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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
70101-70150 / 86044 show all | |||||||||||||||
| anovak-vg | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 77.8733 | 76.5766 | 79.2148 | 62.9281 | 340 | 104 | 343 | 90 | 54 | 60.0000 | |
| anovak-vg | INDEL | I6_15 | segdup | * | 45.2111 | 40.5714 | 51.0490 | 89.3838 | 71 | 104 | 73 | 70 | 55 | 78.5714 | |
| astatham-gatk | INDEL | D6_15 | HG002complexvar | * | 98.3071 | 98.0385 | 98.5771 | 58.5385 | 5198 | 104 | 5196 | 75 | 68 | 90.6667 | |
| ckim-dragen | SNP | ti | map_l250_m1_e0 | * | 97.2516 | 97.7288 | 96.7791 | 88.9718 | 4475 | 104 | 4477 | 149 | 18 | 12.0805 | |
| cchapple-custom | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.3555 | 99.2863 | 97.4421 | 79.1072 | 14467 | 104 | 14476 | 380 | 19 | 5.0000 | |
| cchapple-custom | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.3555 | 99.2863 | 97.4421 | 79.1072 | 14467 | 104 | 14476 | 380 | 19 | 5.0000 | |
| ciseli-custom | INDEL | I1_5 | map_siren | hetalt | 0.0000 | 7.1429 | 0.0000 | 0.0000 | 8 | 104 | 0 | 0 | 0 | ||
| ckim-gatk | SNP | * | HG002compoundhet | homalt | 99.4644 | 99.0354 | 99.8971 | 35.0629 | 10678 | 104 | 10677 | 11 | 10 | 90.9091 | |
| ckim-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.8791 | 99.2863 | 98.4753 | 80.3955 | 14467 | 104 | 14467 | 224 | 14 | 6.2500 | |
| ckim-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.8791 | 99.2863 | 98.4753 | 80.3955 | 14467 | 104 | 14467 | 224 | 14 | 6.2500 | |
| ckim-dragen | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 99.3007 | 99.0279 | 99.5750 | 78.5377 | 10696 | 105 | 10777 | 46 | 21 | 45.6522 | |
| ciseli-custom | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | hetalt | 0.0000 | 6.2500 | 0.0000 | 0.0000 | 7 | 105 | 0 | 0 | 0 | ||
| ckim-gatk | INDEL | * | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 99.7343 | 99.6285 | 99.8404 | 58.9273 | 28155 | 105 | 28158 | 45 | 20 | 44.4444 | |
| eyeh-varpipe | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 92.9382 | 92.2964 | 93.5890 | 71.7186 | 1258 | 105 | 1708 | 117 | 101 | 86.3248 | |
| gduggal-bwavard | SNP | * | lowcmp_SimpleRepeat_homopolymer_6to10 | homalt | 99.0887 | 98.2753 | 99.9156 | 51.4864 | 5983 | 105 | 5919 | 5 | 4 | 80.0000 | |
| gduggal-snapfb | INDEL | * | HG002compoundhet | homalt | 22.9146 | 84.6939 | 13.2497 | 72.0594 | 581 | 105 | 581 | 3804 | 3669 | 96.4511 | |
| gduggal-bwaplat | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 93.4823 | 87.7622 | 100.0000 | 53.9683 | 753 | 105 | 754 | 0 | 0 | ||
| jli-custom | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 98.9179 | 98.5780 | 99.2602 | 53.6895 | 7279 | 105 | 7245 | 54 | 49 | 90.7407 | |
| ltrigg-rtg1 | INDEL | * | map_l125_m2_e1 | * | 97.1606 | 95.2809 | 99.1159 | 83.1609 | 2120 | 105 | 2130 | 19 | 3 | 15.7895 | |
| ltrigg-rtg1 | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 98.9876 | 98.4366 | 99.5448 | 47.2044 | 6611 | 105 | 6561 | 30 | 6 | 20.0000 | |
| ltrigg-rtg1 | INDEL | I16_PLUS | HG002complexvar | het | 91.1805 | 84.2105 | 99.4083 | 47.5155 | 560 | 105 | 504 | 3 | 2 | 66.6667 | |
| jpowers-varprowl | INDEL | I1_5 | segdup | * | 91.1537 | 90.0850 | 92.2481 | 94.2204 | 954 | 105 | 952 | 80 | 67 | 83.7500 | |
| jpowers-varprowl | SNP | tv | lowcmp_SimpleRepeat_diTR_11to50 | het | 96.2010 | 96.5997 | 95.8055 | 76.3827 | 2983 | 105 | 3015 | 132 | 4 | 3.0303 | |
| jmaeng-gatk | SNP | * | HG002compoundhet | homalt | 99.4551 | 99.0262 | 99.8877 | 35.0471 | 10677 | 105 | 10676 | 12 | 11 | 91.6667 | |
