PrecisionFDA
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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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
68901-68950 / 86044 show all | |||||||||||||||
| jli-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | hetalt | 94.8006 | 90.6323 | 99.3707 | 28.9674 | 1548 | 160 | 1579 | 10 | 9 | 90.0000 | |
| astatham-gatk | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 96.5247 | 93.9357 | 99.2605 | 36.0262 | 1549 | 100 | 1745 | 13 | 13 | 100.0000 | |
| ltrigg-rtg2 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | hetalt | 94.6844 | 90.6909 | 99.0458 | 31.4136 | 1549 | 159 | 1557 | 15 | 15 | 100.0000 | |
| mlin-fermikit | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 98.9788 | 98.1646 | 99.8066 | 46.6460 | 1551 | 29 | 1548 | 3 | 1 | 33.3333 | |
| jpowers-varprowl | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 57.4031 | 85.2666 | 43.2650 | 71.4286 | 1551 | 268 | 1561 | 2047 | 2030 | 99.1695 | |
| jpowers-varprowl | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 57.4031 | 85.2666 | 43.2650 | 71.4286 | 1551 | 268 | 1561 | 2047 | 2030 | 99.1695 | |
| hfeng-pmm2 | INDEL | D16_PLUS | HG002complexvar | * | 96.3580 | 94.4005 | 98.3985 | 65.2184 | 1551 | 92 | 1536 | 25 | 15 | 60.0000 | |
| hfeng-pmm3 | INDEL | I16_PLUS | * | homalt | 98.1968 | 99.4234 | 97.0000 | 68.6397 | 1552 | 9 | 1552 | 48 | 45 | 93.7500 | |
| mlin-fermikit | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 91.1134 | 93.7764 | 88.5975 | 54.4652 | 1552 | 103 | 1554 | 200 | 192 | 96.0000 | |
| cchapple-custom | SNP | ti | map_l250_m1_e0 | homalt | 98.2278 | 96.5775 | 99.9356 | 83.5174 | 1552 | 55 | 1551 | 1 | 1 | 100.0000 | |
| anovak-vg | INDEL | * | map_l100_m2_e0 | het | 70.9065 | 67.2735 | 74.9542 | 86.8513 | 1552 | 755 | 1637 | 547 | 155 | 28.3364 | |
| gduggal-snapplat | INDEL | D1_5 | map_l100_m2_e1 | * | 85.3151 | 80.0413 | 91.3330 | 91.1809 | 1552 | 387 | 1802 | 171 | 33 | 19.2982 | |
| dgrover-gatk | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 96.6211 | 94.1176 | 99.2614 | 36.3011 | 1552 | 97 | 1747 | 13 | 13 | 100.0000 | |
| egarrison-hhga | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 96.3335 | 96.2182 | 96.4490 | 61.4990 | 1552 | 61 | 1521 | 56 | 30 | 53.5714 | |
| jpowers-varprowl | SNP | ti | map_l250_m1_e0 | homalt | 98.1979 | 96.6397 | 99.8072 | 88.8547 | 1553 | 54 | 1553 | 3 | 3 | 100.0000 | |
| ghariani-varprowl | SNP | ti | map_l250_m1_e0 | homalt | 98.1979 | 96.6397 | 99.8072 | 87.4354 | 1553 | 54 | 1553 | 3 | 3 | 100.0000 | |
| hfeng-pmm2 | INDEL | I16_PLUS | * | homalt | 98.0751 | 99.5516 | 96.6418 | 69.9214 | 1554 | 7 | 1554 | 54 | 51 | 94.4444 | |
| jlack-gatk | INDEL | I16_PLUS | * | homalt | 95.7191 | 99.5516 | 92.1708 | 70.2698 | 1554 | 7 | 1554 | 132 | 127 | 96.2121 | |
| gduggal-bwavard | INDEL | * | lowcmp_SimpleRepeat_triTR_11to50 | homalt | 83.7592 | 72.2584 | 99.6141 | 35.3161 | 1555 | 597 | 1549 | 6 | 4 | 66.6667 | |
| ckim-vqsr | INDEL | I16_PLUS | * | homalt | 97.7080 | 99.6797 | 95.8128 | 71.8495 | 1556 | 5 | 1556 | 68 | 67 | 98.5294 | |
| astatham-gatk | INDEL | I16_PLUS | * | homalt | 97.6467 | 99.6797 | 95.6950 | 72.0858 | 1556 | 5 | 1556 | 70 | 68 | 97.1429 | |
| ckim-dragen | INDEL | I16_PLUS | * | homalt | 97.0983 | 99.6797 | 94.6472 | 70.1850 | 1556 | 5 | 1556 | 88 | 85 | 96.5909 | |
| ckim-gatk | INDEL | I16_PLUS | * | homalt | 97.7080 | 99.6797 | 95.8128 | 71.8495 | 1556 | 5 | 1556 | 68 | 67 | 98.5294 | |
| hfeng-pmm1 | INDEL | I16_PLUS | * | homalt | 98.2323 | 99.6797 | 96.8264 | 69.2499 | 1556 | 5 | 1556 | 51 | 49 | 96.0784 | |
