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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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
74551-74600 / 86044 show all | |||||||||||||||
jlack-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 95.6093 | 91.9316 | 99.5935 | 30.0616 | 10209 | 896 | 10290 | 42 | 37 | 88.0952 | |
jlack-gatk | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_51to200 | het | 67.8262 | 71.8519 | 64.2276 | 75.9766 | 97 | 38 | 79 | 44 | 37 | 84.0909 | |
jlack-gatk | INDEL | D6_15 | * | hetalt | 94.6900 | 90.3964 | 99.4119 | 33.6937 | 7389 | 785 | 7438 | 44 | 37 | 84.0909 | |
jlack-gatk | INDEL | D6_15 | HG002complexvar | hetalt | 92.4487 | 89.3386 | 95.7831 | 48.0438 | 905 | 108 | 954 | 42 | 37 | 88.0952 | |
hfeng-pmm2 | INDEL | I6_15 | HG002complexvar | * | 98.1553 | 97.1411 | 99.1910 | 57.4123 | 4655 | 137 | 4659 | 38 | 37 | 97.3684 | |
hfeng-pmm3 | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | het | 98.3558 | 97.1558 | 99.5859 | 47.3310 | 10111 | 296 | 10101 | 42 | 37 | 88.0952 | |
hfeng-pmm1 | SNP | * | map_l100_m0_e0 | * | 99.3989 | 99.1931 | 99.6055 | 67.8013 | 32576 | 265 | 32572 | 129 | 37 | 28.6822 | |
hfeng-pmm1 | SNP | * | map_l150_m1_e0 | * | 99.3336 | 99.1016 | 99.5666 | 73.6726 | 30334 | 275 | 30328 | 132 | 37 | 28.0303 | |
hfeng-pmm1 | SNP | * | map_l150_m2_e0 | * | 99.3518 | 99.1272 | 99.5773 | 75.1179 | 31574 | 278 | 31568 | 134 | 37 | 27.6119 | |
hfeng-pmm1 | SNP | * | map_l150_m2_e1 | * | 99.3543 | 99.1307 | 99.5789 | 75.1677 | 31930 | 280 | 31924 | 135 | 37 | 27.4074 | |
hfeng-pmm1 | SNP | * | map_siren | het | 99.5907 | 99.3571 | 99.8255 | 53.5727 | 90406 | 585 | 90392 | 158 | 38 | 24.0506 | |
hfeng-pmm2 | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 99.5103 | 99.5446 | 99.4760 | 35.3827 | 7214 | 33 | 7214 | 38 | 38 | 100.0000 | |
hfeng-pmm2 | INDEL | I1_5 | HG002complexvar | * | 99.5522 | 99.2597 | 99.8464 | 56.6743 | 33116 | 247 | 33159 | 51 | 38 | 74.5098 | |
jlack-gatk | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.4946 | 98.2087 | 98.7822 | 76.6731 | 6305 | 115 | 6246 | 77 | 38 | 49.3506 | |
jlack-gatk | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.4946 | 98.2087 | 98.7822 | 76.6731 | 6305 | 115 | 6246 | 77 | 38 | 49.3506 | |
jlack-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 94.6208 | 90.1948 | 99.5035 | 32.1162 | 8380 | 911 | 8417 | 42 | 38 | 90.4762 | |
jlack-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 94.6208 | 90.1948 | 99.5035 | 32.1162 | 8380 | 911 | 8417 | 42 | 38 | 90.4762 | |
hfeng-pmm3 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 97.1733 | 95.1598 | 99.2739 | 61.8292 | 6016 | 306 | 6016 | 44 | 38 | 86.3636 | |
hfeng-pmm3 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 97.1733 | 95.1598 | 99.2739 | 61.8292 | 6016 | 306 | 6016 | 44 | 38 | 86.3636 | |
hfeng-pmm2 | SNP | ti | HG002complexvar | * | 99.8914 | 99.8002 | 99.9829 | 17.3851 | 507420 | 1016 | 507361 | 87 | 38 | 43.6782 | |
hfeng-pmm3 | INDEL | * | lowcmp_SimpleRepeat_diTR_51to200 | homalt | 90.5350 | 91.9220 | 89.1892 | 48.1793 | 330 | 29 | 330 | 40 | 38 | 95.0000 | |
hfeng-pmm3 | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_51to200 | * | 91.7813 | 89.3878 | 94.3066 | 53.8098 | 657 | 78 | 646 | 39 | 38 | 97.4359 | |
hfeng-pmm1 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 94.2991 | 91.8816 | 96.8472 | 60.7800 | 1211 | 107 | 1198 | 39 | 38 | 97.4359 | |
hfeng-pmm1 | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_51to200 | * | 91.7813 | 89.3878 | 94.3066 | 53.8721 | 657 | 78 | 646 | 39 | 38 | 97.4359 | |
