PrecisionFDA
Truth Challenge
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Explore HG002 comparison results
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| Entry | Type | Subtype | Subset | Genotype | F-score | Recall | Precision | Frac_NA | Truth TP | Truth FN | Query TP | Query FP | FP gt | % FP ma | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
26051-26100 / 86044 show all | |||||||||||||||
| ltrigg-rtg1 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 97.1952 | 95.9411 | 98.4824 | 66.8225 | 1891 | 80 | 1817 | 28 | 10 | 35.7143 | |
| ltrigg-rtg1 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 97.1952 | 95.9411 | 98.4824 | 66.8225 | 1891 | 80 | 1817 | 28 | 10 | 35.7143 | |
| jli-custom | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 97.2142 | 96.8491 | 97.5820 | 71.1510 | 584 | 19 | 565 | 14 | 5 | 35.7143 | |
| hfeng-pmm3 | SNP | ti | map_l125_m0_e0 | homalt | 99.6659 | 99.6437 | 99.6881 | 69.8765 | 4475 | 16 | 4475 | 14 | 5 | 35.7143 | |
| jli-custom | INDEL | * | map_l100_m1_e0 | * | 98.4897 | 98.1595 | 98.8222 | 83.0077 | 3520 | 66 | 3524 | 42 | 15 | 35.7143 | |
| hfeng-pmm1 | SNP | ti | map_l125_m0_e0 | homalt | 99.6547 | 99.6215 | 99.6881 | 70.0040 | 4474 | 17 | 4474 | 14 | 5 | 35.7143 | |
| hfeng-pmm2 | SNP | tv | map_l100_m1_e0 | homalt | 99.8507 | 99.8562 | 99.8452 | 62.5538 | 9030 | 13 | 9030 | 14 | 5 | 35.7143 | |
| hfeng-pmm2 | SNP | tv | map_l100_m2_e0 | homalt | 99.8535 | 99.8589 | 99.8481 | 64.9206 | 9201 | 13 | 9201 | 14 | 5 | 35.7143 | |
| hfeng-pmm2 | SNP | tv | map_l100_m2_e1 | homalt | 99.8549 | 99.8602 | 99.8495 | 64.9261 | 9289 | 13 | 9289 | 14 | 5 | 35.7143 | |
| hfeng-pmm2 | SNP | tv | map_l125_m1_e0 | homalt | 99.7782 | 99.7952 | 99.7612 | 67.4839 | 5848 | 12 | 5848 | 14 | 5 | 35.7143 | |
| hfeng-pmm2 | SNP | tv | map_l125_m2_e0 | homalt | 99.7840 | 99.8006 | 99.7674 | 69.8673 | 6005 | 12 | 6005 | 14 | 5 | 35.7143 | |
| hfeng-pmm2 | SNP | tv | map_l125_m2_e1 | homalt | 99.7860 | 99.8024 | 99.7696 | 69.9104 | 6062 | 12 | 6062 | 14 | 5 | 35.7143 | |
| cchapple-custom | INDEL | C6_15 | HG002compoundhet | * | 0.0000 | 0.0000 | 88.1356 | 86.5143 | 0 | 0 | 104 | 14 | 5 | 35.7143 | |
| cchapple-custom | INDEL | C6_15 | HG002compoundhet | het | 0.0000 | 0.0000 | 88.0342 | 86.0382 | 0 | 0 | 103 | 14 | 5 | 35.7143 | |
| cchapple-custom | INDEL | C6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 0.0000 | 0.0000 | 84.2697 | 96.2668 | 0 | 0 | 75 | 14 | 5 | 35.7143 | |
| cchapple-custom | INDEL | C6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 0.0000 | 0.0000 | 78.4615 | 96.6234 | 0 | 0 | 51 | 14 | 5 | 35.7143 | |
| ckim-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 97.4013 | 96.9970 | 97.8091 | 88.3245 | 646 | 20 | 625 | 14 | 5 | 35.7143 | |
| ckim-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 97.4013 | 96.9970 | 97.8091 | 88.3245 | 646 | 20 | 625 | 14 | 5 | 35.7143 | |
| rpoplin-dv42 | INDEL | * | map_l150_m1_e0 | het | 97.5275 | 96.7251 | 98.3432 | 88.8109 | 827 | 28 | 831 | 14 | 5 | 35.7143 | |
| rpoplin-dv42 | INDEL | * | map_l150_m2_e0 | het | 97.6106 | 96.7991 | 98.4358 | 89.4308 | 877 | 29 | 881 | 14 | 5 | 35.7143 | |
| ndellapenna-hhga | SNP | * | map_l250_m0_e0 | het | 96.7742 | 94.6215 | 99.0271 | 92.2359 | 1425 | 81 | 1425 | 14 | 5 | 35.7143 | |
| ndellapenna-hhga | INDEL | * | map_l125_m1_e0 | * | 97.7659 | 97.5320 | 98.0010 | 98.2503 | 2055 | 52 | 2059 | 42 | 15 | 35.7143 | |
| ndellapenna-hhga | INDEL | * | map_l125_m2_e0 | * | 97.8100 | 97.5410 | 98.0804 | 98.3346 | 2142 | 54 | 2146 | 42 | 15 | 35.7143 | |
