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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
69601-69650 / 86044 show all | |||||||||||||||
jpowers-varprowl | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 54.4398 | 38.5882 | 92.3944 | 62.6316 | 328 | 522 | 328 | 27 | 21 | 77.7778 | |
jpowers-varprowl | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 81.8991 | 87.2340 | 77.1791 | 62.6848 | 492 | 72 | 487 | 144 | 112 | 77.7778 | |
jmaeng-gatk | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 97.2881 | 95.5213 | 99.1216 | 64.1698 | 5076 | 238 | 5078 | 45 | 35 | 77.7778 | |
jmaeng-gatk | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 93.1298 | 100.0000 | 87.1429 | 91.5459 | 61 | 0 | 61 | 9 | 7 | 77.7778 | |
anovak-vg | INDEL | I16_PLUS | * | homalt | 55.6761 | 71.2364 | 45.6948 | 36.9604 | 1112 | 449 | 1141 | 1356 | 1055 | 77.8024 | |
ciseli-custom | SNP | tv | map_l150_m2_e0 | homalt | 85.5692 | 82.9537 | 88.3551 | 74.3676 | 3387 | 696 | 3384 | 446 | 347 | 77.8027 | |
ndellapenna-hhga | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 76.3516 | 67.9439 | 87.1341 | 64.1684 | 2181 | 1029 | 2262 | 334 | 260 | 77.8443 | |
qzeng-custom | SNP | ti | map_l100_m2_e0 | het | 87.5433 | 79.2078 | 97.8395 | 80.9563 | 24255 | 6367 | 24137 | 533 | 415 | 77.8612 | |
qzeng-custom | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 93.8870 | 94.9500 | 92.8476 | 48.1847 | 7972 | 424 | 15305 | 1179 | 918 | 77.8626 | |
gduggal-snapfb | INDEL | I1_5 | HG002compoundhet | hetalt | 85.0180 | 77.5969 | 94.0087 | 72.7861 | 8673 | 2504 | 4111 | 262 | 204 | 77.8626 | |
ckim-dragen | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 96.7279 | 96.7327 | 96.7231 | 79.7872 | 3908 | 132 | 3601 | 122 | 95 | 77.8689 | |
ciseli-custom | SNP | tv | map_l125_m2_e0 | homalt | 87.1292 | 84.9759 | 89.3945 | 70.0273 | 5113 | 904 | 5108 | 606 | 472 | 77.8878 | |
gduggal-snapvard | SNP | * | map_siren | homalt | 98.0593 | 96.3449 | 99.8358 | 52.8740 | 53140 | 2016 | 52295 | 86 | 67 | 77.9070 | |
cchapple-custom | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | het | 98.9656 | 98.4786 | 99.4574 | 53.6403 | 10939 | 169 | 15763 | 86 | 67 | 77.9070 | |
gduggal-snapvard | INDEL | I6_15 | map_l125_m2_e0 | * | 60.0321 | 64.1509 | 56.4103 | 82.6087 | 34 | 19 | 88 | 68 | 53 | 77.9412 | |
gduggal-snapvard | INDEL | I6_15 | map_l125_m2_e0 | het | 66.1017 | 86.6667 | 53.4247 | 82.5150 | 26 | 4 | 78 | 68 | 53 | 77.9412 | |
gduggal-snapvard | INDEL | I6_15 | map_l125_m2_e1 | * | 60.1890 | 64.1509 | 56.6879 | 82.9162 | 34 | 19 | 89 | 68 | 53 | 77.9412 | |
gduggal-snapvard | INDEL | I6_15 | map_l125_m2_e1 | het | 66.1017 | 86.6667 | 53.4247 | 82.9240 | 26 | 4 | 78 | 68 | 53 | 77.9412 | |
jpowers-varprowl | SNP | tv | HG002complexvar | homalt | 99.4724 | 99.9411 | 99.0081 | 25.6082 | 95055 | 56 | 95130 | 953 | 743 | 77.9643 | |
rpoplin-dv42 | SNP | tv | HG002complexvar | het | 99.8928 | 99.8249 | 99.9608 | 21.2882 | 150467 | 264 | 150382 | 59 | 46 | 77.9661 | |
mlin-fermikit | SNP | tv | lowcmp_SimpleRepeat_quadTR_11to50 | * | 98.1967 | 97.8663 | 98.5292 | 39.4229 | 7293 | 159 | 7302 | 109 | 85 | 77.9817 | |
gduggal-snapplat | INDEL | D6_15 | HG002complexvar | hetalt | 48.9308 | 33.8598 | 88.1797 | 67.9303 | 343 | 670 | 373 | 50 | 39 | 78.0000 | |
gduggal-bwaplat | INDEL | D16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 81.6262 | 69.9242 | 98.0323 | 76.4744 | 2490 | 1071 | 2491 | 50 | 39 | 78.0000 | |
jli-custom | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 97.0535 | 95.4837 | 98.6758 | 53.2615 | 3721 | 176 | 3726 | 50 | 39 | 78.0000 | |
anovak-vg | INDEL | D6_15 | * | het | 76.4820 | 81.7202 | 71.8750 | 45.3746 | 9473 | 2119 | 11523 | 4509 | 3518 | 78.0217 | |
