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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
17701-17750 / 86044 show all | |||||||||||||||
| ndellapenna-hhga | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 99.2704 | 99.1149 | 99.4264 | 74.8452 | 5375 | 48 | 5373 | 31 | 27 | 87.0968 | |
| ndellapenna-hhga | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 99.2704 | 99.1149 | 99.4264 | 74.8452 | 5375 | 48 | 5373 | 31 | 27 | 87.0968 | |
| ndellapenna-hhga | SNP | tv | lowcmp_SimpleRepeat_diTR_11to50 | * | 98.8620 | 98.3731 | 99.3556 | 61.7355 | 4777 | 79 | 4780 | 31 | 21 | 67.7419 | |
| ndellapenna-hhga | SNP | tv | map_l150_m1_e0 | het | 98.5385 | 97.5525 | 99.5446 | 72.4747 | 6776 | 170 | 6776 | 31 | 13 | 41.9355 | |
| qzeng-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 98.5178 | 99.1870 | 97.8576 | 69.7090 | 1342 | 11 | 1416 | 31 | 10 | 32.2581 | |
| qzeng-custom | INDEL | * | map_l150_m0_e0 | het | 80.0048 | 71.5543 | 90.7186 | 97.0277 | 244 | 97 | 303 | 31 | 16 | 51.6129 | |
| qzeng-custom | INDEL | * | map_l250_m2_e1 | het | 76.6254 | 69.1943 | 85.8447 | 98.2768 | 146 | 65 | 188 | 31 | 16 | 51.6129 | |
| qzeng-custom | INDEL | I6_15 | lowcmp_SimpleRepeat_diTR_51to200 | * | 44.0143 | 35.8696 | 56.9444 | 58.6207 | 33 | 59 | 41 | 31 | 27 | 87.0968 | |
| qzeng-custom | INDEL | I6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | het | 87.2528 | 88.5714 | 85.9729 | 64.5833 | 31 | 4 | 190 | 31 | 20 | 64.5161 | |
| mlin-fermikit | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 97.9660 | 97.1407 | 98.8054 | 65.3168 | 2582 | 76 | 2564 | 31 | 30 | 96.7742 | |
| ndellapenna-hhga | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 82.7487 | 71.4392 | 98.3125 | 49.4079 | 1916 | 766 | 1806 | 31 | 20 | 64.5161 | |
| ndellapenna-hhga | INDEL | * | map_l100_m0_e0 | het | 97.0778 | 97.1596 | 96.9961 | 85.3472 | 992 | 29 | 1001 | 31 | 4 | 12.9032 | |
| ndellapenna-hhga | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | het | 93.0643 | 93.0175 | 93.1111 | 72.1190 | 373 | 28 | 419 | 31 | 26 | 83.8710 | |
| ndellapenna-hhga | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 63.3251 | 46.6890 | 98.3795 | 37.6873 | 2228 | 2544 | 1882 | 31 | 28 | 90.3226 | |
| ndellapenna-hhga | INDEL | D6_15 | lowcmp_SimpleRepeat_triTR_51to200 | * | 70.8955 | 66.9014 | 75.3968 | 42.7273 | 95 | 47 | 95 | 31 | 29 | 93.5484 | |
| ndellapenna-hhga | INDEL | I16_PLUS | HG002complexvar | het | 92.9757 | 90.9774 | 95.0637 | 67.1720 | 605 | 60 | 597 | 31 | 15 | 48.3871 | |
| ltrigg-rtg2 | SNP | ti | segdup | homalt | 99.7804 | 99.9734 | 99.5881 | 87.6176 | 7503 | 2 | 7496 | 31 | 31 | 100.0000 | |
| mlin-fermikit | INDEL | D16_PLUS | map_l100_m0_e0 | * | 45.7741 | 60.7143 | 36.7347 | 93.3243 | 17 | 11 | 18 | 31 | 4 | 12.9032 | |
| mlin-fermikit | INDEL | D16_PLUS | map_siren | het | 71.4286 | 76.9231 | 66.6667 | 92.1980 | 60 | 18 | 62 | 31 | 14 | 45.1613 | |
| qzeng-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 94.1085 | 98.8889 | 89.7690 | 62.4535 | 267 | 3 | 272 | 31 | 1 | 3.2258 | |
| qzeng-custom | INDEL | D16_PLUS | segdup | * | 76.3496 | 93.1034 | 64.7059 | 94.9525 | 54 | 4 | 55 | 30 | 6 | 20.0000 | |
| qzeng-custom | INDEL | D1_5 | map_l100_m0_e0 | * | 86.8238 | 79.0267 | 96.3280 | 91.0593 | 682 | 181 | 787 | 30 | 23 | 76.6667 | |
| qzeng-custom | INDEL | I16_PLUS | map_l100_m1_e0 | het | 54.2158 | 72.2222 | 43.3962 | 80.2974 | 13 | 5 | 23 | 30 | 0 | 0.0000 | |
| qzeng-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 99.3593 | 99.4891 | 99.2298 | 79.0524 | 3895 | 20 | 3865 | 30 | 20 | 66.6667 | |
| raldana-dualsentieon | INDEL | * | map_l100_m0_e0 | * | 97.7226 | 97.3768 | 98.0707 | 83.8643 | 1522 | 41 | 1525 | 30 | 4 | 13.3333 | |
