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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
9001-9050 / 86044 show all | |||||||||||||||
ckim-isaac | SNP | * | * | het | 98.6547 | 97.3796 | 99.9637 | 16.8583 | 1824505 | 49096 | 1825101 | 663 | 63 | 9.5023 | |
ckim-vqsr | INDEL | * | HG002complexvar | hetalt | 91.5318 | 85.7259 | 98.1813 | 66.4504 | 3171 | 528 | 3401 | 63 | 63 | 100.0000 | |
dgrover-gatk | INDEL | * | HG002complexvar | hetalt | 96.4173 | 94.5931 | 98.3131 | 68.7891 | 3499 | 200 | 3730 | 64 | 63 | 98.4375 | |
dgrover-gatk | INDEL | D16_PLUS | HG002compoundhet | het | 89.2587 | 99.2593 | 81.0888 | 59.0856 | 402 | 3 | 283 | 66 | 63 | 95.4545 | |
dgrover-gatk | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 96.2346 | 98.8722 | 93.7341 | 83.8197 | 1315 | 15 | 1107 | 74 | 63 | 85.1351 | |
egarrison-hhga | INDEL | I6_15 | * | hetalt | 95.1738 | 91.5448 | 99.1023 | 37.9004 | 7828 | 723 | 7838 | 71 | 63 | 88.7324 | |
gduggal-bwafb | INDEL | I6_15 | HG002compoundhet | hetalt | 82.7582 | 72.8242 | 95.8306 | 40.7336 | 6217 | 2320 | 1471 | 64 | 63 | 98.4375 | |
gduggal-bwavard | INDEL | * | map_l100_m0_e0 | het | 87.7147 | 97.5514 | 79.6800 | 90.8905 | 996 | 25 | 996 | 254 | 63 | 24.8031 | |
gduggal-bwavard | INDEL | D6_15 | map_l100_m2_e1 | * | 67.9623 | 66.1818 | 69.8413 | 89.4073 | 182 | 93 | 176 | 76 | 63 | 82.8947 | |
gduggal-bwavard | INDEL | D6_15 | map_l100_m2_e1 | het | 77.2912 | 99.2593 | 63.2850 | 90.3316 | 134 | 1 | 131 | 76 | 63 | 82.8947 | |
gduggal-bwaplat | INDEL | I16_PLUS | HG002compoundhet | * | 76.7851 | 64.4424 | 94.9759 | 53.5783 | 1381 | 762 | 1380 | 73 | 63 | 86.3014 | |
gduggal-bwaplat | SNP | ti | map_l100_m2_e0 | het | 87.1494 | 77.7546 | 99.1265 | 83.6970 | 23810 | 6812 | 23832 | 210 | 63 | 30.0000 | |
gduggal-bwaplat | SNP | ti | map_l100_m2_e1 | het | 87.2661 | 77.9360 | 99.1339 | 83.6711 | 24129 | 6831 | 24151 | 211 | 63 | 29.8578 | |
eyeh-varpipe | INDEL | I6_15 | HG002compoundhet | hetalt | 42.7960 | 27.4218 | 97.4089 | 29.0841 | 2341 | 6196 | 2406 | 64 | 63 | 98.4375 | |
gduggal-bwavard | SNP | ti | lowcmp_SimpleRepeat_quadTR_11to50 | het | 96.8600 | 98.1613 | 95.5927 | 59.3604 | 6620 | 124 | 6572 | 303 | 63 | 20.7921 | |
gduggal-bwavard | SNP | tv | map_l125_m1_e0 | het | 93.0274 | 98.3804 | 88.2269 | 82.2633 | 9962 | 164 | 9937 | 1326 | 63 | 4.7511 | |
eyeh-varpipe | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 97.3719 | 99.6869 | 95.1620 | 62.9872 | 17513 | 55 | 16385 | 833 | 63 | 7.5630 | |
gduggal-bwafb | SNP | ti | map_l100_m0_e0 | het | 98.5173 | 98.5983 | 98.4365 | 72.6281 | 13787 | 196 | 13788 | 219 | 63 | 28.7671 | |
gduggal-bwafb | SNP | ti | map_l150_m1_e0 | het | 98.3399 | 98.4074 | 98.2724 | 78.0641 | 12173 | 197 | 12173 | 214 | 63 | 29.4393 | |
gduggal-bwafb | SNP | ti | map_l150_m2_e0 | het | 98.3596 | 98.4551 | 98.2644 | 79.4915 | 12682 | 199 | 12682 | 224 | 63 | 28.1250 | |
gduggal-bwaplat | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 82.2027 | 72.0883 | 95.6186 | 70.2749 | 5323 | 2061 | 5325 | 244 | 63 | 25.8197 | |
gduggal-bwaplat | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 79.0601 | 66.9823 | 96.4515 | 82.5174 | 3749 | 1848 | 3751 | 138 | 63 | 45.6522 | |
ltrigg-rtg2 | INDEL | D6_15 | HG002compoundhet | * | 97.5434 | 95.9362 | 99.2054 | 30.5780 | 8664 | 367 | 8615 | 69 | 63 | 91.3043 | |
ndellapenna-hhga | INDEL | D16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 91.6601 | 95.7237 | 87.9276 | 63.3075 | 873 | 39 | 874 | 120 | 63 | 52.5000 | |
ndellapenna-hhga | INDEL | D1_5 | * | hetalt | 77.7578 | 64.1093 | 98.7893 | 70.8854 | 6568 | 3677 | 6120 | 75 | 63 | 84.0000 | |
