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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
12401-12450 / 86044 show all | |||||||||||||||
gduggal-bwaplat | INDEL | I16_PLUS | lowcmp_SimpleRepeat_diTR_11to50 | * | 72.0169 | 58.7500 | 93.0233 | 81.0095 | 282 | 198 | 280 | 21 | 14 | 66.6667 | |
eyeh-varpipe | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 11.2554 | 6.1611 | 65.0000 | 68.2540 | 13 | 198 | 13 | 7 | 4 | 57.1429 | |
gduggal-bwavard | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 52.9207 | 36.3344 | 97.3684 | 65.7658 | 113 | 198 | 111 | 3 | 3 | 100.0000 | |
gduggal-bwavard | SNP | * | map_l125_m0_e0 | homalt | 98.3897 | 97.0501 | 99.7668 | 70.8893 | 6514 | 198 | 6417 | 15 | 11 | 73.3333 | |
gduggal-bwavard | SNP | ti | map_l125_m0_e0 | het | 92.1685 | 97.6038 | 87.3066 | 84.9758 | 8065 | 198 | 8013 | 1165 | 59 | 5.0644 | |
gduggal-bwafb | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 31.6497 | 19.5122 | 83.7398 | 62.9518 | 48 | 198 | 103 | 20 | 20 | 100.0000 | |
gduggal-bwaplat | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_51to200 | het | 61.6145 | 48.5714 | 84.2342 | 85.1703 | 187 | 198 | 187 | 35 | 5 | 14.2857 | |
gduggal-bwaplat | INDEL | D1_5 | map_l150_m2_e1 | het | 76.1457 | 62.0690 | 98.4802 | 96.0428 | 324 | 198 | 324 | 5 | 1 | 20.0000 | |
ckim-isaac | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | het | 88.0210 | 92.7552 | 83.7467 | 49.6639 | 2535 | 198 | 2195 | 426 | 362 | 84.9765 | |
ckim-vqsr | INDEL | * | map_siren | * | 97.9969 | 97.3279 | 98.6752 | 85.5636 | 7212 | 198 | 7225 | 97 | 19 | 19.5876 | |
egarrison-hhga | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 99.5328 | 99.2846 | 99.7822 | 62.2610 | 27480 | 198 | 27491 | 60 | 36 | 60.0000 | |
astatham-gatk | SNP | tv | * | homalt | 99.9694 | 99.9475 | 99.9912 | 19.9071 | 376925 | 198 | 376910 | 33 | 26 | 78.7879 | |
anovak-vg | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | het | 39.5158 | 40.0000 | 39.0432 | 37.8119 | 132 | 198 | 253 | 395 | 347 | 87.8481 | |
bgallagher-sentieon | INDEL | I16_PLUS | HG002compoundhet | * | 93.0399 | 90.7606 | 95.4367 | 53.0631 | 1945 | 198 | 1945 | 93 | 93 | 100.0000 | |
anovak-vg | INDEL | I6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 28.1418 | 19.8381 | 48.4018 | 54.7521 | 49 | 198 | 106 | 113 | 90 | 79.6460 | |
anovak-vg | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 76.6177 | 84.7222 | 69.9283 | 81.0889 | 1098 | 198 | 1365 | 587 | 286 | 48.7223 | |
astatham-gatk | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 97.9353 | 96.3590 | 99.5640 | 26.8986 | 5240 | 198 | 5252 | 23 | 22 | 95.6522 | |
ltrigg-rtg2 | SNP | * | map_l250_m0_e0 | het | 92.7987 | 86.8526 | 99.6189 | 78.5270 | 1308 | 198 | 1307 | 5 | 0 | 0.0000 | |
qzeng-custom | INDEL | D1_5 | map_l100_m1_e0 | het | 89.6970 | 83.6228 | 96.7227 | 89.7617 | 1011 | 198 | 1151 | 39 | 27 | 69.2308 | |
ndellapenna-hhga | INDEL | D1_5 | lowcmp_SimpleRepeat_triTR_11to50 | * | 95.3412 | 95.1435 | 95.5397 | 38.5245 | 3879 | 198 | 3877 | 181 | 170 | 93.9227 | |
raldana-dualsentieon | SNP | * | map_l125_m0_e0 | het | 98.3431 | 98.4365 | 98.2499 | 76.1833 | 12466 | 198 | 12463 | 222 | 2 | 0.9009 | |
ltrigg-rtg1 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 97.1505 | 94.9192 | 99.4892 | 54.6175 | 3699 | 198 | 3701 | 19 | 11 | 57.8947 | |
ckim-dragen | INDEL | I1_5 | HG002complexvar | * | 99.5809 | 99.4065 | 99.7559 | 56.6825 | 33165 | 198 | 33105 | 81 | 67 | 82.7160 | |
ciseli-custom | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | het | 83.6651 | 85.4732 | 81.9319 | 70.4517 | 1165 | 198 | 1179 | 260 | 119 | 45.7692 | |
