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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
19601-19650 / 86044 show all | |||||||||||||||
ckim-dragen | SNP | ti | map_l100_m2_e1 | homalt | 99.6178 | 99.3565 | 99.8804 | 57.3860 | 18375 | 119 | 18380 | 22 | 20 | 90.9091 | |
cchapple-custom | INDEL | D16_PLUS | HG002compoundhet | homalt | 29.7030 | 75.0000 | 18.5185 | 49.0566 | 6 | 2 | 5 | 22 | 22 | 100.0000 | |
ciseli-custom | SNP | tv | tech_badpromoters | het | 73.5632 | 96.9697 | 59.2593 | 50.0000 | 32 | 1 | 32 | 22 | 0 | 0.0000 | |
ckim-dragen | INDEL | * | map_l150_m0_e0 | het | 95.2381 | 96.7742 | 93.7500 | 93.2991 | 330 | 11 | 330 | 22 | 1 | 4.5455 | |
ckim-dragen | INDEL | D16_PLUS | HG002complexvar | homalt | 95.9866 | 99.3080 | 92.8803 | 75.5924 | 287 | 2 | 287 | 22 | 20 | 90.9091 | |
ciseli-custom | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 27.6134 | 19.4444 | 47.6190 | 91.1579 | 21 | 87 | 20 | 22 | 11 | 50.0000 | |
ciseli-custom | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 26.0012 | 16.8539 | 56.8627 | 86.1789 | 30 | 148 | 29 | 22 | 16 | 72.7273 | |
ciseli-custom | INDEL | I16_PLUS | lowcmp_SimpleRepeat_diTR_11to50 | het | 32.8326 | 22.5000 | 60.7143 | 91.1532 | 36 | 124 | 34 | 22 | 12 | 54.5455 | |
ciseli-custom | INDEL | I1_5 | map_l125_m2_e0 | homalt | 49.9618 | 35.4839 | 84.3972 | 87.4219 | 121 | 220 | 119 | 22 | 19 | 86.3636 | |
ciseli-custom | INDEL | I1_5 | map_l125_m2_e1 | homalt | 50.0650 | 35.5685 | 84.5070 | 87.6843 | 122 | 221 | 120 | 22 | 19 | 86.3636 | |
ciseli-custom | INDEL | I6_15 | map_siren | het | 39.1268 | 27.9720 | 65.0794 | 86.1842 | 40 | 103 | 41 | 22 | 21 | 95.4545 | |
cchapple-custom | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | het | 98.4844 | 97.4321 | 99.5596 | 48.5952 | 1328 | 35 | 4973 | 22 | 19 | 86.3636 | |
cchapple-custom | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 98.1825 | 99.6937 | 96.7164 | 71.0458 | 651 | 2 | 648 | 22 | 21 | 95.4545 | |
cchapple-custom | INDEL | I6_15 | lowcmp_SimpleRepeat_diTR_11to50 | * | 97.4449 | 95.8541 | 99.0894 | 62.1020 | 2312 | 100 | 2394 | 22 | 17 | 77.2727 | |
cchapple-custom | SNP | ti | lowcmp_SimpleRepeat_diTR_11to50 | het | 98.9388 | 98.5705 | 99.3099 | 68.9036 | 3103 | 45 | 3166 | 22 | 16 | 72.7273 | |
cchapple-custom | SNP | tv | lowcmp_SimpleRepeat_diTR_11to50 | * | 99.4664 | 99.3822 | 99.5507 | 61.1367 | 4826 | 30 | 4874 | 22 | 10 | 45.4545 | |
ciseli-custom | INDEL | * | map_l250_m0_e0 | het | 51.9039 | 49.0566 | 55.1020 | 98.7937 | 26 | 27 | 27 | 22 | 5 | 22.7273 | |
hfeng-pmm3 | SNP | tv | map_l250_m2_e0 | het | 98.4472 | 98.0412 | 98.8565 | 88.5422 | 1902 | 38 | 1902 | 22 | 0 | 0.0000 | |
hfeng-pmm3 | SNP | tv | map_l250_m2_e1 | het | 98.4670 | 98.0662 | 98.8712 | 88.6090 | 1927 | 38 | 1927 | 22 | 0 | 0.0000 | |
jlack-gatk | INDEL | D16_PLUS | * | homalt | 98.8194 | 98.9362 | 98.7028 | 69.0115 | 1674 | 18 | 1674 | 22 | 15 | 68.1818 | |
jlack-gatk | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 98.4013 | 98.5588 | 98.2442 | 73.3744 | 1231 | 18 | 1231 | 22 | 15 | 68.1818 | |
jlack-gatk | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 98.4013 | 98.5588 | 98.2442 | 73.3744 | 1231 | 18 | 1231 | 22 | 15 | 68.1818 | |
jlack-gatk | INDEL | D1_5 | HG002complexvar | homalt | 99.8161 | 99.8396 | 99.7926 | 59.1577 | 10581 | 17 | 10588 | 22 | 21 | 95.4545 | |
jlack-gatk | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | het | 94.9497 | 96.6667 | 93.2927 | 74.5736 | 319 | 11 | 306 | 22 | 18 | 81.8182 | |
