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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
22351-22400 / 86044 show all | |||||||||||||||
jli-custom | SNP | ti | map_l250_m2_e0 | * | 98.3980 | 97.5040 | 99.3085 | 86.8596 | 4883 | 125 | 4883 | 34 | 18 | 52.9412 | |
dgrover-gatk | INDEL | I6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 98.7362 | 97.5039 | 100.0000 | 43.6266 | 625 | 16 | 628 | 0 | 0 | ||
ghariani-varprowl | SNP | * | lowcmp_SimpleRepeat_diTR_11to50 | * | 90.8942 | 97.5031 | 85.1244 | 74.2945 | 9450 | 242 | 9545 | 1668 | 246 | 14.7482 | |
cchapple-custom | INDEL | * | map_l100_m2_e1 | homalt | 98.1532 | 97.5020 | 98.8133 | 82.2920 | 1249 | 32 | 1249 | 15 | 11 | 73.3333 | |
ckim-gatk | INDEL | I6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 98.5840 | 97.5019 | 99.6904 | 61.7751 | 1288 | 33 | 1288 | 4 | 2 | 50.0000 | |
gduggal-bwavard | SNP | * | map_l250_m2_e0 | * | 90.6036 | 97.5016 | 84.6171 | 92.0596 | 7688 | 197 | 7613 | 1384 | 44 | 3.1792 | |
gduggal-snapvard | SNP | tv | map_l125_m1_e0 | het | 90.5242 | 97.5015 | 84.4788 | 81.5577 | 9873 | 253 | 9846 | 1809 | 112 | 6.1913 | |
jlack-gatk | SNP | ti | map_l150_m0_e0 | homalt | 98.6081 | 97.5009 | 99.7406 | 73.6452 | 2692 | 69 | 2692 | 7 | 6 | 85.7143 | |
cchapple-custom | SNP | * | map_l100_m2_e0 | homalt | 98.7307 | 97.5003 | 99.9925 | 58.6733 | 26835 | 688 | 26824 | 2 | 2 | 100.0000 | |
rpoplin-dv42 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 98.4151 | 97.5003 | 99.3472 | 47.2567 | 9283 | 238 | 9283 | 61 | 57 | 93.4426 | |
rpoplin-dv42 | INDEL | * | map_l125_m1_e0 | hetalt | 95.1220 | 97.5000 | 92.8571 | 93.4783 | 39 | 1 | 39 | 3 | 0 | 0.0000 | |
qzeng-custom | SNP | * | tech_badpromoters | homalt | 98.0970 | 97.5000 | 98.7013 | 46.1538 | 78 | 2 | 76 | 1 | 1 | 100.0000 | |
rpoplin-dv42 | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | homalt | 98.4848 | 97.5000 | 99.4898 | 65.3710 | 195 | 5 | 195 | 1 | 1 | 100.0000 | |
ckim-vqsr | INDEL | D6_15 | map_siren | het | 96.9741 | 97.5000 | 96.4539 | 89.3222 | 273 | 7 | 272 | 10 | 2 | 20.0000 | |
egarrison-hhga | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 97.2255 | 97.5000 | 96.9526 | 72.5894 | 2925 | 75 | 2927 | 92 | 63 | 68.4783 | |
ckim-dragen | INDEL | I16_PLUS | lowcmp_SimpleRepeat_diTR_11to50 | het | 97.7221 | 97.5000 | 97.9452 | 89.4888 | 156 | 4 | 143 | 3 | 1 | 33.3333 | |
jli-custom | INDEL | D6_15 | map_siren | het | 97.8495 | 97.5000 | 98.2014 | 83.8184 | 273 | 7 | 273 | 5 | 1 | 20.0000 | |
ltrigg-rtg1 | INDEL | D6_15 | map_siren | het | 97.8430 | 97.5000 | 98.1884 | 80.0145 | 273 | 7 | 271 | 5 | 0 | 0.0000 | |
ltrigg-rtg2 | INDEL | D6_15 | map_siren | het | 97.4910 | 97.5000 | 97.4820 | 79.8988 | 273 | 7 | 271 | 7 | 0 | 0.0000 | |
dgrover-gatk | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.4673 | 97.4995 | 99.4544 | 67.8523 | 15675 | 402 | 15676 | 86 | 70 | 81.3953 | |
dgrover-gatk | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.4673 | 97.4995 | 99.4544 | 67.8523 | 15675 | 402 | 15676 | 86 | 70 | 81.3953 | |
qzeng-custom | INDEL | D16_PLUS | * | het | 80.5778 | 97.4992 | 68.6613 | 61.3602 | 3080 | 79 | 4888 | 2231 | 308 | 13.8055 | |
hfeng-pmm3 | INDEL | D16_PLUS | * | het | 97.3472 | 97.4992 | 97.1956 | 74.5540 | 3080 | 79 | 2842 | 82 | 62 | 75.6098 | |
dgrover-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 97.7491 | 97.4988 | 98.0006 | 56.6076 | 36954 | 948 | 36761 | 750 | 723 | 96.4000 | |
egarrison-hhga | INDEL | * | map_l150_m2_e1 | * | 97.7374 | 97.4983 | 97.9777 | 98.7042 | 1403 | 36 | 1405 | 29 | 10 | 34.4828 | |
