PrecisionFDA
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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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
4101-4150 / 86044 show all | |||||||||||||||
| egarrison-hhga | INDEL | I1_5 | HG002compoundhet | * | 96.1134 | 95.0631 | 97.1871 | 62.4825 | 11746 | 610 | 11747 | 340 | 264 | 77.6471 | |
| jlack-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 90.3274 | 94.4904 | 86.5158 | 75.9742 | 2058 | 120 | 1835 | 286 | 264 | 92.3077 | |
| raldana-dualsentieon | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 97.1585 | 95.7079 | 98.6538 | 44.4898 | 19712 | 884 | 19713 | 269 | 264 | 98.1413 | |
| raldana-dualsentieon | INDEL | I1_5 | HG002compoundhet | homalt | 70.9467 | 99.0881 | 55.2542 | 86.1176 | 326 | 3 | 326 | 264 | 264 | 100.0000 | |
| jpowers-varprowl | INDEL | I6_15 | * | homalt | 79.1239 | 68.4565 | 93.7294 | 42.5350 | 4271 | 1968 | 4275 | 286 | 264 | 92.3077 | |
| jpowers-varprowl | SNP | * | map_l100_m2_e0 | het | 97.3254 | 97.0883 | 97.5636 | 74.0402 | 45048 | 1351 | 45050 | 1125 | 264 | 23.4667 | |
| jpowers-varprowl | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 97.3815 | 99.4979 | 95.3533 | 74.7822 | 11494 | 58 | 11512 | 561 | 264 | 47.0588 | |
| jpowers-varprowl | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 97.3815 | 99.4979 | 95.3533 | 74.7822 | 11494 | 58 | 11512 | 561 | 264 | 47.0588 | |
| jpowers-varprowl | SNP | * | map_l100_m1_e0 | het | 97.3402 | 97.0590 | 97.6230 | 72.4758 | 44025 | 1334 | 44027 | 1072 | 263 | 24.5336 | |
| ndellapenna-hhga | INDEL | D16_PLUS | * | het | 92.2712 | 93.4473 | 91.1244 | 67.5886 | 2952 | 207 | 3193 | 311 | 263 | 84.5659 | |
| ndellapenna-hhga | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 87.6321 | 89.4447 | 85.8915 | 75.4124 | 1627 | 192 | 1869 | 307 | 263 | 85.6678 | |
| ndellapenna-hhga | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 87.6321 | 89.4447 | 85.8915 | 75.4124 | 1627 | 192 | 1869 | 307 | 263 | 85.6678 | |
| ckim-dragen | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 97.6040 | 99.7536 | 95.5451 | 59.8944 | 5667 | 14 | 5662 | 264 | 263 | 99.6212 | |
| bgallagher-sentieon | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 98.6696 | 99.8938 | 97.4750 | 45.7112 | 10346 | 11 | 10346 | 268 | 263 | 98.1343 | |
| cchapple-custom | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | het | 98.1220 | 97.1827 | 99.0797 | 47.1607 | 15316 | 444 | 34988 | 325 | 263 | 80.9231 | |
| gduggal-bwaplat | INDEL | D1_5 | HG002compoundhet | * | 81.6558 | 71.3118 | 95.5098 | 73.5540 | 8725 | 3510 | 8721 | 410 | 263 | 64.1463 | |
| gduggal-bwaplat | SNP | ti | HG002compoundhet | * | 89.0817 | 91.8641 | 86.4629 | 42.2720 | 16056 | 1422 | 16121 | 2524 | 263 | 10.4200 | |
| gduggal-bwavard | INDEL | D16_PLUS | HG002complexvar | het | 81.5892 | 88.8889 | 75.3974 | 65.5091 | 984 | 123 | 996 | 325 | 263 | 80.9231 | |
| ghariani-varprowl | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 97.6620 | 99.4893 | 95.9007 | 73.2635 | 11493 | 59 | 11510 | 492 | 263 | 53.4553 | |
| ghariani-varprowl | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 97.6620 | 99.4893 | 95.9007 | 73.2635 | 11493 | 59 | 11510 | 492 | 263 | 53.4553 | |
| gduggal-snapplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 20.4886 | 18.2277 | 23.3898 | 80.8737 | 397 | 1781 | 552 | 1808 | 263 | 14.5465 | |
| ckim-vqsr | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 99.5126 | 99.8992 | 99.1290 | 74.4665 | 30730 | 31 | 30730 | 270 | 263 | 97.4074 | |
| ckim-vqsr | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 97.9357 | 97.2033 | 98.6791 | 48.0009 | 20020 | 576 | 20021 | 268 | 262 | 97.7612 | |
| dgrover-gatk | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 99.4181 | 99.5505 | 99.2861 | 75.9770 | 48054 | 217 | 47844 | 344 | 262 | 76.1628 | |
