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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
26151-26200 / 86044 show all | |||||||||||||||
| asubramanian-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 93.3398 | 93.6585 | 93.0233 | 91.4274 | 192 | 13 | 200 | 15 | 11 | 73.3333 | |
| asubramanian-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 93.3398 | 93.6585 | 93.0233 | 91.4274 | 192 | 13 | 200 | 15 | 11 | 73.3333 | |
| ndellapenna-hhga | SNP | tv | map_l250_m0_e0 | * | 97.2074 | 95.5556 | 98.9175 | 91.4259 | 731 | 34 | 731 | 8 | 4 | 50.0000 | |
| ltrigg-rtg1 | INDEL | I1_5 | map_l250_m1_e0 | het | 91.0871 | 85.0000 | 98.1132 | 91.4239 | 51 | 9 | 52 | 1 | 0 | 0.0000 | |
| jpowers-varprowl | SNP | tv | segdup | homalt | 99.1421 | 99.9074 | 98.3886 | 91.4237 | 3235 | 3 | 3236 | 53 | 29 | 54.7170 | |
| anovak-vg | INDEL | D6_15 | segdup | homalt | 85.5227 | 82.0000 | 89.3617 | 91.4234 | 41 | 9 | 42 | 5 | 3 | 60.0000 | |
| astatham-gatk | INDEL | D6_15 | map_l125_m2_e0 | * | 97.1888 | 96.0317 | 98.3740 | 91.4226 | 121 | 5 | 121 | 2 | 1 | 50.0000 | |
| gduggal-snapplat | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 79.9814 | 83.6479 | 76.6228 | 91.4225 | 3545 | 693 | 3553 | 1084 | 49 | 4.5203 | |
| hfeng-pmm1 | INDEL | * | map_l100_m0_e0 | hetalt | 96.8750 | 93.9394 | 100.0000 | 91.4209 | 31 | 2 | 32 | 0 | 0 | ||
| gduggal-bwavard | INDEL | I6_15 | map_l125_m2_e1 | * | 72.2222 | 73.5849 | 70.9091 | 91.4197 | 39 | 14 | 39 | 16 | 8 | 50.0000 | |
| hfeng-pmm3 | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 91.5663 | 85.9729 | 97.9381 | 91.4197 | 190 | 31 | 190 | 4 | 0 | 0.0000 | |
| jlack-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | homalt | 96.0000 | 100.0000 | 92.3077 | 91.4191 | 24 | 0 | 24 | 2 | 2 | 100.0000 | |
| asubramanian-gatk | INDEL | D1_5 | map_l150_m0_e0 | homalt | 92.6076 | 88.2353 | 97.4359 | 91.4191 | 75 | 10 | 76 | 2 | 1 | 50.0000 | |
| hfeng-pmm3 | INDEL | * | map_l150_m0_e0 | het | 97.3854 | 97.9472 | 96.8300 | 91.4173 | 334 | 7 | 336 | 11 | 1 | 9.0909 | |
| qzeng-custom | INDEL | * | map_l125_m1_e0 | * | 82.7094 | 73.9440 | 93.8324 | 91.4171 | 1558 | 549 | 1993 | 131 | 45 | 34.3511 | |
| gduggal-snapvard | SNP | tv | map_l250_m2_e1 | * | 84.9786 | 95.5761 | 76.4966 | 91.4134 | 2787 | 129 | 2773 | 852 | 31 | 3.6385 | |
| ckim-dragen | SNP | tv | map_l250_m2_e1 | het | 96.2700 | 96.5394 | 96.0020 | 91.4117 | 1897 | 68 | 1897 | 79 | 5 | 6.3291 | |
| ghariani-varprowl | SNP | * | map_l250_m2_e0 | * | 95.6186 | 97.4255 | 93.8776 | 91.4090 | 7682 | 203 | 7682 | 501 | 87 | 17.3653 | |
| ckim-vqsr | SNP | ti | map_l150_m2_e1 | het | 78.3815 | 65.0480 | 98.5906 | 91.4083 | 8466 | 4549 | 8464 | 121 | 2 | 1.6529 | |
| mlin-fermikit | INDEL | I16_PLUS | map_l100_m2_e1 | * | 70.8333 | 65.3846 | 77.2727 | 91.4062 | 17 | 9 | 17 | 5 | 3 | 60.0000 | |
| jli-custom | INDEL | * | map_l100_m0_e0 | hetalt | 90.3728 | 84.8485 | 96.6667 | 91.4040 | 28 | 5 | 29 | 1 | 0 | 0.0000 | |
| ckim-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 94.5736 | 100.0000 | 89.7059 | 91.4033 | 61 | 0 | 61 | 7 | 7 | 100.0000 | |
| ckim-vqsr | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 94.5736 | 100.0000 | 89.7059 | 91.4033 | 61 | 0 | 61 | 7 | 7 | 100.0000 | |
| ghariani-varprowl | INDEL | I6_15 | map_l125_m1_e0 | * | 70.7071 | 66.0377 | 76.0870 | 91.4019 | 35 | 18 | 35 | 11 | 7 | 63.6364 | |
