlin-fermikit | INDEL | D1_5 | map_l150_m0_e0 | homalt | 65.0307 | 62.3529 | 67.9487 | 83.1533 | 53 | 32 | 53 | 25 | 21 | 84.0000 | |
| 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 | |
| hfeng-pmm2 | INDEL | D1_5 | map_l100_m1_e0 | * | 98.7075 | 99.0801 | 98.3378 | 83.1572 | 1831 | 17 | 1834 | 31 | 4 | 12.9032 | |
| ckim-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 100.0000 | 100.0000 | 100.0000 | 83.1579 | 16 | 0 | 16 | 0 | 0 | ||
| bgallagher-sentieon | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 100.0000 | 100.0000 | 100.0000 | 83.1579 | 16 | 0 | 16 | 0 | 0 | ||
| astatham-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 100.0000 | 100.0000 | 100.0000 | 83.1579 | 16 | 0 | 16 | 0 | 0 | ||
| jpowers-varprowl | INDEL | I16_PLUS | map_l100_m2_e1 | het | 70.5882 | 66.6667 | 75.0000 | 83.1579 | 12 | 6 | 12 | 4 | 4 | 100.0000 | |
| ckim-vqsr | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 100.0000 | 100.0000 | 100.0000 | 83.1579 | 16 | 0 | 16 | 0 | 0 | ||
| dgrover-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 100.0000 | 100.0000 | 100.0000 | 83.1579 | 16 | 0 | 16 | 0 | 0 | ||
| ltrigg-rtg1 | INDEL | * | map_l125_m2_e1 | * | 97.1606 | 95.2809 | 99.1159 | 83.1609 | 2120 | 105 | 2130 | 19 | 3 | 15.7895 | |
| jlack-gatk | SNP | ti | map_l100_m2_e1 | hetalt | 93.7500 | 96.7742 | 90.9091 | 83.1633 | 30 | 1 | 30 | 3 | 3 | 100.0000 | |
| astatham-gatk | SNP | tv | map_l150_m0_e0 | * | 93.7784 | 88.8356 | 99.3035 | 83.1642 | 3708 | 466 | 3707 | 26 | 6 | 23.0769 | |
| jmaeng-gatk | INDEL | I16_PLUS | lowcmp_SimpleRepeat_triTR_11to50 | het | 96.9697 | 100.0000 | 94.1176 | 83.1683 | 16 | 0 | 16 | 1 | 0 | 0.0000 | |
| gduggal-snapvard | INDEL | D6_15 | map_l100_m2_e1 | * | 65.5947 | 59.6364 | 72.8758 | 83.1683 | 164 | 111 | 223 | 83 | 59 | 71.0843 | |
| mlin-fermikit | INDEL | D16_PLUS | map_siren | hetalt | 66.6667 | 51.6129 | 94.1176 | 83.1683 | 16 | 15 | 16 | 1 | 0 | 0.0000 | |
| rpoplin-dv42 | INDEL | D6_15 | map_l100_m0_e0 | hetalt | 94.4444 | 89.4737 | 100.0000 | 83.1683 | 17 | 2 | 17 | 0 | 0 | ||
| ciseli-custom | INDEL | D6_15 | map_siren | homalt | 66.5025 | 82.3077 | 55.7895 | 83.1709 | 107 | 23 | 106 | 84 | 76 | 90.4762 | |
| ckim-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.4418 | 99.2664 | 97.6308 | 83.1720 | 9066 | 67 | 9066 | 220 | 10 | 4.5455 | |
| ckim-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.4418 | 99.2664 | 97.6308 | 83.1720 | 9066 | 67 | 9066 | 220 | 10 | 4.5455 | |
| gduggal-snapvard | INDEL | C1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 0.0000 | 0.0000 | 9.2511 | 83.1727 | 0 | 0 | 21 | 206 | 16 | 7.7670 | |
| gduggal-bwafb | INDEL | I6_15 | map_l100_m2_e1 | * | 86.3981 | 76.7241 | 98.8636 | 83.1740 | 89 | 27 | 87 | 1 | 1 | 100.0000 | |
| jli-custom | INDEL | * | map_l100_m1_e0 | het | 98.3638 | 98.1208 | 98.6080 | 83.1747 | 2193 | 42 | 2196 | 31 | 9 | 29.0323 | |
| ltrigg-rtg1 | INDEL | * | map_l125_m0_e0 | * | 95.9750 | 93.1973 | 98.9234 | 83.1757 | 822 | 60 | 827 | 9 | 2 | 22.2222 | |
| anovak-vg | INDEL | * | map_l125_m1_e0 | homalt | 76.2677 | 86.4754 | 68.2154 | 83.1764 | 633 | 99 | 646 | 301 | 277 | 92.0266 | |
| gduggal-bwavard | SNP | * | map_l125_m2_e1 | het | 94.2043 | 97.9082 | 90.7704 | 83.1773 | 29020 | 620 | 28678 | 2916 | 165 | 5.6584 | |
| rpoplin-dv42 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 99.5465 | 99.6219 | 99.4711 | 83.1776 | 2635 | 10 | 2633 | 14 | 8 | 57.1429 | |
| egarrison-hhga | INDEL | I1_5 | map_l100_m2_e1 | homalt | 99.1674 | 99.2593 | 99.0758 | 83.1779 | 536 | 4 | 536 | 5 | 2 | 40.0000 | |