PrecisionFDA
Truth Challenge
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Explore HG002 comparison results
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| Entry | Type | Subtype | Subset | Genotype | F-score | Recall | Precision | Frac_NA | Truth TP | Truth FN | Query TP | Query FP | FP gt | % FP ma | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
4351-4400 / 86044 show all | |||||||||||||||
| qzeng-custom | SNP | tv | * | homalt | 99.5964 | 99.2947 | 99.8999 | 20.4155 | 374463 | 2660 | 372209 | 373 | 242 | 64.8794 | |
| ciseli-custom | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_51to200 | homalt | 52.0907 | 81.7259 | 38.2284 | 55.9096 | 161 | 36 | 164 | 265 | 242 | 91.3208 | |
| bgallagher-sentieon | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 94.2519 | 99.0946 | 89.8604 | 65.5446 | 2189 | 20 | 2189 | 247 | 241 | 97.5709 | |
| qzeng-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 93.5793 | 94.7690 | 92.4191 | 52.4483 | 3569 | 197 | 3572 | 293 | 241 | 82.2526 | |
| qzeng-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 93.5793 | 94.7690 | 92.4191 | 52.4483 | 3569 | 197 | 3572 | 293 | 241 | 82.2526 | |
| ciseli-custom | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_51to200 | * | 22.5601 | 18.5079 | 28.8840 | 55.7171 | 129 | 568 | 132 | 325 | 240 | 73.8462 | |
| cchapple-custom | SNP | * | map_l150_m1_e0 | * | 96.5908 | 96.7363 | 96.4458 | 77.1687 | 29610 | 999 | 29605 | 1091 | 240 | 21.9982 | |
| ciseli-custom | INDEL | * | segdup | * | 85.0497 | 84.0767 | 86.0456 | 94.6455 | 2149 | 407 | 2152 | 349 | 240 | 68.7679 | |
| gduggal-snapvard | INDEL | * | map_l125_m1_e0 | het | 83.6174 | 95.9551 | 74.0909 | 89.7946 | 1281 | 54 | 1793 | 627 | 240 | 38.2775 | |
| gduggal-snapfb | SNP | ti | HG002complexvar | homalt | 99.6542 | 99.7054 | 99.6030 | 19.3776 | 192894 | 570 | 192940 | 769 | 240 | 31.2094 | |
| jlack-gatk | SNP | * | map_l125_m2_e1 | * | 96.2112 | 98.8920 | 93.6720 | 80.3444 | 46679 | 523 | 46673 | 3153 | 240 | 7.6118 | |
| jlack-gatk | SNP | ti | map_siren | * | 98.3403 | 99.3782 | 97.3238 | 62.0115 | 99731 | 624 | 99716 | 2742 | 240 | 8.7527 | |
| jlack-gatk | INDEL | * | lowcmp_SimpleRepeat_diTR_51to200 | het | 63.1909 | 86.1224 | 49.9033 | 76.4142 | 422 | 68 | 258 | 259 | 240 | 92.6641 | |
| jpowers-varprowl | INDEL | D16_PLUS | HG002complexvar | het | 82.6837 | 86.0885 | 79.5380 | 63.2839 | 953 | 154 | 964 | 248 | 240 | 96.7742 | |
| eyeh-varpipe | INDEL | D6_15 | lowcmp_SimpleRepeat_triTR_11to50 | * | 80.6871 | 76.7630 | 85.0340 | 31.9444 | 1328 | 402 | 1375 | 242 | 240 | 99.1736 | |
| gduggal-bwaplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 86.1524 | 77.3435 | 97.2257 | 44.5184 | 8589 | 2516 | 8586 | 245 | 240 | 97.9592 | |
| jlack-gatk | SNP | * | map_l125_m2_e0 | * | 96.1886 | 98.8828 | 93.6372 | 80.3034 | 46201 | 522 | 46195 | 3139 | 239 | 7.6139 | |
| hfeng-pmm3 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 97.7526 | 96.6010 | 98.9320 | 70.8092 | 29444 | 1036 | 28994 | 313 | 239 | 76.3578 | |
| hfeng-pmm3 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 97.7526 | 96.6010 | 98.9320 | 70.8092 | 29444 | 1036 | 28994 | 313 | 239 | 76.3578 | |
| cchapple-custom | SNP | * | map_l150_m1_e0 | het | 95.6722 | 96.8731 | 94.5008 | 80.5876 | 18712 | 604 | 18731 | 1090 | 239 | 21.9266 | |
| qzeng-custom | INDEL | D1_5 | * | homalt | 99.2131 | 98.9883 | 99.4390 | 53.3870 | 48431 | 495 | 48391 | 273 | 239 | 87.5458 | |
| mlin-fermikit | SNP | tv | map_l250_m2_e1 | * | 45.6242 | 32.2702 | 77.8329 | 80.3319 | 941 | 1975 | 941 | 268 | 239 | 89.1791 | |
| mlin-fermikit | SNP | tv | map_l250_m2_e1 | homalt | 50.9001 | 43.3404 | 61.6541 | 74.8392 | 410 | 536 | 410 | 255 | 239 | 93.7255 | |
| rpoplin-dv42 | INDEL | * | * | homalt | 99.5190 | 99.2498 | 99.7896 | 55.3247 | 124233 | 939 | 124240 | 262 | 239 | 91.2214 | |
