PrecisionFDA
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Explore HG002 comparison results
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| Entry | Type | Subtype | Subset | Genotype | F-score | Recall | Precision | Frac_NA | Truth TP | Truth FN | Query TP | Query FP | FP gt | % FP ma | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
13651-13700 / 86044 show all | |||||||||||||||
| ndellapenna-hhga | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 80.6222 | 79.0628 | 82.2442 | 83.6336 | 7964 | 2109 | 8143 | 1758 | 1536 | 87.3720 | |
| mlin-fermikit | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 95.9291 | 98.9219 | 93.1120 | 72.4097 | 16792 | 183 | 16803 | 1243 | 1086 | 87.3693 | |
| mlin-fermikit | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 95.9291 | 98.9219 | 93.1120 | 72.4097 | 16792 | 183 | 16803 | 1243 | 1086 | 87.3693 | |
| mlin-fermikit | SNP | tv | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 98.1641 | 99.7099 | 96.6655 | 41.7144 | 2750 | 8 | 2754 | 95 | 83 | 87.3684 | |
| jpowers-varprowl | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 81.7040 | 72.4326 | 93.6973 | 66.4963 | 22281 | 8480 | 22240 | 1496 | 1307 | 87.3663 | |
| gduggal-snapvard | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 29.6245 | 17.6158 | 93.0702 | 66.7638 | 2023 | 9461 | 2122 | 158 | 138 | 87.3418 | |
| bgallagher-sentieon | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 97.2930 | 95.5286 | 99.1239 | 61.6524 | 8033 | 376 | 8033 | 71 | 62 | 87.3239 | |
| asubramanian-gatk | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 96.0428 | 95.6233 | 96.4659 | 70.2238 | 3889 | 178 | 3876 | 142 | 124 | 87.3239 | |
| gduggal-snapfb | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 73.1196 | 89.0957 | 62.0019 | 58.7223 | 670 | 82 | 669 | 410 | 358 | 87.3171 | |
| gduggal-snapvard | INDEL | D6_15 | HG002compoundhet | * | 59.7955 | 51.4782 | 71.3183 | 33.2912 | 4649 | 4382 | 4896 | 1969 | 1719 | 87.3032 | |
| ciseli-custom | INDEL | D16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 64.5683 | 53.9483 | 80.3942 | 65.4232 | 731 | 624 | 775 | 189 | 165 | 87.3016 | |
| ciseli-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 44.7752 | 41.0011 | 49.3146 | 53.2015 | 5652 | 8133 | 5684 | 5842 | 5100 | 87.2989 | |
| gduggal-snapvard | INDEL | D6_15 | HG002compoundhet | het | 67.0812 | 63.3178 | 71.3203 | 33.1905 | 542 | 314 | 4894 | 1968 | 1718 | 87.2967 | |
| mlin-fermikit | SNP | tv | map_l150_m2_e1 | * | 57.3730 | 43.7750 | 83.2258 | 66.7620 | 5035 | 6467 | 5031 | 1014 | 885 | 87.2781 | |
| gduggal-bwaplat | INDEL | I6_15 | HG002compoundhet | homalt | 29.0909 | 77.4194 | 17.9104 | 80.8845 | 24 | 7 | 24 | 110 | 96 | 87.2727 | |
| egarrison-hhga | INDEL | D1_5 | HG002compoundhet | hetalt | 77.6385 | 63.8117 | 99.1149 | 65.8609 | 6519 | 3697 | 6159 | 55 | 48 | 87.2727 | |
| ckim-isaac | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 81.2534 | 85.2901 | 77.5815 | 56.2165 | 632 | 109 | 571 | 165 | 144 | 87.2727 | |
| ndellapenna-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 77.1879 | 70.9467 | 84.6330 | 51.0225 | 9780 | 4005 | 9952 | 1807 | 1577 | 87.2717 | |
| mlin-fermikit | SNP | tv | map_l150_m2_e0 | * | 57.2030 | 43.5755 | 83.2323 | 66.6536 | 4948 | 6407 | 4944 | 996 | 869 | 87.2490 | |
| cchapple-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 95.6652 | 95.1622 | 96.1736 | 68.5790 | 1731 | 88 | 3745 | 149 | 130 | 87.2483 | |
| cchapple-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 95.6652 | 95.1622 | 96.1736 | 68.5790 | 1731 | 88 | 3745 | 149 | 130 | 87.2483 | |
| egarrison-hhga | INDEL | D16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 90.7286 | 91.6605 | 89.8154 | 74.1565 | 1242 | 113 | 1314 | 149 | 130 | 87.2483 | |
| ghariani-varprowl | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 81.6774 | 94.4237 | 71.9631 | 77.4935 | 6062 | 358 | 6078 | 2368 | 2066 | 87.2466 | |
