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.
EntryTypeSubtypeSubsetGenotypeF-score RecallPrecisionFrac_NATruth TPTruth FNQuery TPQuery FPFP gt% FP ma
57051-57100 / 86044 show all
ckim-isaacINDELD1_5tech_badpromotershomalt
94.1176
88.8889
100.0000
27.2727
81800
egarrison-hhgaINDELD16_PLUSlowcmp_SimpleRepeat_homopolymer_gt10hetalt
94.1176
88.8889
100.0000
85.1852
81800
egarrison-hhgaINDELD1_5tech_badpromotershet
94.1176
100.0000
88.8889
50.0000
80811
100.0000
egarrison-hhgaINDELI16_PLUSlowcmp_SimpleRepeat_homopolymer_6to10het
94.1176
100.0000
88.8889
81.2500
1501620
0.0000
egarrison-hhgaINDELI16_PLUSlowcmp_SimpleRepeat_triTR_11to50homalt
94.1176
100.0000
88.8889
75.0000
80811
100.0000
egarrison-hhgaINDELI1_5map_l250_m1_e0het
94.1176
93.3333
94.9153
96.5698
5645630
0.0000
ckim-vqsrINDELI16_PLUSmap_l100_m0_e0het
94.1176
100.0000
88.8889
96.0177
80810
0.0000
ckim-vqsrINDELI16_PLUSmap_l100_m1_e0*
94.1176
92.3077
96.0000
96.2179
2422410
0.0000
ckim-vqsrINDELI6_15map_l125_m0_e0het
94.1176
88.8889
100.0000
96.9582
81800
ckim-vqsrINDELI6_15map_l125_m1_e0*
94.1176
90.5660
97.9592
93.5948
4854810
0.0000
ckim-vqsrINDELI6_15map_l125_m2_e0*
94.1176
90.5660
97.9592
94.3353
4854810
0.0000
ckim-vqsrINDELI6_15map_l125_m2_e1*
94.1176
90.5660
97.9592
94.4758
4854810
0.0000
dgrover-gatkINDELD6_15map_l150_m2_e1hetalt
94.1176
88.8889
100.0000
92.2330
81800
dgrover-gatkINDELI16_PLUSmap_l100_m0_e0het
94.1176
100.0000
88.8889
95.1351
80810
0.0000
ckim-vqsrINDEL*lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_gt200bp_gt95identity_merged*
94.1176
94.1176
94.1176
99.4642
1611610
0.0000
ckim-vqsrINDEL*map_l150_m0_e0hetalt
94.1176
88.8889
100.0000
95.4286
81800
ckim-vqsrINDELD6_15map_l150_m2_e1hetalt
94.1176
88.8889
100.0000
92.9825
81800
ltrigg-rtg1INDELI6_15map_sirenhetalt
94.1176
88.8889
100.0000
80.5970
6486500
ltrigg-rtg1SNP*lowcmp_Human_Full_Genome_TRDB_hg19_150331hetalt
94.1176
100.0000
88.8889
88.6792
1501622
100.0000
ltrigg-rtg1SNP*lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_mergedhetalt
94.1176
100.0000
88.8889
88.6792
1501622
100.0000
ltrigg-rtg1SNP*lowcmp_SimpleRepeat_triTR_51to200*
94.1176
88.8889
100.0000
95.5975
81700
ltrigg-rtg1SNPtvlowcmp_Human_Full_Genome_TRDB_hg19_150331hetalt
94.1176
100.0000
88.8889
88.6792
1501622
100.0000
ltrigg-rtg1SNPtvlowcmp_Human_Full_Genome_TRDB_hg19_150331_all_mergedhetalt
94.1176
100.0000
88.8889
88.6792
1501622
100.0000
ltrigg-rtg2INDEL*map_l150_m0_e0hetalt
