PrecisionFDA
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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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
18901-18950 / 86044 show all | |||||||||||||||
| dgrover-gatk | INDEL | * | map_l100_m0_e0 | homalt | 98.1391 | 98.4283 | 97.8516 | 85.3798 | 501 | 8 | 501 | 11 | 5 | 45.4545 | |
| gduggal-bwafb | SNP | tv | map_l150_m2_e0 | het | 97.9956 | 98.4280 | 97.5670 | 79.8007 | 7138 | 114 | 7138 | 178 | 33 | 18.5393 | |
| ciseli-custom | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 89.6962 | 98.4278 | 82.3875 | 81.4243 | 2379 | 38 | 2381 | 509 | 127 | 24.9509 | |
| dgrover-gatk | INDEL | D1_5 | map_l150_m2_e0 | * | 98.3008 | 98.4273 | 98.1747 | 90.2973 | 751 | 12 | 753 | 14 | 3 | 21.4286 | |
| jli-custom | INDEL | D1_5 | map_l150_m2_e0 | * | 98.4283 | 98.4273 | 98.4293 | 88.4102 | 751 | 12 | 752 | 12 | 4 | 33.3333 | |
| raldana-dualsentieon | INDEL | * | map_l125_m2_e0 | homalt | 98.6859 | 98.4273 | 98.9460 | 85.1526 | 751 | 12 | 751 | 8 | 3 | 37.5000 | |
| qzeng-custom | INDEL | * | func_cds | * | 95.4248 | 98.4270 | 92.6004 | 43.9573 | 438 | 7 | 438 | 35 | 4 | 11.4286 | |
| mlin-fermikit | INDEL | * | func_cds | * | 98.6486 | 98.4270 | 98.8713 | 35.8900 | 438 | 7 | 438 | 5 | 3 | 60.0000 | |
| rpoplin-dv42 | INDEL | * | func_cds | * | 98.8729 | 98.4270 | 99.3228 | 93.2232 | 438 | 7 | 440 | 3 | 3 | 100.0000 | |
| gduggal-bwavard | INDEL | * | map_l125_m1_e0 | het | 90.3770 | 98.4270 | 83.5443 | 91.2553 | 1314 | 21 | 1320 | 260 | 67 | 25.7692 | |
| hfeng-pmm3 | INDEL | * | map_l125_m2_e1 | * | 98.5832 | 98.4270 | 98.7399 | 86.2184 | 2190 | 35 | 2194 | 28 | 6 | 21.4286 | |
| asubramanian-gatk | INDEL | * | func_cds | * | 98.8729 | 98.4270 | 99.3228 | 86.9360 | 438 | 7 | 440 | 3 | 1 | 33.3333 | |
| bgallagher-sentieon | INDEL | * | map_l125_m1_e0 | het | 97.9174 | 98.4270 | 97.4132 | 88.3493 | 1314 | 21 | 1318 | 35 | 5 | 14.2857 | |
| ghariani-varprowl | SNP | ti | map_l125_m0_e0 | het | 96.8041 | 98.4267 | 95.2342 | 81.7798 | 8133 | 130 | 8133 | 407 | 98 | 24.0786 | |
| gduggal-bwafb | SNP | * | map_l125_m0_e0 | * | 98.4673 | 98.4266 | 98.5079 | 76.7395 | 19080 | 305 | 19080 | 289 | 76 | 26.2976 | |
| ndellapenna-hhga | SNP | * | map_l100_m2_e1 | het | 99.0834 | 98.4264 | 99.7493 | 64.4229 | 46160 | 738 | 46162 | 116 | 41 | 35.3448 | |
| ltrigg-rtg2 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.6532 | 98.4263 | 98.8811 | 62.2592 | 5754 | 92 | 5656 | 64 | 24 | 37.5000 | |
| ltrigg-rtg2 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.6532 | 98.4263 | 98.8811 | 62.2592 | 5754 | 92 | 5656 | 64 | 24 | 37.5000 | |
| ltrigg-rtg1 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 98.0299 | 98.4252 | 97.6378 | 70.6019 | 125 | 2 | 124 | 3 | 0 | 0.0000 | |
| bgallagher-sentieon | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_51to200 | homalt | 92.9368 | 98.4252 | 88.0282 | 53.4426 | 125 | 2 | 125 | 17 | 16 | 94.1176 | |
| dgrover-gatk | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_51to200 | homalt | 94.3396 | 98.4252 | 90.5797 | 53.8462 | 125 | 2 | 125 | 13 | 12 | 92.3077 | |
| egarrison-hhga | INDEL | D1_5 | map_l125_m2_e0 | * | 98.4252 | 98.4252 | 98.4252 | 86.5939 | 1125 | 18 | 1125 | 18 | 5 | 27.7778 | |
| rpoplin-dv42 | INDEL | D1_5 | map_l125_m2_e0 | * | 98.3836 | 98.4252 | 98.3421 | 86.5303 | 1125 | 18 | 1127 | 19 | 8 | 42.1053 | |
| mlin-fermikit | SNP | * | HG002complexvar | homalt | 98.3225 | 98.4247 | 98.2205 | 20.7847 | 284029 | 4546 | 284043 | 5146 | 4990 | 96.9685 | |
