PrecisionFDA
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Explore HG002 comparison results
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| Entry | Type | Subtype | Subset | Genotype | F-score | Recall | Precision | Frac_NA | Truth TP | Truth FN | Query TP | Query FP | FP gt | % FP ma | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
5601-5650 / 86044 show all | |||||||||||||||
| ndellapenna-hhga | INDEL | I1_5 | HG002complexvar | homalt | 99.1510 | 99.0259 | 99.2764 | 48.8027 | 13317 | 131 | 13308 | 97 | 57 | 58.7629 | |
| ltrigg-rtg2 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 98.2211 | 97.0040 | 99.4690 | 43.1148 | 13372 | 413 | 13301 | 71 | 68 | 95.7746 | |
| mlin-fermikit | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 87.6898 | 82.8388 | 93.1443 | 61.7926 | 13318 | 2759 | 13301 | 979 | 950 | 97.0378 | |
| mlin-fermikit | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 87.6898 | 82.8388 | 93.1443 | 61.7926 | 13318 | 2759 | 13301 | 979 | 950 | 97.0378 | |
| qzeng-custom | INDEL | I1_5 | HG002complexvar | homalt | 99.1245 | 98.9887 | 99.2607 | 46.5706 | 13312 | 136 | 13292 | 99 | 61 | 61.6162 | |
| jpowers-varprowl | SNP | * | HG002compoundhet | het | 94.4520 | 92.3614 | 96.6395 | 53.1760 | 13095 | 1083 | 13286 | 462 | 40 | 8.6580 | |
| bgallagher-sentieon | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 96.7404 | 96.3511 | 97.1328 | 51.7215 | 13282 | 503 | 13280 | 392 | 385 | 98.2143 | |
| jpowers-varprowl | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 43.8182 | 41.5354 | 46.3666 | 49.7641 | 13288 | 18704 | 13278 | 15359 | 15221 | 99.1015 | |
| hfeng-pmm2 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.1021 | 96.7944 | 99.4457 | 64.3875 | 13316 | 441 | 13275 | 74 | 59 | 79.7297 | |
| hfeng-pmm2 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.1021 | 96.7944 | 99.4457 | 64.3875 | 13316 | 441 | 13275 | 74 | 59 | 79.7297 | |
| jmaeng-gatk | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 96.8830 | 96.2858 | 97.4877 | 51.4550 | 13273 | 512 | 13271 | 342 | 335 | 97.9532 | |
| gduggal-snapvard | SNP | * | HG002compoundhet | het | 77.1322 | 83.8682 | 71.3978 | 57.2411 | 11890 | 2287 | 13270 | 5316 | 2307 | 43.3973 | |
| hfeng-pmm3 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 96.4523 | 93.1870 | 99.9548 | 33.8499 | 13076 | 956 | 13269 | 6 | 5 | 83.3333 | |
| cchapple-custom | INDEL | I1_5 | HG002compoundhet | * | 96.1801 | 94.5694 | 97.8466 | 66.9542 | 11685 | 671 | 13268 | 292 | 281 | 96.2329 | |
| ckim-dragen | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 96.6346 | 96.2423 | 97.0302 | 52.9948 | 13267 | 518 | 13265 | 406 | 403 | 99.2611 | |
| ckim-isaac | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 94.1491 | 90.4125 | 98.2078 | 67.8829 | 13174 | 1397 | 13261 | 242 | 122 | 50.4132 | |
| ckim-isaac | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 94.1491 | 90.4125 | 98.2078 | 67.8829 | 13174 | 1397 | 13261 | 242 | 122 | 50.4132 | |
| egarrison-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 80.0812 | 74.2799 | 86.8654 | 57.3222 | 13126 | 4545 | 13260 | 2005 | 1766 | 88.0798 | |
| egarrison-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 80.0812 | 74.2799 | 86.8654 | 57.3222 | 13126 | 4545 | 13260 | 2005 | 1766 | 88.0798 | |
| hfeng-pmm3 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.1075 | 96.6926 | 99.5645 | 63.4833 | 13302 | 455 | 13260 | 58 | 44 | 75.8621 | |
| hfeng-pmm3 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.1075 | 96.6926 | 99.5645 | 63.4833 | 13302 | 455 | 13260 | 58 | 44 | 75.8621 | |
| qzeng-custom | SNP | ti | map_l150_m1_e0 | * | 79.6789 | 67.7202 | 96.7669 | 86.5194 | 13349 | 6363 | 13259 | 443 | 380 | 85.7788 | |
| hfeng-pmm1 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.0379 | 96.6562 | 99.4597 | 63.5583 | 13297 | 460 | 13254 | 72 | 47 | 65.2778 | |