94.1176
88.8889
100.0000
96.6777
811000
jmaeng-gatkINDELD16_PLUSsegdup*
94.1176
96.5517
91.8033
97.0113
5625652
40.0000
jmaeng-gatkINDELD6_15map_l150_m2_e1hetalt
94.1176
88.8889
100.0000
92.8571
81800
jmaeng-gatkINDELI16_PLUSmap_l100_m0_e0het
94.1176
100.0000
88.8889
96.2185
80810
0.0000
jmaeng-gatkINDEL*map_l150_m0_e0hetalt
94.1176
88.8889
100.0000
95.6757
81800
jmaeng-gatkINDELD16_PLUSmap_l150_m2_e0het
94.1176
100.0000
88.8889
97.1875
1601620
0.0000
jmaeng-gatkINDELD16_PLUSmap_l150_m2_e1het
94.1176
100.0000
88.8889
97.2435
1601620
0.0000
jmaeng-gatkSNPtvlowcmp_SimpleRepeat_diTR_51to200homalt
94.1176
88.8889
100.0000
95.5801
81800
jpowers-varprowlINDELI1_5map_l250_m0_e0homalt
94.1176
88.8889
100.0000
96.1353
81800
jpowers-varprowlINDELI1_5map_l250_m1_e0homalt
94.1176
90.9091
97.5610
91.9450
4044011
100.0000
jpowers-varprowlSNPtilowcmp_SimpleRepeat_triTR_51to200*
94.1176
100.0000
88.8889
97.0492
80810
0.0000
jpowers-varprowlSNPtvlowcmp_SimpleRepeat_diTR_51to200homalt
94.1176
88.8889
100.0000
96.9697
81800
ltrigg-rtg1INDEL*map_l150_m0_e0hetalt
94.1176
88.8889
100.0000
96.5278
811000
ltrigg-rtg2INDELD16_PLUSmap_l150_m2_e0*
94.1176
94.1176
94.1176
90.5556
1611610
0.0000
ltrigg-rtg2INDELD16_PLUSsegduphetalt
94.1176
88.8889
100.0000
92.6606
81800
ltrigg-rtg2INDELD1_5tech_badpromotershomalt
94.1176
88.8889
100.0000
27.2727
81800
ltrigg-rtg2INDELD6_15map_l150_m2_e1hetalt
94.1176
88.8889
100.0000
92.8571
81800
ltrigg-rtg2INDELI16_PLUSfunc_cdshet
94.1176
88.8889
100.0000
42.8571
81800
ltrigg-rtg2INDELI16_PLUSlowcmp_SimpleRepeat_triTR_11to50homalt
94.1176
100.0000
88.8889
65.3846
80811
100.0000
ltrigg-rtg2INDELI1_5map_l100_m2_e1hetalt
94.1176
88.8889
100.0000
93.7591
4054300
ltrigg-rtg2INDELI1_5tech_badpromotershet
94.1176
100.0000
88.8889
43.7500
80810
0.0000
ltrigg-rtg2SNP*lowcmp_Human_Full_Genome_TRDB_hg19_150331hetalt
94.1176
100.0000
88.8889
88.7500
1501622
100.0000
ltrigg-rtg2SNP*lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_mergedhetalt
94.1176
100.0000
88.8889
88.7500
1501622
100.0000
ltrigg-rtg2SNP*lowcmp_SimpleRepeat_triTR_51to200*
94.1176
88.8889
100.0000
94.9640
81700
ltrigg-rtg2SNPtvlowcmp_Human_Full_Genome_TRDB_hg19_150331hetalt
94.1176
100.0000
88.8889
88.7500
1501622
100.0000
ltrigg-rtg2SNPtvlowcmp_Human_Full_Genome_TRDB_hg19_150331_all_mergedhetalt
94.1176
100.0000
88.8889
88.7500
1501622
100.0000
ltrigg-rtg1INDELD1_5tech_badpromotershomalt
94.1176
88.8889
100.0000
27.2727
81800