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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
1701-1750 / 86044 show all | |||||||||||||||
| mlin-fermikit | INDEL | D6_15 | HG002compoundhet | * | 69.7015 | 65.9174 | 73.9466 | 36.0645 | 5953 | 3078 | 5949 | 2096 | 2075 | 98.9981 | |
| mlin-fermikit | SNP | tv | map_siren | homalt | 81.9952 | 77.9060 | 86.5373 | 48.2163 | 13431 | 3809 | 13428 | 2089 | 1999 | 95.6917 | |
| gduggal-snapfb | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | het | 86.5531 | 82.3858 | 91.1644 | 45.8288 | 12984 | 2776 | 21554 | 2089 | 859 | 41.1202 | |
| mlin-fermikit | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 81.8009 | 78.9787 | 84.8322 | 50.9671 | 11677 | 3108 | 11678 | 2088 | 2070 | 99.1379 | |
| eyeh-varpipe | INDEL | * | HG002complexvar | homalt | 93.9842 | 95.4231 | 92.5880 | 51.8445 | 25790 | 1237 | 26070 | 2087 | 2039 | 97.7000 | |
| gduggal-bwavard | SNP | * | map_l125_m0_e0 | het | 91.2008 | 97.7811 | 85.4502 | 85.0594 | 12383 | 281 | 12251 | 2086 | 87 | 4.1707 | |
| ghariani-varprowl | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 60.3322 | 92.2485 | 44.8239 | 74.0840 | 1678 | 141 | 1693 | 2084 | 2043 | 98.0326 | |
| ghariani-varprowl | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 60.3322 | 92.2485 | 44.8239 | 74.0840 | 1678 | 141 | 1693 | 2084 | 2043 | 98.0326 | |
| ciseli-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 93.5617 | 98.6804 | 88.9479 | 75.7364 | 16751 | 224 | 16756 | 2082 | 698 | 33.5255 | |
| ciseli-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 93.5617 | 98.6804 | 88.9479 | 75.7364 | 16751 | 224 | 16756 | 2082 | 698 | 33.5255 | |
| jpowers-varprowl | INDEL | D16_PLUS | * | het | 70.8402 | 90.6933 | 58.1179 | 67.6572 | 2865 | 294 | 2878 | 2074 | 2042 | 98.4571 | |
| ndellapenna-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 80.0676 | 74.4893 | 86.5491 | 57.6750 | 13163 | 4508 | 13345 | 2074 | 1774 | 85.5352 | |
| ndellapenna-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 80.0676 | 74.4893 | 86.5491 | 57.6750 | 13163 | 4508 | 13345 | 2074 | 1774 | 85.5352 | |
| anovak-vg | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 54.2561 | 49.7820 | 59.6139 | 54.7156 | 1941 | 1958 | 3057 | 2071 | 1674 | 80.8305 | |
| gduggal-snapvard | SNP | tv | map_l100_m2_e1 | * | 94.5392 | 97.0059 | 92.1948 | 76.2078 | 24526 | 757 | 24427 | 2068 | 154 | 7.4468 | |
| cchapple-custom | INDEL | * | * | * | 99.1388 | 98.8448 | 99.4346 | 57.2260 | 340562 | 3980 | 363520 | 2067 | 1592 | 77.0198 | |
| mlin-fermikit | INDEL | D1_5 | * | het | 97.6071 | 97.5792 | 97.6350 | 51.6497 | 85454 | 2120 | 85333 | 2067 | 1958 | 94.7267 | |
| ghariani-varprowl | INDEL | I1_5 | HG002complexvar | * | 92.9673 | 92.2577 | 93.6879 | 54.6199 | 30779 | 2583 | 30650 | 2065 | 1585 | 76.7554 | |
| gduggal-snapvard | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 69.6175 | 73.0888 | 66.4609 | 58.6501 | 2849 | 1049 | 4092 | 2065 | 1377 | 66.6828 | |
| gduggal-snapvard | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 93.0446 | 97.3019 | 89.1441 | 72.7080 | 17094 | 474 | 16957 | 2065 | 141 | 6.8281 | |
| jlack-gatk | SNP | ti | map_l100_m2_e1 | * | 97.5095 | 99.1108 | 95.9591 | 74.4631 | 49045 | 440 | 49038 | 2065 | 195 | 9.4431 | |
| ghariani-varprowl | INDEL | D6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 26.8074 | 23.6447 | 30.9468 | 56.6057 | 929 | 3000 | 925 | 2064 | 2051 | 99.3702 | |
| ciseli-custom | SNP | tv | map_l100_m1_e0 | het | 78.9799 | 73.9962 | 84.6833 | 75.5859 | 11408 | 4009 | 11406 | 2063 | 73 | 3.5385 | |
| qzeng-custom | INDEL | D6_15 | HG002compoundhet | * | 81.7565 | 82.9255 | 80.6200 | 31.3934 | 7489 | 1542 | 8582 | 2063 | 963 | 46.6796 | |
