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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
13151-13200 / 86044 show all | |||||||||||||||
hfeng-pmm2 | INDEL | D1_5 | map_l125_m2_e0 | homalt | 99.4505 | 99.4505 | 99.4505 | 84.6219 | 362 | 2 | 362 | 2 | 2 | 100.0000 | |
hfeng-pmm3 | INDEL | D1_5 | map_l125_m2_e0 | homalt | 99.5873 | 99.4505 | 99.7245 | 83.3867 | 362 | 2 | 362 | 1 | 1 | 100.0000 | |
astatham-gatk | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 99.6839 | 99.4502 | 99.9188 | 54.8820 | 6150 | 34 | 6150 | 5 | 0 | 0.0000 | |
asubramanian-gatk | SNP | ti | func_cds | homalt | 99.7244 | 99.4502 | 100.0000 | 20.1522 | 5246 | 29 | 5246 | 0 | 0 | ||
bgallagher-sentieon | SNP | * | map_l125_m2_e0 | * | 99.2735 | 99.4499 | 99.0978 | 72.9518 | 46466 | 257 | 46460 | 423 | 70 | 16.5485 | |
hfeng-pmm3 | SNP | * | map_l100_m2_e1 | het | 99.5538 | 99.4499 | 99.6580 | 66.2190 | 46640 | 258 | 46629 | 160 | 14 | 8.7500 | |
ltrigg-rtg2 | INDEL | I1_5 | * | het | 99.5106 | 99.4497 | 99.5716 | 56.0879 | 78606 | 435 | 77868 | 335 | 92 | 27.4627 | |
bgallagher-sentieon | INDEL | D1_5 | * | * | 99.5437 | 99.4494 | 99.6383 | 60.2111 | 145937 | 808 | 145993 | 530 | 397 | 74.9057 | |
gduggal-snapfb | SNP | tv | segdup | * | 98.5144 | 99.4491 | 97.5971 | 92.7173 | 8485 | 47 | 8489 | 209 | 12 | 5.7416 | |
rpoplin-dv42 | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 99.3679 | 99.4491 | 99.2868 | 52.6423 | 6679 | 37 | 6682 | 48 | 39 | 81.2500 | |
gduggal-bwafb | SNP | tv | map_siren | homalt | 99.6686 | 99.4490 | 99.8893 | 56.7363 | 17145 | 95 | 17145 | 19 | 11 | 57.8947 | |
ciseli-custom | SNP | ti | func_cds | * | 98.7839 | 99.4488 | 98.1278 | 24.0438 | 13711 | 76 | 13680 | 261 | 31 | 11.8774 | |
hfeng-pmm2 | SNP | tv | map_l100_m2_e0 | het | 99.2723 | 99.4486 | 99.0966 | 70.7844 | 15690 | 87 | 15686 | 143 | 12 | 8.3916 | |
eyeh-varpipe | SNP | ti | map_l250_m2_e1 | * | 99.0209 | 99.4484 | 98.5971 | 90.5779 | 5048 | 28 | 4990 | 71 | 6 | 8.4507 | |
hfeng-pmm2 | SNP | tv | map_l125_m2_e0 | * | 99.2975 | 99.4481 | 99.1474 | 73.9287 | 16398 | 91 | 16396 | 141 | 16 | 11.3475 | |
ltrigg-rtg2 | SNP | * | map_l250_m2_e1 | homalt | 99.6681 | 99.4481 | 99.8891 | 85.6712 | 2703 | 15 | 2703 | 3 | 3 | 100.0000 | |
dgrover-gatk | SNP | ti | map_l100_m2_e1 | het | 99.4091 | 99.4477 | 99.3705 | 70.9092 | 30789 | 171 | 30782 | 195 | 39 | 20.0000 | |
dgrover-gatk | INDEL | * | HG002complexvar | * | 99.5612 | 99.4476 | 99.6751 | 58.4475 | 76513 | 425 | 76380 | 249 | 210 | 84.3373 | |
ltrigg-rtg2 | INDEL | D1_5 | * | het | 99.5293 | 99.4473 | 99.6114 | 53.9225 | 87090 | 484 | 86889 | 339 | 71 | 20.9440 | |
bgallagher-sentieon | SNP | ti | map_l100_m0_e0 | homalt | 99.6648 | 99.4469 | 99.8837 | 59.2653 | 7731 | 43 | 7731 | 9 | 7 | 77.7778 | |
ndellapenna-hhga | SNP | ti | map_l100_m0_e0 | homalt | 99.6905 | 99.4469 | 99.9354 | 59.4017 | 7731 | 43 | 7731 | 5 | 5 | 100.0000 | |
jlack-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 99.6673 | 99.4468 | 99.8889 | 71.7685 | 5393 | 30 | 5393 | 6 | 6 | 100.0000 | |
jlack-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 99.6673 | 99.4468 | 99.8889 | 71.7685 | 5393 | 30 | 5393 | 6 | 6 | 100.0000 | |
dgrover-gatk | SNP | tv | map_l100_m2_e0 | homalt | 99.6791 | 99.4465 | 99.9128 | 62.0923 | 9163 | 51 | 9163 | 8 | 5 | 62.5000 | |