| ghariani-varprowl | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 81.6774 | 94.4237 | 71.9631 | 77.4935 | 6062 | 358 | 6078 | 2368 | 2066 | 87.2466 | |
| ckim-isaac | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 90.5315 | 93.3228 | 87.9023 | 49.1930 | 13641 | 976 | 12701 | 1748 | 1525 | 87.2426 | |
| mlin-fermikit | SNP | tv | map_l150_m1_e0 | * | 56.0020 | 42.3295 | 82.7209 | 62.1223 | 4619 | 6293 | 4615 | 964 | 841 | 87.2407 | |
| anovak-vg | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 63.8608 | 71.3629 | 57.7860 | 51.0477 | 466 | 187 | 783 | 572 | 499 | 87.2378 | |
| ndellapenna-hhga | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | * | 81.6400 | 76.3498 | 87.7178 | 52.8542 | 1004 | 311 | 1007 | 141 | 123 | 87.2340 | |
| jlack-gatk | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | * | 95.3889 | 94.4487 | 96.3481 | 51.8879 | 1242 | 73 | 1240 | 47 | 41 | 87.2340 | |
| egarrison-hhga | INDEL | * | HG002compoundhet | hetalt | 84.8570 | 74.1223 | 99.2275 | 55.5672 | 18664 | 6516 | 18112 | 141 | 123 | 87.2340 | |
| asubramanian-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 97.8063 | 97.1411 | 98.4806 | 47.1994 | 17737 | 522 | 17759 | 274 | 239 | 87.2263 | |
| cchapple-custom | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | * | 98.1110 | 97.3601 | 98.8735 | 45.3846 | 35626 | 966 | 45291 | 516 | 450 | 87.2093 | |
| jlack-gatk | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 95.6982 | 92.8933 | 98.6777 | 52.9173 | 6418 | 491 | 6418 | 86 | 75 | 87.2093 | |
| eyeh-varpipe | INDEL | I1_5 | HG002compoundhet | het | 74.0633 | 83.6471 | 66.4499 | 67.5390 | 711 | 139 | 511 | 258 | 225 | 87.2093 | |
| ndellapenna-hhga | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | het | 95.1353 | 97.1012 | 93.2475 | 55.2934 | 10786 | 322 | 11006 | 797 | 695 | 87.2020 | |
| gduggal-snapvard | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 65.7662 | 77.6219 | 57.0522 | 44.3331 | 11346 | 3271 | 31729 | 23885 | 20828 | 87.2012 | |
| gduggal-snapvard | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 54.3999 | 51.2849 | 57.9178 | 44.7526 | 19438 | 18464 | 33023 | 23994 | 20921 | 87.1926 | |
| egarrison-hhga | INDEL | D6_15 | HG002compoundhet | hetalt | 65.0591 | 48.4726 | 98.9014 | 28.1522 | 3951 | 4200 | 3511 | 39 | 34 | 87.1795 | |
| ckim-isaac | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 89.1201 | 81.4606 | 98.3693 | 34.9531 | 13608 | 3097 | 14116 | 234 | 204 | 87.1795 | |
| ckim-isaac | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 89.1201 | 81.4606 | 98.3693 | 34.9531 | 13608 | 3097 | 14116 | 234 | 204 | 87.1795 | |
| ciseli-custom | INDEL | I16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 33.6634 | 37.7778 | 30.3571 | 77.6000 | 17 | 28 | 17 | 39 | 34 | 87.1795 | |
| mlin-fermikit | INDEL | D1_5 | map_l100_m1_e0 | * | 76.7469 | 67.5325 | 88.8730 | 76.4647 | 1248 | 600 | 1246 | 156 | 136 | 87.1795 | |
| mlin-fermikit | INDEL | I1_5 | map_l100_m2_e0 | * | 72.7673 | 60.4532 | 91.3812 | 78.4780 | 827 | 541 | 827 | 78 | 68 | 87.1795 | |
| anovak-vg | SNP | ti | map_l150_m1_e0 | homalt | 88.1795 | 79.2821 | 99.3263 | 69.9803 | 5809 | 1518 | 5750 | 39 | 34 | 87.1795 | |
| ckim-isaac | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 90.8245 | 87.6365 | 94.2532 | 40.4574 | 33216 | 4686 | 32687 | 1993 | 1737 | 87.1550 | |
| mlin-fermikit | SNP | * | map_l250_m2_e0 | * | 47.3085 | 33.2150 | 82.1776 | 79.9585 | 2619 | 5266 | 2619 | 568 | 495 | 87.1479 | |
| anovak-vg | INDEL | * | HG002complexvar | * | 72.8155 | 71.0364 | 74.6860 | 53.4026 | 54654 | 22284 | 56069 | 19004 | 16560 | 87.1395 | |
| mlin-fermikit | SNP | * | map_l250_m2_e1 | * | 47.5699 | 33.4544 | 82.2913 | 80.2109 | 2672 | 5315 | 2672 | 575 | 501 | 87.1304 | |
| hfeng-pmm2 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 97.5003 | 96.1325 | 98.9076 | 58.5444 | 41659 | 1676 | 41469 | 458 | 399 | 87.1179 | |
| ckim-isaac | INDEL | I6_15 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 79.4104 | 79.0850 | 79.7386 | 67.5159 | 121 | 32 | 122 | 31 | 27 | 87.0968 | |