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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
3951-4000 / 86044 show all | |||||||||||||||
eyeh-varpipe | INDEL | * | HG002complexvar | hetalt | 61.1209 | 45.5799 | 92.7426 | 76.1697 | 1686 | 2013 | 3642 | 285 | 277 | 97.1930 | |
ckim-vqsr | INDEL | I6_15 | * | homalt | 97.7408 | 99.8557 | 95.7136 | 54.8957 | 6230 | 9 | 6230 | 279 | 277 | 99.2832 | |
ghariani-varprowl | SNP | ti | * | het | 99.3626 | 99.8721 | 98.8582 | 25.2183 | 1280237 | 1639 | 1280417 | 14789 | 277 | 1.8730 | |
gduggal-snapplat | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | * | 52.8485 | 46.3538 | 61.4597 | 79.2031 | 2657 | 3075 | 2762 | 1732 | 277 | 15.9931 | |
jpowers-varprowl | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 97.9694 | 99.9307 | 96.0837 | 66.5958 | 10090 | 7 | 10108 | 412 | 277 | 67.2330 | |
jmaeng-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 97.8814 | 97.0742 | 98.7022 | 53.8225 | 21599 | 651 | 21600 | 284 | 276 | 97.1831 | |
egarrison-hhga | INDEL | D6_15 | HG002complexvar | * | 89.5440 | 86.4579 | 92.8586 | 57.3769 | 4584 | 718 | 4590 | 353 | 276 | 78.1870 | |
eyeh-varpipe | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_51to200 | homalt | 44.5283 | 92.9134 | 29.2804 | 23.5294 | 118 | 9 | 118 | 285 | 276 | 96.8421 | |
gduggal-bwavard | INDEL | I16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 43.5803 | 37.0727 | 52.8590 | 78.7470 | 423 | 718 | 416 | 371 | 276 | 74.3935 | |
gduggal-bwaplat | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 83.8912 | 73.6757 | 97.3956 | 82.4238 | 35564 | 12707 | 35564 | 951 | 276 | 29.0221 | |
cchapple-custom | SNP | ti | map_l100_m2_e1 | * | 97.7339 | 97.6781 | 97.7898 | 68.9863 | 48336 | 1149 | 48316 | 1092 | 276 | 25.2747 | |
ciseli-custom | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | het | 54.8008 | 64.3595 | 47.7143 | 68.5676 | 623 | 345 | 668 | 732 | 276 | 37.7049 | |
ckim-dragen | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 88.9231 | 98.9002 | 80.7746 | 59.1871 | 1169 | 13 | 1168 | 278 | 276 | 99.2806 | |
gduggal-snapvard | SNP | * | map_l100_m0_e0 | * | 92.6283 | 96.0476 | 89.4441 | 77.2407 | 31543 | 1298 | 31148 | 3676 | 276 | 7.5082 | |
ghariani-varprowl | INDEL | D16_PLUS | HG002complexvar | * | 77.2722 | 74.0718 | 80.7617 | 66.1856 | 1217 | 426 | 1230 | 293 | 276 | 94.1980 | |
gduggal-snapplat | SNP | tv | map_l100_m0_e0 | * | 92.3781 | 89.7690 | 95.1434 | 82.0623 | 9950 | 1134 | 9952 | 508 | 276 | 54.3307 | |
ghariani-varprowl | SNP | * | map_l125_m2_e1 | * | 97.9668 | 98.7606 | 97.1856 | 77.0392 | 46617 | 585 | 46617 | 1350 | 276 | 20.4444 | |
rpoplin-dv42 | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | * | 96.7018 | 96.4052 | 97.0003 | 44.3991 | 9118 | 340 | 9119 | 282 | 276 | 97.8723 | |
rpoplin-dv42 | SNP | ti | * | * | 99.9621 | 99.9459 | 99.9782 | 17.6958 | 2084383 | 1128 | 2084320 | 454 | 276 | 60.7930 | |
rpoplin-dv42 | INDEL | D16_PLUS | * | het | 94.0655 | 97.4042 | 90.9480 | 71.1818 | 3077 | 82 | 2974 | 296 | 276 | 93.2432 | |
rpoplin-dv42 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 90.1124 | 96.0968 | 84.8297 | 79.1299 | 1748 | 71 | 1644 | 294 | 276 | 93.8776 | |
rpoplin-dv42 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 90.1124 | 96.0968 | 84.8297 | 79.1299 | 1748 | 71 | 1644 | 294 | 276 | 93.8776 | |
qzeng-custom | SNP | tv | map_l125_m2_e1 | * | 85.1190 | 75.5598 | 97.4472 | 83.5794 | 12586 | 4071 | 12559 | 329 | 276 | 83.8906 | |
ndellapenna-hhga | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_51to200 | het | 57.8720 | 92.5676 | 42.0945 | 50.6085 | 137 | 11 | 205 | 282 | 275 | 97.5177 | |
