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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
78251-78300 / 86044 show all | |||||||||||||||
| bgallagher-sentieon | INDEL | D6_15 | HG002compoundhet | hetalt | 96.6337 | 93.8535 | 99.5837 | 23.7576 | 7650 | 501 | 7654 | 32 | 32 | 100.0000 | |
| ckim-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 96.6289 | 93.8110 | 99.6213 | 24.3430 | 7594 | 501 | 7629 | 29 | 29 | 100.0000 | |
| gduggal-bwavard | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 56.2018 | 39.2727 | 98.7842 | 59.4828 | 324 | 501 | 325 | 4 | 4 | 100.0000 | |
| gduggal-bwavard | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 56.2018 | 39.2727 | 98.7842 | 59.4828 | 324 | 501 | 325 | 4 | 4 | 100.0000 | |
| gduggal-snapfb | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 81.4700 | 91.7896 | 73.2362 | 71.7064 | 5601 | 501 | 6436 | 2352 | 386 | 16.4116 | |
| gduggal-snapfb | SNP | ti | map_l125_m1_e0 | het | 96.3921 | 97.2572 | 95.5423 | 70.8639 | 17765 | 501 | 17768 | 829 | 394 | 47.5271 | |
| gduggal-snapfb | SNP | ti | map_l125_m2_e0 | het | 96.4670 | 97.3405 | 95.6090 | 72.9883 | 18374 | 502 | 18377 | 844 | 395 | 46.8009 | |
| gduggal-snapfb | SNP | ti | map_l125_m2_e1 | het | 96.4982 | 97.3699 | 95.6419 | 73.0724 | 18585 | 502 | 18588 | 847 | 395 | 46.6352 | |
| gduggal-snapvard | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 94.7012 | 90.7431 | 99.0204 | 73.2912 | 4921 | 502 | 4852 | 48 | 28 | 58.3333 | |
| gduggal-snapvard | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 94.7012 | 90.7431 | 99.0204 | 73.2912 | 4921 | 502 | 4852 | 48 | 28 | 58.3333 | |
| ndellapenna-hhga | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 79.5169 | 66.3764 | 99.1444 | 42.1411 | 991 | 502 | 927 | 8 | 5 | 62.5000 | |
| gduggal-bwavard | SNP | ti | map_l150_m2_e1 | * | 95.4042 | 97.5776 | 93.3256 | 83.0965 | 20221 | 502 | 20037 | 1433 | 94 | 6.5597 | |
| ckim-vqsr | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 96.6223 | 93.7986 | 99.6213 | 24.3454 | 7593 | 502 | 7628 | 29 | 29 | 100.0000 | |
| cchapple-custom | INDEL | D6_15 | HG002compoundhet | hetalt | 0.0000 | 93.8412 | 0.0000 | 0.0000 | 7649 | 502 | 0 | 0 | 0 | ||
| ciseli-custom | SNP | * | lowcmp_SimpleRepeat_diTR_11to50 | * | 78.8703 | 94.8102 | 67.5188 | 69.4075 | 9189 | 503 | 9350 | 4498 | 362 | 8.0480 | |
| gduggal-snapvard | SNP | * | map_l125_m0_e0 | het | 87.4804 | 96.0281 | 80.3301 | 84.3236 | 12161 | 503 | 12023 | 2944 | 184 | 6.2500 | |
| gduggal-snapvard | SNP | * | map_l150_m2_e0 | homalt | 97.6688 | 95.7005 | 99.7199 | 73.1870 | 11196 | 503 | 11035 | 31 | 25 | 80.6452 | |
| bgallagher-sentieon | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 96.7404 | 96.3511 | 97.1328 | 51.7215 | 13282 | 503 | 13280 | 392 | 385 | 98.2143 | |
| anovak-vg | INDEL | I1_5 | map_l100_m2_e1 | het | 47.7657 | 37.9012 | 64.5714 | 90.0794 | 307 | 503 | 339 | 186 | 31 | 16.6667 | |
| dgrover-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 98.1224 | 97.5578 | 98.6935 | 48.6222 | 20093 | 503 | 20094 | 266 | 260 | 97.7444 | |
| gduggal-bwavard | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 94.0248 | 95.3430 | 92.7426 | 84.9164 | 10298 | 503 | 10121 | 792 | 175 | 22.0960 | |
| gduggal-bwaplat | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 38.9486 | 24.4745 | 95.3216 | 91.4756 | 163 | 503 | 163 | 8 | 2 | 25.0000 | |
| gduggal-bwaplat | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 38.9486 | 24.4745 | 95.3216 | 91.4756 | 163 | 503 | 163 | 8 | 2 | 25.0000 | |
| gduggal-bwafb | INDEL | I6_15 | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 78.6619 | 71.5415 | 87.3563 | 60.2740 | 1267 | 504 | 304 | 44 | 44 | 100.0000 | |
