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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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1501-1550 / 86044 show all | |||||||||||||||
gduggal-snapvard | INDEL | D6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 48.9137 | 52.6535 | 45.6699 | 40.6819 | 506 | 455 | 1176 | 1399 | 1152 | 82.3445 | |
ndellapenna-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 78.2874 | 71.9726 | 85.8170 | 51.6431 | 7976 | 3106 | 8120 | 1342 | 1151 | 85.7675 | |
mlin-fermikit | SNP | ti | map_l150_m1_e0 | * | 56.8574 | 42.3346 | 86.5470 | 60.8408 | 8345 | 11367 | 8344 | 1297 | 1150 | 88.6662 | |
ndellapenna-hhga | INDEL | * | HG002complexvar | * | 97.2866 | 96.6882 | 97.8924 | 67.2163 | 74390 | 2548 | 74363 | 1601 | 1150 | 71.8301 | |
ciseli-custom | SNP | * | map_l150_m2_e0 | * | 78.3493 | 73.8101 | 83.4833 | 81.5713 | 23510 | 8342 | 23473 | 4644 | 1150 | 24.7631 | |
anovak-vg | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 33.8729 | 24.3264 | 55.7519 | 39.1474 | 948 | 2949 | 1735 | 1377 | 1147 | 83.2970 | |
mlin-fermikit | SNP | ti | map_l150_m1_e0 | homalt | 60.2226 | 50.2115 | 75.2198 | 56.9340 | 3679 | 3648 | 3679 | 1212 | 1145 | 94.4719 | |
mlin-fermikit | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | * | 92.9005 | 92.0300 | 93.7875 | 53.5986 | 18279 | 1583 | 18267 | 1210 | 1145 | 94.6281 | |
qzeng-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 87.2372 | 87.9811 | 86.5058 | 47.3544 | 13008 | 1777 | 14193 | 2214 | 1144 | 51.6712 | |
rpoplin-dv42 | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 98.4841 | 98.2647 | 98.7045 | 79.6128 | 92810 | 1639 | 92797 | 1218 | 1144 | 93.9245 | |
jpowers-varprowl | SNP | tv | HG002compoundhet | * | 83.9956 | 84.7697 | 83.2355 | 57.3909 | 7564 | 1359 | 7661 | 1543 | 1144 | 74.1413 | |
anovak-vg | SNP | * | HG002compoundhet | homalt | 80.7165 | 80.5695 | 80.8640 | 38.2684 | 8687 | 2095 | 7974 | 1887 | 1143 | 60.5723 | |
anovak-vg | INDEL | * | lowcmp_SimpleRepeat_triTR_11to50 | het | 75.1577 | 77.7747 | 72.7110 | 36.3946 | 2845 | 813 | 4074 | 1529 | 1142 | 74.6893 | |
ciseli-custom | SNP | * | map_l100_m0_e0 | * | 81.1632 | 76.8673 | 85.9677 | 74.4366 | 25244 | 7597 | 25198 | 4113 | 1141 | 27.7413 | |
anovak-vg | INDEL | I1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | homalt | 70.9064 | 96.1777 | 56.1521 | 58.9971 | 931 | 37 | 1506 | 1176 | 1140 | 96.9388 | |
gduggal-bwavard | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 58.2911 | 54.3260 | 62.8805 | 55.6252 | 2003 | 1684 | 2004 | 1183 | 1139 | 96.2806 | |
ciseli-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 70.4680 | 75.1615 | 66.3261 | 61.3642 | 2908 | 961 | 3246 | 1648 | 1139 | 69.1141 | |
gduggal-bwavard | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 72.6802 | 97.7039 | 57.8610 | 56.5116 | 1617 | 38 | 1623 | 1182 | 1138 | 96.2775 | |
ghariani-varprowl | SNP | tv | HG002compoundhet | * | 76.9891 | 85.1395 | 70.2629 | 63.5595 | 7597 | 1326 | 7724 | 3269 | 1134 | 34.6895 | |
ghariani-varprowl | INDEL | D1_5 | HG002complexvar | het | 95.4621 | 98.5649 | 92.5488 | 58.7032 | 20467 | 298 | 20407 | 1643 | 1130 | 68.7766 | |
jpowers-varprowl | INDEL | D1_5 | HG002complexvar | het | 95.6155 | 96.8360 | 94.4254 | 57.0236 | 20108 | 657 | 20072 | 1185 | 1127 | 95.1055 | |
jpowers-varprowl | SNP | tv | HG002compoundhet | homalt | 83.3558 | 99.8524 | 71.5372 | 51.1753 | 3383 | 5 | 3388 | 1348 | 1126 | 83.5312 | |
ckim-isaac | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | het | 91.9145 | 93.3439 | 90.5282 | 50.5104 | 14711 | 1049 | 14002 | 1465 | 1126 | 76.8601 | |
ciseli-custom | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 67.2347 | 77.6447 | 59.2860 | 62.9451 | 4345 | 1251 | 4683 | 3216 | 1125 | 34.9813 | |