jlack-gatk | INDEL | I16_PLUS | HG002complexvar | homalt | 96.5625 | 100.0000 | 93.3535 | 69.9091 | 309 | 0 | 309 | 22 | 21 | 95.4545 | |
jlack-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 95.4677 | 94.4444 | 96.5135 | 88.1879 | 629 | 37 | 609 | 22 | 5 | 22.7273 | |
hfeng-pmm1 | INDEL | I1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 95.3233 | 94.2598 | 96.4111 | 77.4217 | 624 | 38 | 591 | 22 | 8 | 36.3636 | |
hfeng-pmm1 | SNP | * | map_l150_m0_e0 | homalt | 99.5848 | 99.7065 | 99.4633 | 76.6851 | 4077 | 12 | 4077 | 22 | 7 | 31.8182 | |
hfeng-pmm1 | SNP | ti | map_l100_m1_e0 | homalt | 99.8580 | 99.8385 | 99.8775 | 60.1505 | 17931 | 29 | 17931 | 22 | 12 | 54.5455 | |
hfeng-pmm1 | SNP | ti | map_l100_m2_e0 | homalt | 99.8607 | 99.8416 | 99.8798 | 62.5925 | 18280 | 29 | 18280 | 22 | 12 | 54.5455 | |
hfeng-pmm1 | SNP | ti | map_l100_m2_e1 | homalt | 99.8621 | 99.8432 | 99.8810 | 62.5754 | 18465 | 29 | 18465 | 22 | 12 | 54.5455 | |
hfeng-pmm2 | INDEL | * | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 99.7892 | 99.6568 | 99.9219 | 57.6377 | 28163 | 97 | 28165 | 22 | 14 | 63.6364 | |
hfeng-pmm2 | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 99.7285 | 99.8188 | 99.6383 | 55.6923 | 6061 | 11 | 6061 | 22 | 22 | 100.0000 | |
jlack-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 95.4677 | 94.4444 | 96.5135 | 88.1879 | 629 | 37 | 609 | 22 | 5 | 22.7273 | |
jlack-gatk | INDEL | I1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 95.8754 | 95.3172 | 96.4401 | 77.6815 | 631 | 31 | 596 | 22 | 12 | 54.5455 | |
jlack-gatk | SNP | * | map_l125_m1_e0 | homalt | 99.2141 | 98.5685 | 99.8681 | 64.3628 | 16663 | 242 | 16663 | 22 | 16 | 72.7273 | |
jlack-gatk | SNP | * | map_l125_m2_e0 | homalt | 99.2238 | 98.5842 | 99.8717 | 66.9110 | 17129 | 246 | 17129 | 22 | 16 | 72.7273 | |
jlack-gatk | SNP | * | map_l125_m2_e1 | homalt | 99.2279 | 98.5911 | 99.8729 | 66.9215 | 17285 | 247 | 17285 | 22 | 16 | 72.7273 | |
jlack-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 98.4529 | 98.4529 | 98.4529 | 88.1815 | 1400 | 22 | 1400 | 22 | 15 | 68.1818 | |
jli-custom | INDEL | * | map_l100_m0_e0 | het | 97.8452 | 97.8452 | 97.8452 | 85.1642 | 999 | 22 | 999 | 22 | 5 | 22.7273 | |
hfeng-pmm3 | INDEL | D6_15 | HG002complexvar | het | 95.8678 | 92.7244 | 99.2318 | 57.2218 | 2893 | 227 | 2842 | 22 | 17 | 77.2727 | |
hfeng-pmm3 | SNP | * | HG002compoundhet | het | 96.0659 | 92.5730 | 99.8327 | 43.9121 | 13125 | 1053 | 13125 | 22 | 5 | 22.7273 | |
hfeng-pmm3 | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 98.3756 | 97.0003 | 99.7905 | 79.9603 | 10477 | 324 | 10478 | 22 | 4 | 18.1818 | |
hfeng-pmm3 | SNP | * | map_l150_m0_e0 | homalt | 99.5725 | 99.6821 | 99.4632 | 76.5815 | 4076 | 13 | 4076 | 22 | 7 | 31.8182 | |
hfeng-pmm3 | SNP | ti | map_l100_m1_e0 | homalt | 99.8636 | 99.8497 | 99.8775 | 60.0521 | 17933 | 27 | 17933 | 22 | 12 | 54.5455 | |
hfeng-pmm3 | SNP | ti | map_l100_m2_e0 | homalt | 99.8662 | 99.8525 | 99.8798 | 62.5049 | 18282 | 27 | 18282 | 22 | 12 | 54.5455 | |
hfeng-pmm3 | SNP | ti | map_l100_m2_e1 | homalt | 99.8675 | 99.8540 | 99.8810 | 62.4833 | 18467 | 27 | 18467 | 22 | 12 | 54.5455 | |
hfeng-pmm3 | SNP | ti | map_l250_m0_e0 | * | 98.5053 | 98.6131 | 98.3977 | 92.9205 | 1351 | 19 | 1351 | 22 | 3 | 13.6364 | |
hfeng-pmm2 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 97.9112 | 96.9995 | 98.8403 | 60.5859 | 1875 | 58 | 1875 | 22 | 21 | 95.4545 | |
hfeng-pmm2 | INDEL | D1_5 | map_l100_m0_e0 | het | 97.5803 | 98.8156 | 96.3756 | 85.7277 | 584 | 7 | 585 | 22 | 1 | 4.5455 |