| ndellapenna-hhga | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 98.9147 | 98.8772 | 98.9521 | 56.9032 | 1321 | 15 | 1322 | 14 | 5 | 35.7143 | |
| qzeng-custom | INDEL | * | map_l125_m1_e0 | homalt | 83.3361 | 73.4973 | 96.2162 | 85.8482 | 538 | 194 | 712 | 28 | 10 | 35.7143 | |
| ghariani-varprowl | INDEL | * | map_l100_m0_e0 | homalt | 94.7686 | 92.5344 | 97.1134 | 82.2993 | 471 | 38 | 471 | 14 | 5 | 35.7143 | |
| ghariani-varprowl | INDEL | * | map_l125_m2_e0 | homalt | 95.6347 | 93.3159 | 98.0716 | 83.8343 | 712 | 51 | 712 | 14 | 5 | 35.7143 | |
| ghariani-varprowl | INDEL | * | map_l125_m2_e1 | homalt | 95.5600 | 93.1525 | 98.0952 | 83.9590 | 721 | 53 | 721 | 14 | 5 | 35.7143 | |
| gduggal-snapplat | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | homalt | 70.0566 | 57.5000 | 89.6296 | 82.8897 | 115 | 85 | 121 | 14 | 5 | 35.7143 | |
| ghariani-varprowl | INDEL | I1_5 | map_siren | homalt | 95.6739 | 94.8845 | 96.4765 | 70.7843 | 1150 | 62 | 1150 | 42 | 15 | 35.7143 | |
| gduggal-snapfb | SNP | ti | HG002compoundhet | homalt | 96.6035 | 99.0803 | 94.2476 | 38.7254 | 7326 | 68 | 7340 | 448 | 160 | 35.7143 | |
| gduggal-snapvard | INDEL | C1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 0.0000 | 0.0000 | 70.8333 | 94.2446 | 0 | 0 | 34 | 14 | 5 | 35.7143 | |
| 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 | |
| gduggal-bwaplat | SNP | ti | map_l150_m2_e0 | * | 70.0796 | 54.1244 | 99.3737 | 90.4802 | 11102 | 9410 | 11106 | 70 | 25 | 35.7143 | |
| gduggal-bwaplat | SNP | ti | map_l150_m2_e1 | * | 70.2141 | 54.2827 | 99.3818 | 90.4903 | 11249 | 9474 | 11253 | 70 | 25 | 35.7143 | |
| gduggal-bwaplat | SNP | tv | map_l125_m0_e0 | * | 61.5481 | 44.5483 | 99.5283 | 92.9610 | 2954 | 3677 | 2954 | 14 | 5 | 35.7143 | |
| gduggal-bwaplat | SNP | tv | map_l125_m0_e0 | het | 64.9641 | 48.2618 | 99.3452 | 94.0434 | 2124 | 2277 | 2124 | 14 | 5 | 35.7143 | |
| gduggal-bwavard | INDEL | C16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 0.0000 | 0.0000 | 33.3333 | 96.7593 | 0 | 0 | 7 | 14 | 5 | 35.7143 | |
| gduggal-bwaplat | INDEL | D1_5 | map_l100_m2_e0 | het | 84.9116 | 74.6019 | 98.5279 | 92.8459 | 937 | 319 | 937 | 14 | 5 | 35.7143 | |
| gduggal-bwaplat | INDEL | D1_5 | map_l100_m2_e1 | het | 84.9192 | 74.6057 | 98.5417 | 92.9073 | 946 | 322 | 946 | 14 | 5 | 35.7143 | |
| gduggal-bwavard | INDEL | I16_PLUS | lowcmp_SimpleRepeat_triTR_11to50 | het | 66.6667 | 93.7500 | 51.7241 | 86.8778 | 15 | 1 | 15 | 14 | 5 | 35.7143 | |
| anovak-vg | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | homalt | 70.4500 | 58.7209 | 88.0342 | 68.5484 | 101 | 71 | 103 | 14 | 5 | 35.7143 | |
| anovak-vg | SNP | * | lowcmp_SimpleRepeat_quadTR_51to200 | * | 62.2688 | 72.0280 | 54.8387 | 90.2559 | 103 | 40 | 119 | 98 | 35 | 35.7143 | |
| asubramanian-gatk | SNP | ti | map_l125_m1_e0 | * | 47.1088 | 30.8267 | 99.8454 | 90.8763 | 9043 | 20292 | 9041 | 14 | 5 | 35.7143 | |
| asubramanian-gatk | SNP | ti | map_l125_m1_e0 | het | 50.2744 | 33.6034 | 99.7724 | 92.0217 | 6138 | 12128 | 6136 | 14 | 5 | 35.7143 | |
| asubramanian-gatk | INDEL | * | segdup | * | 98.4487 | 98.0047 | 98.8968 | 98.3850 | 2505 | 51 | 2510 | 28 | 10 | 35.7143 | |
| egarrison-hhga | SNP | tv | map_l150_m0_e0 | het | 98.6520 | 97.8192 | 99.4991 | 79.4500 | 2781 | 62 | 2781 | 14 | 5 | 35.7143 | |
| eyeh-varpipe | INDEL | C1_5 | map_siren | * | 0.0000 | 0.0000 | 88.0342 | 95.2993 | 0 | 0 | 103 | 14 | 5 | 35.7143 | |
| egarrison-hhga | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 98.3381 | 97.7256 | 98.9583 | 75.2486 | 1332 | 31 | 1330 | 14 | 5 | 35.7143 | |