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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
14801-14850 / 86044 show all | |||||||||||||||
dgrover-gatk | SNP | ti | map_l150_m2_e1 | * | 99.2396 | 99.1990 | 99.2803 | 78.3146 | 20557 | 166 | 20553 | 149 | 36 | 24.1611 | |
ltrigg-rtg1 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 99.5979 | 99.1989 | 100.0000 | 79.0898 | 1486 | 12 | 1507 | 0 | 0 | ||
asubramanian-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 99.5646 | 99.1989 | 99.9329 | 79.3662 | 1486 | 12 | 1490 | 1 | 1 | 100.0000 | |
eyeh-varpipe | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 98.8358 | 99.1988 | 98.4754 | 71.0733 | 16839 | 136 | 16083 | 249 | 72 | 28.9157 | |
eyeh-varpipe | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 98.8358 | 99.1988 | 98.4754 | 71.0733 | 16839 | 136 | 16083 | 249 | 72 | 28.9157 | |
ckim-gatk | SNP | * | * | homalt | 99.5941 | 99.1985 | 99.9929 | 17.5422 | 1170702 | 9459 | 1170679 | 83 | 52 | 62.6506 | |
ndellapenna-hhga | SNP | * | lowcmp_SimpleRepeat_triTR_11to50 | het | 99.5327 | 99.1984 | 99.8692 | 31.8675 | 4579 | 37 | 4580 | 6 | 1 | 16.6667 | |
qzeng-custom | SNP | ti | * | het | 99.4567 | 99.1981 | 99.7166 | 23.5601 | 1271618 | 10279 | 1269681 | 3608 | 520 | 14.4124 | |
ckim-dragen | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.6551 | 99.1981 | 98.1180 | 73.7453 | 19422 | 157 | 19551 | 375 | 40 | 10.6667 | |
ckim-dragen | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.6551 | 99.1981 | 98.1180 | 73.7453 | 19422 | 157 | 19551 | 375 | 40 | 10.6667 | |
asubramanian-gatk | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | homalt | 99.4638 | 99.1979 | 99.7312 | 59.5652 | 371 | 3 | 371 | 1 | 0 | 0.0000 | |
qzeng-custom | SNP | * | lowcmp_SimpleRepeat_triTR_11to50 | * | 99.4064 | 99.1978 | 99.6159 | 41.7997 | 7296 | 59 | 7261 | 28 | 6 | 21.4286 | |
ckim-dragen | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 99.3235 | 99.1976 | 99.4496 | 87.1665 | 2349 | 19 | 2349 | 13 | 13 | 100.0000 | |
gduggal-bwaplat | SNP | * | func_cds | homalt | 99.5972 | 99.1976 | 100.0000 | 22.2746 | 6923 | 56 | 6923 | 0 | 0 | ||
jmaeng-gatk | SNP | tv | segdup | homalt | 99.4735 | 99.1970 | 99.7516 | 89.7966 | 3212 | 26 | 3212 | 8 | 8 | 100.0000 | |
ckim-gatk | SNP | tv | segdup | homalt | 99.5043 | 99.1970 | 99.8135 | 89.9144 | 3212 | 26 | 3212 | 6 | 6 | 100.0000 | |
qzeng-custom | SNP | tv | lowcmp_SimpleRepeat_diTR_11to50 | * | 98.5273 | 99.1969 | 97.8668 | 72.2743 | 4817 | 39 | 4863 | 106 | 20 | 18.8679 | |
egarrison-hhga | SNP | tv | * | hetalt | 99.1394 | 99.1963 | 99.0826 | 48.4024 | 864 | 7 | 864 | 8 | 8 | 100.0000 | |
egarrison-hhga | SNP | * | * | hetalt | 99.1394 | 99.1963 | 99.0826 | 48.4024 | 864 | 7 | 864 | 8 | 8 | 100.0000 | |
ckim-dragen | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.4729 | 99.1955 | 97.7608 | 76.5892 | 28481 | 231 | 28728 | 658 | 53 | 8.0547 | |
ckim-dragen | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.4729 | 99.1955 | 97.7608 | 76.5892 | 28481 | 231 | 28728 | 658 | 53 | 8.0547 | |
raldana-dualsentieon | SNP | * | map_l100_m1_e0 | het | 99.0827 | 99.1953 | 98.9703 | 66.7199 | 44994 | 365 | 44983 | 468 | 7 | 1.4957 | |
bgallagher-sentieon | SNP | * | map_l125_m0_e0 | * | 98.8636 | 99.1953 | 98.5342 | 75.8607 | 19229 | 156 | 19226 | 286 | 50 | 17.4825 | |
ndellapenna-hhga | SNP | * | map_siren | * | 99.5283 | 99.1937 | 99.8651 | 53.0102 | 145049 | 1179 | 145051 | 196 | 89 | 45.4082 | |
