PrecisionFDA
Truth Challenge
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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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
48801-48850 / 86044 show all | |||||||||||||||
| ciseli-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 60.8751 | 59.9982 | 61.7781 | 66.5944 | 39207 | 26140 | 39525 | 24454 | 17134 | 70.0662 | |
| gduggal-bwavard | SNP | tv | map_l125_m1_e0 | homalt | 98.7755 | 97.7645 | 99.8076 | 66.5926 | 5729 | 131 | 5706 | 11 | 9 | 81.8182 | |
| mlin-fermikit | INDEL | D16_PLUS | lowcmp_SimpleRepeat_triTR_11to50 | * | 89.9023 | 87.8981 | 92.0000 | 66.5924 | 138 | 19 | 138 | 12 | 11 | 91.6667 | |
| ltrigg-rtg2 | SNP | tv | map_l125_m0_e0 | homalt | 99.7066 | 99.4597 | 99.9548 | 66.5911 | 2209 | 12 | 2209 | 1 | 0 | 0.0000 | |
| jlack-gatk | INDEL | D16_PLUS | HG002complexvar | * | 96.5938 | 96.2264 | 96.9641 | 66.5839 | 1581 | 62 | 1565 | 49 | 36 | 73.4694 | |
| hfeng-pmm1 | SNP | * | map_l125_m1_e0 | homalt | 99.8048 | 99.7870 | 99.8225 | 66.5790 | 16869 | 36 | 16869 | 30 | 12 | 40.0000 | |
| gduggal-snapplat | INDEL | D6_15 | HG002complexvar | * | 44.3210 | 31.1015 | 77.0858 | 66.5750 | 1649 | 3653 | 1312 | 390 | 129 | 33.0769 | |
| jlack-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 99.7048 | 99.4757 | 99.9349 | 66.5658 | 16886 | 89 | 16886 | 11 | 11 | 100.0000 | |
| jlack-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 99.7048 | 99.4757 | 99.9349 | 66.5658 | 16886 | 89 | 16886 | 11 | 11 | 100.0000 | |
| eyeh-varpipe | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 95.3296 | 99.8474 | 91.2029 | 66.5610 | 3925 | 6 | 3753 | 362 | 12 | 3.3149 | |
| hfeng-pmm2 | SNP | tv | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 96.9477 | 94.4556 | 99.5749 | 66.5601 | 937 | 55 | 937 | 4 | 0 | 0.0000 | |
| ckim-dragen | SNP | tv | lowcmp_SimpleRepeat_diTR_11to50 | * | 99.7426 | 99.6705 | 99.8147 | 66.5588 | 4840 | 16 | 4849 | 9 | 8 | 88.8889 | |
| hfeng-pmm2 | INDEL | D16_PLUS | HG002complexvar | het | 95.7182 | 93.4959 | 98.0488 | 66.5579 | 1035 | 72 | 804 | 16 | 7 | 43.7500 | |
| jlack-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 98.9286 | 99.8558 | 98.0184 | 66.5562 | 1385 | 2 | 1385 | 28 | 1 | 3.5714 | |
| anovak-vg | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 52.6463 | 45.0798 | 63.2653 | 66.5529 | 339 | 413 | 372 | 216 | 150 | 69.4444 | |
| qzeng-custom | INDEL | * | HG002compoundhet | homalt | 47.3681 | 97.3761 | 31.2960 | 66.5488 | 668 | 18 | 681 | 1495 | 1295 | 86.6221 | |
| jmaeng-gatk | INDEL | I1_5 | HG002compoundhet | * | 94.6029 | 91.9877 | 97.3711 | 66.5483 | 11366 | 990 | 11371 | 307 | 304 | 99.0228 | |
| hfeng-pmm3 | INDEL | I6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 92.9204 | 87.9187 | 98.5255 | 66.5471 | 735 | 101 | 735 | 11 | 9 | 81.8182 | |
| ckim-dragen | INDEL | I16_PLUS | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 96.5177 | 93.9068 | 99.2780 | 66.5459 | 262 | 17 | 275 | 2 | 2 | 100.0000 | |
| gduggal-bwaplat | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 93.4119 | 88.3559 | 99.0817 | 66.5438 | 2155 | 284 | 2158 | 20 | 6 | 30.0000 | |
| ndellapenna-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 95.3676 | 96.3218 | 94.4321 | 66.5425 | 419 | 16 | 424 | 25 | 17 | 68.0000 | |
| dgrover-gatk | INDEL | I1_5 | lowcmp_SimpleRepeat_triTR_11to50 | homalt | 99.6269 | 100.0000 | 99.2565 | 66.5423 | 267 | 0 | 267 | 2 | 2 | 100.0000 | |
| ndellapenna-hhga | SNP | * | lowcmp_SimpleRepeat_diTR_11to50 | het | 98.2992 | 97.3060 | 99.3129 | 66.5408 | 6068 | 168 | 6071 | 42 | 21 | 50.0000 | |
| asubramanian-gatk | INDEL | I6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 91.8400 | 87.9187 | 96.1276 | 66.5396 | 735 | 101 | 844 | 34 | 30 | 88.2353 | |
