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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
10901-10950 / 86044 show all | |||||||||||||||
mlin-fermikit | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 95.6677 | 96.0493 | 95.2892 | 79.6573 | 6394 | 263 | 6392 | 316 | 202 | 63.9241 | |
ndellapenna-hhga | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 94.1695 | 90.0530 | 98.6804 | 37.0620 | 2381 | 263 | 2393 | 32 | 28 | 87.5000 | |
ndellapenna-hhga | SNP | ti | map_l125_m0_e0 | * | 98.8454 | 97.9392 | 99.7685 | 71.9216 | 12499 | 263 | 12499 | 29 | 16 | 55.1724 | |
ghariani-varprowl | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 86.5865 | 98.1950 | 77.4326 | 84.5229 | 14308 | 263 | 14380 | 4191 | 196 | 4.6767 | |
ghariani-varprowl | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 86.5865 | 98.1950 | 77.4326 | 84.5229 | 14308 | 263 | 14380 | 4191 | 196 | 4.6767 | |
raldana-dualsentieon | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | hetalt | 92.2212 | 85.5653 | 100.0000 | 31.5699 | 1559 | 263 | 1591 | 0 | 0 | ||
dgrover-gatk | SNP | ti | HG002complexvar | het | 99.9452 | 99.9164 | 99.9739 | 17.0118 | 314503 | 263 | 314449 | 82 | 32 | 39.0244 | |
dgrover-gatk | SNP | tv | * | het | 99.8830 | 99.9556 | 99.8105 | 23.6829 | 591433 | 263 | 591362 | 1123 | 57 | 5.0757 | |
eyeh-varpipe | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 14.8482 | 8.0420 | 96.6292 | 50.2793 | 23 | 263 | 86 | 3 | 3 | 100.0000 | |
gduggal-bwafb | SNP | ti | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 98.2991 | 99.0593 | 97.5505 | 61.1472 | 27696 | 263 | 27758 | 697 | 164 | 23.5294 | |
gduggal-bwavard | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 86.6216 | 88.8936 | 84.4628 | 86.9345 | 2105 | 263 | 2044 | 376 | 124 | 32.9787 | |
jli-custom | SNP | ti | map_l100_m2_e0 | het | 99.3179 | 99.1411 | 99.4953 | 64.3096 | 30359 | 263 | 30357 | 154 | 38 | 24.6753 | |
jli-custom | SNP | ti | map_l100_m2_e1 | het | 99.3237 | 99.1505 | 99.4976 | 64.3340 | 30697 | 263 | 30695 | 155 | 38 | 24.5161 | |
jli-custom | INDEL | D6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 95.0957 | 93.3062 | 96.9553 | 51.5459 | 3666 | 263 | 3662 | 115 | 107 | 93.0435 | |
jli-custom | INDEL | I6_15 | * | het | 98.3728 | 97.3787 | 99.3875 | 54.1020 | 9770 | 263 | 9736 | 60 | 34 | 56.6667 | |
jpowers-varprowl | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 87.8581 | 97.1203 | 80.2087 | 86.4645 | 8870 | 263 | 8916 | 2200 | 30 | 1.3636 | |
jpowers-varprowl | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 87.8581 | 97.1203 | 80.2087 | 86.4645 | 8870 | 263 | 8916 | 2200 | 30 | 1.3636 | |
jmaeng-gatk | INDEL | D1_5 | * | het | 99.4941 | 99.6997 | 99.2893 | 60.9724 | 87311 | 263 | 87316 | 625 | 129 | 20.6400 | |
ltrigg-rtg1 | INDEL | D1_5 | HG002complexvar | het | 99.1733 | 98.7383 | 99.6122 | 51.3027 | 20503 | 262 | 20294 | 79 | 31 | 39.2405 | |
jli-custom | SNP | ti | map_l100_m1_e0 | het | 99.3190 | 99.1250 | 99.5138 | 62.5391 | 29680 | 262 | 29678 | 145 | 38 | 26.2069 | |
ltrigg-rtg1 | SNP | ti | map_l150_m0_e0 | * | 98.1783 | 96.6671 | 99.7375 | 70.0220 | 7599 | 262 | 7598 | 20 | 11 | 55.0000 | |
gduggal-snapfb | SNP | ti | map_l150_m0_e0 | het | 94.2863 | 94.8597 | 93.7197 | 77.7514 | 4835 | 262 | 4835 | 324 | 174 | 53.7037 | |
gduggal-snapvard | SNP | tv | map_l125_m0_e0 | * | 89.3998 | 96.0489 | 83.6117 | 82.4411 | 6369 | 262 | 6357 | 1246 | 62 | 4.9759 | |
gduggal-snapvard | SNP | tv | map_l125_m2_e0 | het | 90.6936 | 97.4909 | 84.7824 | 82.7072 | 10180 | 262 | 10151 | 1822 | 114 | 6.2569 | |