| hfeng-pmm1 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.0379 | 96.6562 | 99.4597 | 63.5583 | 13297 | 460 | 13254 | 72 | 47 | 65.2778 | |
| ltrigg-rtg1 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 96.0483 | 92.8307 | 99.4969 | 46.1918 | 13026 | 1006 | 13250 | 67 | 66 | 98.5075 | |
| ckim-isaac | SNP | ti | map_l100_m0_e0 | * | 75.5708 | 60.8148 | 99.7815 | 66.9687 | 13240 | 8531 | 13241 | 29 | 6 | 20.6897 | |
| raldana-dualsentieon | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 97.7464 | 96.5472 | 98.9758 | 64.1922 | 13282 | 475 | 13239 | 137 | 125 | 91.2409 | |
| raldana-dualsentieon | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 97.7464 | 96.5472 | 98.9758 | 64.1922 | 13282 | 475 | 13239 | 137 | 125 | 91.2409 | |
| ckim-vqsr | SNP | ti | map_l125_m2_e1 | het | 81.5245 | 69.3666 | 98.8501 | 88.6777 | 13240 | 5847 | 13238 | 154 | 3 | 1.9481 | |
| ckim-dragen | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 96.1413 | 92.8877 | 99.6311 | 33.7242 | 13034 | 998 | 13234 | 49 | 49 | 100.0000 | |
| mlin-fermikit | SNP | * | map_l125_m2_e0 | het | 61.8597 | 45.1531 | 98.1895 | 65.2404 | 13238 | 16080 | 13233 | 244 | 8 | 3.2787 | |
| bgallagher-sentieon | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 96.1489 | 92.9019 | 99.6311 | 33.4986 | 13036 | 996 | 13232 | 49 | 48 | 97.9592 | |
| jli-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 97.0877 | 94.7254 | 99.5709 | 28.2155 | 13038 | 726 | 13226 | 57 | 56 | 98.2456 | |
| ckim-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 96.0921 | 92.8093 | 99.6158 | 30.7146 | 13023 | 1009 | 13222 | 51 | 51 | 100.0000 | |
| ckim-vqsr | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 96.0845 | 92.7950 | 99.6157 | 30.7178 | 13021 | 1011 | 13220 | 51 | 51 | 100.0000 | |
| asubramanian-gatk | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 96.4244 | 95.8506 | 97.0051 | 52.0671 | 13213 | 572 | 13215 | 408 | 385 | 94.3627 | |
| ckim-vqsr | SNP | * | map_l150_m2_e1 | het | 78.2150 | 64.9020 | 98.3989 | 91.7124 | 13216 | 7147 | 13213 | 215 | 2 | 0.9302 | |
| qzeng-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 86.6613 | 87.3341 | 85.9988 | 44.9670 | 12039 | 1746 | 13212 | 2151 | 1124 | 52.2548 | |
| gduggal-bwavard | SNP | * | HG002compoundhet | het | 83.4515 | 85.5762 | 81.4296 | 49.6147 | 12133 | 2045 | 13203 | 3011 | 2546 | 84.5566 | |
| dgrover-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 96.9211 | 94.3694 | 99.6146 | 31.5700 | 12989 | 775 | 13182 | 51 | 50 | 98.0392 | |
| gduggal-bwavard | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 92.9844 | 91.6684 | 94.3387 | 81.8623 | 13357 | 1214 | 13181 | 791 | 134 | 16.9406 | |
| gduggal-bwavard | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 92.9844 | 91.6684 | 94.3387 | 81.8623 | 13357 | 1214 | 13181 | 791 | 134 | 16.9406 | |
| jmaeng-gatk | SNP | ti | map_l100_m1_e0 | homalt | 84.6124 | 73.3575 | 99.9469 | 64.1277 | 13175 | 4785 | 13175 | 7 | 7 | 100.0000 | |
| qzeng-custom | SNP | ti | map_l125_m1_e0 | het | 82.7364 | 72.3585 | 96.5897 | 86.1572 | 13217 | 5049 | 13170 | 465 | 385 | 82.7957 | |
| hfeng-pmm1 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 97.1286 | 95.4588 | 98.8579 | 46.1719 | 13159 | 626 | 13157 | 152 | 147 | 96.7105 | |
| gduggal-bwafb | INDEL | I1_5 | HG002complexvar | homalt | 98.3809 | 97.8212 | 98.9471 | 49.0711 | 13155 | 293 | 13156 | 140 | 134 | 95.7143 | |
| anovak-vg | INDEL | I1_5 | HG002complexvar | homalt | 67.3378 | 96.3340 | 51.7586 | 45.0635 | 12955 | 493 | 13156 | 12262 | 11858 | 96.7053 | |
| astatham-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 96.8059 | 94.1587 | 99.6062 | 31.3760 | 12960 | 804 | 13154 | 52 | 51 | 98.0769 | |
| ciseli-custom | SNP | ti | map_l125_m1_e0 | het | 77.4977 | 72.0300 | 83.8636 | 79.8833 | 13157 | 5109 | 13154 | 2531 | 72 | 2.8447 | |
| ndellapenna-hhga | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 86.0688 | 96.6376 | 77.5838 | 51.2369 | 12100 | 421 | 13152 | 3800 | 3663 | 96.3947 | |