ndellapenna-hhga | SNP | * | map_l100_m2_e0 | * | 99.3385 | 98.8697 | 99.8117 | 63.7221 | 73128 | 836 | 73130 | 138 | 63 | 45.6522 | |
ndellapenna-hhga | SNP | * | map_l100_m2_e1 | * | 99.3413 | 98.8761 | 99.8109 | 63.7314 | 73897 | 840 | 73899 | 140 | 63 | 45.0000 | |
mlin-fermikit | INDEL | D1_5 | map_l150_m2_e0 | * | 66.8704 | 54.9148 | 85.4806 | 82.9140 | 419 | 344 | 418 | 71 | 63 | 88.7324 | |
mlin-fermikit | SNP | ti | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 96.5257 | 96.6749 | 96.3770 | 70.3153 | 3140 | 108 | 3139 | 118 | 63 | 53.3898 | |
qzeng-custom | INDEL | D16_PLUS | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 81.1561 | 92.0082 | 72.5938 | 67.9226 | 449 | 39 | 445 | 168 | 63 | 37.5000 | |
qzeng-custom | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 94.4318 | 96.0944 | 92.8258 | 50.7186 | 3543 | 144 | 3597 | 278 | 63 | 22.6619 | |
jpowers-varprowl | INDEL | I16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | het | 71.1111 | 76.1905 | 66.6667 | 71.4710 | 128 | 40 | 128 | 64 | 63 | 98.4375 | |
jpowers-varprowl | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 87.3821 | 92.4855 | 82.8125 | 68.7551 | 320 | 26 | 318 | 66 | 63 | 95.4545 | |
ltrigg-rtg1 | INDEL | D6_15 | HG002compoundhet | * | 96.2411 | 93.4780 | 99.1726 | 30.6557 | 8442 | 589 | 8390 | 70 | 63 | 90.0000 | |
ltrigg-rtg1 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 97.5965 | 95.7727 | 99.4912 | 45.8166 | 14160 | 625 | 14078 | 72 | 63 | 87.5000 | |
jli-custom | INDEL | D16_PLUS | * | * | 98.0920 | 97.4499 | 98.7427 | 65.2664 | 6611 | 173 | 6597 | 84 | 63 | 75.0000 | |
jli-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 97.5168 | 96.7193 | 98.3276 | 70.0415 | 4835 | 164 | 4821 | 82 | 63 | 76.8293 | |
jli-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 97.5168 | 96.7193 | 98.3276 | 70.0415 | 4835 | 164 | 4821 | 82 | 63 | 76.8293 | |
jmaeng-gatk | INDEL | I16_PLUS | HG002compoundhet | homalt | 8.5714 | 100.0000 | 4.4776 | 73.9300 | 3 | 0 | 3 | 64 | 63 | 98.4375 | |
jmaeng-gatk | SNP | ti | map_l100_m1_e0 | * | 89.7569 | 82.4247 | 98.5209 | 77.3729 | 39507 | 8424 | 39500 | 593 | 63 | 10.6239 | |
jpowers-varprowl | INDEL | D1_5 | map_l100_m1_e0 | * | 93.6112 | 92.3701 | 94.8860 | 83.6796 | 1707 | 141 | 1707 | 92 | 63 | 68.4783 | |
jpowers-varprowl | INDEL | D1_5 | map_l100_m2_e0 | * | 93.7318 | 92.5326 | 94.9625 | 84.4045 | 1772 | 143 | 1772 | 94 | 63 | 67.0213 | |
rpoplin-dv42 | SNP | * | map_siren | homalt | 99.7831 | 99.6882 | 99.8783 | 53.6066 | 54984 | 172 | 54983 | 67 | 63 | 94.0299 | |
raldana-dualsentieon | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 92.7674 | 88.8428 | 97.0548 | 55.8776 | 2142 | 269 | 2142 | 65 | 63 | 96.9231 | |
raldana-dualsentieon | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_51to200 | homalt | 82.1053 | 96.8944 | 71.2329 | 36.7052 | 156 | 5 | 156 | 63 | 63 | 100.0000 | |
rpoplin-dv42 | SNP | tv | map_l100_m0_e0 | * | 98.7643 | 98.7911 | 98.7375 | 67.3276 | 10950 | 134 | 10949 | 140 | 63 | 45.0000 | |
bgallagher-sentieon | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 97.2443 | 95.7292 | 98.8082 | 63.2331 | 6052 | 270 | 6052 | 73 | 63 | 86.3014 | |
bgallagher-sentieon | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 97.2443 | 95.7292 | 98.8082 | 63.2331 | 6052 | 270 | 6052 | 73 | 63 | 86.3014 | |
bgallagher-sentieon | SNP | * | map_l100_m1_e0 | het | 99.2217 | 99.5084 | 98.9366 | 68.7750 | 45136 | 223 | 45125 | 485 | 63 | 12.9897 | |
bgallagher-sentieon | SNP | * | map_l100_m2_e0 | het | 99.2145 | 99.5129 | 98.9179 | 70.0977 | 46173 | 226 | 46162 | 505 | 63 | 12.4752 |