gduggal-snapplat | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 90.3941 | 93.8999 | 87.1407 | 79.9532 | 4033 | 262 | 4032 | 595 | 11 | 1.8487 | |
anovak-vg | INDEL | I6_15 | lowcmp_SimpleRepeat_triTR_11to50 | * | 47.4248 | 37.3206 | 65.0316 | 30.6257 | 156 | 262 | 411 | 221 | 186 | 84.1629 | |
jlack-gatk | INDEL | * | * | homalt | 99.2685 | 99.7907 | 98.7518 | 57.7386 | 124910 | 262 | 124923 | 1579 | 1542 | 97.6567 | |
hfeng-pmm1 | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 99.1947 | 98.5087 | 99.8903 | 63.5767 | 17306 | 262 | 17297 | 19 | 5 | 26.3158 | |
mlin-fermikit | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 95.6924 | 96.0989 | 95.2894 | 42.1888 | 6454 | 262 | 6453 | 319 | 300 | 94.0439 | |
mlin-fermikit | INDEL | I16_PLUS | * | het | 86.1646 | 90.3606 | 82.3411 | 68.6094 | 2456 | 262 | 2448 | 525 | 508 | 96.7619 | |
mlin-fermikit | INDEL | I1_5 | map_siren | homalt | 84.8214 | 78.3828 | 92.4125 | 74.4596 | 950 | 262 | 950 | 78 | 75 | 96.1538 | |
mlin-fermikit | SNP | ti | map_l250_m0_e0 | homalt | 50.6550 | 39.9083 | 69.3227 | 79.0659 | 174 | 262 | 174 | 77 | 71 | 92.2078 | |
gduggal-bwaplat | INDEL | I6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 60.2985 | 43.5345 | 98.0583 | 86.3666 | 202 | 262 | 202 | 4 | 2 | 50.0000 | |
raldana-dualsentieon | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 96.4344 | 93.1143 | 100.0000 | 27.8227 | 3543 | 262 | 3567 | 0 | 0 | ||
rpoplin-dv42 | SNP | ti | map_l100_m2_e0 | het | 99.3487 | 99.1444 | 99.5539 | 65.6465 | 30360 | 262 | 30352 | 136 | 82 | 60.2941 | |
raldana-dualsentieon | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | hetalt | 91.7274 | 84.7190 | 100.0000 | 29.6719 | 1447 | 261 | 1479 | 0 | 0 | ||
jlack-gatk | SNP | * | HG002complexvar | homalt | 99.9456 | 99.9096 | 99.9816 | 19.7398 | 288313 | 261 | 288284 | 53 | 46 | 86.7925 | |
ghariani-varprowl | SNP | * | map_l100_m0_e0 | het | 97.0530 | 98.7692 | 95.3955 | 77.5266 | 20944 | 261 | 20946 | 1011 | 206 | 20.3759 | |
gduggal-snapplat | INDEL | * | map_l100_m0_e0 | het | 80.0362 | 74.4368 | 86.5466 | 93.5607 | 760 | 261 | 817 | 127 | 18 | 14.1732 | |
jmaeng-gatk | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 96.6279 | 93.5220 | 99.9473 | 22.3450 | 3768 | 261 | 3793 | 2 | 2 | 100.0000 | |
ciseli-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 45.1028 | 77.9188 | 31.7367 | 57.3110 | 921 | 261 | 921 | 1981 | 1814 | 91.5699 | |
ciseli-custom | SNP | tv | map_l150_m0_e0 | homalt | 82.2034 | 80.3464 | 84.1483 | 77.4538 | 1067 | 261 | 1067 | 201 | 160 | 79.6020 | |
anovak-vg | SNP | * | HG002complexvar | hetalt | 0.0000 | 15.8065 | 0.0000 | 0.0000 | 49 | 261 | 0 | 0 | 0 | ||
anovak-vg | SNP | tv | HG002complexvar | hetalt | 0.0000 | 15.8065 | 0.0000 | 0.0000 | 49 | 261 | 0 | 0 | 0 | ||
gduggal-bwaplat | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 95.8427 | 93.9232 | 97.8424 | 72.3914 | 4034 | 261 | 4036 | 89 | 6 | 6.7416 | |
gduggal-bwafb | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 51.1783 | 36.9565 | 83.1933 | 65.7061 | 153 | 261 | 99 | 20 | 20 | 100.0000 | |
mlin-fermikit | INDEL | I1_5 | map_l125_m2_e0 | het | 63.7838 | 47.4849 | 97.1193 | 82.2238 | 236 | 261 | 236 | 7 | 4 | 57.1429 | |
ltrigg-rtg2 | SNP | tv | map_l150_m2_e0 | het | 98.0436 | 96.4010 | 99.7431 | 60.6061 | 6991 | 261 | 6989 | 18 | 1 | 5.5556 | |
ltrigg-rtg2 | SNP | tv | map_l150_m2_e1 | het | 98.0696 | 96.4480 | 99.7466 | 60.6896 | 7087 | 261 | 7085 | 18 | 1 | 5.5556 | |
dgrover-gatk | SNP | * | map_l150_m1_e0 | * | 99.1521 | 99.1473 | 99.1569 | 77.1188 | 30348 | 261 | 30342 | 258 | 59 | 22.8682 |