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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
15251-15300 / 86044 show all | |||||||||||||||
| ndellapenna-hhga | SNP | * | map_l150_m0_e0 | * | 98.5596 | 97.5316 | 99.6095 | 77.4194 | 11735 | 297 | 11735 | 46 | 22 | 47.8261 | |
| ndellapenna-hhga | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 93.8135 | 92.0290 | 95.6685 | 83.4063 | 1016 | 88 | 1016 | 46 | 28 | 60.8696 | |
| ndellapenna-hhga | SNP | ti | map_l125_m2_e0 | het | 98.8804 | 98.0239 | 99.7520 | 70.6633 | 18503 | 373 | 18503 | 46 | 20 | 43.4783 | |
| ndellapenna-hhga | SNP | ti | map_l125_m2_e1 | het | 98.8822 | 98.0248 | 99.7547 | 70.7116 | 18710 | 377 | 18710 | 46 | 20 | 43.4783 | |
| ndellapenna-hhga | SNP | tv | map_l125_m2_e1 | * | 99.1365 | 98.5592 | 99.7206 | 69.3660 | 16417 | 240 | 16417 | 46 | 22 | 47.8261 | |
| ndellapenna-hhga | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 92.9959 | 91.7476 | 94.2786 | 67.1300 | 756 | 68 | 758 | 46 | 41 | 89.1304 | |
| ndellapenna-hhga | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 64.4666 | 47.9448 | 98.3624 | 43.7187 | 3266 | 3546 | 2763 | 46 | 36 | 78.2609 | |
| jli-custom | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 99.6216 | 99.8758 | 99.3687 | 35.8426 | 7238 | 9 | 7241 | 46 | 44 | 95.6522 | |
| jmaeng-gatk | INDEL | * | map_l150_m0_e0 | * | 94.4555 | 97.4708 | 91.6211 | 94.8011 | 501 | 13 | 503 | 46 | 4 | 8.6957 | |
| jmaeng-gatk | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 90.3229 | 98.3425 | 83.5125 | 84.0206 | 356 | 6 | 233 | 46 | 44 | 95.6522 | |
| jmaeng-gatk | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_51to200 | het | 76.2887 | 100.0000 | 61.6667 | 83.5391 | 169 | 0 | 74 | 46 | 45 | 97.8261 | |
| jpowers-varprowl | INDEL | D6_15 | segdup | * | 67.5255 | 63.3508 | 72.2892 | 93.4978 | 121 | 70 | 120 | 46 | 46 | 100.0000 | |
| ltrigg-rtg1 | INDEL | D6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 94.2071 | 90.0993 | 98.7075 | 49.5392 | 3540 | 389 | 3513 | 46 | 33 | 71.7391 | |
| ltrigg-rtg2 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 98.4583 | 97.2091 | 99.7401 | 57.5217 | 17659 | 507 | 17653 | 46 | 39 | 84.7826 | |
| ltrigg-rtg2 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 98.4583 | 97.2091 | 99.7401 | 57.5217 | 17659 | 507 | 17653 | 46 | 39 | 84.7826 | |
| jmaeng-gatk | SNP | * | HG002compoundhet | * | 99.3502 | 98.8847 | 99.8202 | 41.8705 | 25534 | 288 | 25531 | 46 | 39 | 84.7826 | |
| anovak-vg | INDEL | I6_15 | lowcmp_SimpleRepeat_triTR_11to50 | homalt | 76.2700 | 83.0508 | 70.5128 | 33.8983 | 49 | 10 | 110 | 46 | 45 | 97.8261 | |
| anovak-vg | SNP | * | func_cds | homalt | 99.1150 | 98.8967 | 99.3342 | 20.4124 | 6902 | 77 | 6863 | 46 | 41 | 89.1304 | |
| anovak-vg | SNP | * | lowcmp_SimpleRepeat_triTR_11to50 | homalt | 97.9828 | 97.6625 | 98.3051 | 30.8535 | 2674 | 64 | 2668 | 46 | 33 | 71.7391 | |
| anovak-vg | SNP | tv | segdup | homalt | 98.7340 | 98.8882 | 98.5802 | 89.2441 | 3202 | 36 | 3194 | 46 | 38 | 82.6087 | |
| bgallagher-sentieon | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 99.5462 | 99.5186 | 99.5739 | 79.3195 | 10749 | 52 | 10749 | 46 | 13 | 28.2609 | |
| anovak-vg | INDEL | C1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 0.0000 | 0.0000 | 14.8148 | 81.5068 | 0 | 0 | 8 | 46 | 3 | 6.5217 | |
| anovak-vg | INDEL | C1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 0.0000 | 0.0000 | 14.8148 | 80.1471 | 0 | 0 | 8 | 46 | 3 | 6.5217 | |
| astatham-gatk | SNP | ti | map_l100_m0_e0 | * | 92.5350 | 86.2891 | 99.7557 | 72.1287 | 18786 | 2985 | 18783 | 46 | 24 | 52.1739 | |
| asubramanian-gatk | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | homalt | 94.6012 | 97.7642 | 91.6364 | 62.8378 | 481 | 11 | 504 | 46 | 23 | 50.0000 | |
