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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
12601-12650 / 86044 show all | |||||||||||||||
bgallagher-sentieon | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 99.1996 | 99.5127 | 98.8884 | 74.7272 | 14500 | 71 | 14500 | 163 | 14 | 8.5890 | |
bgallagher-sentieon | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 96.9121 | 99.5122 | 94.4444 | 91.3008 | 204 | 1 | 204 | 12 | 10 | 83.3333 | |
bgallagher-sentieon | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 96.9121 | 99.5122 | 94.4444 | 91.3008 | 204 | 1 | 204 | 12 | 10 | 83.3333 | |
jmaeng-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 95.1049 | 99.5122 | 91.0714 | 91.1567 | 204 | 1 | 204 | 20 | 15 | 75.0000 | |
jmaeng-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 95.1049 | 99.5122 | 91.0714 | 91.1567 | 204 | 1 | 204 | 20 | 15 | 75.0000 | |
raldana-dualsentieon | SNP | * | map_l150_m1_e0 | homalt | 99.7067 | 99.5121 | 99.9020 | 67.3803 | 11218 | 55 | 11218 | 11 | 8 | 72.7273 | |
dgrover-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 99.4424 | 99.5121 | 99.3729 | 70.5814 | 45479 | 223 | 45479 | 287 | 31 | 10.8014 | |
dgrover-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 99.4424 | 99.5121 | 99.3729 | 70.5814 | 45479 | 223 | 45479 | 287 | 31 | 10.8014 | |
ckim-vqsr | INDEL | I1_5 | * | het | 99.5998 | 99.5116 | 99.6881 | 61.9903 | 78655 | 386 | 78634 | 246 | 145 | 58.9431 | |
ckim-vqsr | SNP | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 99.4006 | 99.5116 | 99.2899 | 63.6333 | 35246 | 173 | 35235 | 252 | 21 | 8.3333 | |
ckim-dragen | SNP | tv | map_l100_m2_e0 | homalt | 99.6739 | 99.5116 | 99.8367 | 60.2338 | 9169 | 45 | 9169 | 15 | 13 | 86.6667 | |
asubramanian-gatk | INDEL | * | HG002complexvar | homalt | 99.4823 | 99.5116 | 99.4530 | 57.3903 | 26895 | 132 | 26910 | 148 | 101 | 68.2432 | |
jlack-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 97.4266 | 99.5114 | 95.4273 | 42.4504 | 5092 | 25 | 5092 | 244 | 244 | 100.0000 | |
hfeng-pmm1 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 99.2980 | 99.5114 | 99.0854 | 41.3691 | 5092 | 25 | 5092 | 47 | 47 | 100.0000 | |
ckim-gatk | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 98.2901 | 99.5113 | 97.0984 | 68.6486 | 3258 | 16 | 3246 | 97 | 94 | 96.9072 | |
gduggal-snapfb | SNP | tv | lowcmp_SimpleRepeat_homopolymer_6to10 | homalt | 99.4469 | 99.5112 | 99.3827 | 62.5253 | 3868 | 19 | 3864 | 24 | 9 | 37.5000 | |
asubramanian-gatk | SNP | tv | func_cds | het | 99.4171 | 99.5107 | 99.3236 | 42.1899 | 2644 | 13 | 2643 | 18 | 0 | 0.0000 | |
mlin-fermikit | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 98.3026 | 99.5107 | 97.1234 | 41.8851 | 6712 | 33 | 6719 | 199 | 180 | 90.4523 | |
jlack-gatk | SNP | tv | map_siren | het | 95.9855 | 99.5106 | 92.7015 | 72.5215 | 28469 | 140 | 28464 | 2241 | 108 | 4.8193 | |
egarrison-hhga | SNP | * | lowcmp_SimpleRepeat_triTR_11to50 | * | 99.7071 | 99.5105 | 99.9045 | 32.0412 | 7319 | 36 | 7321 | 7 | 2 | 28.5714 | |
ndellapenna-hhga | SNP | tv | map_l150_m2_e0 | homalt | 99.6933 | 99.5102 | 99.8771 | 72.6980 | 4063 | 20 | 4063 | 5 | 4 | 80.0000 | |
ltrigg-rtg2 | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | het | 98.7965 | 99.5102 | 98.0929 | 39.5838 | 11377 | 56 | 11419 | 222 | 6 | 2.7027 | |
jmaeng-gatk | SNP | ti | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 99.7543 | 99.5098 | 100.0000 | 59.5752 | 1218 | 6 | 1218 | 0 | 0 | ||
raldana-dualsentieon | SNP | ti | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 99.7543 | 99.5098 | 100.0000 | 58.1874 | 1218 | 6 | 1218 | 0 | 0 | ||
