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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
75251-75300 / 86044 show all | |||||||||||||||
| ghariani-varprowl | SNP | ti | map_l250_m2_e0 | * | 96.2305 | 97.3642 | 95.1229 | 91.2925 | 4876 | 132 | 4876 | 250 | 52 | 20.8000 | |
| mlin-fermikit | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 82.8097 | 70.7958 | 99.7345 | 26.8052 | 4875 | 2011 | 4883 | 13 | 13 | 100.0000 | |
| jli-custom | SNP | ti | map_l250_m2_e0 | * | 98.3980 | 97.5040 | 99.3085 | 86.8596 | 4883 | 125 | 4883 | 34 | 18 | 52.9412 | |
| jpowers-varprowl | SNP | * | map_l250_m2_e0 | het | 93.5184 | 94.0316 | 93.0109 | 92.2727 | 4884 | 310 | 4884 | 367 | 88 | 23.9782 | |
| ciseli-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 47.2088 | 43.9090 | 51.0447 | 54.2294 | 4866 | 6216 | 4886 | 4686 | 4047 | 86.3636 | |
| ckim-isaac | SNP | tv | map_l100_m2_e0 | homalt | 69.2951 | 53.0280 | 99.9591 | 61.2002 | 4886 | 4328 | 4886 | 2 | 2 | 100.0000 | |
| qzeng-custom | INDEL | D16_PLUS | * | het | 80.5778 | 97.4992 | 68.6613 | 61.3602 | 3080 | 79 | 4888 | 2231 | 308 | 13.8055 | |
| egarrison-hhga | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 94.4732 | 91.9834 | 97.1014 | 61.6929 | 4888 | 426 | 4891 | 146 | 111 | 76.0274 | |
| rpoplin-dv42 | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 95.1465 | 92.0399 | 98.4702 | 62.7698 | 4891 | 423 | 4892 | 76 | 70 | 92.1053 | |
| gduggal-bwafb | SNP | ti | map_l250_m2_e0 | * | 98.0365 | 97.7037 | 98.3715 | 89.9163 | 4893 | 115 | 4893 | 81 | 24 | 29.6296 | |
| gduggal-snapvard | INDEL | D6_15 | HG002compoundhet | het | 67.0812 | 63.3178 | 71.3203 | 33.1905 | 542 | 314 | 4894 | 1968 | 1718 | 87.2967 | |
| gduggal-snapvard | INDEL | D6_15 | HG002compoundhet | * | 59.7955 | 51.4782 | 71.3183 | 33.2912 | 4649 | 4382 | 4896 | 1969 | 1719 | 87.3032 | |
| gduggal-bwavard | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 95.4306 | 91.4992 | 99.7150 | 67.7457 | 4962 | 461 | 4898 | 14 | 5 | 35.7143 | |
| gduggal-bwavard | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 95.4306 | 91.4992 | 99.7150 | 67.7457 | 4962 | 461 | 4898 | 14 | 5 | 35.7143 | |
| mlin-fermikit | INDEL | I6_15 | HG002compoundhet | * | 62.8773 | 55.7315 | 72.1249 | 36.3543 | 4891 | 3885 | 4898 | 1893 | 1888 | 99.7359 | |
| ckim-dragen | SNP | ti | map_l250_m2_e0 | * | 97.3484 | 97.8435 | 96.8583 | 89.6841 | 4900 | 108 | 4902 | 159 | 19 | 11.9497 | |
| ndellapenna-hhga | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 94.3185 | 92.1152 | 96.6299 | 62.4649 | 4895 | 419 | 4903 | 171 | 122 | 71.3450 | |
| anovak-vg | SNP | tv | map_l125_m2_e1 | homalt | 89.1235 | 80.9516 | 99.1306 | 69.1627 | 4917 | 1157 | 4903 | 43 | 32 | 74.4186 | |
| gduggal-bwafb | INDEL | D6_15 | HG002complexvar | * | 93.2387 | 90.0604 | 96.6496 | 53.7803 | 4775 | 527 | 4904 | 170 | 143 | 84.1176 | |
| egarrison-hhga | SNP | ti | map_l250_m2_e0 | * | 98.8124 | 98.0232 | 99.6144 | 88.6331 | 4909 | 99 | 4909 | 19 | 9 | 47.3684 | |
| jlack-gatk | SNP | ti | map_l250_m2_e0 | * | 94.3425 | 98.0631 | 90.8939 | 92.7804 | 4911 | 97 | 4911 | 492 | 44 | 8.9431 | |
| ciseli-custom | SNP | tv | map_l100_m0_e0 | het | 74.3908 | 68.0559 | 82.0260 | 79.9973 | 4915 | 2307 | 4915 | 1077 | 42 | 3.8997 | |
| rpoplin-dv42 | SNP | ti | map_l250_m2_e0 | * | 98.5577 | 98.2428 | 98.8746 | 88.2672 | 4920 | 88 | 4920 | 56 | 37 | 66.0714 | |
| ndellapenna-hhga | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 96.6400 | 96.0539 | 97.2332 | 85.1791 | 4917 | 202 | 4920 | 140 | 101 | 72.1429 | |
