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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
65801-65850 / 86044 show all | |||||||||||||||
| jli-custom | INDEL | * | map_l150_m2_e1 | * | 98.2943 | 98.0542 | 98.5356 | 89.3280 | 1411 | 28 | 1413 | 21 | 8 | 38.0952 | |
| hfeng-pmm2 | SNP | * | map_l150_m0_e0 | homalt | 99.5726 | 99.7065 | 99.4390 | 76.7349 | 4077 | 12 | 4077 | 23 | 8 | 34.7826 | |
| hfeng-pmm2 | SNP | ti | map_l150_m0_e0 | het | 98.5736 | 98.9994 | 98.1514 | 83.2987 | 5046 | 51 | 5044 | 95 | 8 | 8.4211 | |
| hfeng-pmm2 | SNP | tv | HG002complexvar | het | 99.7540 | 99.5389 | 99.9700 | 20.7785 | 150036 | 695 | 149957 | 45 | 8 | 17.7778 | |
| hfeng-pmm3 | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_51to200 | * | 96.9392 | 95.2922 | 98.6441 | 64.3073 | 587 | 29 | 582 | 8 | 8 | 100.0000 | |
| hfeng-pmm3 | INDEL | D1_5 | HG002complexvar | homalt | 99.8962 | 99.8773 | 99.9151 | 58.2388 | 10585 | 13 | 10590 | 9 | 8 | 88.8889 | |
| hfeng-pmm1 | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 99.2017 | 98.7689 | 99.6382 | 66.9061 | 3851 | 48 | 3856 | 14 | 8 | 57.1429 | |
| hfeng-pmm1 | INDEL | I6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 91.9355 | 96.6102 | 87.6923 | 75.7463 | 57 | 2 | 57 | 8 | 8 | 100.0000 | |
| hfeng-pmm1 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 97.8839 | 96.6007 | 99.2017 | 74.1149 | 1904 | 67 | 1864 | 15 | 8 | 53.3333 | |
| hfeng-pmm1 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 97.0946 | 96.0916 | 98.1187 | 71.9562 | 713 | 29 | 678 | 13 | 8 | 61.5385 | |
| hfeng-pmm1 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 97.1748 | 95.9660 | 98.4145 | 72.9224 | 904 | 38 | 869 | 14 | 8 | 57.1429 | |
| hfeng-pmm1 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 97.8839 | 96.6007 | 99.2017 | 74.1149 | 1904 | 67 | 1864 | 15 | 8 | 53.3333 | |
| hfeng-pmm1 | SNP | ti | HG002compoundhet | * | 98.2873 | 96.6987 | 99.9291 | 34.1329 | 16901 | 577 | 16902 | 12 | 8 | 66.6667 | |
| hfeng-pmm1 | SNP | ti | map_l150_m0_e0 | het | 98.8393 | 98.5874 | 99.0925 | 80.9472 | 5025 | 72 | 5023 | 46 | 8 | 17.3913 | |
| hfeng-pmm1 | SNP | ti | map_l250_m1_e0 | het | 98.6671 | 98.5175 | 98.8172 | 88.8014 | 2924 | 44 | 2924 | 35 | 8 | 22.8571 | |
| hfeng-pmm1 | SNP | ti | map_l250_m2_e0 | het | 98.7844 | 98.6478 | 98.9214 | 88.9993 | 3210 | 44 | 3210 | 35 | 8 | 22.8571 | |
| hfeng-pmm1 | SNP | ti | map_l250_m2_e1 | het | 98.7703 | 98.6056 | 98.9355 | 89.0938 | 3253 | 46 | 3253 | 35 | 8 | 22.8571 | |
| hfeng-pmm1 | SNP | tv | map_siren | homalt | 99.8956 | 99.8898 | 99.9014 | 56.0205 | 17221 | 19 | 17219 | 17 | 8 | 47.0588 | |
| hfeng-pmm2 | INDEL | * | map_l100_m0_e0 | * | 97.7482 | 98.4645 | 97.0422 | 86.4304 | 1539 | 24 | 1542 | 47 | 8 | 17.0213 | |
| hfeng-pmm2 | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_51to200 | * | 96.7687 | 94.9675 | 98.6395 | 64.7059 | 585 | 31 | 580 | 8 | 8 | 100.0000 | |
| hfeng-pmm2 | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_51to200 | het | 81.1947 | 74.8148 | 88.7640 | 73.9003 | 101 | 34 | 79 | 10 | 8 | 80.0000 | |
| hfeng-pmm2 | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 99.8228 | 99.8636 | 99.7820 | 48.9282 | 3661 | 5 | 3661 | 8 | 8 | 100.0000 | |
| hfeng-pmm2 | INDEL | I16_PLUS | HG002complexvar | * | 98.3417 | 97.4026 | 99.2991 | 67.2031 | 1275 | 34 | 1275 | 9 | 8 | 88.8889 | |
| hfeng-pmm2 | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 96.6507 | 98.5366 | 94.8357 | 90.7270 | 202 | 3 | 202 | 11 | 8 | 72.7273 | |
| hfeng-pmm2 | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 96.6507 | 98.5366 | 94.8357 | 90.7270 | 202 | 3 | 202 | 11 | 8 | 72.7273 | |
