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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5851-5900 / 86044 show all | |||||||||||||||
ckim-isaac | INDEL | * | map_siren | homalt | 82.0615 | 69.8682 | 99.4105 | 72.7551 | 1855 | 800 | 1855 | 11 | 7 | 63.6364 | |
cchapple-custom | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 98.8427 | 98.3427 | 99.3479 | 69.0114 | 47471 | 800 | 76325 | 501 | 389 | 77.6447 | |
eyeh-varpipe | INDEL | I16_PLUS | HG002complexvar | * | 52.3530 | 38.8846 | 80.0955 | 45.7686 | 509 | 800 | 503 | 125 | 124 | 99.2000 | |
ndellapenna-hhga | INDEL | * | lowcmp_SimpleRepeat_diTR_51to200 | * | 64.5816 | 61.9705 | 67.4224 | 73.1294 | 1302 | 799 | 1368 | 661 | 606 | 91.6793 | |
hfeng-pmm3 | INDEL | I6_15 | * | * | 97.8954 | 96.7812 | 99.0356 | 49.5509 | 24024 | 799 | 24029 | 234 | 222 | 94.8718 | |
gduggal-snapplat | SNP | tv | HG002compoundhet | het | 71.6435 | 82.9018 | 63.0774 | 69.0248 | 3874 | 799 | 3919 | 2294 | 156 | 6.8004 | |
gduggal-snapvard | SNP | ti | map_l150_m2_e0 | * | 92.6480 | 96.1047 | 89.4313 | 82.4164 | 19713 | 799 | 19530 | 2308 | 189 | 8.1889 | |
gduggal-snapvard | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 82.0117 | 91.2515 | 74.4710 | 86.1394 | 8334 | 799 | 8235 | 2823 | 102 | 3.6132 | |
gduggal-snapvard | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 82.0117 | 91.2515 | 74.4710 | 86.1394 | 8334 | 799 | 8235 | 2823 | 102 | 3.6132 | |
ciseli-custom | INDEL | * | map_l125_m1_e0 | * | 67.4524 | 62.0788 | 73.8444 | 90.3002 | 1308 | 799 | 1310 | 464 | 300 | 64.6552 | |
ckim-gatk | SNP | tv | map_l250_m2_e0 | het | 72.7389 | 58.8660 | 95.1667 | 96.8726 | 1142 | 798 | 1142 | 58 | 1 | 1.7241 | |
ckim-dragen | INDEL | I1_5 | * | hetalt | 96.2953 | 92.8718 | 99.9809 | 60.6438 | 10397 | 798 | 10451 | 2 | 2 | 100.0000 | |
qzeng-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 97.6793 | 98.2539 | 97.1113 | 81.2381 | 44904 | 798 | 44812 | 1333 | 148 | 11.1028 | |
qzeng-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 97.6793 | 98.2539 | 97.1113 | 81.2381 | 44904 | 798 | 44812 | 1333 | 148 | 11.1028 | |
gduggal-bwaplat | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 92.5120 | 87.0957 | 98.6467 | 70.2422 | 5386 | 798 | 5394 | 74 | 11 | 14.8649 | |
gduggal-bwavard | INDEL | D1_5 | lowcmp_SimpleRepeat_triTR_11to50 | * | 82.7813 | 80.4513 | 85.2502 | 40.8125 | 3280 | 797 | 3254 | 563 | 503 | 89.3428 | |
ciseli-custom | INDEL | * | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 92.4417 | 95.1488 | 89.8844 | 58.8124 | 15632 | 797 | 15630 | 1759 | 720 | 40.9323 | |
jlack-gatk | SNP | * | HG002complexvar | * | 99.9118 | 99.8944 | 99.9292 | 19.3948 | 753584 | 797 | 753425 | 534 | 201 | 37.6404 | |
dgrover-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 96.8950 | 94.3201 | 99.6144 | 34.3188 | 13235 | 797 | 13433 | 52 | 50 | 96.1538 | |
mlin-fermikit | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 94.6745 | 93.2968 | 96.0934 | 44.0771 | 11079 | 796 | 11069 | 450 | 425 | 94.4444 | |
rpoplin-dv42 | INDEL | D6_15 | * | * | 97.4536 | 96.9493 | 97.9633 | 52.8335 | 25296 | 796 | 25300 | 526 | 501 | 95.2471 | |
gduggal-snapfb | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | het | 93.4534 | 92.3513 | 94.5822 | 43.0987 | 9611 | 796 | 14228 | 815 | 315 | 38.6503 | |
ckim-dragen | INDEL | I1_5 | HG002compoundhet | hetalt | 96.3036 | 92.8872 | 99.9808 | 55.1746 | 10382 | 795 | 10432 | 2 | 2 | 100.0000 | |
ckim-isaac | INDEL | I16_PLUS | HG002complexvar | * | 52.2963 | 39.2666 | 78.2675 | 62.9505 | 514 | 795 | 515 | 143 | 46 | 32.1678 | |