| jmaeng-gatk | SNP | ti | HG002compoundhet | het | 99.3342 | 98.8953 | 99.7771 | 40.7782 | 9400 | 105 | 9400 | 21 | 17 | 80.9524 | |
| mlin-fermikit | INDEL | D1_5 | map_l250_m2_e0 | * | 56.5892 | 42.9348 | 82.9787 | 91.5996 | 79 | 105 | 78 | 16 | 14 | 87.5000 | |
| ndellapenna-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 92.7491 | 96.2553 | 89.4894 | 50.3947 | 2699 | 105 | 2699 | 317 | 129 | 40.6940 | |
| ltrigg-rtg2 | INDEL | D6_15 | * | het | 99.2141 | 99.0942 | 99.3342 | 52.7094 | 11487 | 105 | 11339 | 76 | 26 | 34.2105 | |
| ltrigg-rtg2 | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 98.1878 | 96.9931 | 99.4123 | 51.7989 | 3387 | 105 | 3383 | 20 | 14 | 70.0000 | |
| qzeng-custom | INDEL | * | map_l250_m1_e0 | * | 75.5265 | 65.5738 | 89.0411 | 97.9332 | 200 | 105 | 260 | 32 | 16 | 50.0000 | |
| qzeng-custom | INDEL | D1_5 | HG002compoundhet | het | 92.9212 | 93.9236 | 91.9400 | 64.3165 | 1623 | 105 | 11042 | 968 | 705 | 72.8306 | |
| qzeng-custom | INDEL | I16_PLUS | HG002complexvar | hetalt | 80.5997 | 68.6567 | 97.5728 | 58.5513 | 230 | 105 | 201 | 5 | 5 | 100.0000 | |
| hfeng-pmm2 | INDEL | I1_5 | * | homalt | 99.7668 | 99.8262 | 99.7075 | 52.8322 | 60323 | 105 | 60327 | 177 | 174 | 98.3051 | |
| hfeng-pmm3 | INDEL | I1_5 | HG002compoundhet | het | 91.3786 | 87.6471 | 95.4420 | 86.4242 | 745 | 105 | 691 | 33 | 27 | 81.8182 | |
| jlack-gatk | INDEL | I6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 91.4321 | 87.4402 | 95.8060 | 67.3513 | 731 | 105 | 731 | 32 | 29 | 90.6250 | |
| jlack-gatk | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | hetalt | 91.3157 | 84.9354 | 98.7324 | 37.8284 | 592 | 105 | 701 | 9 | 9 | 100.0000 | |
| ghariani-varprowl | INDEL | * | map_l100_m2_e1 | homalt | 94.7241 | 91.8033 | 97.8369 | 80.2368 | 1176 | 105 | 1176 | 26 | 9 | 34.6154 | |
| gduggal-snapplat | INDEL | * | map_l250_m2_e0 | * | 76.4380 | 68.2779 | 86.8132 | 98.1240 | 226 | 105 | 237 | 36 | 5 | 13.8889 | |
| gduggal-snapplat | INDEL | * | map_l250_m2_e1 | * | 76.5945 | 68.4685 | 86.9091 | 98.1619 | 228 | 105 | 239 | 36 | 5 | 13.8889 | |
| gduggal-snapplat | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 89.8295 | 94.2654 | 85.7923 | 82.5729 | 1726 | 105 | 1727 | 286 | 3 | 1.0490 | |
| ghariani-varprowl | SNP | * | map_l250_m1_e0 | het | 94.1868 | 97.7918 | 90.8381 | 91.9418 | 4650 | 105 | 4650 | 469 | 80 | 17.0576 | |
| astatham-gatk | INDEL | D16_PLUS | HG002compoundhet | hetalt | 97.0065 | 94.5539 | 99.5897 | 26.4429 | 1823 | 105 | 1942 | 8 | 8 | 100.0000 | |
| astatham-gatk | INDEL | D1_5 | map_siren | * | 97.9977 | 97.0247 | 98.9905 | 82.3184 | 3424 | 105 | 3432 | 35 | 6 | 17.1429 | |
| anovak-vg | SNP | * | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 94.8271 | 96.9609 | 92.7851 | 60.5360 | 3350 | 105 | 3498 | 272 | 223 | 81.9853 | |
| anovak-vg | SNP | ti | segdup | homalt | 98.8024 | 98.6009 | 99.0047 | 87.1313 | 7400 | 105 | 7361 | 74 | 73 | 98.6486 | |
| anovak-vg | INDEL | D1_5 | segdup | * | 91.5860 | 90.4805 | 92.7189 | 94.7590 | 998 | 105 | 1006 | 79 | 52 | 65.8228 | |
| anovak-vg | INDEL | I16_PLUS | HG002complexvar | homalt | 54.3276 | 66.0194 | 46.1538 | 39.2523 | 204 | 105 | 210 | 245 | 216 | 88.1633 | |
| astatham-gatk | SNP | ti | map_l125_m2_e0 | homalt | 99.4872 | 99.0755 | 99.9023 | 65.7910 | 11253 | 105 | 11253 | 11 | 10 | 90.9091 | |
| astatham-gatk | SNP | ti | map_l125_m2_e1 | homalt | 99.4917 | 99.0836 | 99.9032 | 65.8143 | 11353 | 105 | 11353 | 11 | 10 | 90.9091 | |
| raldana-dualsentieon | INDEL | I6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 92.4731 | 87.4402 | 98.1208 | 65.4453 | 731 | 105 | 731 | 14 | 12 | 85.7143 | |