| asubramanian-gatk | INDEL | D16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 96.8698 | 97.4170 | 96.3288 | 83.1947 | 1320 | 35 | 1207 | 46 | 34 | 73.9130 | |
| asubramanian-gatk | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_11to50 | * | 97.1461 | 96.8750 | 97.4186 | 69.7659 | 1736 | 56 | 1736 | 46 | 39 | 84.7826 | |
| asubramanian-gatk | SNP | * | map_l100_m1_e0 | * | 60.2018 | 43.0908 | 99.8527 | 84.6729 | 31199 | 41204 | 31193 | 46 | 12 | 26.0870 | |
| astatham-gatk | INDEL | D16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 97.8462 | 99.3358 | 96.4006 | 82.8203 | 1346 | 9 | 1232 | 46 | 29 | 63.0435 | |
| astatham-gatk | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 99.0587 | 99.3353 | 98.7837 | 71.2941 | 3736 | 25 | 3736 | 46 | 45 | 97.8261 | |
| astatham-gatk | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 99.0587 | 99.3353 | 98.7837 | 71.2941 | 3736 | 25 | 3736 | 46 | 45 | 97.8261 | |
| rpoplin-dv42 | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | het | 91.5617 | 96.6667 | 86.9688 | 73.4387 | 319 | 11 | 307 | 46 | 35 | 76.0870 | |
| rpoplin-dv42 | SNP | tv | map_l250_m1_e0 | * | 97.8376 | 97.4311 | 98.2476 | 86.7964 | 2579 | 68 | 2579 | 46 | 30 | 65.2174 | |
| raldana-dualsentieon | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 93.7500 | 98.9446 | 89.0736 | 60.1703 | 375 | 4 | 375 | 46 | 46 | 100.0000 | |
| raldana-dualsentieon | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 95.4252 | 92.3274 | 98.7380 | 54.1740 | 3598 | 299 | 3599 | 46 | 39 | 84.7826 | |
| raldana-dualsentieon | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_51to200 | het | 73.3937 | 95.8580 | 59.4595 | 79.8913 | 162 | 7 | 66 | 45 | 45 | 100.0000 | |
| rpoplin-dv42 | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 90.9269 | 85.8170 | 96.6839 | 77.1395 | 1313 | 217 | 1312 | 45 | 41 | 91.1111 | |
| rpoplin-dv42 | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 90.9269 | 85.8170 | 96.6839 | 77.1395 | 1313 | 217 | 1312 | 45 | 41 | 91.1111 | |
| rpoplin-dv42 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 98.7353 | 98.9667 | 98.5050 | 75.1773 | 2969 | 31 | 2965 | 45 | 33 | 73.3333 | |
| rpoplin-dv42 | INDEL | * | map_l100_m2_e1 | het | 97.6450 | 97.2258 | 98.0678 | 84.3523 | 2278 | 65 | 2284 | 45 | 20 | 44.4444 | |
| rpoplin-dv42 | INDEL | D1_5 | HG002complexvar | hetalt | 94.1845 | 91.9379 | 96.5438 | 71.6833 | 1243 | 109 | 1257 | 45 | 44 | 97.7778 | |
| hfeng-pmm2 | SNP | tv | HG002complexvar | het | 99.7540 | 99.5389 | 99.9700 | 20.7785 | 150036 | 695 | 149957 | 45 | 8 | 17.7778 | |
| hfeng-pmm3 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 98.9613 | 99.3365 | 98.5889 | 49.3810 | 3144 | 21 | 3144 | 45 | 43 | 95.5556 | |
| jlack-gatk | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 89.3112 | 100.0000 | 80.6867 | 66.4748 | 188 | 0 | 188 | 45 | 44 | 97.7778 | |
| jlack-gatk | SNP | * | map_siren | homalt | 99.6008 | 99.2857 | 99.9179 | 50.5286 | 54762 | 394 | 54753 | 45 | 30 | 66.6667 | |
| jli-custom | INDEL | * | map_l100_m2_e0 | * | 98.4246 | 98.0774 | 98.7742 | 83.9477 | 3622 | 71 | 3626 | 45 | 15 | 33.3333 | |
| jli-custom | INDEL | * | map_l100_m2_e1 | * | 98.4239 | 98.0564 | 98.7942 | 84.0281 | 3683 | 73 | 3687 | 45 | 15 | 33.3333 | |
| jlack-gatk | INDEL | D1_5 | HG002complexvar | hetalt | 93.7719 | 91.1243 | 96.5779 | 72.4607 | 1232 | 120 | 1270 | 45 | 42 | 93.3333 | |
| hfeng-pmm1 | SNP | * | map_siren | homalt | 99.8994 | 99.8803 | 99.9184 | 53.4037 | 55090 | 66 | 55084 | 45 | 26 | 57.7778 | |
| hfeng-pmm1 | SNP | ti | * | homalt | 99.9926 | 99.9908 | 99.9944 | 16.6970 | 802964 | 74 | 802957 | 45 | 35 | 77.7778 | |