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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
11551-11600 / 86044 show all | |||||||||||||||
dgrover-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 97.1571 | 94.8660 | 99.5615 | 32.7282 | 8814 | 477 | 8855 | 39 | 37 | 94.8718 | |
dgrover-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 97.1571 | 94.8660 | 99.5615 | 32.7282 | 8814 | 477 | 8855 | 39 | 37 | 94.8718 | |
dgrover-gatk | INDEL | D6_15 | HG002complexvar | hetalt | 94.7256 | 93.1885 | 96.3143 | 48.2949 | 944 | 69 | 993 | 38 | 37 | 97.3684 | |
egarrison-hhga | INDEL | D16_PLUS | lowcmp_SimpleRepeat_quadTR_11to50 | het | 91.7104 | 93.2668 | 90.2050 | 72.1800 | 374 | 27 | 396 | 43 | 37 | 86.0465 | |
bgallagher-sentieon | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 96.5254 | 93.7213 | 99.5026 | 29.5295 | 7553 | 506 | 7601 | 38 | 37 | 97.3684 | |
bgallagher-sentieon | SNP | ti | map_l150_m2_e0 | * | 99.1869 | 99.3321 | 99.0422 | 77.0287 | 20375 | 137 | 20371 | 197 | 37 | 18.7817 | |
bgallagher-sentieon | SNP | ti | map_l150_m2_e1 | * | 99.1904 | 99.3389 | 99.0424 | 77.0978 | 20586 | 137 | 20582 | 199 | 37 | 18.5930 | |
astatham-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 97.0603 | 94.6723 | 99.5719 | 32.5070 | 8796 | 495 | 8838 | 38 | 37 | 97.3684 | |
astatham-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 97.0603 | 94.6723 | 99.5719 | 32.5070 | 8796 | 495 | 8838 | 38 | 37 | 97.3684 | |
astatham-gatk | INDEL | D6_15 | HG002complexvar | hetalt | 94.7783 | 93.2873 | 96.3178 | 48.2447 | 945 | 68 | 994 | 38 | 37 | 97.3684 | |
asubramanian-gatk | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 95.7489 | 95.0355 | 96.4732 | 75.4199 | 1340 | 70 | 1313 | 48 | 37 | 77.0833 | |
bgallagher-sentieon | INDEL | D6_15 | HG002complexvar | hetalt | 94.0808 | 91.9052 | 96.3618 | 47.7926 | 931 | 82 | 980 | 37 | 37 | 100.0000 | |
bgallagher-sentieon | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 96.5254 | 93.7213 | 99.5026 | 29.5295 | 7553 | 506 | 7601 | 38 | 37 | 97.3684 | |
ltrigg-rtg1 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 97.8994 | 96.0896 | 99.7786 | 37.7218 | 17545 | 714 | 17577 | 39 | 37 | 94.8718 | |
jli-custom | INDEL | D16_PLUS | * | het | 97.9648 | 97.7208 | 98.2100 | 73.1193 | 3087 | 72 | 2853 | 52 | 37 | 71.1538 | |
jli-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 96.6502 | 96.4816 | 96.8193 | 81.9352 | 1755 | 64 | 1522 | 50 | 37 | 74.0000 | |
jli-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 96.6502 | 96.4816 | 96.8193 | 81.9352 | 1755 | 64 | 1522 | 50 | 37 | 74.0000 | |
jli-custom | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_51to200 | * | 87.1637 | 81.3486 | 93.8742 | 45.8781 | 567 | 130 | 567 | 37 | 37 | 100.0000 | |
jli-custom | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 99.4256 | 99.8900 | 98.9654 | 59.3515 | 3634 | 4 | 3635 | 38 | 37 | 97.3684 | |
ltrigg-rtg1 | INDEL | * | lowcmp_SimpleRepeat_diTR_51to200 | * | 85.8472 | 76.6302 | 97.5845 | 55.5436 | 1610 | 491 | 1616 | 40 | 37 | 92.5000 | |
jmaeng-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 96.4888 | 93.5852 | 99.5783 | 30.8129 | 8695 | 596 | 8738 | 37 | 37 | 100.0000 | |
jmaeng-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 96.4888 | 93.5852 | 99.5783 | 30.8129 | 8695 | 596 | 8738 | 37 | 37 | 100.0000 | |
jmaeng-gatk | INDEL | D6_15 | * | hetalt | 96.4840 | 93.6261 | 99.5219 | 32.9957 | 7653 | 521 | 7702 | 37 | 37 | 100.0000 | |
jmaeng-gatk | INDEL | D6_15 | HG002complexvar | hetalt | 93.2190 | 90.3258 | 96.3037 | 47.2880 | 915 | 98 | 964 | 37 | 37 | 100.0000 | |