ndellapenna-hhga | INDEL | D1_5 | map_l125_m2_e1 | homalt | 99.0604 | 99.1935 | 98.9276 | 85.4807 | 369 | 3 | 369 | 4 | 4 | 100.0000 | |
rpoplin-dv42 | SNP | tv | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 99.3435 | 99.1935 | 99.4939 | 70.5690 | 984 | 8 | 983 | 5 | 1 | 20.0000 | |
bgallagher-sentieon | INDEL | D1_5 | map_l150_m2_e1 | homalt | 99.1935 | 99.1935 | 99.1935 | 88.0424 | 246 | 2 | 246 | 2 | 2 | 100.0000 | |
astatham-gatk | INDEL | D1_5 | map_l150_m2_e1 | homalt | 99.1935 | 99.1935 | 99.1935 | 88.1510 | 246 | 2 | 246 | 2 | 2 | 100.0000 | |
ckim-gatk | INDEL | D1_5 | map_l100_m2_e1 | homalt | 99.3538 | 99.1935 | 99.5146 | 84.2025 | 615 | 5 | 615 | 3 | 2 | 66.6667 | |
ckim-gatk | INDEL | D1_5 | map_l125_m2_e1 | homalt | 99.3271 | 99.1935 | 99.4609 | 86.4599 | 369 | 3 | 369 | 2 | 2 | 100.0000 | |
jli-custom | INDEL | D1_5 | map_l100_m2_e1 | homalt | 99.3538 | 99.1935 | 99.5146 | 82.8286 | 615 | 5 | 615 | 3 | 3 | 100.0000 | |
jli-custom | INDEL | D1_5 | map_l125_m2_e1 | homalt | 99.3271 | 99.1935 | 99.4609 | 85.1719 | 369 | 3 | 369 | 2 | 2 | 100.0000 | |
hfeng-pmm2 | INDEL | D1_5 | map_l150_m2_e1 | homalt | 99.1935 | 99.1935 | 99.1935 | 86.9679 | 246 | 2 | 246 | 2 | 2 | 100.0000 | |
egarrison-hhga | INDEL | D1_5 | map_l100_m2_e1 | homalt | 99.1935 | 99.1935 | 99.1935 | 83.6066 | 615 | 5 | 615 | 5 | 4 | 80.0000 | |
dgrover-gatk | INDEL | D1_5 | map_l100_m2_e1 | homalt | 99.4341 | 99.1935 | 99.6759 | 84.1347 | 615 | 5 | 615 | 2 | 2 | 100.0000 | |
ckim-vqsr | INDEL | D1_5 | map_l100_m2_e1 | homalt | 99.3538 | 99.1935 | 99.5146 | 84.2025 | 615 | 5 | 615 | 3 | 2 | 66.6667 | |
ckim-vqsr | INDEL | D1_5 | map_l125_m2_e1 | homalt | 99.3271 | 99.1935 | 99.4609 | 86.4599 | 369 | 3 | 369 | 2 | 2 | 100.0000 | |
hfeng-pmm1 | INDEL | D1_5 | map_l125_m2_e1 | homalt | 99.4609 | 99.1935 | 99.7297 | 84.2620 | 369 | 3 | 369 | 1 | 1 | 100.0000 | |
bgallagher-sentieon | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 99.0727 | 99.1931 | 98.9527 | 67.4865 | 13646 | 111 | 13605 | 144 | 128 | 88.8889 | |
bgallagher-sentieon | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 99.0727 | 99.1931 | 98.9527 | 67.4865 | 13646 | 111 | 13605 | 144 | 128 | 88.8889 | |
hfeng-pmm1 | SNP | * | map_l100_m0_e0 | * | 99.3989 | 99.1931 | 99.6055 | 67.8013 | 32576 | 265 | 32572 | 129 | 37 | 28.6822 | |
jli-custom | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 99.4849 | 99.1930 | 99.7786 | 75.9411 | 1352 | 11 | 1352 | 3 | 1 | 33.3333 | |
rpoplin-dv42 | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 99.1930 | 99.1930 | 99.1930 | 76.9218 | 1352 | 11 | 1352 | 11 | 7 | 63.6364 | |
ndellapenna-hhga | SNP | * | map_l150_m0_e0 | homalt | 99.5215 | 99.1930 | 99.8523 | 72.7346 | 4056 | 33 | 4056 | 6 | 5 | 83.3333 | |
raldana-dualsentieon | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 99.5215 | 99.1930 | 99.8523 | 76.2248 | 1352 | 11 | 1352 | 2 | 2 | 100.0000 | |
ckim-gatk | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | het | 99.4085 | 99.1930 | 99.6249 | 78.2367 | 1352 | 11 | 1328 | 5 | 3 | 60.0000 | |
jmaeng-gatk | INDEL | D1_5 | HG002complexvar | * | 99.4486 | 99.1930 | 99.7055 | 58.6476 | 32451 | 264 | 32505 | 96 | 76 | 79.1667 | |
egarrison-hhga | INDEL | D1_5 | * | homalt | 99.1875 | 99.1927 | 99.1824 | 59.4207 | 48531 | 395 | 48522 | 400 | 203 | 50.7500 | |
hfeng-pmm2 | SNP | ti | map_l150_m2_e0 | het | 99.0233 | 99.1926 | 98.8546 | 79.5912 | 12777 | 104 | 12773 | 148 | 13 | 8.7838 | |
hfeng-pmm3 | INDEL | * | * | het | 99.4705 | 99.1923 | 99.7504 | 58.0356 | 192565 | 1568 | 192191 | 481 | 313 | 65.0728 |