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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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
26951-27000 / 86044 show all | |||||||||||||||
hfeng-pmm3 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 96.9803 | 95.8192 | 98.1699 | 71.2843 | 4790 | 209 | 4774 | 89 | 69 | 77.5281 | |
hfeng-pmm3 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 96.9803 | 95.8192 | 98.1699 | 71.2843 | 4790 | 209 | 4774 | 89 | 69 | 77.5281 | |
jli-custom | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | * | 97.0712 | 95.8175 | 98.3581 | 49.4267 | 1260 | 55 | 1258 | 21 | 13 | 61.9048 | |
hfeng-pmm1 | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 97.2475 | 95.8170 | 98.7214 | 83.8109 | 1466 | 64 | 1467 | 19 | 9 | 47.3684 | |
hfeng-pmm1 | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 97.2475 | 95.8170 | 98.7214 | 83.8109 | 1466 | 64 | 1467 | 19 | 9 | 47.3684 | |
dgrover-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 96.3472 | 95.8165 | 96.8839 | 75.3835 | 710 | 31 | 684 | 22 | 19 | 86.3636 | |
bgallagher-sentieon | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 96.2794 | 95.8165 | 96.7468 | 75.0088 | 710 | 31 | 684 | 23 | 20 | 86.9565 | |
cchapple-custom | SNP | tv | map_l250_m2_e1 | * | 95.6819 | 95.8162 | 95.5479 | 90.3656 | 2794 | 122 | 2790 | 130 | 24 | 18.4615 | |
dgrover-gatk | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | hetalt | 97.5024 | 95.8159 | 99.2494 | 33.8300 | 1145 | 50 | 1190 | 9 | 8 | 88.8889 | |
gduggal-snapfb | INDEL | D1_5 | map_l150_m1_e0 | * | 95.2145 | 95.8159 | 94.6207 | 88.3889 | 687 | 30 | 686 | 39 | 8 | 20.5128 | |
jli-custom | INDEL | D1_5 | HG002compoundhet | * | 97.1251 | 95.8153 | 98.4712 | 65.0788 | 11723 | 512 | 11723 | 182 | 174 | 95.6044 | |
raldana-dualsentieon | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_11to50 | * | 96.9783 | 95.8147 | 98.1704 | 65.8532 | 1717 | 75 | 1717 | 32 | 26 | 81.2500 | |
dgrover-gatk | INDEL | I6_15 | lowcmp_SimpleRepeat_diTR_11to50 | * | 97.4696 | 95.8126 | 99.1849 | 62.9471 | 2311 | 101 | 2312 | 19 | 14 | 73.6842 | |
ckim-vqsr | INDEL | D6_15 | segdup | * | 96.0630 | 95.8115 | 96.3158 | 95.0955 | 183 | 8 | 183 | 7 | 4 | 57.1429 | |
cchapple-custom | INDEL | D6_15 | segdup | * | 96.8734 | 95.8115 | 97.9592 | 92.6811 | 183 | 8 | 192 | 4 | 4 | 100.0000 | |
jpowers-varprowl | INDEL | D1_5 | map_l125_m2_e0 | het | 94.8187 | 95.8115 | 93.8462 | 88.6430 | 732 | 32 | 732 | 48 | 26 | 54.1667 | |
anovak-vg | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 94.6346 | 95.8110 | 93.4868 | 75.2785 | 3751 | 164 | 3818 | 266 | 220 | 82.7068 | |
gduggal-bwafb | INDEL | * | map_l125_m2_e0 | * | 96.9636 | 95.8106 | 98.1447 | 86.9397 | 2104 | 92 | 2116 | 40 | 8 | 20.0000 | |
gduggal-bwavard | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 94.3224 | 95.8089 | 92.8813 | 84.3204 | 6378 | 279 | 6315 | 484 | 93 | 19.2149 | |
gduggal-snapfb | SNP | ti | map_l125_m1_e0 | homalt | 97.7417 | 95.8081 | 99.7549 | 73.6978 | 10582 | 463 | 10583 | 26 | 14 | 53.8462 | |
astatham-gatk | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 97.3915 | 95.8068 | 99.0295 | 51.2175 | 2856 | 125 | 2857 | 28 | 23 | 82.1429 | |
ckim-dragen | INDEL | I1_5 | map_l125_m0_e0 | * | 95.6449 | 95.8065 | 95.4839 | 89.2324 | 297 | 13 | 296 | 14 | 4 | 28.5714 | |
gduggal-snapvard | INDEL | D1_5 | map_l150_m2_e0 | * | 87.0891 | 95.8060 | 79.8261 | 90.0965 | 731 | 32 | 918 | 232 | 55 | 23.7069 | |
ghariani-varprowl | INDEL | D1_5 | map_l150_m2_e0 | * | 90.8639 | 95.8060 | 86.4066 | 91.3346 | 731 | 32 | 731 | 115 | 21 | 18.2609 | |