| jpowers-varprowl | INDEL | I1_5 | map_l125_m0_e0 | het | 93.6170 | 91.6667 | 95.6522 | 91.4019 | 176 | 16 | 176 | 8 | 5 | 62.5000 | |
| gduggal-snapvard | INDEL | I6_15 | map_l150_m0_e0 | het | 74.4186 | 100.0000 | 59.2593 | 91.4013 | 4 | 0 | 16 | 11 | 8 | 72.7273 | |
| qzeng-custom | INDEL | * | map_l100_m2_e1 | hetalt | 85.7143 | 75.0000 | 100.0000 | 91.4013 | 99 | 33 | 27 | 0 | 0 | ||
| anovak-vg | INDEL | D6_15 | map_l150_m1_e0 | * | 80.4282 | 79.4521 | 81.4286 | 91.4005 | 58 | 15 | 57 | 13 | 8 | 61.5385 | |
| rpoplin-dv42 | INDEL | I6_15 | segdup | * | 98.2659 | 97.1429 | 99.4152 | 91.3984 | 170 | 5 | 170 | 1 | 1 | 100.0000 | |
| ghariani-varprowl | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 12.5000 | 8.3333 | 25.0000 | 91.3978 | 2 | 22 | 2 | 6 | 6 | 100.0000 | |
| gduggal-snapvard | INDEL | I6_15 | segdup | het | 71.6829 | 85.5422 | 61.6883 | 91.3966 | 71 | 12 | 95 | 59 | 50 | 84.7458 | |
| gduggal-bwaplat | INDEL | I1_5 | map_l125_m1_e0 | homalt | 68.1452 | 51.6820 | 100.0000 | 91.3951 | 169 | 158 | 169 | 0 | 0 | ||
| jmaeng-gatk | INDEL | I16_PLUS | lowcmp_SimpleRepeat_quadTR_51to200 | * | 89.3617 | 80.7692 | 100.0000 | 91.3934 | 21 | 5 | 21 | 0 | 0 | ||
| asubramanian-gatk | SNP | ti | segdup | * | 98.1992 | 96.8521 | 99.5842 | 91.3917 | 18922 | 615 | 18920 | 79 | 8 | 10.1266 | |
| ckim-gatk | INDEL | I1_5 | map_l100_m0_e0 | het | 96.2697 | 98.4663 | 94.1691 | 91.3906 | 321 | 5 | 323 | 20 | 0 | 0.0000 | |
| jmaeng-gatk | INDEL | D1_5 | map_l125_m1_e0 | het | 94.9786 | 98.7603 | 91.4758 | 91.3901 | 717 | 9 | 719 | 67 | 4 | 5.9702 | |
| astatham-gatk | SNP | * | segdup | het | 98.7752 | 97.7998 | 99.7702 | 91.3893 | 16936 | 381 | 16930 | 39 | 2 | 5.1282 | |
| ckim-vqsr | INDEL | I16_PLUS | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 93.8838 | 90.5263 | 97.5000 | 91.3886 | 86 | 9 | 78 | 2 | 0 | 0.0000 | |
| ckim-dragen | INDEL | D6_15 | map_l125_m1_e0 | * | 96.1373 | 95.7265 | 96.5517 | 91.3883 | 112 | 5 | 112 | 4 | 1 | 25.0000 | |
| gduggal-bwavard | SNP | tv | map_l250_m1_e0 | * | 88.5182 | 97.6199 | 80.9689 | 91.3881 | 2584 | 63 | 2574 | 605 | 16 | 2.6446 | |
| ckim-vqsr | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 97.6744 | 96.7105 | 98.6577 | 91.3873 | 147 | 5 | 147 | 2 | 2 | 100.0000 | |
| ndellapenna-hhga | INDEL | D16_PLUS | map_l125_m2_e1 | het | 95.4545 | 100.0000 | 91.3043 | 91.3858 | 20 | 0 | 21 | 2 | 0 | 0.0000 | |
| gduggal-snapvard | INDEL | C16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 0.0000 | 0.0000 | 21.7391 | 91.3858 | 0 | 0 | 5 | 18 | 3 | 16.6667 | |
| gduggal-snapvard | INDEL | C16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 0.0000 | 0.0000 | 21.7391 | 91.3858 | 0 | 0 | 5 | 18 | 3 | 16.6667 | |
| asubramanian-gatk | INDEL | D1_5 | map_l125_m0_e0 | * | 91.3934 | 89.9194 | 92.9167 | 91.3840 | 446 | 50 | 446 | 34 | 2 | 5.8824 | |
| jpowers-varprowl | INDEL | I16_PLUS | segdup | * | 76.3282 | 68.0851 | 86.8421 | 91.3832 | 32 | 15 | 33 | 5 | 5 | 100.0000 | |
| ckim-vqsr | SNP | tv | map_l150_m1_e0 | homalt | 36.1636 | 22.0730 | 100.0000 | 91.3831 | 871 | 3075 | 871 | 0 | 0 | ||
| hfeng-pmm2 | SNP | tv | segdup | * | 99.6780 | 99.8125 | 99.5439 | 91.3819 | 8516 | 16 | 8512 | 39 | 4 | 10.2564 | |
| ckim-gatk | INDEL | * | map_l125_m2_e1 | * | 96.6536 | 98.5169 | 94.8596 | 91.3812 | 2192 | 33 | 2196 | 119 | 11 | 9.2437 | |
| ckim-dragen | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 98.0107 | 96.7105 | 99.3464 | 91.3803 | 147 | 5 | 152 | 1 | 1 | 100.0000 | |