| gduggal-bwafb | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 94.3271 | 95.6499 | 93.0405 | 79.9739 | 27463 | 1249 | 27553 | 2061 | 214 | 10.3833 | |
| gduggal-bwafb | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 94.3271 | 95.6499 | 93.0405 | 79.9739 | 27463 | 1249 | 27553 | 2061 | 214 | 10.3833 | |
| gduggal-snapvard | SNP | tv | map_l100_m2_e0 | * | 94.5205 | 97.0079 | 92.1574 | 76.1726 | 24284 | 749 | 24195 | 2059 | 151 | 7.3337 | |
| ciseli-custom | INDEL | D6_15 | HG002complexvar | * | 60.6154 | 60.3471 | 60.8861 | 55.7398 | 3199 | 2102 | 3202 | 2057 | 1257 | 61.1084 | |
| jlack-gatk | SNP | ti | map_l100_m2_e0 | * | 97.4962 | 99.1075 | 95.9365 | 74.4561 | 48524 | 437 | 48517 | 2055 | 194 | 9.4404 | |
| ckim-vqsr | SNP | * | * | het | 99.4736 | 99.0611 | 99.8894 | 26.9578 | 1855996 | 17591 | 1855876 | 2054 | 101 | 4.9172 | |
| gduggal-snapvard | SNP | tv | map_l100_m2_e1 | het | 92.6451 | 97.4464 | 88.2947 | 79.7695 | 15531 | 407 | 15471 | 2051 | 143 | 6.9722 | |
| ciseli-custom | SNP | ti | map_l150_m1_e0 | het | 73.8384 | 68.2296 | 80.4520 | 83.6682 | 8440 | 3930 | 8437 | 2050 | 62 | 3.0244 | |
| ghariani-varprowl | SNP | ti | * | homalt | 99.8530 | 99.9608 | 99.7455 | 17.9110 | 802720 | 315 | 802769 | 2048 | 1014 | 49.5117 | |
| gduggal-snapvard | SNP | tv | map_l100_m1_e0 | * | 94.4568 | 97.0001 | 92.0434 | 74.6951 | 23766 | 735 | 23680 | 2047 | 149 | 7.2789 | |
| jpowers-varprowl | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 57.4031 | 85.2666 | 43.2650 | 71.4286 | 1551 | 268 | 1561 | 2047 | 2030 | 99.1695 | |
| jpowers-varprowl | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 57.4031 | 85.2666 | 43.2650 | 71.4286 | 1551 | 268 | 1561 | 2047 | 2030 | 99.1695 | |
| anovak-vg | INDEL | * | map_siren | * | 72.9885 | 73.1309 | 72.8467 | 79.6324 | 5419 | 1991 | 5489 | 2046 | 1378 | 67.3509 | |
| jlack-gatk | SNP | ti | map_l100_m2_e1 | het | 96.4266 | 99.2506 | 93.7588 | 78.7315 | 30728 | 232 | 30721 | 2045 | 177 | 8.6553 | |
| ghariani-varprowl | INDEL | D6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 44.3050 | 88.6576 | 29.5314 | 54.8186 | 852 | 109 | 857 | 2045 | 2032 | 99.3643 | |
| gduggal-snapvard | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 74.2485 | 93.1298 | 61.7328 | 60.2144 | 1586 | 117 | 3299 | 2045 | 1364 | 66.6993 | |
| ciseli-custom | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 46.1795 | 45.3564 | 47.0329 | 65.4087 | 1807 | 2177 | 1815 | 2044 | 1056 | 51.6634 | |
| gduggal-snapvard | SNP | tv | map_l100_m2_e0 | het | 92.6002 | 97.4203 | 88.2346 | 79.7371 | 15370 | 407 | 15314 | 2042 | 140 | 6.8560 | |
| egarrison-hhga | INDEL | D6_15 | * | * | 86.6592 | 82.4007 | 91.3819 | 53.7350 | 21500 | 4592 | 21631 | 2040 | 1771 | 86.8137 | |
| gduggal-snapplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 64.1957 | 56.1798 | 74.8799 | 61.8437 | 4700 | 3666 | 6078 | 2039 | 1497 | 73.4183 | |
| jlack-gatk | SNP | ti | map_l100_m2_e0 | het | 96.4036 | 99.2424 | 93.7226 | 78.7202 | 30390 | 232 | 30383 | 2035 | 176 | 8.6487 | |
| mlin-fermikit | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 80.9211 | 77.9906 | 84.0804 | 49.2093 | 10751 | 3034 | 10748 | 2035 | 2023 | 99.4103 | |
| anovak-vg | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 37.5716 | 28.2822 | 55.9480 | 46.5176 | 1788 | 4534 | 2582 | 2033 | 1650 | 81.1608 | |
| anovak-vg | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 37.5716 | 28.2822 | 55.9480 | 46.5176 | 1788 | 4534 | 2582 | 2033 | 1650 | 81.1608 | |
| gduggal-snapvard | SNP | tv | map_l100_m1_e0 | het | 92.4877 | 97.3990 | 88.0480 | 78.4967 | 15016 | 401 | 14962 | 2031 | 139 | 6.8439 | |
| ghariani-varprowl | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 65.9654 | 55.6526 | 80.9698 | 74.3202 | 8669 | 6908 | 8633 | 2029 | 1680 | 82.7994 | |