qzeng-custom | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 82.9227 | 78.1124 | 88.3643 | 60.1791 | 3112 | 872 | 3182 | 419 | 327 | 78.0430 | |
cchapple-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 97.1515 | 96.1503 | 98.1737 | 71.9585 | 2073 | 83 | 2204 | 41 | 32 | 78.0488 | |
gduggal-bwaplat | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_11to50 | * | 81.9324 | 70.9821 | 96.8774 | 72.2175 | 1272 | 520 | 1272 | 41 | 32 | 78.0488 | |
ciseli-custom | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | het | 63.3990 | 50.8728 | 84.1085 | 55.4404 | 204 | 197 | 217 | 41 | 32 | 78.0488 | |
ckim-isaac | INDEL | I6_15 | * | homalt | 87.6777 | 79.9968 | 96.9903 | 41.8473 | 4991 | 1248 | 4995 | 155 | 121 | 78.0645 | |
asubramanian-gatk | INDEL | D16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 97.5183 | 97.1076 | 97.9326 | 72.3189 | 3458 | 103 | 3458 | 73 | 57 | 78.0822 | |
ciseli-custom | INDEL | * | map_l125_m2_e0 | homalt | 67.2566 | 59.7641 | 76.8971 | 88.5455 | 456 | 307 | 456 | 137 | 107 | 78.1022 | |
ciseli-custom | INDEL | * | map_l125_m2_e1 | homalt | 67.5872 | 60.0775 | 77.2425 | 88.5833 | 465 | 309 | 465 | 137 | 107 | 78.1022 | |
anovak-vg | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 58.8351 | 54.0163 | 64.5980 | 47.2721 | 4519 | 3847 | 5600 | 3069 | 2397 | 78.1036 | |
asubramanian-gatk | INDEL | D16_PLUS | * | homalt | 98.2891 | 98.4634 | 98.1154 | 70.9396 | 1666 | 26 | 1666 | 32 | 25 | 78.1250 | |
asubramanian-gatk | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 97.7654 | 98.0785 | 97.4543 | 75.1188 | 1225 | 24 | 1225 | 32 | 25 | 78.1250 | |
asubramanian-gatk | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 97.7654 | 98.0785 | 97.4543 | 75.1188 | 1225 | 24 | 1225 | 32 | 25 | 78.1250 | |
ndellapenna-hhga | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | homalt | 94.4612 | 95.3252 | 93.6128 | 55.7029 | 469 | 23 | 469 | 32 | 25 | 78.1250 | |
hfeng-pmm1 | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 96.9107 | 94.4420 | 99.5119 | 50.8251 | 6525 | 384 | 6524 | 32 | 25 | 78.1250 | |
gduggal-bwaplat | INDEL | I1_5 | HG002complexvar | homalt | 95.0189 | 90.9429 | 99.4774 | 52.2999 | 12230 | 1218 | 12183 | 64 | 50 | 78.1250 | |
mlin-fermikit | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | * | 88.3125 | 86.2357 | 90.4918 | 71.6894 | 827 | 132 | 828 | 87 | 68 | 78.1609 | |
gduggal-snapvard | INDEL | * | HG002compoundhet | het | 60.5436 | 68.6950 | 54.1215 | 56.4812 | 2811 | 1281 | 24103 | 20432 | 15973 | 78.1764 | |
rpoplin-dv42 | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | * | 94.9354 | 94.1445 | 95.7397 | 51.4296 | 1238 | 77 | 1236 | 55 | 43 | 78.1818 | |
ckim-dragen | INDEL | D1_5 | HG002complexvar | * | 99.5269 | 99.3917 | 99.6625 | 58.3864 | 32516 | 199 | 32478 | 110 | 86 | 78.1818 | |
egarrison-hhga | INDEL | D6_15 | HG002complexvar | * | 89.5440 | 86.4579 | 92.8586 | 57.3769 | 4584 | 718 | 4590 | 353 | 276 | 78.1870 | |
qzeng-custom | SNP | * | HG002complexvar | homalt | 99.2256 | 98.6350 | 99.8233 | 20.2251 | 284636 | 3939 | 274538 | 486 | 380 | 78.1893 | |
ciseli-custom | INDEL | * | map_l125_m1_e0 | homalt | 66.8206 | 59.2896 | 76.5432 | 87.7564 | 434 | 298 | 434 | 133 | 104 | 78.1955 | |
gduggal-snapvard | INDEL | I6_15 | HG002complexvar | het | 67.8635 | 76.9851 | 60.6744 | 48.9450 | 1813 | 542 | 2393 | 1551 | 1213 | 78.2076 | |
ciseli-custom | INDEL | * | map_l100_m0_e0 | homalt | 66.3988 | 59.5285 | 75.0617 | 86.5938 | 303 | 206 | 304 | 101 | 79 | 78.2178 | |
gduggal-snapplat | INDEL | D1_5 | HG002complexvar | hetalt | 53.4943 | 40.5325 | 78.6432 | 87.0210 | 548 | 804 | 626 | 170 | 133 | 78.2353 |