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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
83701-83750 / 86044 show all | |||||||||||||||
qzeng-custom | INDEL | I6_15 | * | * | 88.1501 | 86.9073 | 89.4289 | 48.1019 | 21573 | 3250 | 21640 | 2558 | 1057 | 41.3213 | |
ckim-isaac | SNP | ti | map_l125_m0_e0 | het | 75.4138 | 60.6559 | 99.6620 | 78.2483 | 5012 | 3251 | 5012 | 17 | 2 | 11.7647 | |
ltrigg-rtg2 | SNP | * | * | * | 99.8749 | 99.8935 | 99.8562 | 17.0058 | 3051374 | 3252 | 3051531 | 4395 | 283 | 6.4391 | |
astatham-gatk | SNP | ti | map_l150_m2_e1 | * | 91.3679 | 84.3025 | 99.7259 | 80.0126 | 17470 | 3253 | 17466 | 48 | 27 | 56.2500 | |
ckim-gatk | SNP | tv | map_l100_m0_e0 | * | 81.7454 | 70.6424 | 96.9896 | 85.6470 | 7830 | 3254 | 7829 | 243 | 11 | 4.5268 | |
ckim-gatk | SNP | ti | map_l150_m2_e1 | homalt | 73.1394 | 57.6758 | 99.9324 | 81.1976 | 4437 | 3256 | 4437 | 3 | 2 | 66.6667 | |
jpowers-varprowl | INDEL | I16_PLUS | * | * | 56.3839 | 48.9258 | 66.5246 | 59.4066 | 3120 | 3257 | 3122 | 1571 | 1564 | 99.5544 | |
ciseli-custom | SNP | ti | map_l125_m0_e0 | * | 78.8823 | 74.4554 | 83.8690 | 80.0753 | 9502 | 3260 | 9499 | 1827 | 513 | 28.0788 | |
anovak-vg | SNP | ti | map_l100_m0_e0 | * | 81.1499 | 85.0168 | 77.6195 | 74.1271 | 18509 | 3262 | 18364 | 5295 | 1408 | 26.5911 | |
ciseli-custom | SNP | tv | map_l150_m2_e1 | * | 76.7644 | 71.6136 | 82.7136 | 82.0895 | 8237 | 3265 | 8230 | 1720 | 402 | 23.3721 | |
gduggal-snapplat | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | hetalt | 25.0124 | 14.6182 | 86.5625 | 67.4300 | 559 | 3265 | 554 | 86 | 66 | 76.7442 | |
anovak-vg | INDEL | D1_5 | HG002complexvar | * | 91.1523 | 90.0107 | 92.3232 | 54.8532 | 29447 | 3268 | 29789 | 2477 | 1674 | 67.5818 | |
gduggal-snapvard | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 65.7662 | 77.6219 | 57.0522 | 44.3331 | 11346 | 3271 | 31729 | 23885 | 20828 | 87.2012 | |
asubramanian-gatk | SNP | tv | map_l150_m2_e0 | homalt | 33.1085 | 19.8384 | 100.0000 | 92.7263 | 810 | 3273 | 810 | 0 | 0 | ||
eyeh-varpipe | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 61.4597 | 44.8804 | 97.4636 | 72.8689 | 2665 | 3273 | 4957 | 129 | 121 | 93.7984 | |
ckim-vqsr | SNP | tv | map_l125_m2_e0 | het | 80.8052 | 68.6171 | 98.2581 | 89.8954 | 7165 | 3277 | 7164 | 127 | 1 | 0.7874 | |
gduggal-bwavard | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 52.7219 | 35.8609 | 99.5087 | 32.6223 | 1835 | 3282 | 1823 | 9 | 8 | 88.8889 | |
ciseli-custom | SNP | ti | * | homalt | 98.8778 | 99.5909 | 98.1749 | 17.4213 | 799754 | 3285 | 797240 | 14821 | 7334 | 49.4838 | |
ckim-gatk | SNP | ti | map_l150_m0_e0 | * | 72.8820 | 58.1733 | 97.5459 | 92.0553 | 4573 | 3288 | 4571 | 115 | 19 | 16.5217 | |
ciseli-custom | SNP | tv | map_l125_m2_e0 | het | 74.6164 | 68.4639 | 81.9839 | 81.7497 | 7149 | 3293 | 7149 | 1571 | 62 | 3.9465 | |
ghariani-varprowl | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 45.3666 | 30.7174 | 86.7262 | 43.9252 | 1460 | 3293 | 1457 | 223 | 197 | 88.3408 | |
jpowers-varprowl | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 45.4140 | 30.7174 | 87.0736 | 43.4900 | 1460 | 3293 | 1455 | 216 | 197 | 91.2037 | |
ckim-isaac | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 89.4545 | 89.1929 | 89.7177 | 61.8267 | 27186 | 3294 | 25967 | 2976 | 2168 | 72.8495 | |
ckim-isaac | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 89.4545 | 89.1929 | 89.7177 | 61.8267 | 27186 | 3294 | 25967 | 2976 | 2168 | 72.8495 | |
