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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
18051-18100 / 86044 show all | |||||||||||||||
hfeng-pmm3 | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 97.0452 | 94.5372 | 99.6899 | 70.9197 | 623 | 36 | 643 | 2 | 2 | 100.0000 | |
hfeng-pmm3 | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 97.0452 | 94.5372 | 99.6899 | 70.9197 | 623 | 36 | 643 | 2 | 2 | 100.0000 | |
ltrigg-rtg1 | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 99.2265 | 98.7673 | 99.6899 | 57.2281 | 641 | 8 | 643 | 2 | 1 | 50.0000 | |
ndellapenna-hhga | SNP | ti | map_l125_m0_e0 | het | 98.4376 | 97.2165 | 99.6897 | 74.3678 | 8033 | 230 | 8033 | 25 | 12 | 48.0000 | |
ckim-isaac | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 96.0776 | 92.7182 | 99.6894 | 66.0081 | 2241 | 176 | 2247 | 7 | 6 | 85.7143 | |
ltrigg-rtg2 | SNP | tv | map_l125_m2_e1 | het | 98.4798 | 97.2993 | 99.6893 | 57.3735 | 10268 | 285 | 10267 | 32 | 2 | 6.2500 | |
jmaeng-gatk | SNP | ti | * | het | 99.6655 | 99.6418 | 99.6893 | 25.0371 | 1277299 | 4592 | 1277249 | 3981 | 127 | 3.1902 | |
rpoplin-dv42 | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | homalt | 99.5344 | 99.3802 | 99.6891 | 63.3219 | 962 | 6 | 962 | 3 | 3 | 100.0000 | |
hfeng-pmm3 | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 98.3153 | 96.9789 | 99.6891 | 57.4040 | 1605 | 50 | 1603 | 5 | 2 | 40.0000 | |
hfeng-pmm2 | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 96.8846 | 94.2337 | 99.6890 | 71.2433 | 621 | 38 | 641 | 2 | 2 | 100.0000 | |
hfeng-pmm2 | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 96.8846 | 94.2337 | 99.6890 | 71.2433 | 621 | 38 | 641 | 2 | 2 | 100.0000 | |
astatham-gatk | SNP | * | map_l150_m2_e0 | * | 91.4701 | 84.5033 | 99.6888 | 80.0769 | 26916 | 4936 | 26910 | 84 | 40 | 47.6190 | |
ltrigg-rtg1 | SNP | * | map_l100_m2_e1 | het | 99.0006 | 98.3219 | 99.6887 | 57.1362 | 46111 | 787 | 46109 | 144 | 12 | 8.3333 | |
egarrison-hhga | SNP | * | map_l150_m0_e0 | * | 99.0549 | 98.4292 | 99.6886 | 78.8145 | 11843 | 189 | 11843 | 37 | 16 | 43.2432 | |
ltrigg-rtg2 | INDEL | I1_5 | map_l125_m1_e0 | homalt | 99.3846 | 99.0826 | 99.6885 | 78.7135 | 324 | 3 | 320 | 1 | 0 | 0.0000 | |
gduggal-snapfb | SNP | * | map_l100_m1_e0 | homalt | 98.4097 | 97.1633 | 99.6885 | 68.9633 | 26237 | 766 | 26239 | 82 | 29 | 35.3659 | |
hfeng-pmm3 | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 98.8615 | 98.0480 | 99.6885 | 70.4692 | 1306 | 26 | 1280 | 4 | 2 | 50.0000 | |
jlack-gatk | INDEL | I1_5 | HG002complexvar | homalt | 99.7623 | 99.8364 | 99.6883 | 53.0964 | 13426 | 22 | 13432 | 42 | 40 | 95.2381 | |
hfeng-pmm3 | SNP | tv | map_l100_m2_e0 | * | 99.6443 | 99.6005 | 99.6881 | 66.3015 | 24933 | 100 | 24929 | 78 | 10 | 12.8205 | |
hfeng-pmm3 | SNP | ti | map_l125_m0_e0 | homalt | 99.6659 | 99.6437 | 99.6881 | 69.8765 | 4475 | 16 | 4475 | 14 | 5 | 35.7143 | |
hfeng-pmm1 | SNP | ti | map_l125_m0_e0 | homalt | 99.6547 | 99.6215 | 99.6881 | 70.0040 | 4474 | 17 | 4474 | 14 | 5 | 35.7143 | |
hfeng-pmm1 | SNP | ti | segdup | * | 99.7442 | 99.8004 | 99.6881 | 88.7407 | 19498 | 39 | 19496 | 61 | 5 | 8.1967 | |
ltrigg-rtg1 | INDEL | I1_5 | HG002complexvar | het | 99.2372 | 98.7905 | 99.6881 | 51.9353 | 17969 | 220 | 17257 | 54 | 28 | 51.8519 | |
ckim-vqsr | INDEL | I1_5 | * | het | 99.5998 | 99.5116 | 99.6881 | 61.9903 | 78655 | 386 | 78634 | 246 | 145 | 58.9431 | |
ckim-dragen | INDEL | D1_5 | HG002complexvar | homalt | 99.7544 | 99.8207 | 99.6881 | 60.4958 | 10579 | 19 | 10549 | 33 | 30 | 90.9091 | |