hfeng-pmm1 | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | het | 98.2885 | 97.1365 | 99.4681 | 47.3280 | 10109 | 298 | 10098 | 54 | 38 | 70.3704 | |
ndellapenna-hhga | INDEL | * | map_l100_m1_e0 | * | 97.2875 | 96.9325 | 97.6451 | 97.5899 | 3476 | 110 | 3483 | 84 | 38 | 45.2381 | |
ndellapenna-hhga | INDEL | * | map_l100_m2_e0 | * | 97.3112 | 96.9402 | 97.6852 | 97.7103 | 3580 | 113 | 3587 | 85 | 38 | 44.7059 | |
ndellapenna-hhga | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | * | 85.7237 | 78.9364 | 93.7881 | 67.9922 | 757 | 202 | 770 | 51 | 38 | 74.5098 | |
ltrigg-rtg2 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 97.9633 | 96.4517 | 99.5230 | 36.1107 | 7883 | 290 | 7929 | 38 | 38 | 100.0000 | |
ltrigg-rtg2 | INDEL | I1_5 | * | homalt | 99.7495 | 99.5797 | 99.9200 | 48.8836 | 60173 | 254 | 59955 | 48 | 38 | 79.1667 | |
ltrigg-rtg2 | SNP | * | map_siren | * | 99.4570 | 99.1479 | 99.7681 | 47.8411 | 144981 | 1246 | 144975 | 337 | 38 | 11.2760 | |
qzeng-custom | SNP | ti | map_l150_m2_e1 | homalt | 80.1365 | 67.1910 | 99.2610 | 72.9055 | 5169 | 2524 | 5104 | 38 | 38 | 100.0000 | |
mlin-fermikit | INDEL | D6_15 | lowcmp_SimpleRepeat_triTR_51to200 | * | 60.2317 | 54.9296 | 66.6667 | 46.3303 | 78 | 64 | 78 | 39 | 38 | 97.4359 | |
mlin-fermikit | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 73.7321 | 76.6917 | 70.9924 | 82.6490 | 102 | 31 | 93 | 38 | 38 | 100.0000 | |
mlin-fermikit | INDEL | I1_5 | HG002compoundhet | hetalt | 79.4743 | 66.1627 | 99.4916 | 57.4825 | 7395 | 3782 | 7437 | 38 | 38 | 100.0000 | |
mlin-fermikit | SNP | ti | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 99.0073 | 98.6439 | 99.3734 | 43.8166 | 6183 | 85 | 6185 | 39 | 38 | 97.4359 | |
mlin-fermikit | SNP | ti | lowcmp_SimpleRepeat_homopolymer_6to10 | homalt | 98.8267 | 99.3639 | 98.2952 | 44.3446 | 2187 | 14 | 2191 | 38 | 38 | 100.0000 | |
ndellapenna-hhga | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 97.1729 | 95.2004 | 99.2289 | 61.5550 | 5653 | 285 | 5662 | 44 | 38 | 86.3636 | |
ndellapenna-hhga | INDEL | I6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 88.1449 | 83.3732 | 93.4959 | 66.1468 | 697 | 139 | 690 | 48 | 38 | 79.1667 | |
ndellapenna-hhga | SNP | ti | map_l100_m1_e0 | * | 99.3542 | 98.8671 | 99.8462 | 61.3943 | 47388 | 543 | 47390 | 73 | 38 | 52.0548 | |
jmaeng-gatk | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 97.0103 | 94.5783 | 99.5706 | 64.1494 | 8792 | 504 | 8811 | 38 | 38 | 100.0000 | |
jli-custom | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_51to200 | homalt | 88.2022 | 97.5155 | 80.5128 | 34.1216 | 157 | 4 | 157 | 38 | 38 | 100.0000 | |
ltrigg-rtg1 | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 97.0900 | 94.8591 | 99.4283 | 33.0075 | 6532 | 354 | 6609 | 38 | 38 | 100.0000 | |
ltrigg-rtg1 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 96.1659 | 93.1102 | 99.4290 | 31.4906 | 6622 | 490 | 6617 | 38 | 38 | 100.0000 | |
jli-custom | SNP | ti | map_l100_m1_e0 | het | 99.3190 | 99.1250 | 99.5138 | 62.5391 | 29680 | 262 | 29678 | 145 | 38 | 26.2069 | |
jli-custom | SNP | ti | map_l100_m2_e0 | het | 99.3179 | 99.1411 | 99.4953 | 64.3096 | 30359 | 263 | 30357 | 154 | 38 | 24.6753 | |
jli-custom | SNP | ti | map_l100_m2_e1 | het | 99.3237 | 99.1505 | 99.4976 | 64.3340 | 30697 | 263 | 30695 | 155 | 38 | 24.5161 | |
ltrigg-rtg1 | SNP | * | map_l100_m2_e0 | * | 99.3059 | 98.8413 | 99.7748 | 59.2762 | 73107 | 857 | 73104 | 165 | 38 | 23.0303 | |
ltrigg-rtg1 | SNP | * | map_l100_m2_e1 | * | 99.3071 | 98.8520 | 99.7664 | 59.3097 | 73879 | 858 | 73876 | 173 | 38 | 21.9653 | |
ltrigg-rtg1 | SNP | ti | map_siren | * | 99.5060 | 99.2556 | 99.7576 | 49.1435 | 99607 | 747 | 99601 | 242 | 38 | 15.7025 |