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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
71351-71400 / 86044 show all | |||||||||||||||
ckim-dragen | SNP | * | HG002compoundhet | * | 99.7929 | 99.7831 | 99.8027 | 41.5217 | 25766 | 56 | 25804 | 51 | 26 | 50.9804 | |
ciseli-custom | SNP | tv | lowcmp_SimpleRepeat_diTR_51to200 | homalt | 25.1497 | 77.7778 | 15.0000 | 88.4393 | 7 | 2 | 9 | 51 | 2 | 3.9216 | |
ciseli-custom | SNP | tv | map_l250_m0_e0 | homalt | 73.5751 | 73.5751 | 73.5751 | 93.4487 | 142 | 51 | 142 | 51 | 33 | 64.7059 | |
ckim-dragen | INDEL | * | map_l150_m1_e0 | * | 96.2243 | 96.2631 | 96.1855 | 90.5619 | 1288 | 50 | 1286 | 51 | 9 | 17.6471 | |
cchapple-custom | SNP | tv | HG002compoundhet | * | 99.1131 | 98.7784 | 99.4501 | 47.4326 | 8814 | 109 | 9224 | 51 | 34 | 66.6667 | |
ciseli-custom | INDEL | D6_15 | lowcmp_SimpleRepeat_triTR_51to200 | homalt | 40.0000 | 85.7143 | 26.0870 | 33.0097 | 18 | 3 | 18 | 51 | 51 | 100.0000 | |
ciseli-custom | INDEL | D6_15 | map_l125_m1_e0 | * | 54.5455 | 53.8462 | 55.2632 | 91.9718 | 63 | 54 | 63 | 51 | 28 | 54.9020 | |
ciseli-custom | INDEL | I16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | * | 17.8423 | 11.0825 | 45.7447 | 82.7206 | 43 | 345 | 43 | 51 | 42 | 82.3529 | |
ckim-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 96.1540 | 92.9308 | 99.6088 | 28.2869 | 12791 | 973 | 12985 | 51 | 51 | 100.0000 | |
ckim-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 96.0921 | 92.8093 | 99.6158 | 30.7146 | 13023 | 1009 | 13222 | 51 | 51 | 100.0000 | |
ckim-gatk | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | * | 97.3063 | 96.6102 | 98.0125 | 68.8327 | 2565 | 90 | 2515 | 51 | 39 | 76.4706 | |
ckim-gatk | INDEL | * | map_l150_m0_e0 | het | 92.1979 | 98.2405 | 86.8557 | 95.3544 | 335 | 6 | 337 | 51 | 1 | 1.9608 | |
gduggal-bwavard | INDEL | C6_15 | HG002compoundhet | * | 0.0000 | 0.0000 | 27.1429 | 91.0026 | 0 | 0 | 19 | 51 | 23 | 45.0980 | |
gduggal-bwavard | INDEL | D16_PLUS | map_l100_m2_e1 | * | 55.1438 | 57.7320 | 52.7778 | 93.1122 | 56 | 41 | 57 | 51 | 23 | 45.0980 | |
gduggal-bwaplat | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 88.1401 | 80.0632 | 98.0294 | 59.0247 | 2534 | 631 | 2537 | 51 | 48 | 94.1176 | |
gduggal-bwaplat | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 80.8933 | 68.5041 | 98.7531 | 57.3514 | 4039 | 1857 | 4039 | 51 | 49 | 96.0784 | |
gduggal-bwaplat | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 80.8933 | 68.5041 | 98.7531 | 57.3514 | 4039 | 1857 | 4039 | 51 | 49 | 96.0784 | |
gduggal-bwafb | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 76.5760 | 87.0968 | 68.3230 | 91.5441 | 108 | 16 | 110 | 51 | 5 | 9.8039 | |
gduggal-bwaplat | INDEL | D1_5 | HG002complexvar | hetalt | 80.5939 | 70.0444 | 94.8847 | 81.8132 | 947 | 405 | 946 | 51 | 50 | 98.0392 | |
gduggal-bwaplat | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_51to200 | * | 75.2576 | 62.8247 | 93.8257 | 69.9746 | 774 | 458 | 775 | 51 | 20 | 39.2157 | |
gduggal-bwafb | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | homalt | 86.7133 | 96.8750 | 78.4810 | 46.7416 | 186 | 6 | 186 | 51 | 50 | 98.0392 | |
jpowers-varprowl | INDEL | D1_5 | map_l125_m1_e0 | * | 94.5370 | 93.8419 | 95.2425 | 86.5208 | 1021 | 67 | 1021 | 51 | 27 | 52.9412 | |
jpowers-varprowl | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 67.1394 | 62.6794 | 72.2826 | 73.6011 | 131 | 78 | 133 | 51 | 50 | 98.0392 | |
jli-custom | SNP | * | HG002complexvar | homalt | 99.9614 | 99.9404 | 99.9823 | 19.9145 | 288402 | 172 | 288385 | 51 | 37 | 72.5490 | |