| raldana-dualsentieon | SNP | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 99.0144 | 98.4246 | 99.6113 | 60.1683 | 34861 | 558 | 34851 | 136 | 14 | 10.2941 | |
| rpoplin-dv42 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 98.3066 | 98.4234 | 98.1900 | 73.3092 | 437 | 7 | 434 | 8 | 4 | 50.0000 | |
| qzeng-custom | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 97.7758 | 98.4234 | 97.1366 | 86.2132 | 437 | 7 | 441 | 13 | 9 | 69.2308 | |
| raldana-dualsentieon | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 98.9787 | 98.4234 | 99.5402 | 73.1978 | 437 | 7 | 433 | 2 | 0 | 0.0000 | |
| qzeng-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 76.8774 | 98.4234 | 63.0705 | 60.7279 | 437 | 7 | 456 | 267 | 5 | 1.8727 | |
| jli-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 99.2054 | 98.4234 | 100.0000 | 72.6469 | 437 | 7 | 433 | 0 | 0 | ||
| mlin-fermikit | SNP | * | HG002compoundhet | homalt | 92.6523 | 98.4233 | 87.5206 | 41.6338 | 10612 | 170 | 10618 | 1514 | 1310 | 86.5258 | |
| mlin-fermikit | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 85.0654 | 98.4227 | 74.9004 | 87.7501 | 936 | 15 | 940 | 315 | 251 | 79.6825 | |
| gduggal-bwavard | INDEL | I1_5 | map_l150_m2_e1 | het | 93.4841 | 98.4227 | 89.0173 | 93.4950 | 312 | 5 | 308 | 38 | 14 | 36.8421 | |
| hfeng-pmm2 | SNP | tv | map_l250_m2_e1 | * | 98.3213 | 98.4225 | 98.2204 | 89.7650 | 2870 | 46 | 2870 | 52 | 7 | 13.4615 | |
| hfeng-pmm1 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 99.2048 | 98.4221 | 100.0000 | 85.8880 | 499 | 8 | 499 | 0 | 0 | ||
| cchapple-custom | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 99.1030 | 98.4221 | 99.7934 | 73.4358 | 499 | 8 | 483 | 1 | 1 | 100.0000 | |
| jmaeng-gatk | INDEL | * | map_siren | * | 97.8625 | 98.4211 | 97.3103 | 85.3526 | 7293 | 117 | 7308 | 202 | 30 | 14.8515 | |
| dgrover-gatk | SNP | ti | map_l250_m2_e1 | homalt | 99.1191 | 98.4199 | 99.8283 | 86.6233 | 1744 | 28 | 1744 | 3 | 2 | 66.6667 | |
| ndellapenna-hhga | SNP | ti | map_l100_m2_e0 | het | 99.1023 | 98.4194 | 99.7947 | 64.2605 | 30138 | 484 | 30140 | 62 | 24 | 38.7097 | |
| ndellapenna-hhga | INDEL | I1_5 | map_l150_m1_e0 | * | 98.6139 | 98.4190 | 98.8095 | 88.8938 | 498 | 8 | 498 | 6 | 1 | 16.6667 | |
| egarrison-hhga | INDEL | I1_5 | map_l150_m1_e0 | * | 98.3218 | 98.4190 | 98.2249 | 89.3800 | 498 | 8 | 498 | 9 | 2 | 22.2222 | |
| hfeng-pmm3 | INDEL | I1_5 | map_l150_m1_e0 | * | 98.4221 | 98.4190 | 98.4252 | 87.6729 | 498 | 8 | 500 | 8 | 2 | 25.0000 | |
| bgallagher-sentieon | INDEL | I1_5 | map_l150_m1_e0 | * | 98.3253 | 98.4190 | 98.2318 | 89.1587 | 498 | 8 | 500 | 9 | 2 | 22.2222 | |
| ckim-gatk | INDEL | I1_5 | map_l150_m1_e0 | * | 96.8962 | 98.4190 | 95.4198 | 92.2035 | 498 | 8 | 500 | 24 | 3 | 12.5000 | |
| qzeng-custom | SNP | tv | HG002complexvar | * | 99.0948 | 98.4189 | 99.7800 | 23.2771 | 242263 | 3892 | 238613 | 526 | 243 | 46.1977 | |
| bgallagher-sentieon | INDEL | * | map_l125_m2_e0 | het | 97.9642 | 98.4184 | 97.5142 | 89.0844 | 1369 | 22 | 1373 | 35 | 5 | 14.2857 | |
| gduggal-bwavard | INDEL | * | map_l125_m2_e0 | het | 90.4577 | 98.4184 | 83.6884 | 91.8376 | 1369 | 22 | 1375 | 268 | 70 | 26.1194 | |
| ndellapenna-hhga | SNP | * | map_l100_m2_e0 | het | 99.0800 | 98.4181 | 99.7510 | 64.4052 | 45665 | 734 | 45667 | 114 | 41 | 35.9649 | |
| mlin-fermikit | SNP | ti | HG002compoundhet | homalt | 93.7665 | 98.4176 | 89.5352 | 35.5677 | 7277 | 117 | 7281 | 851 | 725 | 85.1939 | |
| asubramanian-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 92.4411 | 98.4169 | 87.1495 | 60.2600 | 373 | 6 | 373 | 55 | 54 | 98.1818 | |