| rpoplin-dv42 | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | het | 95.1084 | 98.7559 | 91.7206 | 61.9079 | 2699 | 34 | 2692 | 243 | 239 | 98.3539 | |
| asubramanian-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 97.8063 | 97.1411 | 98.4806 | 47.1994 | 17737 | 522 | 17759 | 274 | 239 | 87.2263 | |
| anovak-vg | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 31.4802 | 22.9894 | 49.9162 | 51.5028 | 303 | 1015 | 298 | 299 | 239 | 79.9331 | |
| anovak-vg | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 78.1375 | 85.3261 | 72.0660 | 79.7424 | 942 | 162 | 1179 | 457 | 238 | 52.0788 | |
| qzeng-custom | SNP | tv | map_l150_m2_e0 | * | 82.9982 | 72.7081 | 96.6811 | 87.1519 | 8256 | 3099 | 8244 | 283 | 238 | 84.0989 | |
| ciseli-custom | SNP | tv | map_l125_m0_e0 | homalt | 85.0153 | 83.7461 | 86.3236 | 70.9690 | 1860 | 361 | 1862 | 295 | 238 | 80.6780 | |
| jlack-gatk | SNP | * | map_l125_m1_e0 | * | 96.1255 | 98.8638 | 93.5349 | 78.9418 | 44812 | 515 | 44806 | 3097 | 238 | 7.6849 | |
| ghariani-varprowl | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 83.1025 | 78.7956 | 87.9076 | 66.5360 | 2787 | 750 | 2777 | 382 | 238 | 62.3037 | |
| gduggal-snapfb | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 67.8720 | 57.3310 | 83.1622 | 50.3568 | 2002 | 1490 | 1215 | 246 | 238 | 96.7480 | |
| ghariani-varprowl | SNP | * | map_l125_m2_e1 | het | 97.3535 | 98.9777 | 95.7818 | 79.7151 | 29337 | 303 | 29337 | 1292 | 237 | 18.3437 | |
| ndellapenna-hhga | INDEL | D16_PLUS | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 75.3565 | 68.2801 | 84.0693 | 69.0324 | 1453 | 675 | 1504 | 285 | 237 | 83.1579 | |
| mlin-fermikit | SNP | tv | map_l250_m2_e0 | * | 45.2311 | 31.9223 | 77.5717 | 80.1107 | 920 | 1962 | 920 | 266 | 237 | 89.0977 | |
| mlin-fermikit | SNP | tv | map_l250_m2_e0 | homalt | 50.5025 | 42.9029 | 61.3740 | 74.4739 | 402 | 535 | 402 | 253 | 237 | 93.6759 | |
| gduggal-snapfb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 73.1048 | 71.1289 | 75.1936 | 73.0650 | 2577 | 1046 | 2622 | 865 | 237 | 27.3988 | |
| eyeh-varpipe | INDEL | I16_PLUS | * | homalt | 74.9769 | 69.1864 | 81.8251 | 30.1275 | 1080 | 481 | 1076 | 239 | 237 | 99.1632 | |
| cchapple-custom | INDEL | * | lowcmp_SimpleRepeat_diTR_51to200 | * | 84.8454 | 79.2480 | 91.2936 | 44.8269 | 1665 | 436 | 2590 | 247 | 237 | 95.9514 | |
| ltrigg-rtg1 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 97.3301 | 95.6145 | 99.1085 | 62.8544 | 62485 | 2866 | 62808 | 565 | 237 | 41.9469 | |
| ltrigg-rtg1 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 97.3301 | 95.6145 | 99.1085 | 62.8544 | 62485 | 2866 | 62808 | 565 | 237 | 41.9469 | |
| jmaeng-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 98.4732 | 98.9378 | 98.0130 | 65.7049 | 12388 | 133 | 12233 | 248 | 237 | 95.5645 | |
| jpowers-varprowl | SNP | * | map_l100_m0_e0 | * | 97.2063 | 96.7297 | 97.6876 | 74.3551 | 31767 | 1074 | 31768 | 752 | 236 | 31.3830 | |
| gduggal-bwaplat | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 83.7356 | 73.4530 | 97.3658 | 70.5818 | 11787 | 4260 | 11791 | 319 | 236 | 73.9812 | |
| gduggal-bwavard | SNP | * | map_l100_m1_e0 | * | 96.4277 | 97.4269 | 95.4487 | 73.9277 | 70540 | 1863 | 69564 | 3317 | 236 | 7.1149 | |
| qzeng-custom | SNP | tv | map_l150_m1_e0 | * | 82.5382 | 72.0674 | 96.5687 | 86.5523 | 7864 | 3048 | 7852 | 279 | 236 | 84.5878 | |
| ghariani-varprowl | SNP | * | map_l125_m2_e0 | het | 97.3365 | 98.9699 | 95.7561 | 79.6531 | 29016 | 302 | 29016 | 1286 | 236 | 18.3515 | |
| gduggal-snapfb | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 62.0729 | 98.0650 | 45.4073 | 82.4158 | 10592 | 209 | 10757 | 12933 | 236 | 1.8248 | |
| ckim-dragen | SNP | * | HG002complexvar | * | 99.9301 | 99.9223 | 99.9379 | 19.4552 | 753795 | 586 | 754278 | 469 | 236 | 50.3198 | |