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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
20551-20600 / 86044 show all | |||||||||||||||
jlack-gatk | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | * | 98.1723 | 98.0188 | 98.3264 | 71.8409 | 940 | 19 | 940 | 16 | 9 | 56.2500 | |
gduggal-snapvard | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 98.5864 | 98.0186 | 99.1607 | 45.3115 | 841 | 17 | 827 | 7 | 4 | 57.1429 | |
astatham-gatk | INDEL | I6_15 | HG002complexvar | * | 98.5836 | 98.0175 | 99.1563 | 57.7225 | 4697 | 95 | 4701 | 40 | 39 | 97.5000 | |
jlack-gatk | SNP | * | map_l250_m2_e0 | het | 91.0733 | 98.0169 | 85.0484 | 94.0579 | 5091 | 103 | 5091 | 895 | 58 | 6.4805 | |
egarrison-hhga | SNP | tv | HG002compoundhet | * | 98.7023 | 98.0164 | 99.3979 | 47.2112 | 8746 | 177 | 8749 | 53 | 39 | 73.5849 | |
gduggal-bwafb | INDEL | D1_5 | map_siren | * | 98.1690 | 98.0164 | 98.3220 | 81.5743 | 3459 | 70 | 3457 | 59 | 15 | 25.4237 | |
hfeng-pmm1 | INDEL | I1_5 | map_l125_m2_e0 | * | 98.5925 | 98.0163 | 99.1755 | 86.0408 | 840 | 17 | 842 | 7 | 2 | 28.5714 | |
gduggal-snapfb | SNP | ti | map_l100_m1_e0 | het | 97.3515 | 98.0162 | 96.6958 | 65.8783 | 29348 | 594 | 29352 | 1003 | 436 | 43.4696 | |
ckim-dragen | INDEL | D1_5 | map_l100_m2_e0 | * | 97.6319 | 98.0157 | 97.2510 | 85.8443 | 1877 | 38 | 1875 | 53 | 6 | 11.3208 | |
raldana-dualsentieon | INDEL | D1_5 | map_l100_m2_e0 | * | 98.5570 | 98.0157 | 99.1043 | 82.2749 | 1877 | 38 | 1881 | 17 | 5 | 29.4118 | |
jli-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.2104 | 98.0157 | 98.4058 | 67.0172 | 5730 | 116 | 5679 | 92 | 83 | 90.2174 | |
jli-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.2104 | 98.0157 | 98.4058 | 67.0172 | 5730 | 116 | 5679 | 92 | 83 | 90.2174 | |
egarrison-hhga | INDEL | D1_5 | map_l100_m2_e0 | * | 98.1438 | 98.0157 | 98.2723 | 83.6389 | 1877 | 38 | 1877 | 33 | 12 | 36.3636 | |
dgrover-gatk | SNP | tv | map_l250_m2_e1 | het | 97.7665 | 98.0153 | 97.5190 | 91.3080 | 1926 | 39 | 1926 | 49 | 9 | 18.3673 | |
ckim-vqsr | SNP | tv | HG002complexvar | het | 98.9859 | 98.0150 | 99.9763 | 22.4456 | 147739 | 2992 | 147662 | 35 | 14 | 40.0000 | |
ckim-dragen | INDEL | D1_5 | map_l100_m1_e0 | het | 96.9291 | 98.0149 | 95.8671 | 85.7209 | 1185 | 24 | 1183 | 51 | 4 | 7.8431 | |
ckim-vqsr | INDEL | D6_15 | HG002compoundhet | het | 89.9917 | 98.0140 | 83.1832 | 68.8202 | 839 | 17 | 831 | 168 | 166 | 98.8095 | |
jmaeng-gatk | INDEL | D6_15 | HG002compoundhet | het | 88.9799 | 98.0140 | 81.4706 | 68.2342 | 839 | 17 | 831 | 189 | 187 | 98.9418 | |
egarrison-hhga | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 97.7893 | 98.0137 | 97.5659 | 71.4911 | 30150 | 611 | 30142 | 752 | 362 | 48.1383 | |
ltrigg-rtg2 | SNP | * | map_l100_m1_e0 | het | 98.8659 | 98.0136 | 99.7330 | 50.5607 | 44458 | 901 | 44456 | 119 | 8 | 6.7227 | |
jlack-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 96.7207 | 98.0134 | 95.4617 | 70.0763 | 17465 | 354 | 17080 | 812 | 691 | 85.0985 | |
hfeng-pmm3 | INDEL | * | map_l150_m2_e0 | het | 97.9638 | 98.0132 | 97.9144 | 88.9709 | 888 | 18 | 892 | 19 | 3 | 15.7895 | |
jli-custom | INDEL | * | map_l150_m2_e0 | het | 98.1776 | 98.0132 | 98.3425 | 89.4239 | 888 | 18 | 890 | 15 | 4 | 26.6667 | |
dgrover-gatk | INDEL | * | map_l150_m2_e0 | het | 97.8027 | 98.0132 | 97.5930 | 91.8342 | 888 | 18 | 892 | 22 | 3 | 13.6364 | |
jli-custom | INDEL | D6_15 | HG002complexvar | het | 98.7528 | 98.0128 | 99.5040 | 56.9844 | 3058 | 62 | 3009 | 15 | 10 | 66.6667 | |