ltrigg-rtg2 | INDEL | * | map_l125_m1_e0 | het | 97.3392 | 95.8052 | 98.9231 | 79.2399 | 1279 | 56 | 1286 | 14 | 0 | 0.0000 | |
cchapple-custom | INDEL | I6_15 | map_siren | het | 96.0059 | 95.8042 | 96.2085 | 84.5308 | 137 | 6 | 203 | 8 | 2 | 25.0000 | |
ckim-gatk | INDEL | I6_15 | map_siren | het | 96.8198 | 95.8042 | 97.8571 | 88.4774 | 137 | 6 | 137 | 3 | 1 | 33.3333 | |
ckim-gatk | INDEL | D16_PLUS | map_siren | * | 93.4849 | 95.8042 | 91.2752 | 95.1513 | 137 | 6 | 136 | 13 | 2 | 15.3846 | |
ckim-vqsr | INDEL | D16_PLUS | map_siren | * | 93.8073 | 95.8042 | 91.8919 | 95.1823 | 137 | 6 | 136 | 12 | 2 | 16.6667 | |
rpoplin-dv42 | SNP | * | lowcmp_SimpleRepeat_quadTR_51to200 | * | 96.1404 | 95.8042 | 96.4789 | 92.5654 | 137 | 6 | 137 | 5 | 4 | 80.0000 | |
ltrigg-rtg1 | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 97.7725 | 95.8037 | 99.8239 | 42.4645 | 4452 | 195 | 4535 | 8 | 8 | 100.0000 | |
ckim-dragen | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 97.5871 | 95.8024 | 99.4396 | 50.7631 | 5683 | 249 | 5678 | 32 | 30 | 93.7500 | |
cchapple-custom | SNP | tv | map_l250_m2_e0 | * | 95.6656 | 95.8015 | 95.5301 | 90.2861 | 2761 | 121 | 2757 | 129 | 24 | 18.6047 | |
gduggal-snapvard | SNP | tv | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 97.1847 | 95.8015 | 98.6083 | 75.1972 | 502 | 22 | 496 | 7 | 4 | 57.1429 | |
jpowers-varprowl | SNP | * | map_l150_m1_e0 | het | 96.1124 | 95.8014 | 96.4254 | 81.4447 | 18505 | 811 | 18505 | 686 | 205 | 29.8834 | |
hfeng-pmm1 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 97.3881 | 95.8010 | 99.0287 | 53.0662 | 16929 | 742 | 16924 | 166 | 154 | 92.7711 | |
hfeng-pmm1 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 97.3881 | 95.8010 | 99.0287 | 53.0662 | 16929 | 742 | 16924 | 166 | 154 | 92.7711 | |
asubramanian-gatk | INDEL | D16_PLUS | HG002complexvar | * | 96.5513 | 95.8004 | 97.3142 | 67.2463 | 1574 | 69 | 1558 | 43 | 31 | 72.0930 | |
mlin-fermikit | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 96.1180 | 95.8000 | 96.4382 | 69.3543 | 2874 | 126 | 2870 | 106 | 91 | 85.8491 | |
ckim-isaac | SNP | tv | segdup | homalt | 97.8395 | 95.7999 | 99.9678 | 86.9397 | 3102 | 136 | 3102 | 1 | 1 | 100.0000 | |
ltrigg-rtg1 | INDEL | I1_5 | map_l125_m2_e0 | * | 97.5042 | 95.7993 | 99.2710 | 82.8542 | 821 | 36 | 817 | 6 | 1 | 16.6667 | |
jli-custom | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 97.7642 | 95.7991 | 99.8117 | 30.3607 | 2098 | 92 | 2120 | 4 | 4 | 100.0000 | |
ciseli-custom | SNP | * | HG002complexvar | het | 95.7970 | 95.7987 | 95.7952 | 20.3525 | 445943 | 19557 | 439539 | 19293 | 621 | 3.2188 | |
jpowers-varprowl | INDEL | I1_5 | func_cds | homalt | 97.4359 | 95.7983 | 99.1304 | 27.2152 | 114 | 5 | 114 | 1 | 1 | 100.0000 | |
anovak-vg | INDEL | I1_5 | func_cds | homalt | 87.3563 | 95.7983 | 80.2817 | 31.0680 | 114 | 5 | 114 | 28 | 26 | 92.8571 | |
ghariani-varprowl | INDEL | I1_5 | func_cds | homalt | 97.0213 | 95.7983 | 98.2759 | 29.2683 | 114 | 5 | 114 | 2 | 1 | 50.0000 | |
gduggal-snapplat | SNP | * | map_siren | * | 96.8913 | 95.7977 | 98.0103 | 67.7918 | 140083 | 6145 | 140139 | 2845 | 1340 | 47.1002 | |
qzeng-custom | INDEL | I6_15 | HG002complexvar | het | 94.4892 | 95.7962 | 93.2173 | 56.1507 | 2256 | 99 | 2625 | 191 | 60 | 31.4136 | |
rpoplin-dv42 | INDEL | * | map_l250_m2_e1 | * | 96.3746 | 95.7958 | 96.9605 | 99.6645 | 319 | 14 | 319 | 10 | 5 | 50.0000 | |
jmaeng-gatk | INDEL | * | map_l250_m2_e1 | * | 93.2749 | 95.7958 | 90.8832 | 97.4381 | 319 | 14 | 319 | 32 | 4 | 12.5000 |