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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
80551-80600 / 86044 show all | |||||||||||||||
gduggal-bwafb | SNP | * | map_l150_m1_e0 | het | 98.1968 | 98.3951 | 97.9994 | 78.1832 | 19006 | 310 | 19006 | 388 | 96 | 24.7423 | |
gduggal-bwafb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 89.3164 | 86.6966 | 92.0994 | 71.2589 | 4438 | 681 | 4523 | 388 | 351 | 90.4639 | |
gduggal-snapplat | SNP | * | HG002compoundhet | homalt | 94.8523 | 93.4799 | 96.2656 | 42.1750 | 10079 | 703 | 10002 | 388 | 273 | 70.3608 | |
gduggal-snapfb | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 85.4858 | 93.1258 | 79.0043 | 75.2743 | 1436 | 106 | 1460 | 388 | 46 | 11.8557 | |
qzeng-custom | SNP | tv | map_l100_m2_e1 | * | 88.3100 | 80.2832 | 98.1201 | 78.5916 | 20298 | 4985 | 20251 | 388 | 306 | 78.8660 | |
jpowers-varprowl | SNP | tv | map_l125_m1_e0 | het | 96.3069 | 96.4448 | 96.1694 | 78.7859 | 9766 | 360 | 9766 | 389 | 92 | 23.6504 | |
jlack-gatk | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 95.9315 | 98.6064 | 93.3978 | 71.5802 | 5519 | 78 | 5503 | 389 | 233 | 59.8972 | |
gduggal-snapvard | INDEL | * | segdup | het | 85.9532 | 91.8827 | 80.7426 | 95.9123 | 1347 | 119 | 1631 | 389 | 289 | 74.2931 | |
gduggal-snapplat | INDEL | D6_15 | HG002complexvar | * | 44.3210 | 31.1015 | 77.0858 | 66.5750 | 1649 | 3653 | 1312 | 390 | 129 | 33.0769 | |
jpowers-varprowl | SNP | ti | map_l150_m2_e0 | * | 97.3631 | 96.6654 | 98.0710 | 80.0739 | 19828 | 684 | 19828 | 390 | 140 | 35.8974 | |
jpowers-varprowl | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 88.9148 | 94.6211 | 83.8576 | 74.5711 | 2023 | 115 | 2026 | 390 | 381 | 97.6923 | |
eyeh-varpipe | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 83.0949 | 95.8388 | 73.3424 | 87.1802 | 1451 | 63 | 1073 | 390 | 39 | 10.0000 | |
gduggal-bwafb | SNP | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 95.3543 | 98.5726 | 92.3394 | 77.6916 | 4696 | 68 | 4701 | 390 | 34 | 8.7180 | |
bgallagher-sentieon | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.2203 | 97.7012 | 98.7450 | 60.3971 | 30686 | 722 | 30686 | 390 | 372 | 95.3846 | |
bgallagher-sentieon | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.2203 | 97.7012 | 98.7450 | 60.3971 | 30686 | 722 | 30686 | 390 | 372 | 95.3846 | |
egarrison-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 75.3115 | 93.4534 | 63.0682 | 57.8947 | 571 | 40 | 666 | 390 | 384 | 98.4615 | |
qzeng-custom | SNP | tv | map_siren | het | 91.9469 | 86.2561 | 98.4416 | 72.2639 | 24677 | 3932 | 24636 | 390 | 264 | 67.6923 | |
rpoplin-dv42 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 97.1121 | 98.7732 | 95.5059 | 60.7561 | 8293 | 103 | 8288 | 390 | 362 | 92.8205 | |
rpoplin-dv42 | INDEL | D1_5 | HG002compoundhet | * | 95.7563 | 94.7855 | 96.7473 | 62.2778 | 11597 | 638 | 11600 | 390 | 380 | 97.4359 | |
eyeh-varpipe | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 91.3228 | 88.0846 | 94.8081 | 46.5735 | 2166 | 293 | 7140 | 391 | 343 | 87.7238 | |
gduggal-snapplat | SNP | tv | map_l125_m0_e0 | het | 89.8264 | 88.7753 | 90.9027 | 88.4354 | 3907 | 494 | 3907 | 391 | 205 | 52.4297 | |
bgallagher-sentieon | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 99.3343 | 99.9317 | 98.7440 | 74.3514 | 30740 | 21 | 30740 | 391 | 384 | 98.2097 | |
asubramanian-gatk | INDEL | C1_5 | * | * | 0.0000 | 80.0000 | 0.0000 | 77.6571 | 8 | 2 | 0 | 391 | 0 | 0.0000 | |
ndellapenna-hhga | INDEL | D6_15 | HG002complexvar | * | 88.9462 | 85.9864 | 92.1169 | 57.7872 | 4559 | 743 | 4569 | 391 | 292 | 74.6803 | |
