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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
84451-84500 / 86044 show all | |||||||||||||||
eyeh-varpipe | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 44.0002 | 28.5292 | 96.1301 | 45.3174 | 2029 | 5083 | 2335 | 94 | 92 | 97.8723 | |
ghariani-varprowl | INDEL | I1_5 | * | homalt | 94.4302 | 91.5834 | 97.4597 | 39.6857 | 55342 | 5086 | 55284 | 1441 | 928 | 64.3997 | |
mlin-fermikit | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 77.1546 | 63.0485 | 99.3919 | 33.0569 | 8678 | 5086 | 8826 | 54 | 53 | 98.1481 | |
ndellapenna-hhga | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 79.7416 | 66.9975 | 98.4728 | 66.8746 | 10329 | 5088 | 9672 | 150 | 125 | 83.3333 | |
gduggal-bwaplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 81.0947 | 69.5121 | 97.3091 | 55.1710 | 11612 | 5093 | 11608 | 321 | 314 | 97.8193 | |
gduggal-bwaplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 81.0947 | 69.5121 | 97.3091 | 55.1710 | 11612 | 5093 | 11608 | 321 | 314 | 97.8193 | |
gduggal-snapplat | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 59.5098 | 45.1054 | 87.4307 | 85.0479 | 4193 | 5103 | 4257 | 612 | 532 | 86.9281 | |
ciseli-custom | SNP | tv | map_siren | het | 84.4100 | 82.1595 | 86.7874 | 65.3031 | 23505 | 5104 | 23489 | 3576 | 93 | 2.6007 | |
qzeng-custom | SNP | ti | map_l125_m2_e0 | het | 83.1453 | 72.9498 | 96.6538 | 86.6306 | 13770 | 5106 | 13720 | 475 | 387 | 81.4737 | |
ciseli-custom | SNP | ti | map_l125_m1_e0 | het | 77.4977 | 72.0300 | 83.8636 | 79.8833 | 13157 | 5109 | 13154 | 2531 | 72 | 2.8447 | |
ciseli-custom | SNP | ti | map_l150_m2_e0 | * | 79.2695 | 75.0926 | 83.9385 | 81.3448 | 15403 | 5109 | 15396 | 2946 | 753 | 25.5601 | |
mlin-fermikit | SNP | * | map_l100_m0_e0 | homalt | 62.9127 | 56.0069 | 71.7609 | 49.3097 | 6508 | 5112 | 6508 | 2561 | 2415 | 94.2991 | |
jmaeng-gatk | SNP | * | map_l150_m0_e0 | * | 72.2268 | 57.5050 | 97.0803 | 92.6384 | 6919 | 5113 | 6916 | 208 | 23 | 11.0577 | |
ckim-gatk | SNP | * | map_l150_m0_e0 | * | 72.2501 | 57.4634 | 97.2832 | 92.5200 | 6914 | 5118 | 6911 | 193 | 26 | 13.4715 | |
gduggal-bwaplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 76.8144 | 64.9791 | 93.9211 | 77.3415 | 9498 | 5119 | 9502 | 615 | 178 | 28.9431 | |
gduggal-bwaplat | SNP | ti | map_l150_m2_e1 | het | 75.2791 | 60.6685 | 99.1595 | 91.7406 | 7896 | 5119 | 7904 | 67 | 22 | 32.8358 | |
eyeh-varpipe | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 61.3581 | 44.8472 | 97.1096 | 76.3054 | 4169 | 5127 | 5006 | 149 | 142 | 95.3020 | |
eyeh-varpipe | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 52.8397 | 49.0718 | 57.2344 | 61.3327 | 4943 | 5130 | 5716 | 4271 | 3848 | 90.0960 | |
qzeng-custom | SNP | ti | map_l125_m2_e1 | het | 83.2669 | 73.1126 | 96.6968 | 86.6188 | 13955 | 5132 | 13905 | 475 | 387 | 81.4737 | |
eyeh-varpipe | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 43.9004 | 28.4500 | 96.0776 | 48.1986 | 2041 | 5133 | 2376 | 97 | 95 | 97.9381 | |
gduggal-bwavard | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | * | 74.7445 | 74.1265 | 75.3730 | 58.4574 | 14723 | 5139 | 14700 | 4803 | 4251 | 88.5072 | |
ciseli-custom | INDEL | I1_5 | HG002complexvar | * | 86.2012 | 84.5873 | 87.8779 | 52.9140 | 28220 | 5142 | 27874 | 3845 | 2974 | 77.3472 | |
ciseli-custom | SNP | tv | map_l100_m1_e0 | * | 82.8010 | 79.0049 | 86.9802 | 71.6783 | 19357 | 5144 | 19347 | 2896 | 701 | 24.2058 | |
gduggal-bwavard | SNP | tv | * | het | 99.1377 | 99.1291 | 99.1462 | 30.0519 | 586551 | 5153 | 584089 | 5030 | 1454 | 28.9066 | |