jmaeng-gatk | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 96.2878 | 93.9576 | 98.7365 | 52.3236 | 3281 | 211 | 3282 | 42 | 37 | 88.0952 | |
jmaeng-gatk | SNP | ti | map_l100_m0_e0 | * | 83.3904 | 72.5047 | 98.1224 | 83.1489 | 15785 | 5986 | 15782 | 302 | 37 | 12.2517 | |
jli-custom | SNP | * | HG002complexvar | homalt | 99.9614 | 99.9404 | 99.9823 | 19.9145 | 288402 | 172 | 288385 | 51 | 37 | 72.5490 | |
ckim-dragen | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | het | 99.4368 | 99.3178 | 99.5561 | 50.0867 | 10336 | 71 | 10317 | 46 | 37 | 80.4348 | |
ckim-dragen | INDEL | D6_15 | * | hetalt | 96.4645 | 93.5894 | 99.5217 | 32.8589 | 7650 | 524 | 7699 | 37 | 37 | 100.0000 | |
ckim-dragen | INDEL | D6_15 | HG002complexvar | homalt | 98.2293 | 99.6578 | 96.8412 | 63.9172 | 1165 | 4 | 1165 | 38 | 37 | 97.3684 | |
ckim-dragen | SNP | * | map_l125_m0_e0 | het | 97.3570 | 98.4523 | 96.2857 | 80.0772 | 12468 | 196 | 12469 | 481 | 37 | 7.6923 | |
ckim-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 96.6722 | 93.9296 | 99.5798 | 30.8791 | 8727 | 564 | 8769 | 37 | 37 | 100.0000 | |
ckim-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 96.6722 | 93.9296 | 99.5798 | 30.8791 | 8727 | 564 | 8769 | 37 | 37 | 100.0000 | |
ckim-gatk | INDEL | D6_15 | HG002complexvar | hetalt | 93.7593 | 91.3129 | 96.3403 | 47.3985 | 925 | 88 | 974 | 37 | 37 | 100.0000 | |
cchapple-custom | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_11to50 | * | 96.7046 | 95.7031 | 97.7273 | 60.0519 | 1715 | 77 | 1806 | 42 | 37 | 88.0952 | |
ciseli-custom | INDEL | C6_15 | HG002complexvar | * | 35.4067 | 50.0000 | 27.4074 | 91.9258 | 2 | 2 | 37 | 98 | 37 | 37.7551 | |
ciseli-custom | INDEL | C6_15 | HG002complexvar | homalt | 0.0000 | 0.0000 | 19.6429 | 91.7708 | 0 | 0 | 22 | 90 | 37 | 41.1111 | |
ciseli-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 80.7504 | 86.1111 | 76.0181 | 63.2280 | 496 | 80 | 504 | 159 | 37 | 23.2704 | |
ciseli-custom | INDEL | D6_15 | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 53.0778 | 74.8120 | 41.1290 | 71.0280 | 199 | 67 | 204 | 292 | 37 | 12.6712 | |
ciseli-custom | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 28.5347 | 18.3183 | 64.5161 | 91.0058 | 122 | 544 | 120 | 66 | 37 | 56.0606 | |
ciseli-custom | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 28.5347 | 18.3183 | 64.5161 | 91.0058 | 122 | 544 | 120 | 66 | 37 | 56.0606 | |
cchapple-custom | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 97.9217 | 96.6692 | 99.2071 | 63.7791 | 5137 | 177 | 5380 | 43 | 37 | 86.0465 | |
cchapple-custom | SNP | ti | map_l250_m1_e0 | het | 95.4232 | 95.5189 | 95.3277 | 91.2575 | 2835 | 133 | 2836 | 139 | 37 | 26.6187 | |
ciseli-custom | SNP | ti | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 97.0190 | 98.4844 | 95.5966 | 46.9536 | 6173 | 95 | 6209 | 286 | 37 | 12.9371 | |
ckim-dragen | INDEL | D16_PLUS | HG002complexvar | * | 97.0671 | 97.2002 | 96.9344 | 67.2029 | 1597 | 46 | 1581 | 50 | 37 | 74.0000 | |
ckim-gatk | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 96.6974 | 94.6626 | 98.8216 | 55.5793 | 3689 | 208 | 3690 | 44 | 37 | 84.0909 | |
ckim-gatk | SNP | ti | map_l100_m0_e0 | * | 83.4318 | 72.5369 | 98.1781 | 82.8871 | 15792 | 5979 | 15789 | 293 | 37 | 12.6280 | |
ckim-isaac | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 89.1293 | 81.6555 | 98.1092 | 39.4326 | 2190 | 492 | 2283 | 44 | 37 | 84.0909 | |
cchapple-custom | INDEL | D16_PLUS | HG002complexvar | het | 95.3100 | 93.9476 | 96.7125 | 59.3663 | 1040 | 67 | 1265 | 43 | 36 | 83.7209 | |
cchapple-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 97.0940 | 96.7742 | 97.4160 | 59.9171 | 510 | 17 | 1508 | 40 | 36 | 90.0000 |