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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
27101-27150 / 86044 show all | |||||||||||||||
| ltrigg-rtg2 | INDEL | I1_5 | map_l150_m2_e0 | het | 96.5090 | 94.1748 | 98.9619 | 84.5620 | 291 | 18 | 286 | 3 | 0 | 0.0000 | |
| ltrigg-rtg2 | INDEL | I1_5 | map_l150_m2_e1 | het | 96.5995 | 94.3218 | 98.9899 | 84.6986 | 299 | 18 | 294 | 3 | 0 | 0.0000 | |
| ltrigg-rtg2 | INDEL | I6_15 | HG002complexvar | homalt | 98.9542 | 98.5173 | 99.3950 | 43.5610 | 1196 | 18 | 1150 | 7 | 4 | 57.1429 | |
| ltrigg-rtg2 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 99.0937 | 98.8111 | 99.3780 | 84.1286 | 1496 | 18 | 1438 | 9 | 0 | 0.0000 | |
| ndellapenna-hhga | INDEL | D16_PLUS | map_l100_m2_e1 | * | 83.7401 | 81.4433 | 86.1702 | 87.8866 | 79 | 18 | 81 | 13 | 6 | 46.1538 | |
| ndellapenna-hhga | INDEL | D1_5 | lowcmp_SimpleRepeat_triTR_51to200 | hetalt | 76.3171 | 63.2653 | 96.1538 | 23.5294 | 31 | 18 | 25 | 1 | 0 | 0.0000 | |
| ndellapenna-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | hetalt | 68.6649 | 53.8462 | 94.7368 | 73.6111 | 21 | 18 | 18 | 1 | 1 | 100.0000 | |
| ndellapenna-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | hetalt | 80.4348 | 67.2727 | 100.0000 | 66.6667 | 37 | 18 | 36 | 0 | 0 | ||
| ndellapenna-hhga | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 92.7536 | 89.8876 | 95.8084 | 77.0289 | 160 | 18 | 160 | 7 | 5 | 71.4286 | |
| mlin-fermikit | INDEL | D6_15 | map_l150_m1_e0 | het | 62.9857 | 53.8462 | 75.8621 | 84.2391 | 21 | 18 | 22 | 7 | 4 | 57.1429 | |
| mlin-fermikit | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 79.4582 | 83.0189 | 76.1905 | 81.2500 | 88 | 18 | 80 | 25 | 25 | 100.0000 | |
| mlin-fermikit | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | hetalt | 79.0698 | 65.3846 | 100.0000 | 61.5385 | 34 | 18 | 35 | 0 | 0 | ||
| mlin-fermikit | INDEL | I6_15 | map_l100_m0_e0 | * | 57.9710 | 45.4545 | 80.0000 | 87.8049 | 15 | 18 | 16 | 4 | 3 | 75.0000 | |
| mlin-fermikit | SNP | ti | map_l100_m1_e0 | hetalt | 55.0000 | 37.9310 | 100.0000 | 70.2703 | 11 | 18 | 11 | 0 | 0 | ||
| mlin-fermikit | SNP | ti | map_l100_m2_e0 | hetalt | 57.1429 | 40.0000 | 100.0000 | 72.0930 | 12 | 18 | 12 | 0 | 0 | ||
| mlin-fermikit | SNP | ti | map_l100_m2_e1 | hetalt | 59.0909 | 41.9355 | 100.0000 | 71.1111 | 13 | 18 | 13 | 0 | 0 | ||
| mlin-fermikit | SNP | ti | map_l125_m1_e0 | hetalt | 40.0000 | 25.0000 | 100.0000 | 68.4211 | 6 | 18 | 6 | 0 | 0 | ||
| mlin-fermikit | SNP | ti | map_l125_m2_e0 | hetalt | 40.0000 | 25.0000 | 100.0000 | 77.7778 | 6 | 18 | 6 | 0 | 0 | ||
| mlin-fermikit | SNP | ti | map_l125_m2_e1 | hetalt | 40.0000 | 25.0000 | 100.0000 | 78.5714 | 6 | 18 | 6 | 0 | 0 | ||
| mlin-fermikit | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 99.0251 | 98.7500 | 99.3017 | 67.9499 | 1422 | 18 | 1422 | 10 | 10 | 100.0000 | |
| mlin-fermikit | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 99.0055 | 98.0306 | 100.0000 | 65.5504 | 896 | 18 | 895 | 0 | 0 | ||
| ltrigg-rtg2 | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 90.6003 | 88.1579 | 93.1818 | 89.0638 | 134 | 18 | 123 | 9 | 1 | 11.1111 | |
| ltrigg-rtg2 | SNP | ti | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 99.8244 | 99.7128 | 99.9361 | 40.9541 | 6250 | 18 | 6259 | 4 | 3 | 75.0000 | |
| 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 | I6_15 | map_l125_m1_e0 | * | 66.0697 | 66.0377 | 66.1017 | 87.0756 | 35 | 18 | 78 | 40 | 3 | 7.5000 | |
