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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
77351-77400 / 86044 show all | |||||||||||||||
gduggal-snapvard | INDEL | I1_5 | map_l125_m2_e0 | het | 88.5120 | 98.7928 | 80.1693 | 90.7999 | 491 | 6 | 663 | 164 | 68 | 41.4634 | |
gduggal-snapvard | INDEL | I1_5 | segdup | * | 91.3324 | 90.4627 | 92.2190 | 95.0889 | 958 | 101 | 960 | 81 | 68 | 83.9506 | |
gduggal-snapvard | SNP | ti | map_l250_m1_e0 | * | 86.1545 | 95.0207 | 78.8017 | 91.2590 | 4351 | 228 | 4327 | 1164 | 68 | 5.8419 | |
ghariani-varprowl | INDEL | D16_PLUS | * | homalt | 72.0773 | 58.8061 | 93.0841 | 70.1867 | 995 | 697 | 996 | 74 | 68 | 91.8919 | |
ghariani-varprowl | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 94.5086 | 98.3261 | 90.9764 | 72.8370 | 1351 | 23 | 1351 | 134 | 68 | 50.7463 | |
ghariani-varprowl | SNP | * | map_l100_m2_e1 | homalt | 99.3161 | 99.0071 | 99.6271 | 64.4501 | 27520 | 276 | 27520 | 103 | 68 | 66.0194 | |
ghariani-varprowl | SNP | tv | map_l125_m0_e0 | * | 96.2771 | 98.0848 | 94.5349 | 81.3241 | 6504 | 127 | 6504 | 376 | 68 | 18.0851 | |
eyeh-varpipe | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 97.4514 | 96.5009 | 98.4209 | 44.2767 | 6481 | 235 | 7230 | 116 | 68 | 58.6207 | |
eyeh-varpipe | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_51to200 | homalt | 0.0000 | 0.0000 | 13.8298 | 27.6923 | 0 | 0 | 13 | 81 | 68 | 83.9506 | |
gduggal-snapfb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | hetalt | 52.3244 | 38.4502 | 81.8636 | 44.8624 | 1047 | 1676 | 492 | 109 | 68 | 62.3853 | |
rpoplin-dv42 | INDEL | I6_15 | * | homalt | 97.7056 | 96.5700 | 98.8683 | 48.6914 | 6025 | 214 | 6028 | 69 | 68 | 98.5507 | |
rpoplin-dv42 | SNP | * | map_l250_m2_e0 | * | 98.3456 | 98.0089 | 98.6847 | 88.0100 | 7728 | 157 | 7728 | 103 | 68 | 66.0194 | |
rpoplin-dv42 | SNP | ti | map_l150_m2_e0 | het | 99.0005 | 98.8200 | 99.1816 | 75.9652 | 12729 | 152 | 12725 | 105 | 68 | 64.7619 | |
rpoplin-dv42 | SNP | ti | map_l150_m2_e1 | het | 98.9954 | 98.8167 | 99.1746 | 76.0502 | 12861 | 154 | 12857 | 107 | 68 | 63.5514 | |
rpoplin-dv42 | INDEL | * | HG002complexvar | hetalt | 94.3915 | 91.0246 | 98.0170 | 68.2440 | 3367 | 332 | 3460 | 70 | 68 | 97.1429 | |
rpoplin-dv42 | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 96.2570 | 93.3938 | 99.3014 | 31.9625 | 9783 | 692 | 9808 | 69 | 68 | 98.5507 | |
ckim-isaac | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 92.6853 | 87.1155 | 99.0159 | 25.1484 | 7052 | 1043 | 7244 | 72 | 68 | 94.4444 | |
dgrover-gatk | INDEL | * | * | hetalt | 96.9073 | 94.2584 | 99.7094 | 58.4640 | 23788 | 1449 | 24018 | 70 | 68 | 97.1429 | |
dgrover-gatk | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 92.7974 | 97.3813 | 88.6256 | 72.0653 | 595 | 16 | 561 | 72 | 68 | 94.4444 | |
dgrover-gatk | SNP | * | map_l125_m1_e0 | * | 99.3215 | 99.3139 | 99.3291 | 72.7346 | 45016 | 311 | 45010 | 304 | 68 | 22.3684 | |
dgrover-gatk | SNP | ti | map_siren | * | 99.6765 | 99.6403 | 99.7128 | 55.1320 | 99994 | 361 | 99979 | 288 | 68 | 23.6111 | |
egarrison-hhga | INDEL | * | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 99.4966 | 99.3171 | 99.6769 | 61.8156 | 28067 | 193 | 28070 | 91 | 68 | 74.7253 | |
ckim-isaac | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 82.8671 | 76.7932 | 89.9844 | 83.5648 | 1092 | 330 | 1150 | 128 | 68 | 53.1250 | |
egarrison-hhga | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 95.5535 | 97.1688 | 93.9910 | 58.3407 | 3535 | 103 | 3535 | 226 | 68 | 30.0885 | |