| jmaeng-gatk | INDEL | I16_PLUS | * | homalt | 97.5243 | 99.6797 | 95.4601 | 72.0843 | 1556 | 5 | 1556 | 74 | 69 | 93.2432 | |
| raldana-dualsentieon | INDEL | D16_PLUS | HG002complexvar | * | 96.5485 | 94.7048 | 98.4655 | 65.1748 | 1556 | 87 | 1540 | 24 | 18 | 75.0000 | |
| raldana-dualsentieon | INDEL | I16_PLUS | * | homalt | 97.4343 | 99.7438 | 95.2294 | 67.8023 | 1557 | 4 | 1557 | 78 | 76 | 97.4359 | |
| bgallagher-sentieon | INDEL | I16_PLUS | * | homalt | 97.0698 | 99.7438 | 94.5355 | 72.0279 | 1557 | 4 | 1557 | 90 | 87 | 96.6667 | |
| jpowers-varprowl | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 98.4208 | 98.5443 | 98.2976 | 60.8492 | 1557 | 23 | 1559 | 27 | 0 | 0.0000 | |
| jmaeng-gatk | SNP | tv | map_l250_m2_e0 | * | 69.2000 | 54.0250 | 96.2299 | 96.4918 | 1557 | 1325 | 1557 | 61 | 2 | 3.2787 | |
| qzeng-custom | INDEL | * | map_l125_m1_e0 | * | 82.7094 | 73.9440 | 93.8324 | 91.4171 | 1558 | 549 | 1993 | 131 | 45 | 34.3511 | |
| ckim-isaac | INDEL | D16_PLUS | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 80.2126 | 73.2143 | 88.6901 | 63.6383 | 1558 | 570 | 1537 | 196 | 162 | 82.6531 | |
| dgrover-gatk | INDEL | I16_PLUS | * | homalt | 97.7415 | 99.8078 | 95.7591 | 72.2497 | 1558 | 3 | 1558 | 69 | 66 | 95.6522 | |
| cchapple-custom | INDEL | I16_PLUS | * | homalt | 98.0326 | 99.8078 | 96.3194 | 65.1446 | 1558 | 3 | 1544 | 59 | 57 | 96.6102 | |
| raldana-dualsentieon | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | hetalt | 92.2212 | 85.5653 | 100.0000 | 31.5699 | 1559 | 263 | 1591 | 0 | 0 | ||
| gduggal-snapfb | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 81.7047 | 98.6709 | 69.7171 | 59.9362 | 1559 | 21 | 1577 | 685 | 12 | 1.7518 | |
| mlin-fermikit | INDEL | D6_15 | lowcmp_SimpleRepeat_triTR_11to50 | * | 91.7166 | 90.1734 | 93.3134 | 34.6469 | 1560 | 170 | 1563 | 112 | 110 | 98.2143 | |
| gduggal-snapvard | SNP | ti | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 94.7982 | 92.4763 | 97.2396 | 66.7223 | 1561 | 127 | 1550 | 44 | 15 | 34.0909 | |
| raldana-dualsentieon | INDEL | I1_5 | HG002complexvar | hetalt | 94.9524 | 90.4403 | 99.9382 | 69.6987 | 1561 | 165 | 1618 | 1 | 1 | 100.0000 | |
| ckim-isaac | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 92.1781 | 91.6618 | 92.7003 | 64.7784 | 1561 | 142 | 1562 | 123 | 54 | 43.9024 | |
| hfeng-pmm2 | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 97.8835 | 96.7762 | 99.0164 | 72.2070 | 1561 | 52 | 1510 | 15 | 11 | 73.3333 | |
| hfeng-pmm3 | INDEL | D16_PLUS | HG002complexvar | * | 96.9227 | 95.0700 | 98.8491 | 64.9955 | 1562 | 81 | 1546 | 18 | 11 | 61.1111 | |
| gduggal-bwavard | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | homalt | 98.5178 | 97.0789 | 100.0000 | 47.9893 | 1562 | 47 | 1552 | 0 | 0 | ||
| gduggal-bwavard | SNP | ti | map_l250_m1_e0 | homalt | 98.2992 | 97.1998 | 99.4238 | 87.2438 | 1562 | 45 | 1553 | 9 | 6 | 66.6667 | |
| ckim-gatk | SNP | tv | map_l250_m2_e0 | * | 69.3914 | 54.1985 | 96.4198 | 96.4303 | 1562 | 1320 | 1562 | 58 | 1 | 1.7241 | |
| ckim-isaac | SNP | ti | map_l250_m1_e0 | het | 68.7954 | 52.6280 | 99.3007 | 91.8721 | 1562 | 1406 | 1562 | 11 | 0 | 0.0000 | |
| anovak-vg | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 44.1057 | 39.2068 | 50.4037 | 54.9961 | 1562 | 2422 | 1748 | 1720 | 1273 | 74.0116 | |
| anovak-vg | INDEL | * | map_l125_m1_e0 | * | 72.5033 | 74.1813 | 70.8995 | 87.0946 | 1563 | 544 | 1608 | 660 | 372 | 56.3636 | |
| hfeng-pmm3 | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 98.0428 | 96.9002 | 99.2126 | 71.4874 | 1563 | 50 | 1512 | 12 | 7 | 58.3333 | |
| gduggal-snapplat | INDEL | * | map_l125_m1_e0 | * | 81.4439 | 74.1813 | 90.2830 | 92.9787 | 1563 | 544 | 1691 | 182 | 25 | 13.7363 | |