ciseli-custom | SNP | ti | map_l150_m2_e1 | * | 79.2822 | 75.1146 | 83.9394 | 81.3843 | 15566 | 5157 | 15559 | 2977 | 763 | 25.6298 | |
ciseli-custom | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | * | 73.3978 | 74.0332 | 72.7731 | 56.7536 | 14703 | 5157 | 14714 | 5505 | 3111 | 56.5123 | |
asubramanian-gatk | SNP | tv | map_l150_m1_e0 | het | 40.8243 | 25.6695 | 99.6644 | 95.4254 | 1783 | 5163 | 1782 | 6 | 1 | 16.6667 | |
anovak-vg | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 60.1585 | 64.6439 | 56.2551 | 36.6040 | 9449 | 5168 | 18693 | 14536 | 11429 | 78.6255 | |
gduggal-bwavard | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 55.1982 | 38.2022 | 99.4371 | 43.8652 | 3196 | 5170 | 3180 | 18 | 16 | 88.8889 | |
ghariani-varprowl | INDEL | D1_5 | * | homalt | 93.4710 | 89.4248 | 97.9006 | 50.1151 | 43752 | 5174 | 43695 | 937 | 631 | 67.3426 | |
gduggal-snapfb | INDEL | D1_5 | * | * | 96.2520 | 96.4735 | 96.0315 | 60.0578 | 141570 | 5175 | 142868 | 5904 | 2222 | 37.6355 | |
jpowers-varprowl | INDEL | D1_5 | * | homalt | 93.6510 | 89.4228 | 98.2990 | 49.9719 | 43751 | 5175 | 43688 | 756 | 634 | 83.8624 | |
mlin-fermikit | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 77.1804 | 63.0915 | 99.3707 | 35.9250 | 8853 | 5179 | 9000 | 57 | 56 | 98.2456 | |
ciseli-custom | SNP | tv | map_l100_m2_e0 | * | 83.0120 | 79.3073 | 87.0798 | 73.4407 | 19853 | 5180 | 19842 | 2944 | 713 | 24.2188 | |
gduggal-bwaplat | SNP | ti | map_l100_m0_e0 | het | 76.9732 | 62.9193 | 99.1113 | 88.0688 | 8798 | 5185 | 8810 | 79 | 24 | 30.3797 | |
ckim-vqsr | SNP | tv | map_l100_m0_e0 | * | 69.0592 | 53.2118 | 98.3492 | 88.9281 | 5898 | 5186 | 5898 | 99 | 1 | 1.0101 | |
egarrison-hhga | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 79.2993 | 66.3164 | 98.6030 | 66.3016 | 10224 | 5193 | 9740 | 138 | 125 | 90.5797 | |
ciseli-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 0.0000 | 4.3582 | 0.0000 | 0.0000 | 237 | 5201 | 0 | 0 | 0 | ||
ciseli-custom | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 49.3606 | 38.1496 | 69.9029 | 67.8340 | 3208 | 5201 | 3024 | 1302 | 965 | 74.1167 | |
ciseli-custom | SNP | ti | map_l125_m2_e0 | het | 77.8322 | 72.4359 | 84.0972 | 81.0572 | 13673 | 5203 | 13670 | 2585 | 72 | 2.7853 | |
ckim-isaac | SNP | * | map_l125_m0_e0 | het | 74.0171 | 58.8677 | 99.6658 | 78.7645 | 7455 | 5209 | 7455 | 25 | 3 | 12.0000 | |
gduggal-bwaplat | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 84.2998 | 74.7038 | 96.7245 | 58.1245 | 15386 | 5210 | 15385 | 521 | 324 | 62.1881 | |
ndellapenna-hhga | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 76.2491 | 62.1404 | 98.6463 | 36.1300 | 8553 | 5211 | 7870 | 108 | 94 | 87.0370 | |
ciseli-custom | SNP | tv | map_l100_m2_e1 | * | 83.0739 | 79.3893 | 87.1172 | 73.4544 | 20072 | 5211 | 20057 | 2966 | 720 | 24.2751 | |
mlin-fermikit | SNP | ti | map_l150_m0_e0 | * | 48.0167 | 33.6471 | 83.8086 | 63.2254 | 2645 | 5216 | 2645 | 511 | 462 | 90.4110 | |
qzeng-custom | SNP | ti | HG002complexvar | het | 99.0720 | 98.3388 | 99.8162 | 18.0479 | 309537 | 5229 | 307433 | 566 | 153 | 27.0318 | |
ckim-isaac | INDEL | I6_15 | * | * | 86.2978 | 78.9268 | 95.1875 | 41.9911 | 19592 | 5231 | 19601 | 991 | 727 | 73.3602 | |
ckim-vqsr | SNP | * | map_l125_m0_e0 | homalt | 36.1328 | 22.0501 | 100.0000 | 90.6459 | 1480 | 5232 | 1480 | 0 | 0 | ||
ciseli-custom | SNP | * | map_l125_m0_e0 | * | 77.7410 | 73.0049 | 83.1343 | 80.5630 | 14152 | 5233 | 14132 | 2867 | 775 | 27.0317 | |
ciseli-custom | SNP | ti | map_l125_m2_e1 | het | 77.9434 | 72.5730 | 84.1721 | 81.0539 | 13852 | 5235 | 13848 | 2604 | 72 | 2.7650 |