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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
70051-70100 / 86044 show all | |||||||||||||||
ndellapenna-hhga | SNP | ti | map_l125_m1_e0 | * | 99.1869 | 98.5512 | 99.8308 | 67.6959 | 28910 | 425 | 28910 | 49 | 27 | 55.1020 | |
ckim-isaac | SNP | * | map_siren | het | 87.0731 | 77.2065 | 99.8309 | 53.7836 | 70251 | 20740 | 70263 | 119 | 18 | 15.1261 | |
ltrigg-rtg2 | SNP | tv | map_l150_m1_e0 | * | 98.6367 | 97.4707 | 99.8310 | 62.1132 | 10636 | 276 | 10635 | 18 | 2 | 11.1111 | |
gduggal-snapplat | SNP | * | segdup | homalt | 99.4486 | 99.0692 | 99.8310 | 88.7280 | 10643 | 100 | 10636 | 18 | 13 | 72.2222 | |
eyeh-varpipe | SNP | ti | HG002complexvar | het | 99.8630 | 99.8948 | 99.8311 | 17.2379 | 314435 | 331 | 297366 | 503 | 109 | 21.6700 | |
hfeng-pmm3 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 99.2623 | 98.7000 | 99.8311 | 74.5091 | 2961 | 39 | 2955 | 5 | 1 | 20.0000 | |
egarrison-hhga | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 99.6677 | 99.5048 | 99.8311 | 60.3522 | 10047 | 50 | 10048 | 17 | 14 | 82.3529 | |
ltrigg-rtg2 | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 99.1609 | 98.4997 | 99.8312 | 49.4969 | 5843 | 89 | 5913 | 10 | 6 | 60.0000 | |
ltrigg-rtg1 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 99.3938 | 98.9601 | 99.8314 | 43.2370 | 8279 | 87 | 8291 | 14 | 13 | 92.8571 | |
cchapple-custom | INDEL | * | lowcmp_SimpleRepeat_homopolymer_6to10 | homalt | 99.8050 | 99.7787 | 99.8314 | 54.7146 | 11271 | 25 | 11248 | 19 | 17 | 89.4737 | |
hfeng-pmm3 | SNP | tv | lowcmp_SimpleRepeat_diTR_11to50 | * | 98.6772 | 97.5494 | 99.8314 | 64.0612 | 4737 | 119 | 4737 | 8 | 5 | 62.5000 | |
hfeng-pmm3 | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 99.1846 | 98.5457 | 99.8318 | 70.9620 | 63494 | 937 | 63506 | 107 | 86 | 80.3738 | |
bgallagher-sentieon | INDEL | I1_5 | HG002complexvar | * | 99.6940 | 99.5564 | 99.8319 | 56.9171 | 33215 | 148 | 33263 | 56 | 45 | 80.3571 | |
astatham-gatk | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 99.0127 | 98.2067 | 99.8321 | 79.0112 | 4162 | 76 | 4162 | 7 | 4 | 57.1429 | |
ltrigg-rtg2 | INDEL | I1_5 | map_siren | homalt | 99.5854 | 99.3399 | 99.8321 | 73.3974 | 1204 | 8 | 1189 | 2 | 1 | 50.0000 | |
jpowers-varprowl | SNP | ti | map_l125_m2_e1 | homalt | 99.2450 | 98.6647 | 99.8322 | 70.9730 | 11305 | 153 | 11305 | 19 | 15 | 78.9474 | |
gduggal-bwafb | SNP | * | segdup | homalt | 99.7625 | 99.6928 | 99.8322 | 89.4414 | 10710 | 33 | 10710 | 18 | 18 | 100.0000 | |
ltrigg-rtg1 | SNP | ti | map_l100_m0_e0 | homalt | 99.7102 | 99.5884 | 99.8324 | 61.6545 | 7742 | 32 | 7742 | 13 | 13 | 100.0000 | |
hfeng-pmm2 | INDEL | D1_5 | * | * | 99.4930 | 99.1557 | 99.8326 | 57.8117 | 145506 | 1239 | 145558 | 244 | 146 | 59.8361 | |
hfeng-pmm2 | SNP | ti | map_l125_m2_e0 | homalt | 99.8283 | 99.8239 | 99.8327 | 68.6045 | 11338 | 20 | 11338 | 19 | 9 | 47.3684 | |
hfeng-pmm3 | SNP | * | HG002compoundhet | het | 96.0659 | 92.5730 | 99.8327 | 43.9121 | 13125 | 1053 | 13125 | 22 | 5 | 22.7273 | |
rpoplin-dv42 | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 99.1559 | 98.4882 | 99.8328 | 57.1769 | 3583 | 55 | 3583 | 6 | 4 | 66.6667 | |
egarrison-hhga | SNP | ti | map_l100_m0_e0 | * | 99.3678 | 98.9068 | 99.8331 | 66.9886 | 21533 | 238 | 21534 | 36 | 20 | 55.5556 | |
ltrigg-rtg2 | SNP | * | map_l250_m2_e0 | het | 95.8350 | 92.1448 | 99.8331 | 76.0408 | 4786 | 408 | 4786 | 8 | 1 | 12.5000 | |