| hfeng-pmm2 | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 99.4848 | 99.7183 | 99.2523 | 67.2382 | 1062 | 3 | 1062 | 8 | 8 | 100.0000 | |
| hfeng-pmm2 | INDEL | I6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 91.9355 | 96.6102 | 87.6923 | 76.1029 | 57 | 2 | 57 | 8 | 8 | 100.0000 | |
| hfeng-pmm2 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 97.7268 | 96.3470 | 99.1467 | 74.4062 | 1899 | 72 | 1859 | 16 | 8 | 50.0000 | |
| hfeng-pmm2 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 92.9273 | 88.2463 | 98.1328 | 62.8086 | 473 | 63 | 473 | 9 | 8 | 88.8889 | |
| hfeng-pmm2 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 97.7268 | 96.3470 | 99.1467 | 74.4062 | 1899 | 72 | 1859 | 16 | 8 | 50.0000 | |
| hfeng-pmm2 | INDEL | I6_15 | lowcmp_SimpleRepeat_diTR_11to50 | * | 97.0727 | 94.8590 | 99.3921 | 62.0781 | 2288 | 124 | 2289 | 14 | 8 | 57.1429 | |
| hfeng-pmm3 | SNP | tv | map_siren | homalt | 99.8898 | 99.8724 | 99.9071 | 55.8869 | 17218 | 22 | 17215 | 16 | 8 | 50.0000 | |
| jlack-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 99.2829 | 99.3333 | 99.2326 | 76.5804 | 2980 | 20 | 2974 | 23 | 8 | 34.7826 | |
| jlack-gatk | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | hetalt | 95.9073 | 92.8033 | 99.2261 | 33.2760 | 1109 | 86 | 1154 | 9 | 8 | 88.8889 | |
| jlack-gatk | INDEL | * | map_l100_m0_e0 | het | 91.5391 | 97.8452 | 85.9966 | 90.8195 | 999 | 22 | 1001 | 163 | 8 | 4.9080 | |
| jlack-gatk | INDEL | * | map_l100_m2_e1 | homalt | 98.7114 | 98.6729 | 98.7500 | 83.9418 | 1264 | 17 | 1264 | 16 | 8 | 50.0000 | |
| jlack-gatk | INDEL | * | map_l125_m1_e0 | het | 92.6306 | 98.1273 | 87.7170 | 91.3380 | 1310 | 25 | 1314 | 184 | 8 | 4.3478 | |
| jlack-gatk | INDEL | * | segdup | homalt | 99.3240 | 99.4792 | 99.1693 | 93.4858 | 955 | 5 | 955 | 8 | 8 | 100.0000 | |
| jlack-gatk | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | hetalt | 88.0509 | 79.0340 | 99.3902 | 32.6949 | 1440 | 382 | 1467 | 9 | 8 | 88.8889 | |
| jlack-gatk | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_51to200 | homalt | 97.7556 | 99.4924 | 96.0784 | 58.9537 | 196 | 1 | 196 | 8 | 8 | 100.0000 | |
| jlack-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 93.4254 | 90.8213 | 96.1832 | 73.6419 | 376 | 38 | 378 | 15 | 8 | 53.3333 | |
| ndellapenna-hhga | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 98.0761 | 97.2854 | 98.8798 | 74.4855 | 1326 | 37 | 1324 | 15 | 8 | 53.3333 | |
| ndellapenna-hhga | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 95.4245 | 94.0678 | 96.8208 | 67.3893 | 333 | 21 | 335 | 11 | 8 | 72.7273 | |
| ndellapenna-hhga | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 91.7765 | 90.9091 | 92.6606 | 88.7745 | 100 | 10 | 101 | 8 | 8 | 100.0000 | |
| ndellapenna-hhga | SNP | * | map_l100_m0_e0 | homalt | 99.6765 | 99.4406 | 99.9135 | 60.1441 | 11555 | 65 | 11555 | 10 | 8 | 80.0000 | |
| ndellapenna-hhga | SNP | * | map_l250_m0_e0 | * | 97.4261 | 95.7377 | 99.1752 | 91.7964 | 2044 | 91 | 2044 | 17 | 8 | 47.0588 | |
| ndellapenna-hhga | SNP | tv | map_l250_m1_e0 | het | 97.1755 | 95.2994 | 99.1269 | 86.3845 | 1703 | 84 | 1703 | 15 | 8 | 53.3333 | |
| ndellapenna-hhga | SNP | tv | map_l250_m2_e0 | het | 97.2703 | 95.5155 | 99.0909 | 86.8763 | 1853 | 87 | 1853 | 17 | 8 | 47.0588 | |
| ndellapenna-hhga | SNP | tv | map_l250_m2_e1 | het | 97.3057 | 95.5725 | 99.1029 | 86.9625 | 1878 | 87 | 1878 | 17 | 8 | 47.0588 | |
| ltrigg-rtg2 | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_51to200 | * | 95.7268 | 93.0195 | 98.5965 | 56.9811 | 573 | 43 | 562 | 8 | 8 | 100.0000 | |