gduggal-snapplat | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 58.8151 | 45.7510 | 82.3221 | 66.0165 | 2778 | 3294 | 3772 | 810 | 398 | 49.1358 | |
jmaeng-gatk | SNP | ti | map_l150_m0_e0 | * | 72.7820 | 58.0842 | 97.4381 | 92.2027 | 4566 | 3295 | 4564 | 120 | 17 | 14.1667 | |
anovak-vg | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 86.9581 | 84.9537 | 89.0595 | 73.1224 | 18604 | 3295 | 18674 | 2294 | 1762 | 76.8091 | |
ltrigg-rtg1 | SNP | * | * | * | 99.8754 | 99.8921 | 99.8587 | 17.5113 | 3051330 | 3296 | 3051518 | 4317 | 267 | 6.1849 | |
ckim-vqsr | SNP | tv | map_l125_m2_e1 | het | 80.9165 | 68.7672 | 98.2798 | 89.9018 | 7257 | 3296 | 7256 | 127 | 1 | 0.7874 | |
gduggal-bwavard | SNP | ti | map_siren | * | 97.1130 | 96.7157 | 97.5137 | 63.7053 | 97059 | 3296 | 96090 | 2450 | 278 | 11.3469 | |
anovak-vg | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | hetalt | 0.0000 | 13.6768 | 0.0000 | 0.0000 | 523 | 3301 | 0 | 0 | 0 | ||
ckim-vqsr | SNP | * | map_l150_m0_e0 | homalt | 32.3149 | 19.2712 | 100.0000 | 93.7742 | 788 | 3301 | 788 | 0 | 0 | ||
ciseli-custom | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 76.6853 | 89.2624 | 67.2148 | 71.4466 | 27458 | 3303 | 27386 | 13358 | 11870 | 88.8606 | |
asubramanian-gatk | SNP | tv | map_l150_m2_e1 | homalt | 33.4408 | 20.0774 | 100.0000 | 92.6353 | 830 | 3304 | 830 | 0 | 0 | ||
mlin-fermikit | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 78.2556 | 64.3957 | 99.7182 | 32.7011 | 5983 | 3308 | 6015 | 17 | 17 | 100.0000 | |
mlin-fermikit | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 78.2556 | 64.3957 | 99.7182 | 32.7011 | 5983 | 3308 | 6015 | 17 | 17 | 100.0000 | |
mlin-fermikit | SNP | ti | map_l250_m2_e0 | * | 48.4805 | 33.9257 | 84.9075 | 79.7858 | 1699 | 3309 | 1699 | 302 | 258 | 85.4305 | |
ndellapenna-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 74.0374 | 59.1106 | 99.0498 | 29.9414 | 4785 | 3310 | 4378 | 42 | 35 | 83.3333 | |
ciseli-custom | SNP | tv | map_l125_m2_e1 | het | 74.7394 | 68.6345 | 82.0365 | 81.7503 | 7243 | 3310 | 7243 | 1586 | 64 | 4.0353 | |
gduggal-snapfb | INDEL | D6_15 | HG002compoundhet | * | 72.3856 | 63.3263 | 84.4695 | 30.0529 | 5719 | 3312 | 6592 | 1212 | 1198 | 98.8449 | |
ckim-isaac | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 96.4197 | 94.8503 | 98.0420 | 61.5230 | 61113 | 3318 | 60987 | 1218 | 972 | 79.8030 | |
jmaeng-gatk | SNP | tv | map_siren | homalt | 89.3303 | 80.7367 | 99.9713 | 58.2484 | 13919 | 3321 | 13916 | 4 | 4 | 100.0000 | |
anovak-vg | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 0.0000 | 30.3646 | 0.0000 | 0.0000 | 1449 | 3323 | 0 | 0 | 0 | ||
ndellapenna-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 74.1810 | 59.3050 | 99.0185 | 33.0396 | 4847 | 3326 | 4439 | 44 | 37 | 84.0909 | |
ckim-gatk | SNP | tv | map_siren | homalt | 89.2983 | 80.6845 | 99.9712 | 58.8566 | 13910 | 3330 | 13907 | 4 | 3 | 75.0000 | |
gduggal-bwavard | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 58.4346 | 41.3660 | 99.4845 | 45.9233 | 2350 | 3331 | 2316 | 12 | 11 | 91.6667 | |
qzeng-custom | INDEL | * | * | het | 97.1762 | 98.2811 | 96.0960 | 58.8639 | 190796 | 3337 | 217691 | 8844 | 3946 | 44.6178 | |
mlin-fermikit | INDEL | D1_5 | HG002compoundhet | hetalt | 80.3857 | 67.3160 | 99.7534 | 60.0394 | 6877 | 3339 | 6877 | 17 | 17 | 100.0000 | |
gduggal-snapplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 42.2807 | 34.7724 | 53.9244 | 82.6368 | 1780 | 3339 | 2068 | 1767 | 59 | 3.3390 | |
mlin-fermikit | INDEL | D1_5 | * | hetalt | 80.4314 | 67.3987 | 99.7126 | 64.5076 | 6905 | 3340 | 6939 | 20 | 20 | 100.0000 |