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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
71751-71800 / 86044 show all | |||||||||||||||
| hfeng-pmm1 | SNP | tv | map_l250_m1_e0 | * | 98.5782 | 98.2244 | 98.9346 | 87.7185 | 2600 | 47 | 2600 | 28 | 6 | 21.4286 | |
| jlack-gatk | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 98.0087 | 96.3087 | 99.7699 | 41.5864 | 2583 | 99 | 2601 | 6 | 6 | 100.0000 | |
| eyeh-varpipe | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 94.0198 | 99.8511 | 88.8320 | 71.0242 | 2682 | 4 | 2601 | 327 | 6 | 1.8349 | |
| gduggal-bwafb | INDEL | I6_15 | HG002complexvar | het | 87.7628 | 80.4671 | 96.5134 | 49.2661 | 1895 | 460 | 2602 | 94 | 89 | 94.6809 | |
| hfeng-pmm2 | SNP | tv | map_l250_m1_e0 | * | 98.2628 | 98.3000 | 98.2257 | 89.1399 | 2602 | 45 | 2602 | 47 | 6 | 12.7660 | |
| ltrigg-rtg2 | INDEL | * | map_siren | homalt | 98.9758 | 98.3427 | 99.6172 | 74.6678 | 2611 | 44 | 2602 | 10 | 7 | 70.0000 | |
| ghariani-varprowl | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 68.4840 | 92.9334 | 54.2196 | 86.0939 | 2525 | 192 | 2602 | 2197 | 203 | 9.2399 | |
| gduggal-snapfb | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 84.8725 | 80.8690 | 89.2931 | 75.5803 | 4802 | 1136 | 2602 | 312 | 198 | 63.4615 | |
| rpoplin-dv42 | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 98.2023 | 96.7189 | 99.7319 | 41.3917 | 2594 | 88 | 2604 | 7 | 7 | 100.0000 | |
| gduggal-snapplat | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 52.8724 | 36.5157 | 95.7721 | 51.7559 | 2597 | 4515 | 2605 | 115 | 100 | 86.9565 | |
| cchapple-custom | INDEL | * | map_siren | homalt | 98.6746 | 98.1544 | 99.2003 | 78.4454 | 2606 | 49 | 2605 | 21 | 13 | 61.9048 | |
| hfeng-pmm3 | SNP | tv | map_l250_m1_e0 | * | 98.7121 | 98.4511 | 98.9746 | 87.8091 | 2606 | 41 | 2606 | 27 | 4 | 14.8148 | |
| bgallagher-sentieon | SNP | tv | map_l250_m1_e0 | * | 98.0805 | 98.4511 | 97.7128 | 88.7082 | 2606 | 41 | 2606 | 61 | 12 | 19.6721 | |
| egarrison-hhga | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 98.6941 | 98.1189 | 99.2762 | 66.9104 | 2608 | 50 | 2606 | 19 | 14 | 73.6842 | |
| ndellapenna-hhga | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 98.7132 | 98.1565 | 99.2762 | 66.6200 | 2609 | 49 | 2606 | 19 | 10 | 52.6316 | |
| gduggal-snapvard | INDEL | D1_5 | map_siren | het | 89.3607 | 98.0237 | 82.1046 | 85.3259 | 2232 | 45 | 2606 | 568 | 243 | 42.7817 | |
| jpowers-varprowl | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 85.8875 | 93.5591 | 79.3786 | 89.7033 | 2542 | 175 | 2606 | 677 | 208 | 30.7238 | |
| jlack-gatk | INDEL | I16_PLUS | * | het | 96.8584 | 96.8359 | 96.8808 | 75.4914 | 2632 | 86 | 2609 | 84 | 21 | 25.0000 | |
| gduggal-bwafb | INDEL | * | map_siren | homalt | 98.3408 | 98.1921 | 98.4900 | 81.3372 | 2607 | 48 | 2609 | 40 | 27 | 67.5000 | |
| gduggal-bwavard | SNP | tv | HG002compoundhet | homalt | 92.4344 | 86.2456 | 99.5802 | 40.9644 | 2922 | 466 | 2609 | 11 | 8 | 72.7273 | |
| gduggal-bwavard | SNP | * | map_l250_m2_e1 | homalt | 98.2472 | 97.0935 | 99.4288 | 88.0788 | 2639 | 79 | 2611 | 15 | 10 | 66.6667 | |
| raldana-dualsentieon | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 98.3128 | 96.6816 | 100.0000 | 40.4561 | 2593 | 89 | 2611 | 0 | 0 | ||
| eyeh-varpipe | SNP | * | map_l250_m2_e0 | homalt | 99.7746 | 99.7022 | 99.8472 | 89.1514 | 2678 | 8 | 2613 | 4 | 4 | 100.0000 | |
| gduggal-snapvard | SNP | * | lowcmp_SimpleRepeat_triTR_11to50 | homalt | 98.2185 | 96.7495 | 99.7328 | 29.9465 | 2649 | 89 | 2613 | 7 | 4 | 57.1429 | |