qzeng-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 84.0471 | 96.0902 | 74.6866 | 62.8554 | 1278 | 52 | 2800 | 949 | 275 | 28.9779 | |
eyeh-varpipe | INDEL | I6_15 | HG002complexvar | homalt | 78.9714 | 80.2306 | 77.7510 | 38.7303 | 974 | 240 | 968 | 277 | 275 | 99.2780 | |
gduggal-bwafb | INDEL | * | * | hetalt | 87.6150 | 80.5643 | 96.0183 | 78.7583 | 20332 | 4905 | 6728 | 279 | 275 | 98.5663 | |
gduggal-bwafb | INDEL | D16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 86.1916 | 81.4378 | 91.5347 | 58.1069 | 2900 | 661 | 3006 | 278 | 275 | 98.9209 | |
cchapple-custom | SNP | ti | map_l100_m2_e0 | * | 97.7249 | 97.6634 | 97.7865 | 68.9717 | 47817 | 1144 | 47800 | 1082 | 275 | 25.4159 | |
ckim-dragen | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 98.2063 | 99.6651 | 96.7896 | 65.1548 | 8332 | 28 | 8321 | 276 | 275 | 99.6377 | |
ckim-dragen | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 98.2063 | 99.6651 | 96.7896 | 65.1548 | 8332 | 28 | 8321 | 276 | 275 | 99.6377 | |
ghariani-varprowl | SNP | * | map_l125_m2_e0 | * | 97.9545 | 98.7522 | 97.1696 | 76.9826 | 46140 | 583 | 46140 | 1344 | 275 | 20.4613 | |
gduggal-snapplat | SNP | tv | HG002compoundhet | * | 81.2573 | 87.2016 | 76.0717 | 63.0432 | 7781 | 1142 | 7808 | 2456 | 275 | 11.1971 | |
gduggal-snapfb | SNP | * | HG002compoundhet | homalt | 96.1466 | 99.1282 | 93.3392 | 44.8696 | 10688 | 94 | 10692 | 763 | 275 | 36.0419 | |
qzeng-custom | SNP | tv | map_l125_m2_e0 | * | 85.0368 | 75.4382 | 97.4343 | 83.5735 | 12439 | 4050 | 12418 | 327 | 274 | 83.7920 | |
ndellapenna-hhga | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 94.3116 | 95.7208 | 92.9434 | 47.3511 | 8008 | 358 | 8008 | 608 | 274 | 45.0658 | |
astatham-gatk | INDEL | I6_15 | HG002compoundhet | homalt | 18.3976 | 100.0000 | 10.1307 | 62.6829 | 31 | 0 | 31 | 275 | 274 | 99.6364 | |
jlack-gatk | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 92.9723 | 97.9176 | 88.5025 | 64.8041 | 2163 | 46 | 2163 | 281 | 274 | 97.5089 | |
eyeh-varpipe | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 46.0787 | 30.3663 | 95.4861 | 59.9469 | 4261 | 9771 | 6050 | 286 | 274 | 95.8042 | |
cchapple-custom | SNP | ti | HG002complexvar | * | 99.8096 | 99.6932 | 99.9263 | 17.3694 | 506876 | 1560 | 505502 | 373 | 274 | 73.4584 | |
cchapple-custom | SNP | ti | map_l100_m2_e1 | het | 97.1612 | 97.8036 | 96.5271 | 73.0715 | 30280 | 680 | 30296 | 1090 | 274 | 25.1376 | |
gduggal-bwavard | INDEL | I16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 62.0275 | 82.7982 | 49.5879 | 79.0744 | 361 | 75 | 361 | 367 | 274 | 74.6594 | |
gduggal-bwaplat | INDEL | D6_15 | * | * | 86.9684 | 78.1121 | 98.0899 | 65.2244 | 20381 | 5711 | 20387 | 397 | 273 | 68.7657 | |
mlin-fermikit | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 94.7617 | 96.8094 | 92.7988 | 67.6203 | 3641 | 120 | 3634 | 282 | 273 | 96.8085 | |
mlin-fermikit | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 94.7617 | 96.8094 | 92.7988 | 67.6203 | 3641 | 120 | 3634 | 282 | 273 | 96.8085 | |
mlin-fermikit | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 86.4923 | 90.0065 | 83.2423 | 70.9011 | 1387 | 154 | 1371 | 276 | 273 | 98.9130 | |
qzeng-custom | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | het | 96.8049 | 97.4163 | 96.2011 | 51.9614 | 10821 | 287 | 18967 | 749 | 273 | 36.4486 | |
mlin-fermikit | INDEL | * | map_l100_m2_e1 | * | 75.3445 | 66.1342 | 87.5352 | 80.6829 | 2484 | 1272 | 2486 | 354 | 273 | 77.1186 | |
jmaeng-gatk | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 99.2241 | 98.9337 | 99.5161 | 74.5848 | 63744 | 687 | 63757 | 310 | 273 | 88.0645 | |
jpowers-varprowl | INDEL | D16_PLUS | HG002complexvar | * | 75.6960 | 71.3329 | 80.6276 | 65.0203 | 1172 | 471 | 1182 | 284 | 273 | 96.1268 |