qzeng-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 64.0961 | 94.0104 | 48.6239 | 70.6199 | 361 | 23 | 371 | 392 | 15 | 3.8265 | |
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 | |
hfeng-pmm1 | SNP | ti | * | het | 99.9312 | 99.8931 | 99.9694 | 16.7684 | 1280521 | 1370 | 1280470 | 392 | 29 | 7.3980 | |
ckim-dragen | INDEL | I1_5 | HG002compoundhet | homalt | 62.2015 | 99.0881 | 45.3278 | 87.8082 | 326 | 3 | 325 | 392 | 391 | 99.7449 | |
cchapple-custom | INDEL | D6_15 | * | * | 97.8623 | 97.1869 | 98.5472 | 48.1960 | 25358 | 734 | 26658 | 393 | 348 | 88.5496 | |
ghariani-varprowl | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 49.4821 | 41.3725 | 61.5460 | 81.3094 | 633 | 897 | 629 | 393 | 384 | 97.7099 | |
ghariani-varprowl | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 49.4821 | 41.3725 | 61.5460 | 81.3094 | 633 | 897 | 629 | 393 | 384 | 97.7099 | |
gduggal-snapfb | SNP | * | map_l250_m2_e1 | het | 94.2221 | 95.7257 | 92.7651 | 87.6052 | 5039 | 225 | 5039 | 393 | 175 | 44.5293 | |
egarrison-hhga | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | het | 79.4418 | 90.8058 | 70.6058 | 71.2226 | 879 | 89 | 944 | 393 | 338 | 86.0051 | |
jlack-gatk | SNP | tv | map_l250_m1_e0 | * | 91.7764 | 97.3933 | 86.7721 | 92.6439 | 2578 | 69 | 2578 | 393 | 24 | 6.1069 | |
gduggal-snapplat | SNP | tv | map_l125_m0_e0 | * | 89.9339 | 86.5631 | 93.5778 | 86.2991 | 5740 | 891 | 5741 | 394 | 208 | 52.7919 | |
jpowers-varprowl | SNP | ti | map_l150_m2_e1 | * | 97.3682 | 96.6752 | 98.0713 | 80.1400 | 20034 | 689 | 20034 | 394 | 141 | 35.7868 | |
qzeng-custom | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 87.7736 | 89.0780 | 86.5068 | 60.4550 | 1256 | 154 | 2526 | 394 | 302 | 76.6497 | |
qzeng-custom | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | * | 98.6752 | 99.5050 | 97.8590 | 48.2393 | 18093 | 90 | 18009 | 394 | 21 | 5.3300 | |
qzeng-custom | SNP | * | map_l250_m2_e0 | * | 75.7461 | 64.0330 | 92.7037 | 95.4455 | 5049 | 2836 | 5006 | 394 | 328 | 83.2487 | |
anovak-vg | INDEL | I1_5 | map_l125_m1_e0 | * | 59.3006 | 61.3253 | 57.4054 | 86.4983 | 509 | 321 | 531 | 394 | 267 | 67.7665 | |
anovak-vg | INDEL | I6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 31.9699 | 22.4138 | 55.7303 | 40.4682 | 104 | 360 | 496 | 394 | 328 | 83.2487 | |
anovak-vg | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | het | 39.5158 | 40.0000 | 39.0432 | 37.8119 | 132 | 198 | 253 | 395 | 347 | 87.8481 | |
bgallagher-sentieon | SNP | * | map_l125_m1_e0 | het | 98.9928 | 99.3695 | 98.6190 | 74.6006 | 28213 | 179 | 28207 | 395 | 55 | 13.9241 | |
ghariani-varprowl | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 73.4052 | 61.1563 | 91.7896 | 37.5114 | 4432 | 2815 | 4416 | 395 | 339 | 85.8228 | |
ciseli-custom | SNP | * | map_l250_m1_e0 | homalt | 80.5510 | 78.2785 | 82.9594 | 86.9401 | 1928 | 535 | 1923 | 395 | 279 | 70.6329 | |
mlin-fermikit | INDEL | D1_5 | HG002complexvar | het | 96.8827 | 95.7525 | 98.0399 | 50.2469 | 19883 | 882 | 19757 | 395 | 351 | 88.8608 | |
ltrigg-rtg2 | SNP | * | segdup | * | 99.1371 | 99.6722 | 98.6078 | 87.3153 | 27975 | 92 | 27977 | 395 | 53 | 13.4177 | |
ndellapenna-hhga | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | * | 83.5594 | 82.2599 | 84.9006 | 82.0181 | 2184 | 471 | 2221 | 395 | 339 | 85.8228 | |
mlin-fermikit | SNP | tv | map_l150_m0_e0 | homalt | 51.4655 | 44.9548 | 60.1815 | 60.0161 | 597 | 731 | 597 | 395 | 356 | 90.1266 | |
ckim-vqsr | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 98.2947 | 98.8383 | 97.7570 | 71.4388 | 17612 | 207 | 17215 | 395 | 354 | 89.6203 |