| ltrigg-rtg2 | INDEL | D16_PLUS | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 93.0557 | 88.2519 | 98.4127 | 61.7176 | 1878 | 250 | 1860 | 30 | 25 | 83.3333 | |
| ltrigg-rtg2 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 96.0537 | 93.9527 | 98.2507 | 73.2824 | 1709 | 110 | 1685 | 30 | 15 | 50.0000 | |
| ltrigg-rtg2 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 95.5306 | 92.3053 | 98.9896 | 52.2438 | 2963 | 247 | 2939 | 30 | 30 | 100.0000 | |
| ltrigg-rtg2 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 96.0537 | 93.9527 | 98.2507 | 73.2824 | 1709 | 110 | 1685 | 30 | 15 | 50.0000 | |
| ltrigg-rtg2 | INDEL | D1_5 | map_siren | * | 98.7460 | 98.3565 | 99.1387 | 75.8494 | 3471 | 58 | 3453 | 30 | 4 | 13.3333 | |
| ltrigg-rtg2 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 99.0708 | 98.8304 | 99.3124 | 59.5757 | 4394 | 52 | 4333 | 30 | 22 | 73.3333 | |
| ltrigg-rtg2 | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 98.2976 | 98.3558 | 98.2394 | 68.7282 | 1675 | 28 | 1674 | 30 | 5 | 16.6667 | |
| qzeng-custom | INDEL | * | map_l250_m2_e0 | het | 76.6664 | 69.0476 | 86.1751 | 98.2597 | 145 | 65 | 187 | 30 | 16 | 53.3333 | |
| ltrigg-rtg2 | SNP | ti | HG002compoundhet | het | 99.3400 | 99.0005 | 99.6817 | 37.0509 | 9410 | 95 | 9396 | 30 | 8 | 26.6667 | |
| mlin-fermikit | INDEL | I1_5 | lowcmp_SimpleRepeat_triTR_11to50 | het | 94.4878 | 95.3191 | 93.6709 | 57.5649 | 448 | 22 | 444 | 30 | 29 | 96.6667 | |
| mlin-fermikit | INDEL | I6_15 | map_siren | * | 81.7172 | 75.7377 | 88.7218 | 80.5981 | 231 | 74 | 236 | 30 | 28 | 93.3333 | |
| mlin-fermikit | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | homalt | 98.5545 | 99.7340 | 97.4026 | 53.7630 | 1125 | 3 | 1125 | 30 | 23 | 76.6667 | |
| mlin-fermikit | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 98.5033 | 98.3901 | 98.6169 | 63.5523 | 2139 | 35 | 2139 | 30 | 19 | 63.3333 | |
| ndellapenna-hhga | INDEL | D6_15 | map_siren | het | 94.0545 | 97.8571 | 90.5363 | 84.7816 | 274 | 6 | 287 | 30 | 16 | 53.3333 | |
| ndellapenna-hhga | INDEL | I16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 86.1423 | 94.2623 | 79.3103 | 80.9461 | 115 | 7 | 115 | 30 | 20 | 66.6667 | |
| gduggal-snapplat | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | homalt | 37.9562 | 27.0833 | 63.4146 | 40.5797 | 52 | 140 | 52 | 30 | 24 | 80.0000 | |
| gduggal-snapvard | INDEL | C1_5 | segdup | * | 0.0000 | 0.0000 | 50.0000 | 98.9717 | 0 | 0 | 30 | 30 | 1 | 3.3333 | |
| gduggal-snapvard | INDEL | C1_5 | segdup | het | 0.0000 | 0.0000 | 40.0000 | 99.0381 | 0 | 0 | 20 | 30 | 1 | 3.3333 | |
| gduggal-snapvard | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | homalt | 79.0433 | 68.6813 | 93.0876 | 67.1461 | 375 | 171 | 404 | 30 | 28 | 93.3333 | |
| gduggal-snapfb | SNP | tv | map_l100_m0_e0 | homalt | 97.1883 | 95.2678 | 99.1879 | 78.6252 | 3664 | 182 | 3664 | 30 | 6 | 20.0000 | |
| ghariani-varprowl | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 98.8939 | 99.9277 | 97.8814 | 65.9861 | 1382 | 1 | 1386 | 30 | 18 | 60.0000 | |
| gduggal-snapvard | INDEL | D6_15 | map_l150_m2_e0 | het | 79.0507 | 91.3043 | 69.6970 | 89.1089 | 42 | 4 | 69 | 30 | 19 | 63.3333 | |
| gduggal-snapvard | INDEL | D6_15 | map_l150_m2_e1 | het | 79.3149 | 91.4894 | 70.0000 | 89.2473 | 43 | 4 | 70 | 30 | 19 | 63.3333 | |
| gduggal-snapvard | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 0.0000 | 0.0000 | 37.5000 | 63.6364 | 0 | 106 | 18 | 30 | 11 | 36.6667 | |
| gduggal-snapvard | INDEL | I6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | * | 20.7177 | 14.5161 | 36.1702 | 74.1758 | 27 | 159 | 17 | 30 | 17 | 56.6667 | |