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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
9651-9700 / 86044 show all | |||||||||||||||
| gduggal-snapfb | SNP | tv | map_l250_m1_e0 | het | 94.3085 | 95.9709 | 92.7027 | 86.6223 | 1715 | 72 | 1715 | 135 | 48 | 35.5556 | |
| gduggal-bwafb | SNP | * | map_l250_m1_e0 | het | 97.0310 | 96.9085 | 97.1537 | 89.8249 | 4608 | 147 | 4608 | 135 | 33 | 24.4444 | |
| eyeh-varpipe | INDEL | D6_15 | * | hetalt | 46.3037 | 30.5358 | 95.7427 | 56.1168 | 2496 | 5678 | 3036 | 135 | 128 | 94.8148 | |
| eyeh-varpipe | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 97.4672 | 95.4477 | 99.5740 | 49.7805 | 2537 | 121 | 31556 | 135 | 135 | 100.0000 | |
| gduggal-bwavard | INDEL | D1_5 | map_l125_m2_e0 | * | 92.6484 | 96.6754 | 88.9435 | 89.1467 | 1105 | 38 | 1086 | 135 | 19 | 14.0741 | |
| gduggal-bwavard | INDEL | D1_5 | map_l125_m2_e1 | het | 91.2581 | 98.8312 | 84.7630 | 90.8034 | 761 | 9 | 751 | 135 | 18 | 13.3333 | |
| gduggal-bwaplat | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 76.6225 | 63.6808 | 96.1659 | 75.3638 | 3384 | 1930 | 3386 | 135 | 45 | 33.3333 | |
| gduggal-bwaplat | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 91.1118 | 85.3688 | 97.6832 | 88.4817 | 5683 | 974 | 5692 | 135 | 24 | 17.7778 | |
| gduggal-bwaplat | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 69.0799 | 55.3552 | 91.8541 | 94.6607 | 1504 | 1213 | 1511 | 134 | 31 | 23.1343 | |
| gduggal-bwavard | INDEL | D1_5 | map_l125_m1_e0 | * | 92.4713 | 96.7831 | 88.5274 | 88.5445 | 1053 | 35 | 1034 | 134 | 19 | 14.1791 | |
| eyeh-varpipe | INDEL | I16_PLUS | lowcmp_SimpleRepeat_diTR_11to50 | het | 32.5233 | 24.3750 | 48.8550 | 47.4950 | 39 | 121 | 128 | 134 | 134 | 100.0000 | |
| mlin-fermikit | INDEL | I16_PLUS | HG002complexvar | * | 84.0504 | 79.8319 | 88.7395 | 68.1648 | 1045 | 264 | 1056 | 134 | 128 | 95.5224 | |
| mlin-fermikit | SNP | ti | map_l125_m1_e0 | het | 61.0167 | 44.2242 | 98.3680 | 59.8543 | 8078 | 10188 | 8077 | 134 | 7 | 5.2239 | |
| mlin-fermikit | INDEL | * | lowcmp_SimpleRepeat_homopolymer_6to10 | homalt | 98.7368 | 98.6632 | 98.8105 | 55.8582 | 11145 | 151 | 11131 | 134 | 133 | 99.2537 | |
| mlin-fermikit | INDEL | * | map_l150_m2_e1 | * | 65.1571 | 52.8145 | 85.0279 | 85.1378 | 760 | 679 | 761 | 134 | 106 | 79.1045 | |
| mlin-fermikit | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 82.2770 | 90.3226 | 75.5474 | 70.8511 | 476 | 51 | 414 | 134 | 133 | 99.2537 | |
| mlin-fermikit | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_51to200 | * | 68.8811 | 63.9610 | 74.6212 | 70.9571 | 394 | 222 | 394 | 134 | 130 | 97.0149 | |
| jli-custom | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 98.7391 | 98.3237 | 99.1580 | 56.4704 | 15778 | 269 | 15780 | 134 | 125 | 93.2836 | |
| jpowers-varprowl | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 91.6782 | 96.9631 | 86.9396 | 76.4300 | 894 | 28 | 892 | 134 | 128 | 95.5224 | |
| ciseli-custom | INDEL | D1_5 | map_l100_m0_e0 | * | 77.3981 | 72.8853 | 82.5065 | 89.4982 | 629 | 234 | 632 | 134 | 63 | 47.0149 | |
| ciseli-custom | INDEL | I6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 45.3431 | 47.6852 | 43.2203 | 58.3774 | 103 | 113 | 102 | 134 | 129 | 96.2687 | |
| ckim-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 98.6391 | 99.8632 | 97.4447 | 51.1732 | 5110 | 7 | 5110 | 134 | 133 | 99.2537 | |
| ckim-dragen | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_51to200 | homalt | 70.6140 | 100.0000 | 54.5763 | 33.4086 | 161 | 0 | 161 | 134 | 134 | 100.0000 | |
| asubramanian-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 98.1287 | 97.8680 | 98.3908 | 64.4221 | 8217 | 179 | 8193 | 134 | 104 | 77.6119 | |