ghariani-varprowl | INDEL | I1_5 | HG002compoundhet | het | 21.0205 | 76.7059 | 12.1791 | 72.5111 | 652 | 198 | 721 | 5199 | 5126 | 98.5959 | |
gduggal-snapvard | INDEL | I1_5 | lowcmp_SimpleRepeat_triTR_11to50 | * | 78.1683 | 81.1429 | 75.4042 | 51.8889 | 852 | 198 | 1306 | 426 | 326 | 76.5258 | |
gduggal-snapvard | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 65.5717 | 86.0759 | 52.9568 | 90.4618 | 1224 | 198 | 1200 | 1066 | 55 | 5.1595 | |
gduggal-snapvard | SNP | tv | map_l150_m2_e1 | het | 88.7208 | 97.3054 | 81.5281 | 85.1064 | 7150 | 198 | 7128 | 1615 | 97 | 6.0062 | |
hfeng-pmm3 | SNP | * | map_l125_m2_e1 | het | 99.4275 | 99.3320 | 99.5233 | 72.3246 | 29442 | 198 | 29436 | 141 | 13 | 9.2199 | |
hfeng-pmm2 | SNP | ti | map_l100_m1_e0 | het | 99.3403 | 99.3387 | 99.3419 | 67.8029 | 29744 | 198 | 29737 | 197 | 16 | 8.1218 | |
hfeng-pmm2 | SNP | * | map_l100_m0_e0 | * | 99.2701 | 99.4001 | 99.1404 | 70.5461 | 32644 | 197 | 32640 | 283 | 34 | 12.0141 | |
hfeng-pmm3 | SNP | * | map_l125_m2_e0 | het | 99.4247 | 99.3281 | 99.5214 | 72.2786 | 29121 | 197 | 29115 | 140 | 13 | 9.2857 | |
hfeng-pmm1 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 96.1118 | 92.5492 | 99.9597 | 37.5723 | 2447 | 197 | 2483 | 1 | 1 | 100.0000 | |
rpoplin-dv42 | SNP | ti | map_l125_m2_e1 | het | 99.1705 | 98.9679 | 99.3738 | 71.8144 | 18890 | 197 | 18886 | 119 | 74 | 62.1849 | |
asubramanian-gatk | INDEL | D1_5 | map_l100_m2_e0 | * | 93.0444 | 89.7128 | 96.6330 | 87.5446 | 1718 | 197 | 1722 | 60 | 7 | 11.6667 | |
bgallagher-sentieon | INDEL | I16_PLUS | * | hetalt | 95.0034 | 90.6101 | 99.8444 | 57.6357 | 1901 | 197 | 1925 | 3 | 3 | 100.0000 | |
gduggal-bwafb | SNP | ti | map_l150_m1_e0 | het | 98.3399 | 98.4074 | 98.2724 | 78.0641 | 12173 | 197 | 12173 | 214 | 63 | 29.4393 | |
gduggal-bwavard | SNP | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 93.9826 | 95.8648 | 92.1728 | 78.1956 | 4567 | 197 | 4522 | 384 | 48 | 12.5000 | |
gduggal-bwavard | SNP | * | map_l250_m2_e0 | * | 90.6036 | 97.5016 | 84.6171 | 92.0596 | 7688 | 197 | 7613 | 1384 | 44 | 3.1792 | |
gduggal-snapfb | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | homalt | 59.9593 | 59.9593 | 59.9593 | 55.8744 | 295 | 197 | 295 | 197 | 173 | 87.8173 | |
egarrison-hhga | INDEL | I16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 87.5573 | 82.7344 | 92.9773 | 75.9228 | 944 | 197 | 940 | 71 | 43 | 60.5634 | |
dgrover-gatk | SNP | ti | map_l125_m1_e0 | * | 99.3758 | 99.3284 | 99.4233 | 72.4326 | 29138 | 197 | 29134 | 169 | 41 | 24.2604 | |
ndellapenna-hhga | SNP | tv | map_l150_m2_e0 | * | 98.9623 | 98.2651 | 99.6695 | 73.4684 | 11158 | 197 | 11158 | 37 | 17 | 45.9459 | |
qzeng-custom | SNP | tv | map_l250_m0_e0 | het | 74.5292 | 65.5594 | 86.3426 | 98.2078 | 375 | 197 | 373 | 59 | 42 | 71.1864 | |
qzeng-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 93.5793 | 94.7690 | 92.4191 | 52.4483 | 3569 | 197 | 3572 | 293 | 241 | 82.2526 | |
qzeng-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 93.5793 | 94.7690 | 92.4191 | 52.4483 | 3569 | 197 | 3572 | 293 | 241 | 82.2526 | |
gduggal-snapvard | SNP | tv | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 98.5877 | 98.1945 | 98.9841 | 59.2905 | 10714 | 197 | 10620 | 109 | 34 | 31.1927 | |
gduggal-snapvard | SNP | tv | map_l150_m2_e0 | het | 88.6343 | 97.2835 | 81.3975 | 85.0700 | 7055 | 197 | 7036 | 1608 | 95 | 5.9080 | |
gduggal-snapplat | INDEL | D6_15 | map_l100_m2_e0 | * | 38.8774 | 25.3788 | 83.0508 | 94.3378 | 67 | 197 | 49 | 10 | 1 | 10.0000 | |
ltrigg-rtg1 | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 97.9702 | 98.9938 | 96.9676 | 70.5278 | 19382 | 197 | 19570 | 612 | 14 | 2.2876 |