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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
4801-4850 / 86044 show all | |||||||||||||||
| ltrigg-rtg1 | SNP | * | map_siren | * | 99.4858 | 99.2395 | 99.7333 | 50.0979 | 145115 | 1112 | 145108 | 388 | 49 | 12.6289 | |
| ckim-isaac | INDEL | * | map_l100_m2_e0 | * | 81.7339 | 69.9161 | 98.3594 | 84.3176 | 2582 | 1111 | 2578 | 43 | 21 | 48.8372 | |
| ckim-isaac | INDEL | I16_PLUS | HG002compoundhet | * | 61.2497 | 48.1568 | 84.1205 | 44.7593 | 1032 | 1111 | 1033 | 195 | 178 | 91.2821 | |
| jpowers-varprowl | SNP | ti | map_l100_m2_e1 | * | 98.2264 | 97.7569 | 98.7004 | 70.3802 | 48375 | 1110 | 48377 | 637 | 193 | 30.2983 | |
| gduggal-bwaplat | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 87.6933 | 79.6065 | 97.6088 | 41.6096 | 4329 | 1109 | 4327 | 106 | 105 | 99.0566 | |
| ltrigg-rtg2 | SNP | * | map_siren | het | 99.2163 | 98.7812 | 99.6552 | 46.0328 | 89881 | 1109 | 89887 | 311 | 15 | 4.8232 | |
| hfeng-pmm2 | SNP | * | HG002compoundhet | * | 97.7436 | 95.7052 | 99.8707 | 39.1925 | 24713 | 1109 | 24713 | 32 | 14 | 43.7500 | |
| mlin-fermikit | SNP | ti | HG002compoundhet | het | 93.4304 | 88.3535 | 99.1262 | 38.1960 | 8398 | 1107 | 8395 | 74 | 14 | 18.9189 | |
| eyeh-varpipe | SNP | * | * | * | 99.4670 | 99.9638 | 98.9751 | 20.3427 | 3053527 | 1107 | 2999712 | 31063 | 471 | 1.5163 | |
| gduggal-snapplat | INDEL | D16_PLUS | HG002complexvar | het | 0.0000 | 0.0000 | 0.0000 | 0 | 1107 | 0 | 0 | 0 | |||
| gduggal-snapvard | SNP | ti | map_l125_m1_e0 | * | 93.7547 | 96.2264 | 91.4068 | 77.7724 | 28228 | 1107 | 27965 | 2629 | 225 | 8.5584 | |
| ghariani-varprowl | SNP | tv | HG002complexvar | * | 98.9457 | 99.5507 | 98.3479 | 26.3760 | 245046 | 1106 | 245266 | 4120 | 790 | 19.1748 | |
| gduggal-bwaplat | SNP | ti | map_l250_m1_e0 | homalt | 47.5332 | 31.1761 | 100.0000 | 95.0135 | 501 | 1106 | 500 | 0 | 0 | ||
| asubramanian-gatk | SNP | ti | map_l250_m0_e0 | * | 32.2936 | 19.2701 | 99.6226 | 98.9715 | 264 | 1106 | 264 | 1 | 1 | 100.0000 | |
| gduggal-bwaplat | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 86.9148 | 78.4053 | 97.4964 | 52.0513 | 4012 | 1105 | 4011 | 103 | 89 | 86.4078 | |
| eyeh-varpipe | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | hetalt | 24.9746 | 14.4074 | 93.6975 | 63.9939 | 186 | 1105 | 223 | 15 | 14 | 93.3333 | |
| raldana-dualsentieon | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 97.7280 | 96.4818 | 99.0068 | 57.7386 | 30303 | 1105 | 30303 | 304 | 291 | 95.7237 | |
| raldana-dualsentieon | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 97.7280 | 96.4818 | 99.0068 | 57.7386 | 30303 | 1105 | 30303 | 304 | 291 | 95.7237 | |
| gduggal-snapfb | INDEL | D16_PLUS | HG002complexvar | het | 0.5405 | 0.2710 | 100.0000 | 0.0000 | 3 | 1104 | 1 | 0 | 0 | ||
| hfeng-pmm3 | INDEL | I1_5 | * | * | 99.5494 | 99.2672 | 99.8332 | 56.8186 | 149560 | 1104 | 149606 | 250 | 187 | 74.8000 | |
| jpowers-varprowl | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | * | 19.1784 | 16.0456 | 23.8312 | 52.5433 | 211 | 1104 | 209 | 668 | 663 | 99.2515 | |
| gduggal-bwaplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 81.6123 | 69.5280 | 98.7810 | 81.8253 | 2519 | 1104 | 2512 | 31 | 13 | 41.9355 | |
| ciseli-custom | SNP | ti | map_l150_m2_e1 | homalt | 87.0667 | 85.6493 | 88.5319 | 72.6293 | 6589 | 1104 | 6585 | 853 | 699 | 81.9461 | |
| anovak-vg | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 49.8333 | 42.9384 | 59.3660 | 55.4700 | 830 | 1103 | 824 | 564 | 402 | 71.2766 | |
| jpowers-varprowl | SNP | ti | map_l100_m2_e0 | * | 98.2207 | 97.7472 | 98.6987 | 70.3702 | 47858 | 1103 | 47860 | 631 | 192 | 30.4279 | |
