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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
84651-84700 / 86044 show all | |||||||||||||||
gduggal-snapfb | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 87.6713 | 88.1806 | 87.1679 | 60.5788 | 12131 | 1626 | 17750 | 2613 | 591 | 22.6177 | |
gduggal-snapfb | INDEL | I1_5 | HG002complexvar | * | 93.5109 | 94.6378 | 92.4106 | 55.4813 | 31574 | 1789 | 31902 | 2620 | 888 | 33.8931 | |
qzeng-custom | INDEL | D6_15 | * | het | 92.5374 | 97.5155 | 88.0429 | 52.4636 | 11304 | 288 | 19299 | 2621 | 996 | 38.0008 | |
anovak-vg | INDEL | D6_15 | HG002compoundhet | het | 52.4874 | 55.7243 | 49.6058 | 30.8102 | 477 | 379 | 2580 | 2621 | 1862 | 71.0416 | |
gduggal-snapvard | SNP | ti | map_l125_m2_e1 | het | 91.7986 | 96.5945 | 87.4564 | 82.3224 | 18437 | 650 | 18295 | 2624 | 207 | 7.8887 | |
ghariani-varprowl | SNP | * | map_siren | * | 98.7774 | 99.3373 | 98.2237 | 61.6367 | 145259 | 969 | 145263 | 2627 | 430 | 16.3685 | |
gduggal-snapvard | SNP | ti | map_l125_m1_e0 | * | 93.7547 | 96.2264 | 91.4068 | 77.7724 | 28228 | 1107 | 27965 | 2629 | 225 | 8.5584 | |
mlin-fermikit | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 88.2321 | 85.5737 | 91.0609 | 53.6742 | 26877 | 4531 | 26832 | 2634 | 2540 | 96.4313 | |
mlin-fermikit | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 88.2321 | 85.5737 | 91.0609 | 53.6742 | 26877 | 4531 | 26832 | 2634 | 2540 | 96.4313 | |
gduggal-snapvard | SNP | ti | map_l125_m2_e0 | * | 93.8841 | 96.2555 | 91.6267 | 79.1557 | 29125 | 1133 | 28856 | 2637 | 225 | 8.5324 | |
mlin-fermikit | SNP | ti | map_l100_m1_e0 | * | 73.0893 | 60.7644 | 91.6861 | 50.6018 | 29125 | 18806 | 29125 | 2641 | 2337 | 88.4892 | |
anovak-vg | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 51.1017 | 43.2290 | 62.4805 | 48.0708 | 1063 | 1396 | 4398 | 2641 | 1993 | 75.4638 | |
gduggal-snapvard | SNP | ti | map_l125_m2_e1 | * | 93.9227 | 96.2838 | 91.6745 | 79.2018 | 29433 | 1136 | 29158 | 2648 | 226 | 8.5347 | |
gduggal-snapfb | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 34.5747 | 92.5000 | 21.2608 | 78.3172 | 666 | 54 | 715 | 2648 | 56 | 2.1148 | |
anovak-vg | SNP | * | map_l250_m1_e0 | het | 70.8783 | 85.8044 | 60.3757 | 91.8863 | 4080 | 675 | 4050 | 2658 | 592 | 22.2724 | |
gduggal-snapvard | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | het | 71.5901 | 79.0706 | 65.4026 | 31.3787 | 2161 | 572 | 5036 | 2664 | 2476 | 92.9429 | |
anovak-vg | SNP | * | map_l250_m1_e0 | * | 74.3435 | 81.2102 | 68.5475 | 91.2491 | 5865 | 1357 | 5819 | 2670 | 600 | 22.4719 | |
gduggal-snapplat | INDEL | D1_5 | HG002complexvar | het | 82.2897 | 77.5921 | 87.5928 | 61.7499 | 16112 | 4653 | 18878 | 2674 | 302 | 11.2939 | |
gduggal-snapvard | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | * | 59.9212 | 54.8636 | 66.0058 | 31.4666 | 5189 | 4269 | 5194 | 2675 | 2487 | 92.9720 | |
gduggal-snapvard | INDEL | * | lowcmp_SimpleRepeat_triTR_11to50 | het | 78.7482 | 91.5528 | 69.0859 | 44.8186 | 3349 | 309 | 5978 | 2675 | 2192 | 81.9439 | |
ghariani-varprowl | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 63.8421 | 54.7304 | 76.5939 | 75.6642 | 8799 | 7278 | 8770 | 2680 | 2299 | 85.7836 | |
ghariani-varprowl | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 63.8421 | 54.7304 | 76.5939 | 75.6642 | 8799 | 7278 | 8770 | 2680 | 2299 | 85.7836 | |
jpowers-varprowl | SNP | * | HG002complexvar | * | 99.4683 | 99.2937 | 99.6435 | 20.7160 | 749051 | 5328 | 749404 | 2681 | 1602 | 59.7538 | |
mlin-fermikit | SNP | ti | map_l100_m2_e0 | * | 73.5756 | 61.3876 | 91.8021 | 54.4848 | 30056 | 18905 | 30056 | 2684 | 2362 | 88.0030 | |
asubramanian-gatk | SNP | * | * | het | 98.9725 | 98.1066 | 99.8538 | 23.0377 | 1838113 | 35474 | 1837999 | 2691 | 109 | 4.0505 | |
