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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
14201-14250 / 86044 show all | |||||||||||||||
cchapple-custom | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 98.5211 | 99.2995 | 97.7547 | 53.9013 | 567 | 4 | 566 | 13 | 13 | 100.0000 | |
ckim-gatk | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 98.5230 | 99.2995 | 97.7586 | 67.1946 | 567 | 4 | 567 | 13 | 13 | 100.0000 | |
astatham-gatk | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 98.4375 | 99.2995 | 97.5904 | 67.0261 | 567 | 4 | 567 | 14 | 14 | 100.0000 | |
ckim-vqsr | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 98.5230 | 99.2995 | 97.7586 | 67.1946 | 567 | 4 | 567 | 13 | 13 | 100.0000 | |
dgrover-gatk | SNP | ti | map_l125_m1_e0 | het | 99.2150 | 99.2992 | 99.1308 | 75.9575 | 18138 | 128 | 18134 | 159 | 33 | 20.7547 | |
ckim-dragen | SNP | tv | map_l250_m1_e0 | homalt | 99.1254 | 99.2991 | 98.9523 | 83.2944 | 850 | 6 | 850 | 9 | 7 | 77.7778 | |
hfeng-pmm3 | SNP | tv | map_l125_m1_e0 | het | 99.3576 | 99.2988 | 99.4165 | 70.9308 | 10055 | 71 | 10053 | 59 | 5 | 8.4746 | |
gduggal-bwaplat | SNP | ti | func_cds | homalt | 99.6481 | 99.2986 | 100.0000 | 20.6003 | 5238 | 37 | 5238 | 0 | 0 | ||
gduggal-snapvard | SNP | ti | func_cds | homalt | 99.6385 | 99.2986 | 99.9808 | 20.4816 | 5238 | 37 | 5217 | 1 | 1 | 100.0000 | |
hfeng-pmm1 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 99.5544 | 99.2984 | 99.8118 | 74.6933 | 2123 | 15 | 2121 | 4 | 1 | 25.0000 | |
gduggal-bwafb | SNP | ti | map_l100_m1_e0 | homalt | 99.5923 | 99.2984 | 99.8880 | 61.5927 | 17834 | 126 | 17834 | 20 | 12 | 60.0000 | |
jli-custom | SNP | tv | map_l100_m1_e0 | * | 99.4197 | 99.2980 | 99.5417 | 62.1631 | 24329 | 172 | 24328 | 112 | 30 | 26.7857 | |
ndellapenna-hhga | SNP | ti | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 99.4850 | 99.2977 | 99.6730 | 35.9284 | 3959 | 28 | 3962 | 13 | 12 | 92.3077 | |
raldana-dualsentieon | SNP | tv | map_l125_m2_e1 | * | 99.2171 | 99.2976 | 99.1368 | 71.9418 | 16540 | 117 | 16538 | 144 | 4 | 2.7778 | |
hfeng-pmm3 | INDEL | * | map_l100_m2_e1 | homalt | 99.2587 | 99.2974 | 99.2200 | 82.2364 | 1272 | 9 | 1272 | 10 | 4 | 40.0000 | |
rpoplin-dv42 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 99.2965 | 99.2968 | 99.2963 | 87.3102 | 1412 | 10 | 1411 | 10 | 6 | 60.0000 | |
ckim-dragen | SNP | ti | map_l100_m2_e1 | * | 98.6777 | 99.2968 | 98.0664 | 68.9837 | 49137 | 348 | 49145 | 969 | 108 | 11.1455 | |
dgrover-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 99.3666 | 99.2968 | 99.4366 | 88.7015 | 1412 | 10 | 1412 | 8 | 7 | 87.5000 | |
jlack-gatk | INDEL | * | HG002complexvar | het | 99.3807 | 99.2967 | 99.4647 | 57.6016 | 45887 | 325 | 45527 | 245 | 124 | 50.6122 | |
ckim-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 99.4326 | 99.2967 | 99.5689 | 75.2558 | 5083 | 36 | 5081 | 22 | 10 | 45.4545 | |
ckim-gatk | INDEL | * | map_l125_m0_e0 | homalt | 98.7741 | 99.2958 | 98.2578 | 88.6874 | 282 | 2 | 282 | 5 | 4 | 80.0000 | |
ckim-vqsr | INDEL | * | map_l125_m0_e0 | homalt | 98.9474 | 99.2958 | 98.6014 | 88.7224 | 282 | 2 | 282 | 4 | 3 | 75.0000 | |
ghariani-varprowl | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 86.2766 | 99.2958 | 76.2757 | 84.3842 | 846 | 6 | 852 | 265 | 167 | 63.0189 | |
ltrigg-rtg1 | INDEL | * | map_l125_m0_e0 | homalt | 98.9449 | 99.2958 | 98.5965 | 86.3047 | 282 | 2 | 281 | 4 | 2 | 50.0000 | |