astatham-gatk | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | * | 99.5288 | 99.4462 | 99.6115 | 59.5139 | 19752 | 110 | 19745 | 77 | 49 | 63.6364 | |
hfeng-pmm3 | SNP | * | map_l100_m2_e0 | het | 99.5523 | 99.4461 | 99.6587 | 66.2016 | 46142 | 257 | 46131 | 158 | 14 | 8.8608 | |
hfeng-pmm2 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | homalt | 99.5839 | 99.4460 | 99.7222 | 61.9048 | 359 | 2 | 359 | 1 | 1 | 100.0000 | |
ltrigg-rtg2 | SNP | tv | lowcmp_SimpleRepeat_quadTR_11to50 | het | 98.5426 | 99.4455 | 97.6559 | 38.3006 | 4663 | 26 | 4666 | 112 | 1 | 0.8929 | |
astatham-gatk | INDEL | * | map_l100_m2_e0 | homalt | 99.2874 | 99.4449 | 99.1304 | 84.8358 | 1254 | 7 | 1254 | 11 | 6 | 54.5455 | |
bgallagher-sentieon | INDEL | * | map_l100_m2_e0 | homalt | 99.1696 | 99.4449 | 98.8959 | 84.6359 | 1254 | 7 | 1254 | 14 | 6 | 42.8571 | |
asubramanian-gatk | INDEL | I1_5 | func_cds | * | 99.1720 | 99.4444 | 98.9011 | 44.5122 | 179 | 1 | 180 | 2 | 0 | 0.0000 | |
rpoplin-dv42 | INDEL | I1_5 | func_cds | * | 99.7214 | 99.4444 | 100.0000 | 35.4839 | 179 | 1 | 180 | 0 | 0 | ||
rpoplin-dv42 | INDEL | I1_5 | map_l100_m2_e1 | homalt | 99.2606 | 99.4444 | 99.0775 | 82.2062 | 537 | 3 | 537 | 5 | 3 | 60.0000 | |
rpoplin-dv42 | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 99.1682 | 99.4444 | 98.8935 | 86.9353 | 716 | 4 | 715 | 8 | 7 | 87.5000 | |
mlin-fermikit | INDEL | I1_5 | func_cds | * | 99.1690 | 99.4444 | 98.8950 | 25.5144 | 179 | 1 | 179 | 2 | 1 | 50.0000 | |
raldana-dualsentieon | INDEL | I1_5 | func_cds | * | 99.1720 | 99.4444 | 98.9011 | 32.5926 | 179 | 1 | 180 | 2 | 0 | 0.0000 | |
qzeng-custom | INDEL | I1_5 | func_cds | * | 99.1720 | 99.4444 | 98.9011 | 34.7670 | 179 | 1 | 180 | 2 | 0 | 0.0000 | |
hfeng-pmm2 | INDEL | I1_5 | func_cds | * | 99.4460 | 99.4444 | 99.4475 | 34.6570 | 179 | 1 | 180 | 1 | 0 | 0.0000 | |
hfeng-pmm3 | INDEL | I1_5 | func_cds | * | 99.7214 | 99.4444 | 100.0000 | 33.8235 | 179 | 1 | 180 | 0 | 0 | ||
hfeng-pmm3 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 99.7214 | 99.4444 | 100.0000 | 67.4027 | 1432 | 8 | 1432 | 0 | 0 | ||
hfeng-pmm1 | INDEL | I1_5 | func_cds | * | 99.7214 | 99.4444 | 100.0000 | 35.2518 | 179 | 1 | 180 | 0 | 0 | ||
hfeng-pmm1 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 99.7214 | 99.4444 | 100.0000 | 67.3953 | 1432 | 8 | 1432 | 0 | 0 | ||
jlack-gatk | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 98.8950 | 99.4444 | 98.3516 | 88.4426 | 716 | 4 | 716 | 12 | 3 | 25.0000 | |
ltrigg-rtg1 | INDEL | I1_5 | map_l100_m2_e1 | homalt | 99.3504 | 99.4444 | 99.2565 | 81.6068 | 537 | 3 | 534 | 4 | 2 | 50.0000 | |
ckim-dragen | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 99.3065 | 99.4444 | 99.1690 | 87.5731 | 716 | 4 | 716 | 6 | 6 | 100.0000 | |
cchapple-custom | INDEL | I1_5 | func_cds | * | 99.4429 | 99.4444 | 99.4413 | 30.0781 | 179 | 1 | 178 | 1 | 0 | 0.0000 | |
ckim-dragen | SNP | tv | map_l150_m2_e1 | homalt | 99.5761 | 99.4436 | 99.7089 | 69.3912 | 4111 | 23 | 4111 | 12 | 10 | 83.3333 | |
ghariani-varprowl | SNP | ti | map_siren | homalt | 99.5932 | 99.4435 | 99.7434 | 52.5183 | 37705 | 211 | 37706 | 97 | 56 | 57.7320 | |
astatham-gatk | INDEL | D1_5 | * | * | 99.5682 | 99.4433 | 99.6934 | 60.4898 | 145928 | 817 | 145983 | 449 | 317 | 70.6013 | |
asubramanian-gatk | INDEL | D1_5 | segdup | homalt | 99.5816 | 99.4429 | 99.7207 | 94.5193 | 357 | 2 | 357 | 1 | 1 | 100.0000 |