ciseli-custom | SNP | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 76.2286 | 96.1797 | 63.1327 | 74.0117 | 4582 | 182 | 4615 | 2695 | 108 | 4.0074 | |
gduggal-snapvard | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 53.8464 | 67.1975 | 44.9213 | 37.7402 | 633 | 309 | 2198 | 2695 | 2403 | 89.1651 | |
mlin-fermikit | SNP | ti | map_l100_m2_e1 | * | 73.7873 | 61.6490 | 91.8775 | 54.5530 | 30507 | 18978 | 30507 | 2697 | 2372 | 87.9496 | |
mlin-fermikit | SNP | * | map_l100_m0_e0 | * | 59.6148 | 45.9548 | 84.8308 | 53.4081 | 15092 | 17749 | 15088 | 2698 | 2419 | 89.6590 | |
gduggal-snapvard | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 43.0132 | 41.0316 | 45.1960 | 37.9193 | 1599 | 2298 | 2225 | 2698 | 2406 | 89.1772 | |
egarrison-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 83.0167 | 98.2183 | 71.8900 | 39.0410 | 6560 | 119 | 6900 | 2698 | 2648 | 98.1468 | |
ciseli-custom | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 62.8906 | 92.3251 | 47.6872 | 81.6922 | 2442 | 203 | 2464 | 2703 | 33 | 1.2209 | |
ndellapenna-hhga | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | * | 88.1593 | 87.4776 | 88.8518 | 37.5644 | 21467 | 3073 | 21551 | 2704 | 2453 | 90.7175 | |
gduggal-bwavard | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 79.0557 | 93.1620 | 68.6595 | 75.7645 | 5981 | 439 | 5926 | 2705 | 2382 | 88.0591 | |
gduggal-bwavard | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 79.0557 | 93.1620 | 68.6595 | 75.7645 | 5981 | 439 | 5926 | 2705 | 2382 | 88.0591 | |
gduggal-bwavard | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 61.8858 | 52.4538 | 75.4536 | 73.3552 | 8433 | 7644 | 8318 | 2706 | 2382 | 88.0266 | |
gduggal-bwavard | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 61.8858 | 52.4538 | 75.4536 | 73.3552 | 8433 | 7644 | 8318 | 2706 | 2382 | 88.0266 | |
jlack-gatk | SNP | ti | map_siren | het | 97.5925 | 99.4357 | 95.8164 | 66.8895 | 62030 | 352 | 62021 | 2708 | 216 | 7.9764 | |
gduggal-snapfb | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 87.5291 | 86.9258 | 88.1409 | 52.6080 | 19341 | 2909 | 20149 | 2711 | 1465 | 54.0391 | |
cchapple-custom | SNP | ti | * | het | 99.8339 | 99.8795 | 99.7883 | 21.7295 | 1280346 | 1545 | 1280384 | 2716 | 443 | 16.3108 | |
gduggal-snapplat | SNP | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 86.1713 | 81.5015 | 91.4087 | 79.3482 | 28867 | 6552 | 28940 | 2720 | 211 | 7.7574 | |
gduggal-snapvard | SNP | tv | HG002complexvar | * | 97.7872 | 96.7504 | 98.8464 | 23.7234 | 238156 | 7999 | 233057 | 2720 | 1012 | 37.2059 | |
gduggal-snapfb | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 74.1073 | 99.0588 | 59.1965 | 64.7074 | 3894 | 37 | 3949 | 2722 | 32 | 1.1756 | |
gduggal-snapvard | INDEL | * | lowcmp_SimpleRepeat_triTR_11to50 | * | 73.1367 | 73.8749 | 72.4131 | 44.0488 | 4974 | 1759 | 7145 | 2722 | 2236 | 82.1455 | |
ghariani-varprowl | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 87.7327 | 97.7687 | 79.5653 | 85.1430 | 10560 | 241 | 10653 | 2736 | 243 | 8.8816 | |
eyeh-varpipe | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 89.1102 | 86.0761 | 92.3660 | 60.6253 | 26236 | 4244 | 33152 | 2740 | 2400 | 87.5912 | |
eyeh-varpipe | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 89.1102 | 86.0761 | 92.3660 | 60.6253 | 26236 | 4244 | 33152 | 2740 | 2400 | 87.5912 | |
jlack-gatk | SNP | ti | map_siren | * | 98.3403 | 99.3782 | 97.3238 | 62.0115 | 99731 | 624 | 99716 | 2742 | 240 | 8.7527 | |
gduggal-snapfb | SNP | tv | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 51.9003 | 97.6253 | 35.3454 | 76.8757 | 1480 | 36 | 1499 | 2742 | 30 | 1.0941 | |
mlin-fermikit | INDEL | * | HG002complexvar | * | 95.4305 | 94.5346 | 96.3436 | 54.3245 | 72733 | 4205 | 72356 | 2746 | 2618 | 95.3387 |