cchapple-custom | SNP | * | * | het | 99.7822 | 99.8765 | 99.6880 | 23.4490 | 1871274 | 2313 | 1871921 | 5859 | 675 | 11.5207 | |
hfeng-pmm1 | SNP | tv | map_l100_m0_e0 | homalt | 99.6880 | 99.6880 | 99.6880 | 65.4385 | 3834 | 12 | 3834 | 12 | 4 | 33.3333 | |
jli-custom | INDEL | I6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 98.1944 | 96.7449 | 99.6880 | 59.3016 | 1278 | 43 | 1278 | 4 | 3 | 75.0000 | |
hfeng-pmm2 | SNP | tv | map_l100_m0_e0 | homalt | 99.6880 | 99.6880 | 99.6880 | 65.5500 | 3834 | 12 | 3834 | 12 | 4 | 33.3333 | |
ckim-dragen | SNP | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 99.7746 | 99.8617 | 99.6878 | 62.5042 | 35370 | 49 | 35441 | 111 | 28 | 25.2252 | |
cchapple-custom | INDEL | D1_5 | * | * | 99.4223 | 99.1584 | 99.6877 | 55.8052 | 145510 | 1235 | 145535 | 456 | 300 | 65.7895 | |
jlack-gatk | INDEL | I1_5 | HG002complexvar | * | 99.5214 | 99.3556 | 99.6877 | 57.0609 | 33148 | 215 | 33197 | 104 | 72 | 69.2308 | |
hfeng-pmm3 | SNP | tv | map_l100_m0_e0 | homalt | 99.6488 | 99.6100 | 99.6877 | 65.3002 | 3831 | 15 | 3831 | 12 | 4 | 33.3333 | |
qzeng-custom | INDEL | D1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 99.4030 | 99.1198 | 99.6877 | 55.5385 | 14640 | 130 | 15005 | 47 | 23 | 48.9362 | |
gduggal-bwaplat | SNP | tv | * | * | 98.5599 | 97.4574 | 99.6876 | 31.4101 | 945035 | 24655 | 945254 | 2962 | 440 | 14.8548 | |
ltrigg-rtg1 | INDEL | D1_5 | map_l125_m0_e0 | het | 95.7836 | 92.1739 | 99.6875 | 74.7036 | 318 | 27 | 319 | 1 | 0 | 0.0000 | |
ltrigg-rtg2 | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 98.8350 | 97.9969 | 99.6875 | 54.5131 | 636 | 13 | 638 | 2 | 1 | 50.0000 | |
raldana-dualsentieon | INDEL | I6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 98.1161 | 96.5935 | 99.6875 | 59.6596 | 1276 | 45 | 1276 | 4 | 3 | 75.0000 | |
jli-custom | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 96.5621 | 93.6267 | 99.6875 | 66.3512 | 617 | 42 | 638 | 2 | 2 | 100.0000 | |
jli-custom | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 96.5621 | 93.6267 | 99.6875 | 66.3512 | 617 | 42 | 638 | 2 | 2 | 100.0000 | |
hfeng-pmm1 | SNP | * | map_l125_m2_e1 | * | 99.4713 | 99.2564 | 99.6872 | 70.6981 | 46851 | 351 | 46845 | 147 | 41 | 27.8912 | |
hfeng-pmm3 | SNP | tv | map_l100_m2_e1 | * | 99.6458 | 99.6045 | 99.6872 | 66.3290 | 25183 | 100 | 25179 | 79 | 10 | 12.6582 | |
ckim-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 96.4002 | 93.3232 | 99.6870 | 67.8894 | 615 | 44 | 637 | 2 | 2 | 100.0000 | |
ckim-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 96.4002 | 93.3232 | 99.6870 | 67.8894 | 615 | 44 | 637 | 2 | 2 | 100.0000 | |
jmaeng-gatk | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 99.6201 | 99.5533 | 99.6870 | 54.4597 | 6686 | 30 | 6688 | 21 | 7 | 33.3333 | |
astatham-gatk | SNP | tv | map_l100_m1_e0 | het | 86.5303 | 76.4416 | 99.6869 | 75.5609 | 11785 | 3632 | 11781 | 37 | 10 | 27.0270 | |
ltrigg-rtg1 | INDEL | * | segdup | homalt | 99.6351 | 99.5833 | 99.6868 | 92.9210 | 956 | 4 | 955 | 3 | 3 | 100.0000 | |
asubramanian-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | homalt | 99.2824 | 98.8813 | 99.6867 | 44.4483 | 1591 | 18 | 1591 | 5 | 1 | 20.0000 | |
ckim-vqsr | SNP | * | func_cds | het | 99.7448 | 99.8029 | 99.6867 | 36.7154 | 11139 | 22 | 11136 | 35 | 0 | 0.0000 | |
hfeng-pmm1 | SNP | * | segdup | * | 99.7400 | 99.7934 | 99.6867 | 89.3409 | 28009 | 58 | 28003 | 88 | 11 | 12.5000 |