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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
25001-25050 / 86044 show all | |||||||||||||||
| hfeng-pmm2 | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 98.7467 | 97.8979 | 99.6103 | 71.3232 | 1304 | 28 | 1278 | 5 | 4 | 80.0000 | |
| hfeng-pmm2 | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | * | 97.9545 | 96.0747 | 99.9093 | 57.3738 | 5507 | 225 | 5507 | 5 | 4 | 80.0000 | |
| hfeng-pmm2 | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 99.5579 | 99.8227 | 99.2945 | 71.7629 | 563 | 1 | 563 | 4 | 4 | 100.0000 | |
| hfeng-pmm2 | INDEL | I1_5 | map_l100_m1_e0 | * | 98.8805 | 98.8051 | 98.9560 | 83.1786 | 1323 | 16 | 1327 | 14 | 4 | 28.5714 | |
| hfeng-pmm2 | INDEL | I1_5 | map_l100_m1_e0 | homalt | 99.5197 | 100.0000 | 99.0440 | 79.1965 | 518 | 0 | 518 | 5 | 4 | 80.0000 | |
| hfeng-pmm2 | INDEL | I1_5 | map_l100_m2_e0 | * | 98.9042 | 98.8304 | 98.9781 | 84.3732 | 1352 | 16 | 1356 | 14 | 4 | 28.5714 | |
| hfeng-pmm2 | INDEL | I1_5 | map_l100_m2_e0 | homalt | 99.5314 | 100.0000 | 99.0672 | 80.7125 | 531 | 0 | 531 | 5 | 4 | 80.0000 | |
| hfeng-pmm2 | INDEL | I1_5 | map_l100_m2_e1 | * | 98.9254 | 98.8530 | 98.9979 | 84.4605 | 1379 | 16 | 1383 | 14 | 4 | 28.5714 | |
| hfeng-pmm2 | INDEL | I1_5 | map_l100_m2_e1 | homalt | 99.5392 | 100.0000 | 99.0826 | 80.8099 | 540 | 0 | 540 | 5 | 4 | 80.0000 | |
| hfeng-pmm2 | INDEL | I1_5 | map_siren | * | 99.2171 | 99.0017 | 99.4335 | 80.3741 | 2975 | 30 | 2984 | 17 | 4 | 23.5294 | |
| hfeng-pmm2 | INDEL | I1_5 | map_siren | homalt | 99.6707 | 99.7525 | 99.5892 | 76.9508 | 1209 | 3 | 1212 | 5 | 4 | 80.0000 | |
| hfeng-pmm2 | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 98.0224 | 96.8202 | 99.2547 | 76.2357 | 1492 | 49 | 1465 | 11 | 4 | 36.3636 | |
| hfeng-pmm2 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 97.3714 | 96.1857 | 98.5866 | 71.6148 | 580 | 23 | 558 | 8 | 4 | 50.0000 | |
| hfeng-pmm2 | INDEL | I6_15 | map_siren | * | 96.6555 | 94.7541 | 98.6348 | 83.9364 | 289 | 16 | 289 | 4 | 4 | 100.0000 | |
| hfeng-pmm2 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.5017 | 97.6560 | 99.3622 | 69.3191 | 28039 | 673 | 28040 | 180 | 4 | 2.2222 | |
| hfeng-pmm2 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.5017 | 97.6560 | 99.3622 | 69.3191 | 28039 | 673 | 28040 | 180 | 4 | 2.2222 | |
| hfeng-pmm2 | SNP | * | lowcmp_SimpleRepeat_diTR_11to50 | het | 97.5045 | 95.2373 | 99.8823 | 66.3421 | 5939 | 297 | 5939 | 7 | 4 | 57.1429 | |
| ckim-isaac | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 84.6065 | 77.2727 | 93.4783 | 86.4507 | 85 | 25 | 86 | 6 | 4 | 66.6667 | |
| ckim-isaac | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 91.5095 | 84.7418 | 99.4521 | 75.3295 | 722 | 130 | 726 | 4 | 4 | 100.0000 | |
| ckim-isaac | SNP | * | lowcmp_SimpleRepeat_quadTR_51to200 | het | 65.6716 | 66.6667 | 64.7059 | 89.5246 | 68 | 34 | 77 | 42 | 4 | 9.5238 | |
| ckim-isaac | SNP | * | map_l150_m0_e0 | * | 69.2458 | 53.0336 | 99.7343 | 81.0939 | 6381 | 5651 | 6381 | 17 | 4 | 23.5294 | |
| ckim-isaac | SNP | * | map_l150_m1_e0 | homalt | 63.2096 | 46.2255 | 99.9233 | 66.9874 | 5211 | 6062 | 5211 | 4 | 4 | 100.0000 | |
| ckim-isaac | SNP | * | map_l150_m2_e0 | homalt | 63.7998 | 46.8587 | 99.9271 | 70.9027 | 5482 | 6217 | 5482 | 4 | 4 | 100.0000 | |
| ckim-isaac | SNP | * | map_l250_m2_e0 | * | 64.4492 | 47.6728 | 99.4444 | 90.9774 | 3759 | 4126 | 3759 | 21 | 4 | 19.0476 | |
