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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
6051-6100 / 86044 show all | |||||||||||||||
gduggal-snapplat | SNP | * | map_l150_m0_e0 | homalt | 89.7981 | 81.5847 | 99.8503 | 78.9397 | 3336 | 753 | 3336 | 5 | 5 | 100.0000 | |
gduggal-snapvard | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 20.0923 | 11.4118 | 83.9506 | 41.7266 | 97 | 753 | 68 | 13 | 13 | 100.0000 | |
gduggal-bwaplat | SNP | tv | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 84.1376 | 72.6976 | 99.8506 | 49.3441 | 2005 | 753 | 2005 | 3 | 3 | 100.0000 | |
ltrigg-rtg2 | SNP | * | map_l150_m2_e1 | * | 98.7491 | 97.6622 | 99.8603 | 65.5073 | 31457 | 753 | 31463 | 44 | 9 | 20.4545 | |
qzeng-custom | INDEL | * | map_l100_m1_e0 | * | 83.9800 | 79.0296 | 89.5920 | 87.4621 | 2834 | 752 | 3667 | 426 | 66 | 15.4930 | |
ckim-gatk | INDEL | * | HG002complexvar | * | 99.3276 | 99.0226 | 99.6345 | 58.1713 | 76186 | 752 | 76048 | 279 | 226 | 81.0036 | |
gduggal-snapplat | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 66.2377 | 71.5690 | 61.6456 | 93.1383 | 1893 | 752 | 1903 | 1184 | 39 | 3.2939 | |
asubramanian-gatk | INDEL | D6_15 | * | * | 97.6552 | 97.1179 | 98.1984 | 55.4499 | 25340 | 752 | 25346 | 465 | 420 | 90.3226 | |
dgrover-gatk | SNP | ti | * | * | 99.9570 | 99.9639 | 99.9500 | 17.7617 | 2084759 | 752 | 2084696 | 1042 | 126 | 12.0921 | |
ckim-isaac | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 91.0304 | 84.2624 | 98.9806 | 25.8726 | 4021 | 751 | 4078 | 42 | 35 | 83.3333 | |
eyeh-varpipe | SNP | * | * | het | 99.1531 | 99.9599 | 98.3592 | 21.9487 | 1872850 | 751 | 1837471 | 30653 | 277 | 0.9037 | |
ltrigg-rtg2 | SNP | * | map_l150_m2_e0 | * | 98.7380 | 97.6422 | 99.8587 | 65.4099 | 31101 | 751 | 31104 | 44 | 9 | 20.4545 | |
anovak-vg | INDEL | D6_15 | HG002complexvar | hetalt | 0.0000 | 25.8638 | 0.0000 | 0.0000 | 262 | 751 | 0 | 0 | 0 | ||
asubramanian-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 97.2830 | 96.3585 | 98.2253 | 48.3467 | 19846 | 750 | 19870 | 359 | 319 | 88.8579 | |
bgallagher-sentieon | INDEL | I6_15 | * | hetalt | 95.3960 | 91.2291 | 99.9618 | 38.0362 | 7801 | 750 | 7841 | 3 | 3 | 100.0000 | |
bgallagher-sentieon | INDEL | I6_15 | HG002compoundhet | hetalt | 95.3997 | 91.2147 | 99.9872 | 29.5092 | 7787 | 750 | 7827 | 1 | 1 | 100.0000 | |
gduggal-bwafb | INDEL | D6_15 | * | het | 96.0906 | 93.5300 | 98.7954 | 45.4106 | 10842 | 750 | 17633 | 215 | 165 | 76.7442 | |
mlin-fermikit | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 83.4868 | 81.5589 | 85.5080 | 68.6930 | 3317 | 750 | 3316 | 562 | 522 | 92.8826 | |
jli-custom | INDEL | I6_15 | * | * | 97.9633 | 96.9786 | 98.9683 | 47.9648 | 24073 | 750 | 24077 | 251 | 222 | 88.4462 | |
ghariani-varprowl | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 83.1025 | 78.7956 | 87.9076 | 66.5360 | 2787 | 750 | 2777 | 382 | 238 | 62.3037 | |
gduggal-snapvard | INDEL | D1_5 | lowcmp_SimpleRepeat_triTR_11to50 | * | 77.9762 | 81.6286 | 74.6367 | 40.5656 | 3328 | 749 | 4314 | 1466 | 1261 | 86.0164 | |
gduggal-snapfb | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 73.1099 | 94.8597 | 59.4736 | 81.1920 | 13822 | 749 | 13965 | 9516 | 255 | 2.6797 | |
gduggal-snapfb | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 73.1099 | 94.8597 | 59.4736 | 81.1920 | 13822 | 749 | 13965 | 9516 | 255 | 2.6797 | |
gduggal-snapvard | SNP | tv | map_l100_m2_e0 | * | 94.5205 | 97.0079 | 92.1574 | 76.1726 | 24284 | 749 | 24195 | 2059 | 151 | 7.3337 | |
anovak-vg | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 0.0000 | 20.6568 | 0.0000 | 0.0000 | 195 | 749 | 0 | 0 | 0 | ||
