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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
21001-21050 / 86044 show all | |||||||||||||||
gduggal-bwafb | SNP | * | * | hetalt | 99.5989 | 99.7704 | 99.4279 | 53.2620 | 869 | 2 | 869 | 5 | 5 | 100.0000 | |
gduggal-bwafb | SNP | tv | * | hetalt | 99.5989 | 99.7704 | 99.4279 | 53.2620 | 869 | 2 | 869 | 5 | 5 | 100.0000 | |
ltrigg-rtg2 | INDEL | I6_15 | * | * | 98.2993 | 97.1961 | 99.4278 | 44.2481 | 24127 | 696 | 23804 | 137 | 83 | 60.5839 | |
rpoplin-dv42 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 98.4857 | 97.5614 | 99.4277 | 64.2143 | 17723 | 443 | 17720 | 102 | 87 | 85.2941 | |
rpoplin-dv42 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 98.4857 | 97.5614 | 99.4277 | 64.2143 | 17723 | 443 | 17720 | 102 | 87 | 85.2941 | |
bgallagher-sentieon | INDEL | * | lowcmp_SimpleRepeat_homopolymer_6to10 | hetalt | 98.0116 | 96.6355 | 99.4275 | 73.3333 | 517 | 18 | 521 | 3 | 3 | 100.0000 | |
gduggal-bwaplat | INDEL | I1_5 | map_l125_m2_e0 | * | 75.4526 | 60.7935 | 99.4275 | 94.2638 | 521 | 336 | 521 | 3 | 1 | 33.3333 | |
gduggal-bwaplat | SNP | tv | map_l100_m1_e0 | * | 80.7967 | 68.0462 | 99.4275 | 83.4681 | 16672 | 7829 | 16673 | 96 | 19 | 19.7917 | |
egarrison-hhga | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 99.5783 | 99.7296 | 99.4274 | 58.3882 | 2951 | 8 | 2952 | 17 | 2 | 11.7647 | |
ckim-vqsr | SNP | tv | segdup | het | 98.9929 | 98.5625 | 99.4272 | 95.9257 | 5211 | 76 | 5207 | 30 | 0 | 0.0000 | |
gduggal-bwaplat | SNP | tv | map_l100_m2_e0 | * | 81.2147 | 68.6414 | 99.4272 | 84.5184 | 17183 | 7850 | 17184 | 99 | 19 | 19.1919 | |
jli-custom | SNP | ti | map_l125_m1_e0 | het | 99.1158 | 98.8065 | 99.4270 | 68.8246 | 18048 | 218 | 18046 | 104 | 33 | 31.7308 | |
ltrigg-rtg2 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 94.6096 | 90.2375 | 99.4269 | 52.7740 | 342 | 37 | 347 | 2 | 2 | 100.0000 | |
egarrison-hhga | INDEL | I1_5 | HG002complexvar | het | 98.9830 | 98.5431 | 99.4269 | 55.1160 | 17924 | 265 | 17869 | 103 | 26 | 25.2427 | |
dgrover-gatk | INDEL | I16_PLUS | HG002complexvar | hetalt | 97.8993 | 96.4179 | 99.4269 | 69.1424 | 323 | 12 | 347 | 2 | 2 | 100.0000 | |
bgallagher-sentieon | INDEL | D1_5 | map_l125_m1_e0 | homalt | 99.4269 | 99.4269 | 99.4269 | 85.2494 | 347 | 2 | 347 | 2 | 2 | 100.0000 | |
astatham-gatk | INDEL | D1_5 | map_l125_m1_e0 | homalt | 99.4269 | 99.4269 | 99.4269 | 85.3484 | 347 | 2 | 347 | 2 | 2 | 100.0000 | |
hfeng-pmm2 | INDEL | D1_5 | map_l125_m1_e0 | homalt | 99.4269 | 99.4269 | 99.4269 | 83.7068 | 347 | 2 | 347 | 2 | 2 | 100.0000 | |
hfeng-pmm1 | INDEL | D6_15 | HG002complexvar | * | 97.1047 | 94.8887 | 99.4267 | 56.6618 | 5031 | 271 | 5029 | 29 | 25 | 86.2069 | |
ltrigg-rtg1 | INDEL | * | map_l100_m1_e0 | homalt | 99.0600 | 98.6960 | 99.4267 | 80.9576 | 1211 | 16 | 1214 | 7 | 4 | 57.1429 | |
gduggal-bwaplat | SNP | ti | map_l250_m2_e0 | het | 59.6085 | 42.5630 | 99.4265 | 97.5359 | 1385 | 1869 | 1387 | 8 | 2 | 25.0000 | |
ltrigg-rtg1 | INDEL | D1_5 | map_l125_m1_e0 | * | 97.4217 | 95.4963 | 99.4264 | 79.7601 | 1039 | 49 | 1040 | 6 | 2 | 33.3333 | |
jmaeng-gatk | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 99.6714 | 99.9177 | 99.4264 | 57.8940 | 6067 | 5 | 6067 | 35 | 34 | 97.1429 | |
ndellapenna-hhga | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 99.2704 | 99.1149 | 99.4264 | 74.8452 | 5375 | 48 | 5373 | 31 | 27 | 87.0968 | |
