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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
82051-82100 / 86044 show all | |||||||||||||||
| mlin-fermikit | SNP | * | map_l250_m2_e1 | homalt | 53.1320 | 43.3775 | 68.5465 | 76.1343 | 1179 | 1539 | 1179 | 541 | 500 | 92.4214 | |
| jpowers-varprowl | INDEL | D6_15 | HG002complexvar | * | 74.6372 | 70.9355 | 78.7466 | 57.5873 | 3761 | 1541 | 3757 | 1014 | 966 | 95.2663 | |
| qzeng-custom | INDEL | D6_15 | HG002compoundhet | * | 81.7565 | 82.9255 | 80.6200 | 31.3934 | 7489 | 1542 | 8582 | 2063 | 963 | 46.6796 | |
| gduggal-bwaplat | SNP | ti | lowcmp_SimpleRepeat_quadTR_11to50 | * | 91.9498 | 85.6224 | 99.2869 | 60.0604 | 9189 | 1543 | 9190 | 66 | 25 | 37.8788 | |
| ghariani-varprowl | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 44.2731 | 30.1494 | 83.2915 | 76.5745 | 666 | 1543 | 663 | 133 | 106 | 79.6992 | |
| jpowers-varprowl | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 44.3323 | 30.1494 | 83.7121 | 76.2590 | 666 | 1543 | 663 | 129 | 106 | 82.1705 | |
| gduggal-bwafb | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 94.8782 | 93.0607 | 96.7682 | 51.4476 | 20706 | 1544 | 21469 | 717 | 639 | 89.1213 | |
| ckim-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.0533 | 97.6374 | 98.4728 | 67.8136 | 63807 | 1544 | 63576 | 986 | 844 | 85.5984 | |
| ckim-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.0533 | 97.6374 | 98.4728 | 67.8136 | 63807 | 1544 | 63576 | 986 | 844 | 85.5984 | |
| cchapple-custom | SNP | ti | * | het | 99.8339 | 99.8795 | 99.7883 | 21.7295 | 1280346 | 1545 | 1280384 | 2716 | 443 | 16.3108 | |
| eyeh-varpipe | INDEL | D16_PLUS | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 33.7995 | 27.2556 | 44.4783 | 55.2641 | 580 | 1548 | 584 | 729 | 693 | 95.0617 | |
| gduggal-snapplat | SNP | * | map_l150_m2_e0 | homalt | 92.8770 | 86.7681 | 99.9113 | 74.6788 | 10151 | 1548 | 10142 | 9 | 9 | 100.0000 | |
| gduggal-snapplat | SNP | * | map_l150_m1_e0 | het | 92.4706 | 91.9807 | 92.9658 | 86.7974 | 17767 | 1549 | 17789 | 1346 | 738 | 54.8291 | |
| gduggal-snapvard | INDEL | I16_PLUS | * | homalt | 1.5180 | 0.7687 | 60.0000 | 43.7086 | 12 | 1549 | 51 | 34 | 22 | 64.7059 | |
| ckim-isaac | SNP | ti | map_l250_m2_e1 | het | 69.1304 | 53.0161 | 99.3186 | 92.2279 | 1749 | 1550 | 1749 | 12 | 1 | 8.3333 | |
| qzeng-custom | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 89.5167 | 81.0229 | 100.0000 | 94.3548 | 6622 | 1551 | 7 | 0 | 0 | ||
| gduggal-snapplat | SNP | ti | lowcmp_SimpleRepeat_quadTR_11to50 | * | 90.3474 | 85.5479 | 95.7174 | 70.9701 | 9181 | 1551 | 9186 | 411 | 54 | 13.1387 | |
| anovak-vg | SNP | ti | map_l150_m2_e0 | homalt | 88.3955 | 79.6350 | 99.3218 | 72.4413 | 6065 | 1551 | 6004 | 41 | 36 | 87.8049 | |
| anovak-vg | SNP | * | map_l125_m0_e0 | het | 76.4858 | 87.7448 | 67.7876 | 82.7028 | 11112 | 1552 | 11006 | 5230 | 1427 | 27.2849 | |
| mlin-fermikit | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 85.0207 | 91.2790 | 79.5656 | 57.4207 | 16265 | 1554 | 15972 | 4102 | 4011 | 97.7816 | |
| mlin-fermikit | SNP | * | map_l250_m0_e0 | * | 40.4330 | 27.1194 | 79.4239 | 82.2628 | 579 | 1556 | 579 | 150 | 132 | 88.0000 | |
| ckim-isaac | SNP | * | map_l250_m2_e0 | homalt | 59.1933 | 42.0700 | 99.8233 | 85.8571 | 1130 | 1556 | 1130 | 2 | 2 | 100.0000 | |
| gduggal-snapvard | INDEL | D16_PLUS | HG002complexvar | * | 9.5470 | 5.2952 | 48.4536 | 72.9428 | 87 | 1556 | 94 | 100 | 53 | 53.0000 | |
| gduggal-snapfb | SNP | ti | * | homalt | 99.7832 | 99.8062 | 99.7602 | 19.1162 | 801483 | 1556 | 801532 | 1927 | 269 | 13.9595 | |