hfeng-pmm3 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 97.2064 | 95.5068 | 98.9676 | 53.3545 | 16877 | 794 | 16872 | 176 | 162 | 92.0455 | |
hfeng-pmm3 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 97.2064 | 95.5068 | 98.9676 | 53.3545 | 16877 | 794 | 16872 | 176 | 162 | 92.0455 | |
ckim-isaac | INDEL | * | HG002compoundhet | het | 56.9247 | 80.6302 | 43.9912 | 64.9439 | 3301 | 793 | 2405 | 3062 | 2738 | 89.4187 | |
gduggal-bwavard | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | hetalt | 0.0000 | 0.0000 | 0.0000 | 0 | 793 | 0 | 0 | 0 | |||
eyeh-varpipe | INDEL | D16_PLUS | HG002complexvar | * | 59.4403 | 51.7955 | 69.7324 | 50.7211 | 851 | 792 | 834 | 362 | 361 | 99.7238 | |
ciseli-custom | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 77.4749 | 88.1419 | 69.1110 | 56.7739 | 5887 | 792 | 6258 | 2797 | 1501 | 53.6646 | |
gduggal-snapvard | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 57.4446 | 41.4634 | 93.4708 | 72.4562 | 561 | 792 | 544 | 38 | 36 | 94.7368 | |
asubramanian-gatk | INDEL | I1_5 | HG002compoundhet | * | 95.2373 | 93.5902 | 96.9436 | 67.0365 | 11564 | 792 | 11577 | 365 | 350 | 95.8904 | |
hfeng-pmm1 | INDEL | I6_15 | * | * | 97.8503 | 96.8134 | 98.9096 | 50.1395 | 24032 | 791 | 24037 | 265 | 246 | 92.8302 | |
ckim-isaac | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 87.7042 | 78.9949 | 98.5719 | 61.4567 | 2971 | 790 | 2968 | 43 | 28 | 65.1163 | |
ckim-isaac | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 87.7042 | 78.9949 | 98.5719 | 61.4567 | 2971 | 790 | 2968 | 43 | 28 | 65.1163 | |
cchapple-custom | INDEL | I6_15 | * | * | 97.7435 | 96.8215 | 98.6833 | 49.3635 | 24034 | 789 | 25632 | 342 | 305 | 89.1813 | |
jpowers-varprowl | INDEL | * | lowcmp_SimpleRepeat_triTR_11to50 | homalt | 76.1858 | 63.3364 | 95.5758 | 44.5914 | 1363 | 789 | 1361 | 63 | 54 | 85.7143 | |
rpoplin-dv42 | INDEL | I1_5 | HG002compoundhet | * | 95.3045 | 93.6144 | 97.0566 | 64.5995 | 11567 | 789 | 11574 | 351 | 345 | 98.2906 | |
ghariani-varprowl | INDEL | * | lowcmp_SimpleRepeat_triTR_11to50 | homalt | 76.1858 | 63.3364 | 95.5758 | 45.0405 | 1363 | 789 | 1361 | 63 | 51 | 80.9524 | |
gduggal-snapplat | INDEL | I6_15 | HG002complexvar | hetalt | 51.2055 | 35.5683 | 91.3793 | 60.4433 | 435 | 788 | 424 | 40 | 34 | 85.0000 | |
ckim-isaac | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 86.2084 | 80.6245 | 92.6232 | 55.4837 | 3279 | 788 | 3252 | 259 | 195 | 75.2896 | |
ckim-isaac | SNP | tv | map_l150_m0_e0 | homalt | 57.8158 | 40.6627 | 100.0000 | 71.4889 | 540 | 788 | 540 | 0 | 0 | ||
gduggal-bwaplat | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 82.5452 | 70.6189 | 99.3183 | 55.6924 | 1894 | 788 | 1894 | 13 | 13 | 100.0000 | |
ghariani-varprowl | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | hetalt | 0.0000 | 0.7566 | 0.0000 | 0.0000 | 6 | 787 | 0 | 0 | 0 | ||
ltrigg-rtg1 | SNP | * | map_l100_m2_e1 | het | 99.0006 | 98.3219 | 99.6887 | 57.1362 | 46111 | 787 | 46109 | 144 | 12 | 8.3333 | |
jpowers-varprowl | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | hetalt | 0.0000 | 0.7566 | 0.0000 | 0.0000 | 6 | 787 | 0 | 0 | 0 | ||
jmaeng-gatk | SNP | * | map_l250_m0_e0 | het | 63.5159 | 47.7424 | 94.8549 | 98.4462 | 719 | 787 | 719 | 39 | 2 | 5.1282 | |
jmaeng-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.1915 | 97.4975 | 98.8955 | 61.4377 | 30622 | 786 | 30622 | 342 | 309 | 90.3509 | |
jmaeng-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.1915 | 97.4975 | 98.8955 | 61.4377 | 30622 | 786 | 30622 | 342 | 309 | 90.3509 | |
ltrigg-rtg1 | SNP | * | map_l100_m2_e0 | het | 98.9994 | 98.3060 | 99.7027 | 57.0672 | 45613 | 786 | 45611 | 136 | 12 | 8.8235 |