egarrison-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 94.2348 | 96.1840 | 92.3630 | 49.0134 | 2697 | 107 | 2697 | 223 | 68 | 30.4933 | |
egarrison-hhga | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 86.0678 | 81.0458 | 91.7533 | 79.3558 | 1240 | 290 | 1235 | 111 | 68 | 61.2613 | |
egarrison-hhga | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 86.0678 | 81.0458 | 91.7533 | 79.3558 | 1240 | 290 | 1235 | 111 | 68 | 61.2613 | |
egarrison-hhga | INDEL | I1_5 | HG002compoundhet | het | 88.5536 | 91.2941 | 85.9729 | 82.4603 | 776 | 74 | 760 | 124 | 68 | 54.8387 | |
eyeh-varpipe | INDEL | * | map_l100_m1_e0 | het | 96.1706 | 95.7494 | 96.5955 | 81.6758 | 2140 | 95 | 2894 | 102 | 68 | 66.6667 | |
eyeh-varpipe | INDEL | * | map_l125_m2_e1 | * | 96.4393 | 96.0449 | 96.8369 | 94.4522 | 2137 | 88 | 2939 | 96 | 68 | 70.8333 | |
astatham-gatk | INDEL | D16_PLUS | HG002compoundhet | het | 88.8320 | 99.5062 | 80.2260 | 58.8850 | 403 | 2 | 284 | 70 | 68 | 97.1429 | |
astatham-gatk | INDEL | D6_15 | HG002complexvar | * | 98.3071 | 98.0385 | 98.5771 | 58.5385 | 5198 | 104 | 5196 | 75 | 68 | 90.6667 | |
astatham-gatk | INDEL | I16_PLUS | * | homalt | 97.6467 | 99.6797 | 95.6950 | 72.0858 | 1556 | 5 | 1556 | 70 | 68 | 97.1429 | |
bgallagher-sentieon | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 94.1847 | 93.8543 | 94.5174 | 64.2660 | 1237 | 81 | 1224 | 71 | 68 | 95.7746 | |
asubramanian-gatk | INDEL | I6_15 | * | hetalt | 94.9273 | 91.1005 | 99.0896 | 39.2643 | 7790 | 761 | 7837 | 72 | 68 | 94.4444 | |
ckim-gatk | SNP | ti | map_l100_m1_e0 | * | 89.7917 | 82.4352 | 98.5900 | 77.1488 | 39512 | 8419 | 39505 | 565 | 68 | 12.0354 | |
ciseli-custom | SNP | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 90.8951 | 98.2838 | 84.5396 | 75.5036 | 1718 | 30 | 1717 | 314 | 68 | 21.6561 | |
ciseli-custom | SNP | ti | lowcmp_SimpleRepeat_diTR_11to50 | het | 71.2738 | 92.2490 | 58.0701 | 68.6719 | 2904 | 244 | 3015 | 2177 | 68 | 3.1236 | |
ckim-dragen | INDEL | * | * | hetalt | 95.9597 | 92.4793 | 99.7124 | 57.0557 | 23339 | 1898 | 23575 | 68 | 68 | 100.0000 | |
ckim-dragen | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_51to200 | * | 90.4159 | 90.6122 | 90.2204 | 58.0347 | 666 | 69 | 655 | 71 | 68 | 95.7746 | |
ckim-gatk | INDEL | D16_PLUS | HG002compoundhet | het | 88.7912 | 99.7531 | 80.0000 | 59.4286 | 404 | 1 | 284 | 71 | 68 | 95.7746 | |
ckim-dragen | SNP | * | map_l150_m1_e0 | het | 97.4659 | 98.6591 | 96.3012 | 80.3004 | 19057 | 259 | 19058 | 732 | 68 | 9.2896 | |
ciseli-custom | INDEL | C1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 0.0000 | 0.0000 | 20.2658 | 93.8269 | 0 | 0 | 61 | 240 | 68 | 28.3333 | |
ciseli-custom | INDEL | C1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 0.0000 | 0.0000 | 20.2658 | 93.8269 | 0 | 0 | 61 | 240 | 68 | 28.3333 | |
cchapple-custom | INDEL | * | map_siren | * | 97.2258 | 97.5978 | 96.8567 | 81.1585 | 7232 | 178 | 7426 | 241 | 69 | 28.6307 | |
ckim-gatk | INDEL | I1_5 | HG002compoundhet | het | 95.1264 | 98.8235 | 91.6959 | 86.6176 | 840 | 10 | 784 | 71 | 69 | 97.1831 | |
ckim-gatk | SNP | * | HG002complexvar | het | 99.7401 | 99.5255 | 99.9558 | 19.1024 | 463288 | 2209 | 463160 | 205 | 69 | 33.6585 | |
ckim-dragen | SNP | tv | map_siren | * | 98.9465 | 99.4753 | 98.4233 | 61.5086 | 45689 | 241 | 45694 | 732 | 69 | 9.4262 | |
ckim-dragen | SNP | * | map_l150_m2_e0 | het | 97.5195 | 98.7086 | 96.3588 | 81.7586 | 19873 | 260 | 19874 | 751 | 69 | 9.1878 | |
ckim-dragen | SNP | ti | map_l150_m2_e1 | * | 98.2199 | 98.8901 | 97.5587 | 78.2933 | 20493 | 230 | 20500 | 513 | 69 | 13.4503 |