| gduggal-snapplat | SNP | * | map_l150_m2_e0 | het | 92.7026 | 92.2615 | 93.1480 | 87.6370 | 18575 | 1558 | 18597 | 1368 | 748 | 54.6784 | |
| gduggal-snapplat | SNP | * | map_l150_m2_e1 | homalt | 92.9111 | 86.8268 | 99.9123 | 74.6875 | 10269 | 1558 | 10259 | 9 | 9 | 100.0000 | |
| anovak-vg | SNP | ti | map_l150_m2_e1 | homalt | 88.4680 | 79.7478 | 99.3294 | 72.4334 | 6135 | 1558 | 6073 | 41 | 36 | 87.8049 | |
| astatham-gatk | INDEL | * | HG002compoundhet | * | 95.0088 | 94.7931 | 95.2256 | 62.9264 | 28400 | 1560 | 28282 | 1418 | 1407 | 99.2243 | |
| jmaeng-gatk | SNP | ti | HG002complexvar | het | 99.7293 | 99.5044 | 99.9553 | 17.6005 | 313206 | 1560 | 313156 | 140 | 49 | 35.0000 | |
| cchapple-custom | SNP | ti | HG002complexvar | * | 99.8096 | 99.6932 | 99.9263 | 17.3694 | 506876 | 1560 | 505502 | 373 | 274 | 73.4584 | |
| ciseli-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 0.0000 | 3.5250 | 0.0000 | 0.0000 | 57 | 1560 | 0 | 0 | 0 | ||
| gduggal-snapplat | SNP | * | lowcmp_SimpleRepeat_diTR_11to50 | het | 76.7313 | 74.9840 | 78.5619 | 87.2292 | 4676 | 1560 | 4720 | 1288 | 113 | 8.7733 | |
| gduggal-snapplat | INDEL | I16_PLUS | * | homalt | 0.0000 | 0.0000 | 0.0000 | 0 | 1561 | 0 | 0 | 0 | |||
| gduggal-snapfb | INDEL | I16_PLUS | * | homalt | 0.0000 | 0.0000 | 0.0000 | 0 | 1561 | 0 | 0 | 0 | |||
| eyeh-varpipe | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | * | 44.1195 | 41.2053 | 47.4772 | 55.2735 | 1094 | 1561 | 1355 | 1499 | 1289 | 85.9907 | |
| anovak-vg | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 56.9297 | 50.5845 | 65.0951 | 55.0427 | 1601 | 1564 | 1712 | 918 | 650 | 70.8061 | |
| eyeh-varpipe | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | hetalt | 24.4790 | 14.1603 | 90.2314 | 68.8301 | 258 | 1564 | 351 | 38 | 31 | 81.5789 | |
| hfeng-pmm3 | INDEL | * | HG002compoundhet | hetalt | 96.7848 | 93.7847 | 99.9831 | 50.6733 | 23615 | 1565 | 23731 | 4 | 2 | 50.0000 | |
| gduggal-snapplat | SNP | * | map_l150_m2_e1 | het | 92.7489 | 92.3145 | 93.1874 | 87.6725 | 18798 | 1565 | 18822 | 1376 | 752 | 54.6512 | |
| ciseli-custom | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 60.2687 | 57.5149 | 63.2995 | 49.8576 | 2120 | 1566 | 2118 | 1228 | 856 | 69.7068 | |
| anovak-vg | SNP | ti | HG002compoundhet | homalt | 82.5870 | 78.8207 | 86.7313 | 34.8753 | 5828 | 1566 | 5275 | 807 | 534 | 66.1710 | |
| anovak-vg | INDEL | * | HG002complexvar | homalt | 75.7278 | 94.2021 | 63.3115 | 49.8629 | 25460 | 1567 | 25940 | 15032 | 14199 | 94.4585 | |
| mlin-fermikit | INDEL | I1_5 | HG002complexvar | * | 96.3771 | 95.3032 | 97.4754 | 51.5661 | 31796 | 1567 | 31622 | 819 | 800 | 97.6801 | |
| ndellapenna-hhga | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | hetalt | 73.5160 | 59.0220 | 97.4456 | 46.9644 | 2257 | 1567 | 2060 | 54 | 42 | 77.7778 | |
| ckim-dragen | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 97.8701 | 97.6006 | 98.1411 | 68.2416 | 63783 | 1568 | 63513 | 1203 | 1069 | 88.8612 | |
| ckim-dragen | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 97.8701 | 97.6006 | 98.1411 | 68.2416 | 63783 | 1568 | 63513 | 1203 | 1069 | 88.8612 | |
| hfeng-pmm3 | INDEL | * | * | het | 99.4705 | 99.1923 | 99.7504 | 58.0356 | 192565 | 1568 | 192191 | 481 | 313 | 65.0728 | |
| hfeng-pmm3 | INDEL | * | * | hetalt | 96.7703 | 93.7869 | 99.9498 | 57.3944 | 23669 | 1568 | 23894 | 12 | 10 | 83.3333 | |
| hfeng-pmm1 | INDEL | * | * | het | 99.4245 | 99.1923 | 99.6578 | 58.3471 | 192565 | 1568 | 192194 | 660 | 374 | 56.6667 | |
| hfeng-pmm1 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 97.3761 | 95.8604 | 98.9406 | 51.0374 | 36333 | 1569 | 36144 | 387 | 350 | 90.4393 | |