hfeng-pmm3 | INDEL | * | map_l125_m0_e0 | homalt | 98.7741 | 99.2958 | 98.2578 | 85.7498 | 282 | 2 | 282 | 5 | 3 | 60.0000 | |
hfeng-pmm2 | INDEL | * | map_l125_m0_e0 | homalt | 98.7741 | 99.2958 | 98.2578 | 86.8469 | 282 | 2 | 282 | 5 | 4 | 80.0000 | |
raldana-dualsentieon | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 99.5294 | 99.2958 | 99.7642 | 84.2672 | 846 | 6 | 846 | 2 | 2 | 100.0000 | |
astatham-gatk | INDEL | * | map_l125_m0_e0 | homalt | 98.6014 | 99.2958 | 97.9167 | 88.3589 | 282 | 2 | 282 | 6 | 4 | 66.6667 | |
bgallagher-sentieon | INDEL | * | map_l125_m0_e0 | homalt | 98.6014 | 99.2958 | 97.9167 | 88.2112 | 282 | 2 | 282 | 6 | 4 | 66.6667 | |
hfeng-pmm1 | INDEL | I1_5 | HG002complexvar | * | 99.5778 | 99.2956 | 99.8615 | 56.6148 | 33128 | 235 | 33171 | 46 | 29 | 63.0435 | |
hfeng-pmm3 | INDEL | I1_5 | HG002complexvar | * | 99.5912 | 99.2956 | 99.8886 | 56.4158 | 33128 | 235 | 33172 | 37 | 24 | 64.8649 | |
ckim-dragen | SNP | ti | map_l100_m2_e0 | * | 98.6738 | 99.2954 | 98.0599 | 68.9474 | 48616 | 345 | 48624 | 962 | 107 | 11.1227 | |
ckim-gatk | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 99.1201 | 99.2954 | 98.9455 | 75.2393 | 1691 | 12 | 1689 | 18 | 3 | 16.6667 | |
gduggal-bwafb | SNP | ti | map_l100_m2_e0 | homalt | 99.5892 | 99.2954 | 99.8846 | 63.9034 | 18180 | 129 | 18180 | 21 | 13 | 61.9048 | |
ckim-dragen | SNP | * | map_l100_m2_e1 | * | 98.6686 | 99.2949 | 98.0501 | 69.8284 | 74210 | 527 | 74221 | 1476 | 153 | 10.3659 | |
ckim-dragen | SNP | ti | map_l100_m1_e0 | * | 98.6835 | 99.2948 | 98.0797 | 66.8879 | 47593 | 338 | 47601 | 932 | 106 | 11.3734 | |
qzeng-custom | SNP | tv | * | homalt | 99.5964 | 99.2947 | 99.8999 | 20.4155 | 374463 | 2660 | 372209 | 373 | 242 | 64.8794 | |
rpoplin-dv42 | SNP | ti | map_l100_m2_e1 | * | 99.4666 | 99.2947 | 99.6390 | 64.7230 | 49136 | 349 | 49129 | 178 | 121 | 67.9775 | |
hfeng-pmm1 | SNP | tv | map_l125_m1_e0 | * | 99.4714 | 99.2945 | 99.6491 | 69.3117 | 15903 | 113 | 15901 | 56 | 16 | 28.5714 | |
hfeng-pmm2 | SNP | tv | map_l150_m1_e0 | * | 99.1035 | 99.2944 | 98.9134 | 76.5808 | 10835 | 77 | 10833 | 119 | 14 | 11.7647 | |
ckim-dragen | SNP | * | map_l100_m2_e0 | * | 98.6634 | 99.2943 | 98.0406 | 69.7855 | 73442 | 522 | 73453 | 1468 | 152 | 10.3542 | |
ltrigg-rtg1 | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 99.5867 | 99.2941 | 99.8810 | 43.2816 | 844 | 6 | 839 | 1 | 0 | 0.0000 | |
jpowers-varprowl | SNP | * | HG002complexvar | * | 99.4683 | 99.2937 | 99.6435 | 20.7160 | 749051 | 5328 | 749404 | 2681 | 1602 | 59.7538 | |
eyeh-varpipe | SNP | ti | map_l150_m0_e0 | het | 98.2368 | 99.2937 | 97.2021 | 84.3948 | 5061 | 36 | 4968 | 143 | 4 | 2.7972 | |
rpoplin-dv42 | SNP | ti | map_l100_m2_e0 | * | 99.4660 | 99.2933 | 99.6392 | 64.7198 | 48615 | 346 | 48608 | 176 | 120 | 68.1818 | |
ckim-dragen | SNP | tv | map_l100_m2_e0 | * | 98.6448 | 99.2929 | 98.0051 | 71.3118 | 24856 | 177 | 24859 | 506 | 45 | 8.8933 | |
astatham-gatk | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 99.6057 | 99.2925 | 99.9209 | 50.5187 | 2526 | 18 | 2526 | 2 | 0 | 0.0000 | |
jpowers-varprowl | SNP | * | func_cds | het | 99.1057 | 99.2922 | 98.9199 | 32.1729 | 11082 | 79 | 11082 | 121 | 2 | 1.6529 | |
ckim-dragen | SNP | tv | map_l100_m2_e1 | * | 98.6522 | 99.2920 | 98.0206 | 71.3656 | 25104 | 179 | 25107 | 507 | 45 | 8.8757 | |
cchapple-custom | SNP | ti | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 99.3846 | 99.2919 | 99.4776 | 66.9410 | 3225 | 23 | 3237 | 17 | 3 | 17.6471 |