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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
3551-3600 / 86044 show all | |||||||||||||||
jmaeng-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 97.7771 | 97.1844 | 98.3771 | 67.7791 | 63511 | 1840 | 63286 | 1044 | 906 | 86.7816 | |
rpoplin-dv42 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 96.2804 | 95.7563 | 96.8102 | 77.5473 | 41496 | 1839 | 41428 | 1365 | 1297 | 95.0183 | |
ltrigg-rtg1 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 97.2969 | 95.1533 | 99.5393 | 51.1225 | 36065 | 1837 | 36299 | 168 | 133 | 79.1667 | |
anovak-vg | INDEL | D16_PLUS | HG002compoundhet | * | 28.7549 | 21.7001 | 42.6065 | 32.2197 | 508 | 1833 | 510 | 687 | 477 | 69.4323 | |
ckim-gatk | SNP | tv | map_l150_m0_e0 | * | 71.0339 | 56.1092 | 96.7755 | 93.2891 | 2342 | 1832 | 2341 | 78 | 7 | 8.9744 | |
ckim-gatk | SNP | tv | map_l150_m2_e0 | het | 83.9328 | 74.7380 | 95.7075 | 90.8782 | 5420 | 1832 | 5418 | 243 | 8 | 3.2922 | |
gduggal-snapvard | SNP | ti | map_l100_m2_e1 | * | 95.1804 | 96.2979 | 94.0886 | 74.3752 | 47653 | 1832 | 47192 | 2965 | 284 | 9.5784 | |
gduggal-bwavard | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 68.5442 | 93.9928 | 53.9399 | 70.1347 | 28649 | 1831 | 28668 | 24480 | 22479 | 91.8260 | |
gduggal-bwavard | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 68.5442 | 93.9928 | 53.9399 | 70.1347 | 28649 | 1831 | 28668 | 24480 | 22479 | 91.8260 | |
ciseli-custom | SNP | ti | HG002complexvar | homalt | 96.5088 | 99.0536 | 94.0915 | 19.4065 | 191633 | 1831 | 189105 | 11875 | 5178 | 43.6042 | |
qzeng-custom | SNP | tv | map_l150_m1_e0 | het | 83.1414 | 73.6683 | 95.4104 | 89.4270 | 5117 | 1829 | 5114 | 246 | 203 | 82.5203 | |
anovak-vg | INDEL | D16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 57.0334 | 48.7504 | 68.7072 | 56.9745 | 1736 | 1825 | 1706 | 777 | 550 | 70.7851 | |
jmaeng-gatk | SNP | tv | map_l150_m2_e1 | het | 84.1017 | 75.1633 | 95.4530 | 91.0507 | 5523 | 1825 | 5521 | 263 | 7 | 2.6616 | |
gduggal-snapvard | SNP | ti | map_l100_m2_e0 | * | 95.1595 | 96.2807 | 94.0641 | 74.3570 | 47140 | 1821 | 46684 | 2946 | 281 | 9.5384 | |
gduggal-snapfb | INDEL | D1_5 | HG002complexvar | * | 94.7329 | 94.4337 | 95.0340 | 57.1180 | 30894 | 1821 | 31423 | 1642 | 692 | 42.1437 | |
gduggal-snapfb | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 78.4631 | 67.4647 | 93.7460 | 41.7311 | 3776 | 1821 | 8829 | 589 | 574 | 97.4533 | |
jmaeng-gatk | SNP | tv | map_l150_m0_e0 | * | 71.1604 | 56.3967 | 96.3949 | 93.3607 | 2354 | 1820 | 2353 | 88 | 6 | 6.8182 | |
ckim-gatk | SNP | tv | map_l150_m1_e0 | het | 83.3287 | 73.7979 | 95.6863 | 90.3850 | 5126 | 1820 | 5124 | 231 | 8 | 3.4632 | |
gduggal-bwaplat | INDEL | * | HG002compoundhet | het | 66.0619 | 55.5447 | 81.4921 | 84.3450 | 2274 | 1820 | 2272 | 516 | 182 | 35.2713 | |
gduggal-snapplat | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 0.0000 | 0.0000 | 0.0000 | 0 | 1819 | 0 | 0 | 0 | |||
gduggal-snapplat | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 0.0000 | 0.0000 | 0.0000 | 0 | 1819 | 0 | 0 | 0 | |||
gduggal-snapvard | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | * | 68.0107 | 68.2833 | 67.7403 | 40.7190 | 3914 | 1818 | 10936 | 5208 | 4870 | 93.5100 | |
gduggal-snapfb | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 0.1099 | 0.0550 | 100.0000 | 0.0000 | 1 | 1818 | 1 | 0 | 0 | ||
gduggal-snapfb | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 0.1099 | 0.0550 | 100.0000 | 0.0000 | 1 | 1818 | 1 | 0 | 0 | ||
