PrecisionFDA
Truth Challenge
Engage and improve DNA test results with our community challenges
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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
23801-23850 / 86044 show all | |||||||||||||||
egarrison-hhga | INDEL | I6_15 | HG002complexvar | homalt | 96.2063 | 97.0346 | 95.3921 | 53.5137 | 1178 | 36 | 1180 | 57 | 43 | 75.4386 | |
mlin-fermikit | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 93.5003 | 97.0335 | 90.2153 | 59.9508 | 8112 | 248 | 8086 | 877 | 859 | 97.9475 | |
mlin-fermikit | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 93.5003 | 97.0335 | 90.2153 | 59.9508 | 8112 | 248 | 8086 | 877 | 859 | 97.9475 | |
asubramanian-gatk | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.1776 | 97.0330 | 99.3494 | 70.2755 | 30219 | 924 | 30236 | 198 | 22 | 11.1111 | |
asubramanian-gatk | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.1776 | 97.0330 | 99.3494 | 70.2755 | 30219 | 924 | 30236 | 198 | 22 | 11.1111 | |
asubramanian-gatk | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 93.7284 | 97.0320 | 90.6425 | 82.6718 | 850 | 26 | 649 | 67 | 66 | 98.5075 | |
mlin-fermikit | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 91.3183 | 97.0313 | 86.2405 | 69.6055 | 3530 | 108 | 3535 | 564 | 553 | 98.0496 | |
anovak-vg | SNP | tv | segdup | het | 97.1722 | 97.0305 | 97.3143 | 94.5962 | 5130 | 157 | 5109 | 141 | 42 | 29.7872 | |
cchapple-custom | INDEL | D1_5 | map_l150_m0_e0 | het | 94.2515 | 97.0297 | 91.6279 | 90.6318 | 196 | 6 | 197 | 18 | 2 | 11.1111 | |
rpoplin-dv42 | INDEL | D1_5 | map_l150_m0_e0 | het | 97.2766 | 97.0297 | 97.5248 | 90.6741 | 196 | 6 | 197 | 5 | 0 | 0.0000 | |
ltrigg-rtg2 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.1456 | 97.0290 | 99.2882 | 49.3199 | 17146 | 525 | 17018 | 122 | 80 | 65.5738 | |
ltrigg-rtg2 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.1456 | 97.0290 | 99.2882 | 49.3199 | 17146 | 525 | 17018 | 122 | 80 | 65.5738 | |
gduggal-bwafb | INDEL | D1_5 | HG002complexvar | * | 98.0343 | 97.0289 | 99.0607 | 56.8977 | 31743 | 972 | 31851 | 302 | 219 | 72.5166 | |
rpoplin-dv42 | SNP | tv | map_l250_m0_e0 | het | 97.0280 | 97.0280 | 97.0280 | 91.3647 | 555 | 17 | 555 | 17 | 12 | 70.5882 | |
hfeng-pmm2 | INDEL | I6_15 | HG002complexvar | het | 98.4267 | 97.0276 | 99.8668 | 58.9949 | 2285 | 70 | 2249 | 3 | 2 | 66.6667 | |
hfeng-pmm1 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 95.2809 | 97.0252 | 93.5982 | 46.7059 | 424 | 13 | 424 | 29 | 29 | 100.0000 | |
astatham-gatk | INDEL | D1_5 | map_siren | * | 97.9977 | 97.0247 | 98.9905 | 82.3184 | 3424 | 105 | 3432 | 35 | 6 | 17.1429 | |
asubramanian-gatk | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 97.4646 | 97.0242 | 97.9090 | 63.2516 | 1565 | 48 | 2669 | 57 | 50 | 87.7193 | |
jmaeng-gatk | INDEL | I16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | het | 96.7145 | 97.0238 | 96.4072 | 78.9673 | 163 | 5 | 161 | 6 | 2 | 33.3333 | |
gduggal-bwafb | INDEL | D1_5 | map_l100_m1_e0 | * | 97.6299 | 97.0238 | 98.2437 | 83.5797 | 1793 | 55 | 1790 | 32 | 6 | 18.7500 | |
ckim-vqsr | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 97.4920 | 97.0234 | 97.9652 | 58.1135 | 17145 | 526 | 17140 | 356 | 338 | 94.9438 | |
ckim-vqsr | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 97.4920 | 97.0234 | 97.9652 | 58.1135 | 17145 | 526 | 17140 | 356 | 338 | 94.9438 | |
cchapple-custom | SNP | tv | map_l150_m2_e0 | * | 96.3013 | 97.0233 | 95.5899 | 79.4079 | 11017 | 338 | 11011 | 508 | 83 | 16.3386 | |