ckim-dragen | SNP | * | HG002compoundhet | homalt | 99.8656 | 99.8980 | 99.8332 | 35.0217 | 10771 | 11 | 10771 | 18 | 18 | 100.0000 | |
hfeng-pmm3 | INDEL | I1_5 | * | * | 99.5494 | 99.2672 | 99.8332 | 56.8186 | 149560 | 1104 | 149606 | 250 | 187 | 74.8000 | |
eyeh-varpipe | SNP | * | map_l250_m1_e0 | homalt | 99.7542 | 99.6752 | 99.8333 | 88.3918 | 2455 | 8 | 2396 | 4 | 4 | 100.0000 | |
ltrigg-rtg1 | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 99.2568 | 98.6869 | 99.8334 | 39.3004 | 10221 | 136 | 10186 | 17 | 16 | 94.1176 | |
hfeng-pmm2 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 99.5711 | 99.3100 | 99.8335 | 74.5893 | 3598 | 25 | 3598 | 6 | 2 | 33.3333 | |
ltrigg-rtg2 | INDEL | D1_5 | map_l100_m2_e0 | homalt | 98.8432 | 97.8723 | 99.8336 | 76.9113 | 598 | 13 | 600 | 1 | 1 | 100.0000 | |
ckim-dragen | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 99.2515 | 98.6760 | 99.8336 | 71.5436 | 2385 | 32 | 2400 | 4 | 4 | 100.0000 | |
ckim-dragen | SNP | tv | map_l100_m1_e0 | homalt | 99.6733 | 99.5134 | 99.8336 | 57.5832 | 8999 | 44 | 8999 | 15 | 13 | 86.6667 | |
hfeng-pmm2 | SNP | tv | HG002compoundhet | * | 96.9561 | 94.2396 | 99.8337 | 46.6519 | 8409 | 514 | 8407 | 14 | 7 | 50.0000 | |
rpoplin-dv42 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 99.7694 | 99.7050 | 99.8338 | 75.7174 | 5407 | 16 | 5407 | 9 | 2 | 22.2222 | |
rpoplin-dv42 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 99.7694 | 99.7050 | 99.8338 | 75.7174 | 5407 | 16 | 5407 | 9 | 2 | 22.2222 | |
ckim-gatk | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 96.3956 | 93.1863 | 99.8338 | 31.7550 | 2366 | 173 | 2403 | 4 | 4 | 100.0000 | |
ckim-vqsr | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 96.3956 | 93.1863 | 99.8338 | 31.7550 | 2366 | 173 | 2403 | 4 | 4 | 100.0000 | |
ltrigg-rtg2 | SNP | * | map_l150_m1_e0 | het | 98.0986 | 96.4227 | 99.8338 | 58.7339 | 18625 | 691 | 18625 | 31 | 2 | 6.4516 | |
ltrigg-rtg2 | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 99.4045 | 98.9789 | 99.8338 | 50.4652 | 6010 | 62 | 6006 | 10 | 5 | 50.0000 | |
asubramanian-gatk | SNP | * | map_l100_m2_e0 | * | 60.9821 | 43.8984 | 99.8339 | 85.3165 | 32469 | 41495 | 32463 | 54 | 14 | 25.9259 | |
cchapple-custom | SNP | * | map_l250_m0_e0 | homalt | 97.6442 | 95.5485 | 99.8339 | 90.2320 | 601 | 28 | 601 | 1 | 1 | 100.0000 | |
asubramanian-gatk | SNP | ti | map_l150_m1_e0 | * | 39.2304 | 24.4115 | 99.8340 | 94.1489 | 4812 | 14900 | 4810 | 8 | 4 | 50.0000 | |
astatham-gatk | SNP | * | HG002compoundhet | het | 98.6981 | 97.5878 | 99.8340 | 46.2177 | 13836 | 342 | 13834 | 23 | 22 | 95.6522 | |
ltrigg-rtg2 | SNP | * | map_l125_m2_e1 | * | 98.9981 | 98.1759 | 99.8341 | 61.4299 | 46341 | 861 | 46349 | 77 | 15 | 19.4805 | |
hfeng-pmm3 | SNP | tv | HG002compoundhet | * | 97.0510 | 94.4189 | 99.8341 | 47.0669 | 8425 | 498 | 8423 | 14 | 7 | 50.0000 | |
ckim-gatk | INDEL | I1_5 | HG002complexvar | * | 99.4404 | 99.0498 | 99.8341 | 56.8511 | 33046 | 317 | 33092 | 55 | 41 | 74.5455 | |
ckim-vqsr | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 99.7375 | 99.6412 | 99.8341 | 75.9622 | 3610 | 13 | 3610 | 6 | 3 | 50.0000 | |
astatham-gatk | SNP | ti | segdup | * | 99.2327 | 98.6385 | 99.8342 | 89.7728 | 19271 | 266 | 19269 | 32 | 6 | 18.7500 | |
qzeng-custom | SNP | * | lowcmp_SimpleRepeat_homopolymer_6to10 | homalt | 99.7774 | 99.7208 | 99.8342 | 53.5684 | 6071 | 17 | 6021 | 10 | 8 | 80.0000 | |
hfeng-pmm3 | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 98.9050 | 97.9929 | 99.8342 | 48.4986 | 3613 | 74 | 3613 | 6 | 3 | 50.0000 |