jli-custom | SNP | tv | map_l125_m0_e0 | * | 98.7959 | 98.3713 | 99.2242 | 70.3527 | 6523 | 108 | 6523 | 51 | 18 | 35.2941 | |
jpowers-varprowl | INDEL | I16_PLUS | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 35.0403 | 26.6990 | 50.9615 | 85.3315 | 55 | 151 | 53 | 51 | 50 | 98.0392 | |
ltrigg-rtg1 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.5300 | 97.9644 | 99.1021 | 62.8102 | 5727 | 119 | 5629 | 51 | 17 | 33.3333 | |
ltrigg-rtg1 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.5300 | 97.9644 | 99.1021 | 62.8102 | 5727 | 119 | 5629 | 51 | 17 | 33.3333 | |
jlack-gatk | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 99.4911 | 99.8188 | 99.1656 | 57.1479 | 6061 | 11 | 6061 | 51 | 49 | 96.0784 | |
jlack-gatk | INDEL | D1_5 | * | hetalt | 95.0041 | 90.9322 | 99.4577 | 62.5612 | 9316 | 929 | 9354 | 51 | 46 | 90.1961 | |
hfeng-pmm2 | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | het | 98.4016 | 97.3287 | 99.4985 | 47.5257 | 10129 | 278 | 10118 | 51 | 47 | 92.1569 | |
hfeng-pmm2 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 98.8127 | 99.4294 | 98.2036 | 48.6526 | 2788 | 16 | 2788 | 51 | 50 | 98.0392 | |
hfeng-pmm2 | INDEL | I1_5 | HG002complexvar | * | 99.5522 | 99.2597 | 99.8464 | 56.6743 | 33116 | 247 | 33159 | 51 | 38 | 74.5098 | |
hfeng-pmm3 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 99.4861 | 99.5813 | 99.3911 | 58.2577 | 8325 | 35 | 8325 | 51 | 50 | 98.0392 | |
hfeng-pmm1 | INDEL | I16_PLUS | * | homalt | 98.2323 | 99.6797 | 96.8264 | 69.2499 | 1556 | 5 | 1556 | 51 | 49 | 96.0784 | |
hfeng-pmm3 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 99.4861 | 99.5813 | 99.3911 | 58.2577 | 8325 | 35 | 8325 | 51 | 50 | 98.0392 | |
hfeng-pmm3 | SNP | * | map_l250_m1_e0 | het | 98.6931 | 98.4648 | 98.9225 | 88.7103 | 4682 | 73 | 4682 | 51 | 3 | 5.8824 | |
hfeng-pmm3 | SNP | tv | map_l125_m0_e0 | * | 99.1700 | 99.1102 | 99.2298 | 75.2152 | 6572 | 59 | 6571 | 51 | 7 | 13.7255 | |
jlack-gatk | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 99.1869 | 99.2134 | 99.1605 | 78.4314 | 6054 | 48 | 6024 | 51 | 24 | 47.0588 | |
jlack-gatk | INDEL | I1_5 | map_l125_m2_e0 | * | 96.2945 | 98.3664 | 94.3080 | 90.1657 | 843 | 14 | 845 | 51 | 5 | 9.8039 | |
jli-custom | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 97.1839 | 94.9785 | 99.4942 | 28.3420 | 9949 | 526 | 10032 | 51 | 50 | 98.0392 | |
qzeng-custom | INDEL | C16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 0.0000 | 0.0000 | 3.7736 | 82.9582 | 0 | 0 | 2 | 51 | 0 | 0.0000 | |
qzeng-custom | INDEL | C16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 0.0000 | 0.0000 | 10.5263 | 92.2343 | 0 | 0 | 6 | 51 | 0 | 0.0000 | |
qzeng-custom | INDEL | C16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 0.0000 | 0.0000 | 10.5263 | 92.2343 | 0 | 0 | 6 | 51 | 0 | 0.0000 | |
ndellapenna-hhga | INDEL | * | segdup | * | 97.8664 | 97.7308 | 98.0024 | 98.7178 | 2498 | 58 | 2502 | 51 | 37 | 72.5490 | |
ndellapenna-hhga | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | * | 85.7237 | 78.9364 | 93.7881 | 67.9922 | 757 | 202 | 770 | 51 | 38 | 74.5098 | |
mlin-fermikit | INDEL | I1_5 | map_l125_m1_e0 | * | 66.7171 | 53.1325 | 89.6341 | 77.6871 | 441 | 389 | 441 | 51 | 46 | 90.1961 | |
mlin-fermikit | INDEL | I1_5 | map_l125_m2_e0 | * | 67.2515 | 53.6756 | 90.0196 | 80.9186 | 460 | 397 | 460 | 51 | 46 | 90.1961 | |
mlin-fermikit | INDEL | I1_5 | map_l125_m2_e1 | * | 67.6724 | 54.1379 | 90.2299 | 81.0664 | 471 | 399 | 471 | 51 | 46 | 90.1961 | |
mlin-fermikit | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 90.3030 | 95.8199 | 85.3868 | 72.4980 | 298 | 13 | 298 | 51 | 50 | 98.0392 |