| qzeng-custom | INDEL | I6_15 | map_l125_m2_e0 | * | 66.8790 | 66.0377 | 67.7419 | 87.6000 | 35 | 18 | 84 | 40 | 3 | 7.5000 | |
| qzeng-custom | INDEL | I6_15 | map_l125_m2_e1 | * | 66.6138 | 66.0377 | 67.2000 | 87.7089 | 35 | 18 | 84 | 41 | 3 | 7.3171 | |
| qzeng-custom | SNP | ti | * | hetalt | 98.0808 | 96.9072 | 99.2832 | 55.8893 | 564 | 18 | 554 | 4 | 4 | 100.0000 | |
| qzeng-custom | SNP | ti | HG002compoundhet | hetalt | 98.4211 | 96.8912 | 100.0000 | 21.9547 | 561 | 18 | 551 | 0 | 0 | ||
| qzeng-custom | SNP | ti | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 99.5851 | 99.5485 | 99.6217 | 39.7050 | 3969 | 18 | 3950 | 15 | 6 | 40.0000 | |
| qzeng-custom | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 94.8561 | 97.7330 | 92.1437 | 91.1616 | 776 | 18 | 821 | 70 | 14 | 20.0000 | |
| qzeng-custom | SNP | tv | lowcmp_SimpleRepeat_triTR_11to50 | het | 99.1334 | 99.1581 | 99.1088 | 47.3320 | 2120 | 18 | 2113 | 19 | 1 | 5.2632 | |
| raldana-dualsentieon | INDEL | * | lowcmp_SimpleRepeat_triTR_11to50 | hetalt | 99.0153 | 98.0498 | 100.0000 | 28.0159 | 905 | 18 | 907 | 0 | 0 | ||
| raldana-dualsentieon | INDEL | * | segdup | het | 99.0763 | 98.7722 | 99.3823 | 94.1484 | 1448 | 18 | 1448 | 9 | 2 | 22.2222 | |
| qzeng-custom | INDEL | D16_PLUS | HG002compoundhet | het | 84.4943 | 95.5556 | 75.7282 | 32.4836 | 387 | 18 | 2106 | 675 | 234 | 34.6667 | |
| qzeng-custom | INDEL | D16_PLUS | map_l100_m2_e1 | * | 36.6856 | 81.4433 | 23.6749 | 89.0986 | 79 | 18 | 67 | 216 | 1 | 0.4630 | |
| qzeng-custom | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 98.7555 | 98.8327 | 98.6784 | 75.6101 | 1524 | 18 | 1568 | 21 | 7 | 33.3333 | |
| qzeng-custom | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 95.3664 | 97.8824 | 92.9766 | 48.8889 | 832 | 18 | 834 | 63 | 21 | 33.3333 | |
| qzeng-custom | INDEL | I6_15 | HG002compoundhet | het | 84.7648 | 91.3462 | 79.0682 | 44.3175 | 190 | 18 | 2274 | 602 | 437 | 72.5914 | |
| ndellapenna-hhga | INDEL | I16_PLUS | map_siren | * | 81.0503 | 79.0698 | 83.1325 | 85.7143 | 68 | 18 | 69 | 14 | 10 | 71.4286 | |
| ndellapenna-hhga | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 98.1778 | 97.6714 | 98.6894 | 75.0164 | 755 | 18 | 753 | 10 | 4 | 40.0000 | |
| ndellapenna-hhga | SNP | * | lowcmp_SimpleRepeat_homopolymer_6to10 | homalt | 99.7617 | 99.7043 | 99.8191 | 54.9748 | 6070 | 18 | 6071 | 11 | 9 | 81.8182 | |
| ndellapenna-hhga | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 99.3092 | 99.1720 | 99.4467 | 63.8078 | 2156 | 18 | 2157 | 12 | 5 | 41.6667 | |
| ndellapenna-hhga | SNP | tv | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 99.4376 | 99.3474 | 99.5280 | 38.8679 | 2740 | 18 | 2741 | 13 | 13 | 100.0000 | |
| ndellapenna-hhga | SNP | tv | map_l125_m0_e0 | homalt | 99.5256 | 99.1896 | 99.8640 | 68.2316 | 2203 | 18 | 2203 | 3 | 2 | 66.6667 | |
| qzeng-custom | INDEL | * | HG002compoundhet | homalt | 47.3681 | 97.3761 | 31.2960 | 66.5488 | 668 | 18 | 681 | 1495 | 1295 | 86.6221 | |
| qzeng-custom | INDEL | * | lowcmp_SimpleRepeat_triTR_11to50 | homalt | 98.0670 | 99.1636 | 96.9944 | 39.3861 | 2134 | 18 | 2969 | 92 | 42 | 45.6522 | |
| ckim-dragen | INDEL | D6_15 | HG002compoundhet | het | 95.5765 | 97.8972 | 93.3633 | 64.0953 | 838 | 18 | 830 | 59 | 57 | 96.6102 | |
| ckim-dragen | INDEL | I6_15 | * | homalt | 96.6294 | 99.7115 | 93.7321 | 54.6498 | 6221 | 18 | 6221 | 416 | 414 | 99.5192 | |
| ckim-dragen | SNP | ti | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 99.8713 | 99.8218 | 99.9208 | 48.8376 | 10084 | 18 | 10093 | 8 | 8 | 100.0000 | |