ltrigg-rtg2 | INDEL | D1_5 | map_l100_m1_e0 | het | 97.9933 | 97.0223 | 98.9839 | 74.5035 | 1173 | 36 | 1169 | 12 | 0 | 0.0000 | |
hfeng-pmm1 | INDEL | D1_5 | map_l100_m1_e0 | het | 98.0780 | 97.0223 | 99.1568 | 79.7611 | 1173 | 36 | 1176 | 10 | 0 | 0.0000 | |
ckim-isaac | SNP | ti | * | homalt | 98.4855 | 97.0214 | 99.9944 | 13.4256 | 779120 | 23919 | 779153 | 44 | 32 | 72.7273 | |
ckim-gatk | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 96.7759 | 97.0213 | 96.5318 | 75.2636 | 1368 | 42 | 1336 | 48 | 39 | 81.2500 | |
jpowers-varprowl | SNP | ti | map_l100_m1_e0 | het | 97.5455 | 97.0209 | 98.0758 | 71.2709 | 29050 | 892 | 29052 | 570 | 164 | 28.7719 | |
ckim-dragen | INDEL | I16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 97.6636 | 97.0202 | 98.3156 | 79.8607 | 1107 | 34 | 1109 | 19 | 14 | 73.6842 | |
anovak-vg | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | * | 96.4963 | 97.0192 | 95.9791 | 41.7450 | 17641 | 542 | 17783 | 745 | 376 | 50.4698 | |
qzeng-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 94.7046 | 97.0188 | 92.4983 | 89.7173 | 2636 | 81 | 2762 | 224 | 60 | 26.7857 | |
eyeh-varpipe | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 98.1071 | 97.0183 | 99.2207 | 69.5547 | 32245 | 991 | 32847 | 258 | 171 | 66.2791 | |
astatham-gatk | SNP | ti | map_l250_m0_e0 | homalt | 98.2578 | 97.0183 | 99.5294 | 90.9651 | 423 | 13 | 423 | 2 | 2 | 100.0000 | |
ltrigg-rtg1 | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | * | 98.2308 | 97.0167 | 99.4755 | 56.4489 | 5561 | 171 | 5690 | 30 | 15 | 50.0000 | |
jpowers-varprowl | INDEL | * | lowcmp_SimpleRepeat_homopolymer_6to10 | homalt | 97.2043 | 97.0166 | 97.3928 | 54.4393 | 10959 | 337 | 10945 | 293 | 257 | 87.7133 | |
cchapple-custom | SNP | ti | map_l125_m2_e1 | * | 97.1333 | 97.0166 | 97.2504 | 74.6114 | 29657 | 912 | 29639 | 838 | 230 | 27.4463 | |
asubramanian-gatk | SNP | ti | segdup | het | 98.1746 | 97.0158 | 99.3614 | 92.7228 | 11671 | 359 | 11669 | 75 | 4 | 5.3333 | |
ckim-isaac | SNP | ti | segdup | het | 98.4687 | 97.0158 | 99.9657 | 87.9143 | 11671 | 359 | 11671 | 4 | 0 | 0.0000 | |
jli-custom | SNP | tv | map_l250_m1_e0 | * | 97.9966 | 97.0155 | 98.9977 | 85.0101 | 2568 | 79 | 2568 | 26 | 11 | 42.3077 | |
ckim-vqsr | INDEL | D6_15 | map_l100_m2_e1 | homalt | 98.4848 | 97.0149 | 100.0000 | 87.3294 | 65 | 2 | 65 | 0 | 0 | ||
ckim-gatk | INDEL | D6_15 | map_l100_m2_e1 | homalt | 98.4848 | 97.0149 | 100.0000 | 87.3294 | 65 | 2 | 65 | 0 | 0 | ||
cchapple-custom | INDEL | I1_5 | map_l150_m0_e0 | homalt | 97.7444 | 97.0149 | 98.4848 | 88.2562 | 65 | 2 | 65 | 1 | 1 | 100.0000 | |
rpoplin-dv42 | INDEL | D6_15 | map_l100_m2_e1 | homalt | 97.7444 | 97.0149 | 98.4848 | 85.8974 | 65 | 2 | 65 | 1 | 0 | 0.0000 | |
asubramanian-gatk | INDEL | I1_5 | map_l150_m0_e0 | homalt | 98.4848 | 97.0149 | 100.0000 | 89.9691 | 65 | 2 | 65 | 0 | 0 | ||
bgallagher-sentieon | INDEL | D6_15 | map_l100_m2_e1 | homalt | 98.4848 | 97.0149 | 100.0000 | 87.1287 | 65 | 2 | 65 | 0 | 0 | ||
astatham-gatk | INDEL | D6_15 | map_l100_m2_e1 | homalt | 98.4848 | 97.0149 | 100.0000 | 87.0518 | 65 | 2 | 65 | 0 | 0 | ||
hfeng-pmm1 | INDEL | D6_15 | map_l100_m2_e1 | homalt | 98.4848 | 97.0149 | 100.0000 | 83.9901 | 65 | 2 | 65 | 0 | 0 | ||
gduggal-snapfb | INDEL | I1_5 | map_l150_m0_e0 | homalt | 97.7329 | 97.0149 | 98.4615 | 94.4869 | 65 | 2 | 64 | 1 | 1 | 100.0000 | |
hfeng-pmm3 | INDEL | D6_15 | map_l100_m2_e1 | homalt | 98.4848 | 97.0149 | 100.0000 | 84.0686 | 65 | 2 | 65 | 0 | 0 | ||
hfeng-pmm3 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 96.7479 | 97.0149 | 96.4824 | 86.9251 | 195 | 6 | 192 | 7 | 1 | 14.2857 |