| bgallagher-sentieon | SNP | * | map_l250_m1_e0 | het | 97.9332 | 98.6540 | 97.2228 | 90.1965 | 4691 | 64 | 4691 | 134 | 24 | 17.9104 | |
| anovak-vg | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 45.1042 | 39.2655 | 52.9825 | 57.7778 | 139 | 215 | 151 | 134 | 99 | 73.8806 | |
| asubramanian-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.2216 | 97.3921 | 99.0654 | 77.9808 | 14191 | 380 | 14204 | 134 | 16 | 11.9403 | |
| asubramanian-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.2216 | 97.3921 | 99.0654 | 77.9808 | 14191 | 380 | 14204 | 134 | 16 | 11.9403 | |
| hfeng-pmm1 | SNP | * | map_l150_m2_e0 | * | 99.3518 | 99.1272 | 99.5773 | 75.1179 | 31574 | 278 | 31568 | 134 | 37 | 27.6119 | |
| hfeng-pmm1 | SNP | ti | map_siren | * | 99.7016 | 99.5376 | 99.8660 | 52.2018 | 99891 | 464 | 99878 | 134 | 42 | 31.3433 | |
| hfeng-pmm1 | INDEL | D1_5 | * | het | 99.5580 | 99.2715 | 99.8461 | 55.4481 | 86936 | 638 | 86940 | 134 | 51 | 38.0597 | |
| gduggal-snapfb | SNP | ti | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 97.7559 | 98.8212 | 96.7133 | 52.5820 | 3940 | 47 | 3943 | 134 | 24 | 17.9104 | |
| ghariani-varprowl | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 94.5086 | 98.3261 | 90.9764 | 72.8370 | 1351 | 23 | 1351 | 134 | 68 | 50.7463 | |
| gduggal-snapplat | SNP | ti | segdup | * | 99.0792 | 98.8483 | 99.3111 | 92.8755 | 19312 | 225 | 19317 | 134 | 17 | 12.6866 | |
| gduggal-snapplat | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_51to200 | * | 24.3587 | 15.4953 | 56.9132 | 61.6995 | 183 | 998 | 177 | 134 | 97 | 72.3881 | |
| gduggal-snapvard | SNP | tv | lowcmp_SimpleRepeat_triTR_11to50 | het | 95.2056 | 96.5856 | 93.8645 | 49.5961 | 2065 | 73 | 2050 | 134 | 7 | 5.2239 | |
| ckim-vqsr | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 99.0685 | 99.1132 | 99.0238 | 69.1438 | 13635 | 122 | 13593 | 134 | 112 | 83.5821 | |
| ckim-vqsr | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 98.6293 | 99.8437 | 97.4442 | 51.1779 | 5109 | 8 | 5109 | 134 | 133 | 99.2537 | |
| ckim-vqsr | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 99.0685 | 99.1132 | 99.0238 | 69.1438 | 13635 | 122 | 13593 | 134 | 112 | 83.5821 | |
| ckim-vqsr | INDEL | D6_15 | * | homalt | 98.8887 | 99.8735 | 97.9231 | 55.6564 | 6318 | 8 | 6318 | 134 | 131 | 97.7612 | |
| ckim-vqsr | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 98.1989 | 99.8938 | 96.5606 | 60.0492 | 3762 | 4 | 3762 | 134 | 131 | 97.7612 | |
| ckim-vqsr | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 98.1989 | 99.8938 | 96.5606 | 60.0492 | 3762 | 4 | 3762 | 134 | 131 | 97.7612 | |
| dgrover-gatk | SNP | * | HG002complexvar | het | 99.9434 | 99.9156 | 99.9712 | 18.5452 | 465104 | 393 | 464974 | 134 | 53 | 39.5522 | |
| dgrover-gatk | SNP | ti | map_l150_m1_e0 | het | 99.0308 | 99.1431 | 98.9188 | 80.0370 | 12264 | 106 | 12260 | 134 | 29 | 21.6418 | |
| eyeh-varpipe | INDEL | C1_5 | HG002complexvar | * | 90.0749 | 85.7143 | 94.9030 | 78.7246 | 6 | 1 | 2495 | 134 | 108 | 80.5970 | |
| ckim-vqsr | INDEL | * | lowcmp_SimpleRepeat_diTR_51to200 | het | 78.0651 | 92.4490 | 67.5545 | 80.7459 | 453 | 37 | 279 | 134 | 129 | 96.2687 | |
| raldana-dualsentieon | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.5826 | 97.8702 | 99.3056 | 66.7018 | 19162 | 417 | 19162 | 134 | 6 | 4.4776 | |
| raldana-dualsentieon | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.5826 | 97.8702 | 99.3056 | 66.7018 | 19162 | 417 | 19162 | 134 | 6 | 4.4776 | |
| raldana-dualsentieon | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 99.6721 | 99.9543 | 99.3915 | 75.2467 | 21889 | 10 | 21889 | 134 | 133 | 99.2537 | |
| rpoplin-dv42 | SNP | * | HG002complexvar | het | 99.8978 | 99.8245 | 99.9712 | 18.3215 | 464680 | 817 | 464534 | 134 | 101 | 75.3731 | |