| asubramanian-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 98.8815 | 98.4877 | 99.2784 | 83.9265 | 2605 | 40 | 2614 | 19 | 9 | 47.3684 | |
| eyeh-varpipe | SNP | tv | map_l250_m1_e0 | * | 98.7000 | 99.5089 | 97.9042 | 90.2532 | 2634 | 13 | 2616 | 56 | 6 | 10.7143 | |
| ltrigg-rtg1 | INDEL | * | map_siren | homalt | 99.1870 | 98.9077 | 99.4679 | 78.0366 | 2626 | 29 | 2617 | 14 | 10 | 71.4286 | |
| jli-custom | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 99.0528 | 98.3446 | 99.7713 | 68.4849 | 2614 | 44 | 2617 | 6 | 4 | 66.6667 | |
| ckim-vqsr | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 99.1094 | 98.3822 | 99.8474 | 70.7576 | 2615 | 43 | 2617 | 4 | 3 | 75.0000 | |
| cchapple-custom | SNP | * | map_l250_m2_e1 | homalt | 98.1075 | 96.3208 | 99.9618 | 85.0801 | 2618 | 100 | 2617 | 1 | 1 | 100.0000 | |
| ndellapenna-hhga | INDEL | * | map_siren | homalt | 98.6802 | 98.5687 | 98.7920 | 79.0989 | 2617 | 38 | 2617 | 32 | 23 | 71.8750 | |
| gduggal-snapplat | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 52.7132 | 36.3814 | 95.6522 | 52.4661 | 2610 | 4564 | 2618 | 119 | 102 | 85.7143 | |
| raldana-dualsentieon | INDEL | I16_PLUS | * | het | 98.2484 | 97.1302 | 99.3926 | 71.9668 | 2640 | 78 | 2618 | 16 | 8 | 50.0000 | |
| mlin-fermikit | SNP | * | map_l250_m2_e0 | * | 47.3085 | 33.2150 | 82.1776 | 79.9585 | 2619 | 5266 | 2619 | 568 | 495 | 87.1479 | |
| jlack-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 98.4586 | 99.0170 | 97.9065 | 84.2545 | 2619 | 26 | 2619 | 56 | 14 | 25.0000 | |
| ckim-vqsr | INDEL | I16_PLUS | * | het | 98.1949 | 97.2774 | 99.1298 | 76.5400 | 2644 | 74 | 2620 | 23 | 10 | 43.4783 | |
| egarrison-hhga | INDEL | * | map_siren | homalt | 98.7934 | 98.6817 | 98.9052 | 79.7136 | 2620 | 35 | 2620 | 29 | 20 | 68.9655 | |
| jmaeng-gatk | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 99.0355 | 98.4951 | 99.5819 | 70.6787 | 2618 | 40 | 2620 | 11 | 3 | 27.2727 | |
| jmaeng-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 99.2612 | 99.0548 | 99.4685 | 84.3994 | 2620 | 25 | 2620 | 14 | 6 | 42.8571 | |
| ckim-gatk | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 99.0730 | 98.4951 | 99.6577 | 70.6945 | 2618 | 40 | 2620 | 9 | 3 | 33.3333 | |
| rpoplin-dv42 | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 98.9427 | 98.5704 | 99.3179 | 69.3175 | 2620 | 38 | 2621 | 18 | 14 | 77.7778 | |
| ckim-isaac | INDEL | * | map_l100_m2_e1 | * | 81.7169 | 69.9148 | 98.3127 | 84.3697 | 2626 | 1130 | 2622 | 45 | 21 | 46.6667 | |
| mlin-fermikit | SNP | tv | func_cds | het | 99.1679 | 98.6827 | 99.6579 | 21.9982 | 2622 | 35 | 2622 | 9 | 0 | 0.0000 | |
| gduggal-bwavard | SNP | tv | func_cds | het | 99.0001 | 98.7956 | 99.2054 | 42.2421 | 2625 | 32 | 2622 | 21 | 9 | 42.8571 | |
| gduggal-snapfb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 73.1048 | 71.1289 | 75.1936 | 73.0650 | 2577 | 1046 | 2622 | 865 | 237 | 27.3988 | |
| gduggal-bwafb | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 87.4269 | 95.5834 | 80.5530 | 88.6814 | 2597 | 120 | 2622 | 633 | 90 | 14.2180 | |
| ckim-vqsr | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 99.2430 | 99.1304 | 99.3558 | 84.2935 | 2622 | 23 | 2622 | 17 | 7 | 41.1765 | |
| gduggal-snapvard | SNP | tv | func_cds | het | 98.7765 | 98.8333 | 98.7199 | 41.1608 | 2626 | 31 | 2622 | 34 | 9 | 26.4706 | |
| ckim-isaac | SNP | tv | func_cds | het | 99.3184 | 98.7204 | 99.9238 | 24.8927 | 2623 | 34 | 2623 | 2 | 0 | 0.0000 | |
| anovak-vg | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 58.8295 | 52.0303 | 67.6729 | 41.0135 | 2473 | 2280 | 2623 | 1253 | 974 | 77.7334 | |