gduggal-snapvard | SNP | tv | map_l125_m2_e1 | het | 90.7385 | 97.4983 | 84.8553 | 82.7554 | 10289 | 264 | 10259 | 1831 | 116 | 6.3353 | |
jmaeng-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.1915 | 97.4975 | 98.8955 | 61.4377 | 30622 | 786 | 30622 | 342 | 309 | 90.3509 | |
jmaeng-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.1915 | 97.4975 | 98.8955 | 61.4377 | 30622 | 786 | 30622 | 342 | 309 | 90.3509 | |
rpoplin-dv42 | INDEL | * | map_l100_m2_e1 | * | 97.9158 | 97.4973 | 98.3378 | 98.2252 | 3662 | 94 | 3668 | 62 | 29 | 46.7742 | |
ckim-vqsr | INDEL | D1_5 | map_siren | het | 97.8636 | 97.4967 | 98.2332 | 85.9953 | 2220 | 57 | 2224 | 40 | 2 | 5.0000 | |
gduggal-bwavard | SNP | * | map_l125_m2_e0 | homalt | 98.6652 | 97.4964 | 99.8623 | 68.6081 | 16940 | 435 | 16685 | 23 | 18 | 78.2609 | |
gduggal-bwavard | SNP | * | map_l250_m2_e1 | * | 90.6461 | 97.4959 | 84.6957 | 92.1274 | 7787 | 200 | 7709 | 1393 | 45 | 3.2304 | |
gduggal-bwafb | SNP | * | map_l250_m2_e1 | * | 97.8266 | 97.4959 | 98.1596 | 89.9363 | 7787 | 200 | 7787 | 146 | 39 | 26.7123 | |
gduggal-snapfb | SNP | tv | map_l150_m2_e1 | het | 95.8395 | 97.4959 | 94.2384 | 77.2735 | 7164 | 184 | 7164 | 438 | 174 | 39.7260 | |
dgrover-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 97.6983 | 97.4954 | 97.9021 | 76.6822 | 2102 | 54 | 2100 | 45 | 20 | 44.4444 | |
gduggal-bwavard | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 54.7290 | 97.4954 | 38.0419 | 50.8575 | 3192 | 82 | 3194 | 5202 | 5186 | 99.6924 | |
rpoplin-dv42 | INDEL | I1_5 | map_l150_m2_e0 | * | 98.1594 | 97.4952 | 98.8327 | 89.9117 | 506 | 13 | 508 | 6 | 2 | 33.3333 | |
ckim-vqsr | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | * | 97.7733 | 97.4942 | 98.0540 | 45.3637 | 9221 | 237 | 9221 | 183 | 179 | 97.8142 | |
ghariani-varprowl | INDEL | * | HG002complexvar | het | 93.2466 | 97.4941 | 89.3538 | 59.7893 | 45053 | 1158 | 45020 | 5364 | 4472 | 83.3706 | |
gduggal-snapfb | INDEL | D1_5 | * | het | 96.7358 | 97.4935 | 95.9898 | 56.7536 | 85379 | 2195 | 91342 | 3816 | 775 | 20.3092 | |
ckim-dragen | INDEL | D1_5 | map_l125_m2_e1 | * | 97.0711 | 97.4935 | 96.6524 | 88.4160 | 1128 | 29 | 1126 | 39 | 5 | 12.8205 | |
gduggal-snapplat | SNP | ti | HG002complexvar | het | 97.6877 | 97.4934 | 97.8828 | 21.8010 | 306876 | 7890 | 307493 | 6651 | 990 | 14.8850 | |
ltrigg-rtg1 | SNP | ti | map_l125_m0_e0 | * | 98.6208 | 97.4926 | 99.7755 | 64.1831 | 12442 | 320 | 12442 | 28 | 12 | 42.8571 | |
jli-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.2520 | 97.4920 | 99.0239 | 63.2840 | 63712 | 1639 | 63508 | 626 | 529 | 84.5048 | |
jli-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.2520 | 97.4920 | 99.0239 | 63.2840 | 63712 | 1639 | 63508 | 626 | 529 | 84.5048 | |
gduggal-snapvard | SNP | tv | map_l125_m2_e0 | het | 90.6936 | 97.4909 | 84.7824 | 82.7072 | 10180 | 262 | 10151 | 1822 | 114 | 6.2569 | |
rpoplin-dv42 | INDEL | D16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 92.7175 | 97.4908 | 88.3898 | 77.5276 | 1321 | 34 | 1279 | 168 | 162 | 96.4286 | |
hfeng-pmm1 | INDEL | * | map_l100_m1_e0 | * | 98.1895 | 97.4902 | 98.8989 | 82.4896 | 3496 | 90 | 3503 | 39 | 9 | 23.0769 | |
ltrigg-rtg1 | SNP | ti | HG002compoundhet | * | 98.6394 | 97.4883 | 99.8180 | 33.8383 | 17039 | 439 | 17003 | 31 | 12 | 38.7097 | |
ciseli-custom | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 87.0437 | 97.4877 | 78.6210 | 66.4142 | 1785 | 46 | 1813 | 493 | 9 | 1.8256 |