rpoplin-dv42 | INDEL | I1_5 | map_l150_m2_e1 | homalt | 99.2665 | 99.5098 | 99.0244 | 88.6364 | 203 | 1 | 203 | 2 | 1 | 50.0000 | |
ndellapenna-hhga | INDEL | I1_5 | map_l150_m2_e1 | homalt | 99.0244 | 99.5098 | 98.5437 | 88.9840 | 203 | 1 | 203 | 3 | 1 | 33.3333 | |
ckim-vqsr | INDEL | I1_5 | map_l150_m2_e1 | homalt | 99.2665 | 99.5098 | 99.0244 | 88.9488 | 203 | 1 | 203 | 2 | 1 | 50.0000 | |
dgrover-gatk | INDEL | I1_5 | map_l150_m2_e1 | homalt | 99.0244 | 99.5098 | 98.5437 | 88.6501 | 203 | 1 | 203 | 3 | 2 | 66.6667 | |
eyeh-varpipe | INDEL | I1_5 | map_l150_m2_e1 | homalt | 99.0279 | 99.5098 | 98.5507 | 88.2373 | 203 | 1 | 340 | 5 | 5 | 100.0000 | |
gduggal-bwafb | INDEL | I1_5 | map_l150_m2_e1 | homalt | 98.7835 | 99.5098 | 98.0676 | 89.3683 | 203 | 1 | 203 | 4 | 1 | 25.0000 | |
hfeng-pmm2 | SNP | ti | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 99.7135 | 99.5098 | 99.9180 | 66.6027 | 1218 | 6 | 1218 | 1 | 0 | 0.0000 | |
ckim-gatk | INDEL | I1_5 | map_l150_m2_e1 | homalt | 99.0244 | 99.5098 | 98.5437 | 88.9009 | 203 | 1 | 203 | 3 | 2 | 66.6667 | |
rpoplin-dv42 | SNP | * | map_siren | * | 99.6224 | 99.5097 | 99.7354 | 54.5067 | 145511 | 717 | 145497 | 386 | 225 | 58.2902 | |
raldana-dualsentieon | SNP | * | map_l150_m2_e1 | homalt | 99.7077 | 99.5096 | 99.9066 | 69.9014 | 11769 | 58 | 11769 | 11 | 8 | 72.7273 | |
qzeng-custom | SNP | tv | lowcmp_SimpleRepeat_quadTR_11to50 | het | 97.1050 | 99.5095 | 94.8139 | 49.1046 | 4666 | 23 | 4662 | 255 | 3 | 1.1765 | |
ckim-vqsr | SNP | tv | lowcmp_SimpleRepeat_quadTR_11to50 | het | 98.2513 | 99.5095 | 97.0246 | 43.7566 | 4666 | 23 | 4663 | 143 | 1 | 0.6993 | |
cchapple-custom | INDEL | D1_5 | lowcmp_SimpleRepeat_triTR_11to50 | * | 99.6803 | 99.5094 | 99.8517 | 35.3111 | 4057 | 20 | 4039 | 6 | 4 | 66.6667 | |
hfeng-pmm3 | SNP | ti | map_l125_m2_e1 | * | 99.5907 | 99.5093 | 99.6723 | 71.0190 | 30419 | 150 | 30415 | 100 | 16 | 16.0000 | |
asubramanian-gatk | INDEL | I1_5 | HG002complexvar | homalt | 99.6538 | 99.5092 | 99.7987 | 52.7938 | 13382 | 66 | 13389 | 27 | 26 | 96.2963 | |
bgallagher-sentieon | INDEL | D1_5 | map_l100_m2_e0 | homalt | 99.5905 | 99.5090 | 99.6721 | 83.7116 | 608 | 3 | 608 | 2 | 2 | 100.0000 | |
astatham-gatk | INDEL | D1_5 | map_l100_m2_e0 | homalt | 99.5090 | 99.5090 | 99.5090 | 83.7888 | 608 | 3 | 608 | 3 | 2 | 66.6667 | |
hfeng-pmm2 | INDEL | D1_5 | map_l100_m2_e0 | homalt | 99.5905 | 99.5090 | 99.6721 | 81.7529 | 608 | 3 | 608 | 2 | 2 | 100.0000 | |
eyeh-varpipe | SNP | tv | map_l250_m1_e0 | * | 98.7000 | 99.5089 | 97.9042 | 90.2532 | 2634 | 13 | 2616 | 56 | 6 | 10.7143 | |
jli-custom | SNP | ti | map_l150_m1_e0 | homalt | 99.7128 | 99.5087 | 99.9178 | 67.3088 | 7291 | 36 | 7291 | 6 | 6 | 100.0000 | |
bgallagher-sentieon | SNP | ti | map_l150_m1_e0 | homalt | 99.6923 | 99.5087 | 99.8767 | 68.0791 | 7291 | 36 | 7291 | 9 | 7 | 77.7778 | |
gduggal-bwafb | SNP | ti | segdup | * | 99.0195 | 99.5086 | 98.5352 | 91.2837 | 19441 | 96 | 19441 | 289 | 16 | 5.5363 | |
ckim-vqsr | INDEL | * | * | het | 99.5204 | 99.5086 | 99.5323 | 62.3713 | 193179 | 954 | 192796 | 906 | 561 | 61.9205 | |
ndellapenna-hhga | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 99.1298 | 99.5085 | 98.7541 | 58.9047 | 1822 | 9 | 1823 | 23 | 1 | 4.3478 | |
gduggal-snapfb | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 83.6454 | 99.5085 | 72.1445 | 74.1800 | 1822 | 9 | 1857 | 717 | 13 | 1.8131 | |
bgallagher-sentieon | SNP | * | map_l100_m1_e0 | het | 99.2217 | 99.5084 | 98.9366 | 68.7750 | 45136 | 223 | 45125 | 485 | 63 | 12.9897 |