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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
15651-15700 / 86044 show all | |||||||||||||||
egarrison-hhga | SNP | ti | map_l150_m0_e0 | homalt | 99.7098 | 99.5654 | 99.8547 | 73.4497 | 2749 | 12 | 2749 | 4 | 4 | 100.0000 | |
ltrigg-rtg2 | SNP | * | map_l250_m2_e1 | * | 97.1847 | 94.6538 | 99.8547 | 80.7686 | 7560 | 427 | 7560 | 11 | 4 | 36.3636 | |
ltrigg-rtg1 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 99.2720 | 98.6962 | 99.8546 | 54.0539 | 8251 | 109 | 8239 | 12 | 12 | 100.0000 | |
ltrigg-rtg1 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 99.2720 | 98.6962 | 99.8546 | 54.0539 | 8251 | 109 | 8239 | 12 | 12 | 100.0000 | |
ckim-dragen | SNP | tv | HG002compoundhet | * | 99.7984 | 99.7422 | 99.8546 | 49.3913 | 8900 | 23 | 8925 | 13 | 8 | 61.5385 | |
ltrigg-rtg2 | INDEL | D6_15 | * | homalt | 99.1477 | 98.4508 | 99.8545 | 42.0407 | 6228 | 98 | 6177 | 9 | 7 | 77.7778 | |
jli-custom | SNP | ti | map_l150_m0_e0 | homalt | 99.6006 | 99.3481 | 99.8544 | 71.0140 | 2743 | 18 | 2743 | 4 | 4 | 100.0000 | |
egarrison-hhga | SNP | tv | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 99.6549 | 99.4561 | 99.8544 | 38.0748 | 2743 | 15 | 2743 | 4 | 4 | 100.0000 | |
ndellapenna-hhga | SNP | ti | map_l150_m0_e0 | homalt | 99.5641 | 99.2756 | 99.8543 | 71.8779 | 2741 | 20 | 2741 | 4 | 4 | 100.0000 | |
rpoplin-dv42 | SNP | ti | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 99.8628 | 99.8712 | 99.8543 | 55.6453 | 17828 | 23 | 17825 | 26 | 14 | 53.8462 | |
gduggal-bwafb | SNP | ti | map_l150_m2_e0 | homalt | 99.3999 | 98.9496 | 99.8542 | 74.6089 | 7536 | 80 | 7536 | 11 | 6 | 54.5455 | |
bgallagher-sentieon | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 99.7450 | 99.6361 | 99.8542 | 72.0228 | 1369 | 5 | 1370 | 2 | 0 | 0.0000 | |
raldana-dualsentieon | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 99.7085 | 99.5633 | 99.8541 | 71.1368 | 1368 | 6 | 1369 | 2 | 0 | 0.0000 | |
egarrison-hhga | SNP | ti | map_l100_m2_e0 | * | 99.5647 | 99.2770 | 99.8541 | 64.5210 | 48607 | 354 | 48608 | 71 | 32 | 45.0704 | |
ltrigg-rtg2 | SNP | ti | map_l150_m0_e0 | homalt | 99.5276 | 99.2032 | 99.8541 | 71.1520 | 2739 | 22 | 2738 | 4 | 4 | 100.0000 | |
ltrigg-rtg2 | SNP | ti | map_l250_m1_e0 | het | 95.8290 | 92.1159 | 99.8541 | 75.2192 | 2734 | 234 | 2737 | 4 | 1 | 25.0000 | |
hfeng-pmm2 | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 99.3792 | 98.9089 | 99.8541 | 63.0972 | 27376 | 302 | 27367 | 40 | 7 | 17.5000 | |
hfeng-pmm3 | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 99.6719 | 99.4905 | 99.8540 | 71.2728 | 1367 | 7 | 1368 | 2 | 0 | 0.0000 | |
hfeng-pmm1 | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 99.6719 | 99.4905 | 99.8540 | 71.6062 | 1367 | 7 | 1368 | 2 | 0 | 0.0000 | |
hfeng-pmm2 | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 99.6719 | 99.4905 | 99.8540 | 71.8223 | 1367 | 7 | 1368 | 2 | 0 | 0.0000 | |
ltrigg-rtg2 | SNP | tv | map_l250_m2_e1 | * | 96.8015 | 93.9300 | 99.8540 | 79.7875 | 2739 | 177 | 2736 | 4 | 0 | 0.0000 | |
ndellapenna-hhga | SNP | * | lowcmp_SimpleRepeat_triTR_11to50 | homalt | 99.8356 | 99.8174 | 99.8539 | 32.2109 | 2733 | 5 | 2734 | 4 | 3 | 75.0000 | |
astatham-gatk | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 99.6719 | 99.4905 | 99.8539 | 72.1465 | 1367 | 7 | 1367 | 2 | 0 | 0.0000 | |
asubramanian-gatk | SNP | * | * | het | 98.9725 | 98.1066 | 99.8538 | 23.0377 | 1838113 | 35474 | 1837999 | 2691 | 109 | 4.0505 | |