gduggal-bwavard | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | hetalt | 0.0000 | 0.2195 | 0.0000 | 0.0000 | 4 | 1818 | 0 | 0 | 0 | ||
ciseli-custom | INDEL | D6_15 | * | het | 77.1133 | 84.3154 | 71.0447 | 55.4839 | 9773 | 1818 | 10153 | 4138 | 1402 | 33.8811 | |
ghariani-varprowl | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | hetalt | 0.0000 | 0.2744 | 0.0000 | 0.0000 | 5 | 1817 | 0 | 0 | 0 | ||
jmaeng-gatk | SNP | tv | map_l150_m2_e0 | het | 83.9830 | 74.9448 | 95.5001 | 91.0642 | 5435 | 1817 | 5433 | 256 | 6 | 2.3438 | |
jpowers-varprowl | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | hetalt | 0.0000 | 0.2744 | 0.0000 | 0.0000 | 5 | 1817 | 0 | 0 | 0 | ||
ckim-gatk | SNP | tv | map_l150_m2_e1 | homalt | 71.8426 | 56.0716 | 99.9569 | 82.3233 | 2318 | 1816 | 2318 | 1 | 0 | 0.0000 | |
ckim-isaac | INDEL | * | map_siren | * | 85.3582 | 75.5331 | 98.1215 | 78.4772 | 5597 | 1813 | 5589 | 107 | 46 | 42.9907 | |
gduggal-snapvard | INDEL | D6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | hetalt | 0.0000 | 23.3728 | 0.0000 | 0.0000 | 553 | 1813 | 0 | 0 | 0 | ||
gduggal-snapvard | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 55.4366 | 50.8272 | 60.9654 | 44.0200 | 1874 | 1813 | 2046 | 1310 | 988 | 75.4198 | |
jlack-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 95.7595 | 95.2166 | 96.3087 | 53.9807 | 36089 | 1813 | 35901 | 1376 | 1269 | 92.2238 | |
ckim-isaac | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 91.0480 | 87.7443 | 94.6101 | 39.6686 | 12973 | 1812 | 12884 | 734 | 647 | 88.1471 | |
jmaeng-gatk | SNP | tv | map_l150_m2_e1 | homalt | 71.9219 | 56.1684 | 99.9570 | 81.5898 | 2322 | 1812 | 2322 | 1 | 1 | 100.0000 | |
jpowers-varprowl | INDEL | I6_15 | * | het | 67.8850 | 81.9496 | 57.9408 | 49.0356 | 8222 | 1811 | 8267 | 6001 | 5983 | 99.7000 | |
gduggal-snapvard | INDEL | I1_5 | HG002complexvar | homalt | 92.5606 | 86.5333 | 99.4905 | 33.4524 | 11637 | 1811 | 10935 | 56 | 51 | 91.0714 | |
mlin-fermikit | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 76.3374 | 62.0495 | 99.1738 | 31.6467 | 2961 | 1811 | 3001 | 25 | 25 | 100.0000 | |
ciseli-custom | SNP | * | map_l150_m2_e1 | homalt | 86.5594 | 84.7045 | 88.4973 | 73.1841 | 10018 | 1809 | 9994 | 1299 | 1047 | 80.6005 | |
eyeh-varpipe | INDEL | D16_PLUS | HG002compoundhet | * | 28.2801 | 22.7680 | 37.3134 | 28.0307 | 533 | 1808 | 525 | 882 | 881 | 99.8866 | |
anovak-vg | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 64.5845 | 75.5146 | 56.4183 | 33.5145 | 5576 | 1808 | 8421 | 6505 | 5048 | 77.6018 | |
cchapple-custom | INDEL | * | HG002compoundhet | * | 95.5576 | 93.9686 | 97.2012 | 57.1714 | 28153 | 1807 | 51191 | 1474 | 1382 | 93.7585 | |
gduggal-snapplat | INDEL | I6_15 | HG002complexvar | het | 33.8586 | 23.3121 | 61.8312 | 60.5350 | 549 | 1806 | 520 | 321 | 10 | 3.1153 | |
gduggal-bwaplat | SNP | tv | map_l250_m1_e0 | * | 48.2541 | 31.8474 | 99.5277 | 97.7346 | 843 | 1804 | 843 | 4 | 1 | 25.0000 | |
jmaeng-gatk | SNP | tv | map_l150_m1_e0 | het | 83.3948 | 74.0426 | 95.4512 | 90.5818 | 5143 | 1803 | 5141 | 245 | 6 | 2.4490 | |
qzeng-custom | SNP | ti | map_l250_m1_e0 | * | 73.1661 | 60.6683 | 92.1490 | 95.6157 | 2778 | 1801 | 2770 | 236 | 199 | 84.3220 | |
ckim-gatk | SNP | tv | map_l150_m2_e0 | homalt | 71.6934 | 55.8903 | 99.9562 | 82.4006 | 2282 | 1801 | 2282 | 1 | 0 | 0.0000 | |
gduggal-snapvard | SNP | ti | map_l100_m1_e0 | * | 95.0911 | 96.2467 | 93.9630 | 72.8656 | 46132 | 1799 | 45682 | 2935 | 278 | 9.4719 | |
jmaeng-gatk | SNP | tv | map_l150_m2_e0 | homalt | 71.7739 | 55.9882 | 99.9563 | 81.6747 | 2286 | 1797 | 2286 | 1 | 1 | 100.0000 |