| mlin-fermikit | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 79.2227 | 71.1825 | 89.3103 | 43.3419 | 4918 | 1991 | 4921 | 589 | 580 | 98.4720 | |
| gduggal-bwavard | SNP | ti | map_l250_m2_e1 | * | 91.4742 | 97.4586 | 86.1821 | 92.2577 | 4947 | 129 | 4921 | 789 | 28 | 3.5488 | |
| eyeh-varpipe | SNP | ti | map_l250_m2_e0 | * | 99.0376 | 99.4409 | 98.6375 | 90.5192 | 4980 | 28 | 4923 | 68 | 6 | 8.8235 | |
| jmaeng-gatk | SNP | * | map_l150_m0_e0 | het | 75.3760 | 62.0529 | 95.9844 | 93.8640 | 4927 | 3013 | 4924 | 206 | 21 | 10.1942 | |
| ndellapenna-hhga | SNP | ti | map_l250_m2_e1 | * | 98.3031 | 97.0055 | 99.6358 | 87.9552 | 4924 | 152 | 4924 | 18 | 9 | 50.0000 | |
| eyeh-varpipe | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 48.9376 | 37.8496 | 69.2135 | 34.1472 | 1475 | 2422 | 4928 | 2192 | 2178 | 99.3613 | |
| ckim-gatk | SNP | * | map_l150_m0_e0 | het | 75.5141 | 62.1285 | 96.2515 | 93.6797 | 4933 | 3007 | 4930 | 192 | 25 | 13.0208 | |
| raldana-dualsentieon | SNP | ti | map_l250_m2_e0 | * | 98.2170 | 98.4425 | 97.9924 | 88.3517 | 4930 | 78 | 4930 | 101 | 3 | 2.9703 | |
| ckim-isaac | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 89.7782 | 82.5984 | 98.3250 | 32.1288 | 4870 | 1026 | 4931 | 84 | 71 | 84.5238 | |
| ckim-isaac | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 89.7782 | 82.5984 | 98.3250 | 32.1288 | 4870 | 1026 | 4931 | 84 | 71 | 84.5238 | |
| gduggal-bwavard | SNP | ti | map_l150_m0_e0 | het | 90.2624 | 97.3906 | 84.1064 | 88.1487 | 4964 | 133 | 4932 | 932 | 44 | 4.7210 | |
| ndellapenna-hhga | SNP | ti | map_l150_m0_e0 | het | 98.1786 | 96.7628 | 99.6364 | 79.7339 | 4932 | 165 | 4932 | 18 | 7 | 38.8889 | |
| dgrover-gatk | SNP | ti | map_l250_m2_e0 | * | 98.6206 | 98.5024 | 98.7390 | 90.3671 | 4933 | 75 | 4933 | 63 | 18 | 28.5714 | |
| ckim-isaac | SNP | tv | map_l100_m2_e1 | homalt | 69.3075 | 53.0424 | 99.9595 | 61.1858 | 4934 | 4368 | 4934 | 2 | 2 | 100.0000 | |
| mlin-fermikit | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 91.9346 | 96.5800 | 87.7156 | 44.0577 | 4942 | 175 | 4934 | 691 | 677 | 97.9740 | |
| asubramanian-gatk | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 95.8269 | 92.5398 | 99.3561 | 30.5284 | 4416 | 356 | 4938 | 32 | 31 | 96.8750 | |
| ghariani-varprowl | SNP | ti | map_l250_m2_e1 | * | 96.1939 | 97.3404 | 95.0741 | 91.3522 | 4941 | 135 | 4941 | 256 | 54 | 21.0938 | |
| ltrigg-rtg1 | SNP | * | map_l250_m2_e1 | het | 96.6928 | 93.8640 | 99.6973 | 80.4597 | 4941 | 323 | 4941 | 15 | 4 | 26.6667 | |
| egarrison-hhga | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 97.0535 | 96.5032 | 97.6101 | 85.2011 | 4940 | 179 | 4942 | 121 | 84 | 69.4215 | |
| eyeh-varpipe | INDEL | * | map_l100_m2_e0 | * | 94.5816 | 93.6637 | 95.5178 | 92.5332 | 3459 | 234 | 4944 | 232 | 182 | 78.4483 | |
| ckim-isaac | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 95.2859 | 91.1304 | 99.8384 | 63.0944 | 4942 | 481 | 4944 | 8 | 5 | 62.5000 | |
| ckim-isaac | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 95.2859 | 91.1304 | 99.8384 | 63.0944 | 4942 | 481 | 4944 | 8 | 5 | 62.5000 | |
| mlin-fermikit | SNP | tv | map_l150_m2_e0 | * | 57.2030 | 43.5755 | 83.2323 | 66.6536 | 4948 | 6407 | 4944 | 996 | 869 | 87.2490 | |
| jli-custom | SNP | ti | map_l250_m2_e1 | * | 98.3796 | 97.4783 | 99.2976 | 86.9545 | 4948 | 128 | 4948 | 35 | 18 | 51.4286 | |
| ltrigg-rtg1 | INDEL | D6_15 | HG002complexvar | * | 97.6527 | 96.5862 | 98.7430 | 52.4974 | 5121 | 181 | 4949 | 63 | 48 | 76.1905 | |
| jpowers-varprowl | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 57.3405 | 87.8864 | 42.5514 | 59.2810 | 4919 | 678 | 4950 | 6683 | 6644 | 99.4164 | |