ndellapenna-hhga | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 99.2704 | 99.1149 | 99.4264 | 74.8452 | 5375 | 48 | 5373 | 31 | 27 | 87.0968 | |
gduggal-bwafb | INDEL | D1_5 | * | het | 98.9590 | 98.4961 | 99.4263 | 56.5657 | 86257 | 1317 | 92550 | 534 | 170 | 31.8352 | |
mlin-fermikit | SNP | tv | func_cds | * | 99.2667 | 99.1078 | 99.4262 | 22.7208 | 4332 | 39 | 4332 | 25 | 14 | 56.0000 | |
asubramanian-gatk | SNP | ti | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 99.1774 | 98.9300 | 99.4261 | 58.2999 | 17660 | 191 | 17671 | 102 | 10 | 9.8039 | |
hfeng-pmm1 | INDEL | I1_5 | map_siren | homalt | 99.6300 | 99.8350 | 99.4258 | 77.3924 | 1210 | 2 | 1212 | 7 | 4 | 57.1429 | |
jli-custom | SNP | ti | map_l125_m2_e1 | het | 99.1383 | 98.8526 | 99.4256 | 70.6228 | 18868 | 219 | 18866 | 109 | 33 | 30.2752 | |
jmaeng-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 98.2955 | 97.1910 | 99.4253 | 81.4499 | 173 | 5 | 173 | 1 | 1 | 100.0000 | |
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 | I6_15 | segdup | * | 99.1404 | 98.8571 | 99.4253 | 92.0693 | 173 | 2 | 173 | 1 | 0 | 0.0000 | |
jli-custom | INDEL | D1_5 | map_l125_m1_e0 | homalt | 99.2826 | 99.1404 | 99.4253 | 84.3102 | 346 | 3 | 346 | 2 | 2 | 100.0000 | |
astatham-gatk | INDEL | I16_PLUS | HG002complexvar | hetalt | 97.7444 | 96.1194 | 99.4253 | 68.9563 | 322 | 13 | 346 | 2 | 2 | 100.0000 | |
ckim-gatk | INDEL | D1_5 | map_l125_m1_e0 | homalt | 99.2826 | 99.1404 | 99.4253 | 85.7785 | 346 | 3 | 346 | 2 | 2 | 100.0000 | |
gduggal-snapplat | INDEL | D6_15 | lowcmp_SimpleRepeat_triTR_11to50 | hetalt | 45.8495 | 29.7945 | 99.4253 | 32.5581 | 174 | 410 | 173 | 1 | 1 | 100.0000 | |
egarrison-hhga | INDEL | D1_5 | map_l125_m1_e0 | homalt | 99.2826 | 99.1404 | 99.4253 | 85.5781 | 346 | 3 | 346 | 2 | 2 | 100.0000 | |
ckim-vqsr | INDEL | D1_5 | map_l125_m1_e0 | homalt | 99.2826 | 99.1404 | 99.4253 | 85.7785 | 346 | 3 | 346 | 2 | 2 | 100.0000 | |
gduggal-snapfb | SNP | * | HG002complexvar | homalt | 99.5552 | 99.6857 | 99.4250 | 21.2913 | 287668 | 907 | 287733 | 1664 | 399 | 23.9784 | |
ckim-dragen | SNP | ti | map_l250_m2_e0 | homalt | 99.1399 | 98.8565 | 99.4250 | 83.6036 | 1729 | 20 | 1729 | 10 | 9 | 90.0000 | |
ckim-isaac | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 96.3802 | 93.5166 | 99.4246 | 60.9201 | 16429 | 1139 | 16588 | 96 | 15 | 15.6250 | |
rpoplin-dv42 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 96.5493 | 93.8357 | 99.4245 | 23.8294 | 7596 | 499 | 7602 | 44 | 43 | 97.7273 | |
hfeng-pmm3 | SNP | ti | map_l150_m2_e0 | het | 99.3316 | 99.2392 | 99.4243 | 76.7413 | 12783 | 98 | 12779 | 74 | 8 | 10.8108 | |
mlin-fermikit | SNP | ti | lowcmp_SimpleRepeat_quadTR_11to50 | het | 98.3589 | 97.3161 | 99.4242 | 37.2504 | 6563 | 181 | 6562 | 38 | 5 | 13.1579 | |
hfeng-pmm3 | SNP | * | segdup | het | 99.5790 | 99.7344 | 99.4241 | 89.8527 | 17271 | 46 | 17265 | 100 | 0 | 0.0000 | |
ckim-isaac | INDEL | D1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 98.9925 | 98.5647 | 99.4241 | 53.5139 | 14558 | 212 | 14501 | 84 | 48 | 57.1429 | |
gduggal-bwaplat | SNP | tv | map_l125_m2_e1 | * | 74.1036 | 59.0623 | 99.4240 | 88.9166 | 9838 | 6819 | 9838 | 57 | 13 | 22.8070 | |
cchapple-custom | INDEL | I6_15 | lowcmp_SimpleRepeat_diTR_11to50 | het | 98.5778 | 97.7459 | 99.4240 | 60.7000 | 477 | 11 | 2244 | 13 | 9 | 69.2308 | |
gduggal-bwavard | SNP | ti | map_l250_m1_e0 | homalt | 98.2992 | 97.1998 | 99.4238 | 87.2438 | 1562 | 45 | 1553 | 9 | 6 | 66.6667 |