ciseli-custom | SNP | * | map_l150_m1_e0 | * | 77.9234 | 73.3052 | 83.1626 | 80.2472 | 22438 | 8171 | 22404 | 4536 | 1124 | 24.7795 | |
ghariani-varprowl | SNP | tv | HG002compoundhet | homalt | 83.7163 | 99.8524 | 72.0698 | 50.4793 | 3383 | 5 | 3388 | 1313 | 1124 | 85.6055 | |
qzeng-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 86.6613 | 87.3341 | 85.9988 | 44.9670 | 12039 | 1746 | 13212 | 2151 | 1124 | 52.2548 | |
anovak-vg | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 55.0866 | 65.0355 | 47.7778 | 51.5804 | 917 | 493 | 1376 | 1504 | 1123 | 74.6676 | |
gduggal-snapvard | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | * | 28.1855 | 22.9755 | 36.4514 | 63.8922 | 610 | 2045 | 982 | 1712 | 1115 | 65.1285 | |
gduggal-snapplat | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | het | 70.5032 | 65.2830 | 76.6308 | 62.2986 | 6794 | 3613 | 8411 | 2565 | 1113 | 43.3918 | |
egarrison-hhga | INDEL | * | HG002complexvar | * | 97.4540 | 96.9352 | 97.9784 | 67.1267 | 74580 | 2358 | 74541 | 1538 | 1113 | 72.3667 | |
gduggal-bwaplat | SNP | * | * | het | 98.8209 | 98.1336 | 99.5179 | 30.8495 | 1838619 | 34968 | 1839500 | 8912 | 1113 | 12.4888 | |
anovak-vg | INDEL | I16_PLUS | * | * | 32.9342 | 25.0588 | 48.0286 | 39.2493 | 1598 | 4779 | 1547 | 1674 | 1112 | 66.4277 | |
gduggal-snapvard | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | het | 37.9373 | 39.6694 | 36.3501 | 63.2242 | 384 | 584 | 976 | 1709 | 1112 | 65.0673 | |
rpoplin-dv42 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 94.9862 | 97.5782 | 92.5283 | 63.5798 | 14263 | 354 | 14130 | 1141 | 1110 | 97.2831 | |
mlin-fermikit | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 95.2752 | 94.6742 | 95.8839 | 71.5291 | 43268 | 2434 | 43282 | 1858 | 1107 | 59.5802 | |
mlin-fermikit | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 95.2752 | 94.6742 | 95.8839 | 71.5291 | 43268 | 2434 | 43282 | 1858 | 1107 | 59.5802 | |
ciseli-custom | INDEL | * | lowcmp_SimpleRepeat_diTR_51to200 | * | 25.2937 | 22.4179 | 29.0158 | 55.9542 | 471 | 1630 | 513 | 1255 | 1101 | 87.7291 | |
ciseli-custom | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 58.2603 | 63.0693 | 54.1327 | 69.0970 | 2548 | 1492 | 2790 | 2364 | 1096 | 46.3621 | |
ciseli-custom | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 75.6587 | 80.6700 | 71.2335 | 62.4381 | 3034 | 727 | 2974 | 1201 | 1094 | 91.0908 | |
ciseli-custom | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 75.6587 | 80.6700 | 71.2335 | 62.4381 | 3034 | 727 | 2974 | 1201 | 1094 | 91.0908 | |
qzeng-custom | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 91.7828 | 89.8112 | 93.8428 | 47.3895 | 19983 | 2267 | 20728 | 1360 | 1094 | 80.4412 | |
ghariani-varprowl | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 77.2126 | 92.3546 | 66.3363 | 73.7008 | 2271 | 188 | 2276 | 1155 | 1093 | 94.6320 | |
gduggal-snapplat | SNP | * | map_l100_m2_e1 | * | 95.5097 | 94.0511 | 97.0142 | 77.3448 | 70291 | 4446 | 70312 | 2164 | 1091 | 50.4159 | |
gduggal-snapvard | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 66.0556 | 65.0014 | 67.1446 | 72.1458 | 2355 | 1268 | 3278 | 1604 | 1089 | 67.8928 | |
anovak-vg | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 60.6700 | 53.9166 | 69.3576 | 54.0626 | 3063 | 2618 | 3239 | 1431 | 1089 | 76.1006 | |
egarrison-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 85.5828 | 97.0678 | 76.5280 | 56.7627 | 3178 | 96 | 3606 | 1106 | 1089 | 98.4629 | |
jlack-gatk | INDEL | * | * | het | 98.8624 | 99.4076 | 98.3232 | 61.7242 | 192983 | 1150 | 192623 | 3285 | 1088 | 33.1202 | |
gduggal-snapplat | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 75.5346 | 70.5119 | 81.3276 | 50.1751 | 5110 | 2137 | 6481 | 1488 | 1088 | 73.1183 | |
mlin-fermikit | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 95.9291 | 98.9219 | 93.1120 | 72.4097 | 16792 | 183 | 16803 | 1243 | 1086 | 87.3693 |