| ckim-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 97.9631 | 97.2567 | 98.6798 | 47.9874 | 20031 | 565 | 20032 | 268 | 262 | 97.7612 | |
| ciseli-custom | INDEL | D16_PLUS | * | het | 73.2078 | 63.1529 | 87.0708 | 54.9379 | 1995 | 1164 | 2054 | 305 | 262 | 85.9016 | |
| ciseli-custom | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 57.3083 | 74.2240 | 46.6718 | 65.6383 | 550 | 191 | 603 | 689 | 262 | 38.0261 | |
| mlin-fermikit | SNP | ti | map_l250_m2_e1 | * | 48.6646 | 34.1017 | 84.9362 | 80.0607 | 1731 | 3345 | 1731 | 307 | 262 | 85.3420 | |
| anovak-vg | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 72.7114 | 67.5333 | 78.7495 | 70.8829 | 2026 | 974 | 2179 | 588 | 262 | 44.5578 | |
| astatham-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 98.0729 | 97.4752 | 98.6779 | 47.9442 | 20076 | 520 | 20077 | 269 | 262 | 97.3978 | |
| gduggal-snapvard | SNP | * | map_l150_m2_e1 | het | 89.6801 | 96.8079 | 83.5299 | 85.0251 | 19713 | 650 | 19475 | 3840 | 262 | 6.8229 | |
| ghariani-varprowl | SNP | ti | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 97.8165 | 99.8119 | 95.8994 | 55.8743 | 10083 | 19 | 10103 | 432 | 262 | 60.6481 | |
| rpoplin-dv42 | INDEL | D16_PLUS | HG002compoundhet | het | 71.2910 | 94.8148 | 57.1195 | 50.0000 | 384 | 21 | 349 | 262 | 262 | 100.0000 | |
| hfeng-pmm3 | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 98.9496 | 98.2541 | 99.6549 | 70.5915 | 92800 | 1649 | 92707 | 321 | 262 | 81.6199 | |
| mlin-fermikit | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | het | 65.2182 | 88.7879 | 51.5371 | 58.1061 | 293 | 37 | 285 | 268 | 261 | 97.3881 | |
| mlin-fermikit | SNP | ti | map_l250_m2_e1 | homalt | 54.4040 | 43.3973 | 72.8910 | 76.6541 | 769 | 1003 | 769 | 286 | 261 | 91.2587 | |
| egarrison-hhga | INDEL | D16_PLUS | * | het | 92.0708 | 92.9408 | 91.2170 | 67.2524 | 2936 | 223 | 3043 | 293 | 261 | 89.0785 | |
| egarrison-hhga | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 87.0530 | 88.5102 | 85.6431 | 75.6731 | 1610 | 209 | 1718 | 288 | 261 | 90.6250 | |
| egarrison-hhga | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 87.0530 | 88.5102 | 85.6431 | 75.6731 | 1610 | 209 | 1718 | 288 | 261 | 90.6250 | |
| jpowers-varprowl | INDEL | I6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 67.3887 | 79.3103 | 58.5827 | 62.2024 | 368 | 96 | 372 | 263 | 261 | 99.2395 | |
| ciseli-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 57.9068 | 46.9489 | 75.5372 | 67.0120 | 854 | 965 | 914 | 296 | 261 | 88.1757 | |
| ciseli-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 57.9068 | 46.9489 | 75.5372 | 67.0120 | 854 | 965 | 914 | 296 | 261 | 88.1757 | |
| cchapple-custom | INDEL | D1_5 | HG002compoundhet | * | 96.3466 | 94.8427 | 97.8989 | 66.1292 | 11604 | 631 | 12627 | 271 | 261 | 96.3100 | |
| astatham-gatk | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 99.5289 | 99.9220 | 99.1388 | 74.4236 | 30737 | 24 | 30737 | 267 | 261 | 97.7528 | |
| gduggal-snapfb | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 64.3216 | 84.4327 | 51.9481 | 54.2348 | 320 | 59 | 320 | 296 | 261 | 88.1757 | |
| jpowers-varprowl | INDEL | I6_15 | HG002compoundhet | homalt | 11.4804 | 61.2903 | 6.3333 | 53.7037 | 19 | 12 | 19 | 281 | 260 | 92.5267 | |
| jmaeng-gatk | INDEL | * | lowcmp_SimpleRepeat_diTR_51to200 | * | 84.2444 | 82.4369 | 86.1329 | 57.6838 | 1732 | 369 | 1646 | 265 | 260 | 98.1132 | |
| qzeng-custom | INDEL | I16_PLUS | HG002compoundhet | * | 72.9335 | 66.6356 | 80.5461 | 47.8493 | 1428 | 715 | 1416 | 342 | 260 | 76.0234 | |
| 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 | |
| ndellapenna-hhga | INDEL | D1_5 | * | homalt | 99.1101 | 99.1497 | 99.0705 | 58.8372 | 48510 | 416 | 48497 | 455 | 260 | 57.1429 | |