ckim-isaac | SNP | ti | map_siren | het | 88.1134 | 78.8433 | 99.8538 | 52.2793 | 49184 | 13198 | 49191 | 72 | 6 | 8.3333 | |
egarrison-hhga | SNP | ti | map_l100_m2_e1 | * | 99.5683 | 99.2846 | 99.8537 | 64.5157 | 49131 | 354 | 49132 | 72 | 32 | 44.4444 | |
dgrover-gatk | SNP | tv | map_l150_m2_e1 | homalt | 99.4413 | 99.0324 | 99.8537 | 71.5870 | 4094 | 40 | 4094 | 6 | 4 | 66.6667 | |
jmaeng-gatk | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_51to200 | hetalt | 86.0332 | 75.5734 | 99.8536 | 26.3215 | 659 | 213 | 682 | 1 | 1 | 100.0000 | |
cchapple-custom | SNP | ti | segdup | homalt | 99.8600 | 99.8668 | 99.8533 | 87.0523 | 7495 | 10 | 7487 | 11 | 11 | 100.0000 | |
ltrigg-rtg2 | SNP | ti | map_l250_m2_e0 | * | 97.3703 | 95.0080 | 99.8532 | 81.1041 | 4758 | 250 | 4761 | 7 | 4 | 57.1429 | |
dgrover-gatk | INDEL | I1_5 | HG002complexvar | * | 99.7285 | 99.6044 | 99.8530 | 57.2674 | 33231 | 132 | 33279 | 49 | 38 | 77.5510 | |
astatham-gatk | SNP | * | lowcmp_SimpleRepeat_diTR_11to50 | het | 98.9155 | 97.9955 | 99.8529 | 70.5060 | 6111 | 125 | 6111 | 9 | 8 | 88.8889 | |
jlack-gatk | INDEL | D1_5 | lowcmp_SimpleRepeat_triTR_11to50 | * | 99.8160 | 99.7792 | 99.8528 | 43.7655 | 4068 | 9 | 4071 | 6 | 1 | 16.6667 | |
ltrigg-rtg2 | SNP | * | map_l250_m2_e0 | * | 97.1607 | 94.6100 | 99.8528 | 80.6416 | 7460 | 425 | 7460 | 11 | 4 | 36.3636 | |
astatham-gatk | INDEL | I1_5 | HG002complexvar | * | 99.6397 | 99.4275 | 99.8527 | 57.1222 | 33172 | 191 | 33219 | 49 | 39 | 79.5918 | |
asubramanian-gatk | SNP | * | map_l100_m1_e0 | * | 60.2018 | 43.0908 | 99.8527 | 84.6729 | 31199 | 41204 | 31193 | 46 | 12 | 26.0870 | |
hfeng-pmm3 | INDEL | D16_PLUS | * | hetalt | 96.6173 | 93.5851 | 99.8525 | 38.5313 | 1809 | 124 | 2031 | 3 | 3 | 100.0000 | |
jli-custom | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 97.3256 | 94.9234 | 99.8525 | 39.2800 | 3347 | 179 | 3385 | 5 | 5 | 100.0000 | |
jli-custom | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 97.3256 | 94.9234 | 99.8525 | 39.2800 | 3347 | 179 | 3385 | 5 | 5 | 100.0000 | |
hfeng-pmm1 | INDEL | D16_PLUS | * | hetalt | 96.6724 | 93.6886 | 99.8525 | 38.6610 | 1811 | 122 | 2031 | 3 | 3 | 100.0000 | |
ckim-dragen | SNP | tv | HG002compoundhet | homalt | 99.8672 | 99.8819 | 99.8524 | 43.2020 | 3384 | 4 | 3383 | 5 | 5 | 100.0000 | |
hfeng-pmm3 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 99.9261 | 100.0000 | 99.8524 | 72.4033 | 1353 | 0 | 1353 | 2 | 0 | 0.0000 | |
hfeng-pmm2 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 99.9261 | 100.0000 | 99.8524 | 72.8729 | 1353 | 0 | 1353 | 2 | 1 | 50.0000 | |
hfeng-pmm3 | SNP | tv | HG002compoundhet | homalt | 99.8376 | 99.8229 | 99.8524 | 42.5250 | 3382 | 6 | 3382 | 5 | 5 | 100.0000 | |
hfeng-pmm3 | SNP | ti | map_siren | * | 99.7701 | 99.6881 | 99.8523 | 52.8057 | 100042 | 313 | 100027 | 148 | 25 | 16.8919 | |
hfeng-pmm2 | INDEL | D16_PLUS | * | hetalt | 96.6998 | 93.7403 | 99.8523 | 39.1187 | 1812 | 121 | 2028 | 3 | 3 | 100.0000 | |
hfeng-pmm1 | SNP | tv | HG002compoundhet | homalt | 99.8229 | 99.7934 | 99.8523 | 42.7460 | 3381 | 7 | 3381 | 5 | 5 | 100.0000 | |
hfeng-pmm1 | SNP | tv | lowcmp_SimpleRepeat_diTR_11to50 | * | 98.6241 | 97.4259 | 99.8523 | 63.8155 | 4731 | 125 | 4731 | 7 | 6 | 85.7143 | |
hfeng-pmm3 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 96.6136 | 93.5785 | 99.8523 | 38.4918 | 1807 | 124 | 2028 | 3 | 3 | 100.0000 | |
hfeng-pmm3 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 96.6136 | 93.5785 | 99.8523 | 38.4918 | 1807 | 124 | 2028 | 3 | 3 | 100.0000 |