anovak-vg | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 32.6056 | 25.2495 | 46.0100 | 54.7659 | 253 | 749 | 369 | 433 | 324 | 74.8268 | |
egarrison-hhga | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 95.6374 | 95.8769 | 95.3990 | 63.4546 | 17417 | 749 | 17417 | 840 | 435 | 51.7857 | |
egarrison-hhga | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 95.6374 | 95.8769 | 95.3990 | 63.4546 | 17417 | 749 | 17417 | 840 | 435 | 51.7857 | |
gduggal-bwaplat | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 83.1319 | 71.6717 | 98.9545 | 46.3244 | 1895 | 749 | 1893 | 20 | 17 | 85.0000 | |
mlin-fermikit | INDEL | D1_5 | map_siren | * | 85.3013 | 78.7759 | 93.0054 | 76.3252 | 2780 | 749 | 2779 | 209 | 185 | 88.5167 | |
ckim-isaac | INDEL | * | map_l125_m1_e0 | * | 77.9687 | 64.4993 | 98.5486 | 87.4682 | 1359 | 748 | 1358 | 20 | 8 | 40.0000 | |
gduggal-snapfb | SNP | ti | map_siren | het | 98.2591 | 98.8009 | 97.7232 | 58.6413 | 61634 | 748 | 61636 | 1436 | 494 | 34.4011 | |
jpowers-varprowl | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 91.9958 | 97.3948 | 87.1640 | 83.7213 | 27964 | 748 | 28079 | 4135 | 89 | 2.1524 | |
jpowers-varprowl | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 91.9958 | 97.3948 | 87.1640 | 83.7213 | 27964 | 748 | 28079 | 4135 | 89 | 2.1524 | |
ltrigg-rtg1 | SNP | ti | map_siren | * | 99.5060 | 99.2556 | 99.7576 | 49.1435 | 99607 | 747 | 99601 | 242 | 38 | 15.7025 | |
ciseli-custom | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_51to200 | * | 39.9506 | 39.3669 | 40.5518 | 64.0084 | 485 | 747 | 485 | 711 | 356 | 50.0703 | |
ciseli-custom | INDEL | D1_5 | lowcmp_SimpleRepeat_triTR_11to50 | * | 80.7660 | 81.6777 | 79.8745 | 42.7070 | 3330 | 747 | 3310 | 834 | 461 | 55.2758 | |
asubramanian-gatk | SNP | tv | map_l250_m1_e0 | homalt | 22.5907 | 12.7336 | 100.0000 | 97.9792 | 109 | 747 | 109 | 0 | 0 | ||
hfeng-pmm3 | SNP | tv | * | het | 99.9161 | 99.8738 | 99.9586 | 21.3235 | 590949 | 747 | 590875 | 245 | 12 | 4.8980 | |
mlin-fermikit | SNP | tv | HG002compoundhet | het | 90.8488 | 84.0146 | 98.8934 | 54.3251 | 3926 | 747 | 3932 | 44 | 8 | 18.1818 | |
ltrigg-rtg2 | SNP | * | map_l150_m1_e0 | * | 98.7010 | 97.5595 | 99.8696 | 62.6893 | 29862 | 747 | 29864 | 39 | 9 | 23.0769 | |
gduggal-snapplat | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 36.9914 | 25.6716 | 66.1677 | 73.1295 | 258 | 747 | 221 | 113 | 5 | 4.4248 | |
gduggal-bwaplat | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 65.6044 | 51.5250 | 90.2715 | 87.2106 | 794 | 747 | 798 | 86 | 3 | 3.4884 | |
gduggal-bwaplat | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 78.4779 | 66.1838 | 96.3816 | 73.7433 | 1462 | 747 | 1465 | 55 | 51 | 92.7273 | |
asubramanian-gatk | SNP | ti | map_l250_m0_e0 | het | 33.4817 | 20.1285 | 99.4709 | 99.1011 | 188 | 746 | 188 | 1 | 1 | 100.0000 | |
ckim-isaac | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 95.8927 | 93.7179 | 98.1709 | 38.9030 | 11129 | 746 | 11110 | 207 | 127 | 61.3527 | |
eyeh-varpipe | INDEL | I1_5 | HG002complexvar | hetalt | 71.6240 | 56.8366 | 96.8118 | 75.7679 | 981 | 745 | 1245 | 41 | 39 | 95.1220 | |
ckim-isaac | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | * | 79.1674 | 71.9397 | 88.0095 | 54.7793 | 1910 | 745 | 1857 | 253 | 201 | 79.4466 | |
anovak-vg | INDEL | I1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | hetalt | 0.0000 | 16.9454 | 0.0000 | 0.0000 | 152 | 745 | 0 | 0 | 0 | ||
anovak-vg | SNP | * | * | hetalt | 0.0000 | 14.4661 | 0.0000 | 0.0000 | 126 | 745 | 0 | 0 | 0 |