| dgrover-gatk | INDEL | I16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 99.4253 | 98.8571 | 100.0000 | 66.5392 | 173 | 2 | 175 | 0 | 0 | ||
| ltrigg-rtg2 | SNP | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 97.2799 | 97.7540 | 96.8105 | 66.5390 | 4657 | 107 | 4735 | 156 | 5 | 3.2051 | |
| jli-custom | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 98.2812 | 96.8927 | 99.7101 | 66.5373 | 343 | 11 | 344 | 1 | 1 | 100.0000 | |
| 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 | |
| ghariani-varprowl | SNP | ti | map_l125_m1_e0 | homalt | 99.2029 | 98.5967 | 99.8167 | 66.5358 | 10890 | 155 | 10890 | 20 | 15 | 75.0000 | |
| hfeng-pmm3 | INDEL | D16_PLUS | HG002complexvar | het | 96.3171 | 94.3089 | 98.4127 | 66.5304 | 1044 | 63 | 806 | 13 | 7 | 53.8462 | |
| hfeng-pmm3 | INDEL | D16_PLUS | * | * | 97.6998 | 96.8013 | 98.6151 | 66.5273 | 6567 | 217 | 6551 | 92 | 69 | 75.0000 | |
| dgrover-gatk | SNP | * | map_l125_m2_e1 | homalt | 99.6110 | 99.3269 | 99.8967 | 66.5258 | 17414 | 118 | 17414 | 18 | 13 | 72.2222 | |
| egarrison-hhga | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 76.9409 | 66.2700 | 91.7077 | 66.5255 | 1281 | 652 | 1305 | 118 | 98 | 83.0508 | |
| raldana-dualsentieon | INDEL | I16_PLUS | HG002compoundhet | homalt | 7.3171 | 100.0000 | 3.7975 | 66.5254 | 3 | 0 | 3 | 76 | 75 | 98.6842 | |
| eyeh-varpipe | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 48.1230 | 32.2658 | 94.6289 | 66.5252 | 5390 | 11315 | 7611 | 432 | 407 | 94.2130 | |
| eyeh-varpipe | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 48.1230 | 32.2658 | 94.6289 | 66.5252 | 5390 | 11315 | 7611 | 432 | 407 | 94.2130 | |
| hfeng-pmm2 | INDEL | D6_15 | HG002compoundhet | het | 82.2726 | 79.2056 | 85.5867 | 66.5243 | 678 | 178 | 671 | 113 | 110 | 97.3451 | |
| ciseli-custom | INDEL | D1_5 | HG002compoundhet | homalt | 8.4350 | 85.5670 | 4.4361 | 66.5215 | 249 | 42 | 249 | 5364 | 5004 | 93.2886 | |
| egarrison-hhga | SNP | * | lowcmp_SimpleRepeat_diTR_11to50 | het | 98.4322 | 97.6427 | 99.2345 | 66.5194 | 6089 | 147 | 6093 | 47 | 18 | 38.2979 | |
| astatham-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 99.6662 | 99.3697 | 99.9644 | 66.5145 | 16868 | 107 | 16868 | 6 | 6 | 100.0000 | |
| astatham-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 99.6662 | 99.3697 | 99.9644 | 66.5145 | 16868 | 107 | 16868 | 6 | 6 | 100.0000 | |
| ckim-isaac | INDEL | I16_PLUS | HG002complexvar | homalt | 50.1099 | 36.8932 | 78.0822 | 66.5138 | 114 | 195 | 114 | 32 | 13 | 40.6250 | |
| ckim-dragen | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 99.7926 | 99.8634 | 99.7220 | 66.5121 | 17544 | 24 | 17576 | 49 | 13 | 26.5306 | |
| gduggal-snapvard | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 2.7557 | 1.4642 | 23.3645 | 66.5102 | 47 | 3163 | 50 | 164 | 113 | 68.9024 | |
| dgrover-gatk | SNP | * | map_l125_m2_e0 | homalt | 99.6075 | 99.3209 | 99.8958 | 66.5083 | 17257 | 118 | 17257 | 18 | 13 | 72.2222 | |
| qzeng-custom | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 93.9750 | 94.3820 | 93.5714 | 66.5072 | 84 | 5 | 131 | 9 | 2 | 22.2222 | |
| egarrison-hhga | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_51to200 | het | 63.7790 | 63.3136 | 64.2512 | 66.5049 | 107 | 62 | 133 | 74 | 74 | 100.0000 | |
| hfeng-pmm3 | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 99.0975 | 98.5381 | 99.6632 | 66.5047 | 3842 | 57 | 3847 | 13 | 7 | 53.8462 | |
| bgallagher-sentieon | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 97.8275 | 97.5066 | 98.1506 | 66.5044 | 743 | 19 | 743 | 14 | 8 | 57.1429 | |
| gduggal-snapvard | SNP | tv | map_l125_m1_e0 | homalt | 98.0991 | 96.4505 | 99.8050 | 66.5043 | 5652 | 208 | 5629 | 11 | 8 | 72.7273 | |