ckim-vqsr | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 98.2939 | 98.0121 | 98.5773 | 60.5225 | 15728 | 319 | 15729 | 227 | 215 | 94.7137 | |
jli-custom | INDEL | * | map_l150_m1_e0 | het | 98.1285 | 98.0117 | 98.2456 | 88.8001 | 838 | 17 | 840 | 15 | 4 | 26.6667 | |
hfeng-pmm3 | INDEL | * | map_l150_m1_e0 | het | 97.9024 | 98.0117 | 97.7933 | 88.3397 | 838 | 17 | 842 | 19 | 3 | 15.7895 | |
jlack-gatk | INDEL | * | map_l150_m1_e0 | het | 91.0230 | 98.0117 | 84.9647 | 93.0437 | 838 | 17 | 842 | 149 | 6 | 4.0269 | |
jmaeng-gatk | INDEL | * | map_l150_m1_e0 | het | 94.3374 | 98.0117 | 90.9287 | 93.7882 | 838 | 17 | 842 | 84 | 6 | 7.1429 | |
jli-custom | INDEL | * | map_l125_m2_e1 | het | 98.3616 | 98.0114 | 98.7143 | 86.9876 | 1380 | 28 | 1382 | 18 | 4 | 22.2222 | |
gduggal-snapfb | SNP | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 52.4956 | 98.0106 | 35.8482 | 76.1642 | 2956 | 60 | 3022 | 5408 | 61 | 1.1280 | |
egarrison-hhga | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 98.6821 | 98.0105 | 99.3631 | 78.4932 | 936 | 19 | 936 | 6 | 3 | 50.0000 | |
egarrison-hhga | SNP | ti | map_l250_m2_e1 | * | 98.8083 | 98.0102 | 99.6195 | 88.7052 | 4975 | 101 | 4975 | 19 | 9 | 47.3684 | |
dgrover-gatk | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 98.3958 | 98.0100 | 98.7847 | 73.2093 | 591 | 12 | 569 | 7 | 3 | 42.8571 | |
ckim-gatk | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 98.4810 | 98.0100 | 98.9565 | 72.9412 | 591 | 12 | 569 | 6 | 2 | 33.3333 | |
cchapple-custom | INDEL | I1_5 | map_l150_m2_e0 | homalt | 98.4949 | 98.0100 | 98.9848 | 87.2244 | 197 | 4 | 195 | 2 | 1 | 50.0000 | |
jmaeng-gatk | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 98.2260 | 98.0100 | 98.4429 | 73.1662 | 591 | 12 | 569 | 9 | 6 | 66.6667 | |
astatham-gatk | INDEL | D16_PLUS | * | * | 97.8775 | 98.0100 | 97.7454 | 70.7802 | 6649 | 135 | 6633 | 153 | 104 | 67.9739 | |
bgallagher-sentieon | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 98.3958 | 98.0100 | 98.7847 | 72.5975 | 591 | 12 | 569 | 7 | 3 | 42.8571 | |
raldana-dualsentieon | INDEL | I1_5 | map_l150_m2_e0 | homalt | 98.5000 | 98.0100 | 98.9950 | 87.6012 | 197 | 4 | 197 | 2 | 1 | 50.0000 | |
ltrigg-rtg2 | SNP | tv | map_l100_m2_e0 | het | 98.8114 | 98.0098 | 99.6262 | 53.3646 | 15463 | 314 | 15459 | 58 | 2 | 3.4483 | |
gduggal-snapfb | SNP | * | HG002compoundhet | * | 83.3987 | 98.0094 | 72.5790 | 48.5976 | 25308 | 514 | 25579 | 9664 | 581 | 6.0120 | |
ltrigg-rtg2 | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 98.5345 | 98.0092 | 99.0654 | 64.3729 | 640 | 13 | 636 | 6 | 5 | 83.3333 | |
rpoplin-dv42 | SNP | * | map_l250_m2_e0 | * | 98.3456 | 98.0089 | 98.6847 | 88.0100 | 7728 | 157 | 7728 | 103 | 68 | 66.0194 | |
hfeng-pmm3 | INDEL | D6_15 | lowcmp_SimpleRepeat_triTR_11to50 | het | 98.7814 | 98.0085 | 99.5665 | 42.6678 | 689 | 14 | 689 | 3 | 2 | 66.6667 | |
hfeng-pmm3 | SNP | * | map_l250_m0_e0 | het | 98.0731 | 98.0080 | 98.1383 | 92.9489 | 1476 | 30 | 1476 | 28 | 1 | 3.5714 | |
hfeng-pmm2 | SNP | * | map_l250_m0_e0 | het | 97.4257 | 98.0080 | 96.8504 | 93.8031 | 1476 | 30 | 1476 | 48 | 4 | 8.3333 | |
jli-custom | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 98.2132 | 98.0073 | 98.4200 | 74.3056 | 2410 | 49 | 2367 | 38 | 26 | 68.4211 | |
asubramanian-gatk | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 97.9777 | 98.0072 | 97.9483 | 86.5329 | 1082 | 22 | 1098 | 23 | 6 | 26.0870 |