| ltrigg-rtg1 | SNP | tv | * | * | 99.8285 | 99.8863 | 99.7709 | 19.9654 | 968593 | 1103 | 968859 | 2225 | 103 | 4.6292 | |
| hfeng-pmm3 | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | * | 98.1954 | 96.9884 | 99.4328 | 50.3319 | 35490 | 1102 | 35413 | 202 | 180 | 89.1089 | |
| gduggal-bwaplat | INDEL | D1_5 | HG002complexvar | homalt | 93.6134 | 89.6018 | 98.0010 | 59.6110 | 9496 | 1102 | 9462 | 193 | 170 | 88.0829 | |
| gduggal-bwaplat | SNP | tv | HG002compoundhet | * | 87.7776 | 87.6611 | 87.8944 | 56.9502 | 7822 | 1101 | 7856 | 1082 | 151 | 13.9556 | |
| egarrison-hhga | INDEL | D16_PLUS | * | hetalt | 60.0179 | 43.0419 | 99.1060 | 48.8235 | 832 | 1101 | 776 | 7 | 6 | 85.7143 | |
| egarrison-hhga | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 59.9599 | 42.9829 | 99.1026 | 48.8525 | 830 | 1101 | 773 | 7 | 6 | 85.7143 | |
| egarrison-hhga | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 59.9599 | 42.9829 | 99.1026 | 48.8525 | 830 | 1101 | 773 | 7 | 6 | 85.7143 | |
| qzeng-custom | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 89.6938 | 81.4584 | 99.7817 | 61.4370 | 4837 | 1101 | 2742 | 6 | 5 | 83.3333 | |
| anovak-vg | INDEL | I1_5 | HG002complexvar | hetalt | 0.0000 | 36.2109 | 0.0000 | 0.0000 | 625 | 1101 | 0 | 0 | 0 | ||
| raldana-dualsentieon | SNP | * | HG002compoundhet | * | 97.7792 | 95.7401 | 99.9071 | 39.6169 | 24722 | 1100 | 24722 | 23 | 15 | 65.2174 | |
| hfeng-pmm1 | INDEL | I1_5 | * | * | 99.5147 | 99.2699 | 99.7606 | 57.3300 | 149564 | 1100 | 149609 | 359 | 252 | 70.1950 | |
| anovak-vg | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 78.6812 | 70.0218 | 89.7846 | 52.4533 | 2567 | 1099 | 2584 | 294 | 213 | 72.4490 | |
| gduggal-bwaplat | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 83.3451 | 73.4925 | 96.2484 | 91.4731 | 3047 | 1099 | 3053 | 119 | 21 | 17.6471 | |
| mlin-fermikit | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | hetalt | 56.8303 | 39.7366 | 99.7333 | 37.6559 | 724 | 1098 | 748 | 2 | 2 | 100.0000 | |
| qzeng-custom | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 86.5391 | 76.3934 | 99.7924 | 26.7984 | 3550 | 1097 | 1442 | 3 | 3 | 100.0000 | |
| anovak-vg | SNP | * | map_l150_m0_e0 | homalt | 84.1702 | 73.1719 | 99.0595 | 77.5693 | 2992 | 1097 | 2949 | 28 | 25 | 89.2857 | |
| egarrison-hhga | INDEL | D16_PLUS | HG002compoundhet | hetalt | 60.1689 | 43.1017 | 99.6134 | 31.8701 | 831 | 1097 | 773 | 3 | 3 | 100.0000 | |
| ghariani-varprowl | SNP | ti | HG002compoundhet | * | 88.8369 | 93.7235 | 84.4347 | 48.3203 | 16381 | 1097 | 16496 | 3041 | 899 | 29.5626 | |
| raldana-dualsentieon | INDEL | I1_5 | HG002compoundhet | * | 94.0016 | 91.1217 | 97.0695 | 64.7141 | 11259 | 1097 | 11262 | 340 | 339 | 99.7059 | |
| ciseli-custom | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 79.3428 | 82.9101 | 76.0698 | 72.6664 | 5322 | 1097 | 5404 | 1700 | 930 | 54.7059 | |
| ciseli-custom | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 79.3428 | 82.9101 | 76.0698 | 72.6664 | 5322 | 1097 | 5404 | 1700 | 930 | 54.7059 | |
| ciseli-custom | INDEL | I16_PLUS | * | homalt | 37.7444 | 29.7886 | 51.4983 | 66.4182 | 465 | 1096 | 464 | 437 | 402 | 91.9908 | |
| ckim-dragen | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 96.4289 | 93.4391 | 99.6164 | 40.1880 | 15609 | 1096 | 15843 | 61 | 61 | 100.0000 | |
| ckim-dragen | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 96.4289 | 93.4391 | 99.6164 | 40.1880 | 15609 | 1096 | 15843 | 61 | 61 | 100.0000 | |
| raldana-dualsentieon | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 95.8428 | 92.0372 | 99.9767 | 29.6938 | 12668 | 1096 | 12856 | 3 | 3 | 100.0000 | |