| hfeng-pmm1 | SNP | tv | HG002compoundhet | * | 97.0546 | 94.3517 | 99.9169 | 46.7711 | 8419 | 504 | 8417 | 7 | 7 | 100.0000 | |
| hfeng-pmm2 | SNP | tv | HG002compoundhet | het | 94.2146 | 89.2146 | 99.8084 | 51.8565 | 4169 | 504 | 4167 | 8 | 2 | 25.0000 | |
| jmaeng-gatk | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 97.0103 | 94.5783 | 99.5706 | 64.1494 | 8792 | 504 | 8811 | 38 | 38 | 100.0000 | |
| bgallagher-sentieon | SNP | * | HG002complexvar | * | 99.9538 | 99.9332 | 99.9744 | 19.0217 | 753877 | 504 | 753722 | 193 | 84 | 43.5233 | |
| gduggal-bwaplat | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | hetalt | 72.8617 | 57.7406 | 98.7124 | 51.8595 | 690 | 505 | 690 | 9 | 9 | 100.0000 | |
| gduggal-bwavard | SNP | ti | map_l100_m1_e0 | homalt | 98.5262 | 97.1882 | 99.9016 | 59.9578 | 17455 | 505 | 17256 | 17 | 13 | 76.4706 | |
| ghariani-varprowl | SNP | ti | HG002compoundhet | het | 88.1728 | 94.6870 | 82.4973 | 54.5571 | 9000 | 505 | 9111 | 1933 | 19 | 0.9829 | |
| hfeng-pmm1 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 97.6600 | 95.4525 | 99.9719 | 30.6839 | 10600 | 505 | 10680 | 3 | 2 | 66.6667 | |
| jmaeng-gatk | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | * | 98.4981 | 97.9421 | 99.0604 | 41.3577 | 24035 | 505 | 24037 | 228 | 220 | 96.4912 | |
| jmaeng-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 93.0147 | 91.6982 | 94.3696 | 64.0306 | 5578 | 505 | 5464 | 326 | 313 | 96.0123 | |
| gduggal-snapfb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 53.0813 | 57.1912 | 49.5224 | 53.3105 | 676 | 506 | 674 | 687 | 585 | 85.1528 | |
| bgallagher-sentieon | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 96.5254 | 93.7213 | 99.5026 | 29.5295 | 7553 | 506 | 7601 | 38 | 37 | 97.3684 | |
| bgallagher-sentieon | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 96.5254 | 93.7213 | 99.5026 | 29.5295 | 7553 | 506 | 7601 | 38 | 37 | 97.3684 | |
| astatham-gatk | INDEL | D1_5 | HG002compoundhet | hetalt | 97.2654 | 95.0470 | 99.5898 | 58.5927 | 9710 | 506 | 9711 | 40 | 39 | 97.5000 | |
| cchapple-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 0.0000 | 93.7213 | 0.0000 | 0.0000 | 7553 | 506 | 0 | 0 | 0 | ||
| cchapple-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 0.0000 | 93.7213 | 0.0000 | 0.0000 | 7553 | 506 | 0 | 0 | 0 | ||
| ciseli-custom | INDEL | * | lowcmp_SimpleRepeat_homopolymer_6to10 | hetalt | 0.0000 | 5.4206 | 0.0000 | 0.0000 | 29 | 506 | 0 | 0 | 0 | ||
| ltrigg-rtg2 | SNP | ti | map_l100_m0_e0 | * | 98.7646 | 97.6758 | 99.8779 | 53.5389 | 21265 | 506 | 21269 | 26 | 7 | 26.9231 | |
| mlin-fermikit | SNP | tv | map_l250_m1_e0 | homalt | 48.6787 | 40.8879 | 60.1375 | 71.4985 | 350 | 506 | 350 | 232 | 216 | 93.1034 | |
| egarrison-hhga | INDEL | D6_15 | HG002complexvar | hetalt | 65.3629 | 50.0494 | 94.1788 | 58.1739 | 507 | 506 | 453 | 28 | 24 | 85.7143 | |
| ckim-isaac | INDEL | D1_5 | map_l100_m2_e0 | * | 84.1952 | 73.5770 | 98.3950 | 83.2672 | 1409 | 506 | 1410 | 23 | 11 | 47.8261 | |
| ckim-vqsr | SNP | ti | map_l250_m0_e0 | het | 62.2449 | 45.7173 | 97.4886 | 98.4812 | 427 | 507 | 427 | 11 | 0 | 0.0000 | |
| bgallagher-sentieon | INDEL | D6_15 | * | hetalt | 96.5632 | 93.7974 | 99.4971 | 32.7057 | 7667 | 507 | 7716 | 39 | 38 | 97.4359 | |
| ltrigg-rtg2 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 98.4583 | 97.2091 | 99.7401 | 57.5217 | 17659 | 507 | 17653 | 46 | 39 | 84.7826 | |
| ltrigg-rtg2 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 98.4583 | 97.2091 | 99.7401 | 57.5217 | 17659 | 507 | 17653 | 46 | 39 | 84.7826 | |
| hfeng-pmm2 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 96.7869 | 93.7966 | 99.9740 | 28.5303 | 7666 | 507 | 7701 | 2 | 1 | 50.0000 | |