| ckim-isaac | SNP | * | map_l250_m2_e1 | * | 64.5467 | 47.7776 | 99.4527 | 91.0189 | 3816 | 4171 | 3816 | 21 | 4 | 19.0476 | |
| ckim-isaac | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 83.0006 | 75.5556 | 92.0732 | 84.2949 | 544 | 176 | 604 | 52 | 4 | 7.6923 | |
| ckim-isaac | SNP | ti | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 95.9870 | 92.7725 | 99.4322 | 50.3135 | 1566 | 122 | 1576 | 9 | 4 | 44.4444 | |
| ckim-isaac | SNP | ti | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 97.8767 | 95.9619 | 99.8695 | 26.2226 | 3826 | 161 | 3827 | 5 | 4 | 80.0000 | |
| ckim-isaac | SNP | ti | lowcmp_SimpleRepeat_quadTR_51to200 | het | 66.2722 | 72.7273 | 60.8696 | 89.6513 | 48 | 18 | 56 | 36 | 4 | 11.1111 | |
| ckim-isaac | SNP | ti | map_l100_m1_e0 | het | 82.8228 | 70.7902 | 99.7835 | 65.4154 | 21196 | 8746 | 21200 | 46 | 4 | 8.6957 | |
| ckim-isaac | SNP | ti | map_l100_m2_e0 | het | 83.0715 | 71.1515 | 99.7894 | 67.1619 | 21788 | 8834 | 21792 | 46 | 4 | 8.6957 | |
| ckim-isaac | SNP | ti | map_l100_m2_e1 | het | 83.1462 | 71.2597 | 99.7920 | 67.1300 | 22062 | 8898 | 22066 | 46 | 4 | 8.6957 | |
| ckim-isaac | SNP | ti | map_l125_m0_e0 | * | 72.1772 | 56.5507 | 99.7374 | 74.7461 | 7217 | 5545 | 7217 | 19 | 4 | 21.0526 | |
| ckim-isaac | SNP | ti | map_l125_m2_e1 | homalt | 69.3119 | 53.0546 | 99.9342 | 64.5595 | 6079 | 5379 | 6079 | 4 | 4 | 100.0000 | |
| ckim-isaac | SNP | ti | map_l150_m2_e1 | homalt | 65.7188 | 48.9666 | 99.8939 | 70.0833 | 3767 | 3926 | 3767 | 4 | 4 | 100.0000 | |
| ckim-isaac | SNP | tv | segdup | * | 97.9382 | 96.0384 | 99.9147 | 88.7225 | 8194 | 338 | 8196 | 7 | 4 | 57.1429 | |
| ckim-vqsr | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 99.5993 | 99.5000 | 99.6988 | 76.7994 | 2985 | 15 | 2979 | 9 | 4 | 44.4444 | |
| ckim-vqsr | INDEL | * | lowcmp_SimpleRepeat_diTR_51to200 | hetalt | 87.5183 | 78.0351 | 99.6251 | 29.7101 | 977 | 275 | 1063 | 4 | 4 | 100.0000 | |
| ckim-vqsr | INDEL | * | lowcmp_SimpleRepeat_triTR_11to50 | homalt | 99.8839 | 99.9535 | 99.8144 | 47.5030 | 2151 | 1 | 2151 | 4 | 4 | 100.0000 | |
| ckim-vqsr | INDEL | * | lowcmp_SimpleRepeat_triTR_51to200 | * | 96.3583 | 95.9459 | 96.7742 | 64.4262 | 213 | 9 | 210 | 7 | 4 | 57.1429 | |
| ckim-vqsr | INDEL | * | map_l100_m0_e0 | homalt | 98.8235 | 99.0177 | 98.6301 | 85.4747 | 504 | 5 | 504 | 7 | 4 | 57.1429 | |
| ckim-vqsr | INDEL | * | map_l125_m0_e0 | * | 96.5169 | 97.3923 | 95.6570 | 93.0361 | 859 | 23 | 859 | 39 | 4 | 10.2564 | |
| ckim-vqsr | INDEL | * | map_l150_m1_e0 | het | 94.8598 | 94.8538 | 94.8658 | 94.1088 | 811 | 44 | 813 | 44 | 4 | 9.0909 | |
| ckim-vqsr | INDEL | * | map_l150_m2_e0 | het | 94.8645 | 94.7020 | 95.0276 | 94.4740 | 858 | 48 | 860 | 45 | 4 | 8.8889 | |
| ckim-vqsr | INDEL | * | map_l150_m2_e1 | het | 94.7936 | 94.4805 | 95.1087 | 94.5035 | 873 | 51 | 875 | 45 | 4 | 8.8889 | |
| ckim-vqsr | INDEL | D16_PLUS | HG002complexvar | homalt | 98.7952 | 99.3080 | 98.2877 | 76.3371 | 287 | 2 | 287 | 5 | 4 | 80.0000 | |
| ckim-vqsr | SNP | ti | map_l125_m1_e0 | * | 70.1902 | 54.3480 | 99.0678 | 87.5048 | 15943 | 13392 | 15941 | 150 | 4 | 2.6667 | |
| ckim-vqsr | SNP | ti | map_siren | homalt | 77.6182 | 63.4297 | 99.9834 | 60.5065 | 24050 | 13866 | 24044 | 4 | 4 | 100.0000 | |
| ckim-vqsr | SNP | ti | segdup | het | 98.9319 | 98.5619 | 99.3047 | 94.5420 | 11857 | 173 | 11855 | 83 | 4 | 4.8193 | |
| ckim-vqsr | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 99.1639 | 98.4142 | 99.9251 | 72.5328 | 5337 | 86 | 5337 | 4 | 4 | 100.0000 | |