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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
7801-7850 / 86044 show all | |||||||||||||||
ltrigg-rtg2 | SNP | ti | map_siren | * | 99.4787 | 99.1669 | 99.7924 | 46.9044 | 99518 | 836 | 99513 | 207 | 30 | 14.4928 | |
mlin-fermikit | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 78.7662 | 69.4733 | 90.9290 | 52.5276 | 2071 | 910 | 2075 | 207 | 206 | 99.5169 | |
qzeng-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 91.8091 | 96.9639 | 87.1747 | 63.5912 | 511 | 16 | 1407 | 207 | 89 | 42.9952 | |
dgrover-gatk | SNP | ti | map_l100_m2_e0 | * | 99.5249 | 99.4730 | 99.5767 | 67.5957 | 48703 | 258 | 48696 | 207 | 50 | 24.1546 | |
eyeh-varpipe | INDEL | * | map_siren | homalt | 94.7726 | 96.1959 | 93.3908 | 81.3483 | 2554 | 101 | 2925 | 207 | 162 | 78.2609 | |
ckim-isaac | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 95.8927 | 93.7179 | 98.1709 | 38.9030 | 11129 | 746 | 11110 | 207 | 127 | 61.3527 | |
dgrover-gatk | SNP | * | map_l125_m0_e0 | het | 98.7051 | 99.0287 | 98.3836 | 80.4812 | 12541 | 123 | 12538 | 206 | 40 | 19.4175 | |
hfeng-pmm2 | SNP | ti | map_l100_m2_e1 | het | 99.3427 | 99.3508 | 99.3346 | 69.0698 | 30759 | 201 | 30752 | 206 | 16 | 7.7670 | |
jlack-gatk | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 99.4496 | 99.8356 | 99.0666 | 73.6565 | 21863 | 36 | 21863 | 206 | 205 | 99.5146 | |
astatham-gatk | SNP | tv | * | het | 99.2722 | 98.5893 | 99.9647 | 23.3815 | 583349 | 8347 | 583282 | 206 | 35 | 16.9903 | |
jli-custom | SNP | * | HG002complexvar | * | 99.9396 | 99.9065 | 99.9727 | 19.0201 | 753676 | 705 | 753565 | 206 | 91 | 44.1748 | |
jmaeng-gatk | SNP | * | map_l150_m0_e0 | het | 75.3760 | 62.0529 | 95.9844 | 93.8640 | 4927 | 3013 | 4924 | 206 | 21 | 10.1942 | |
gduggal-snapvard | INDEL | * | map_l250_m2_e0 | * | 77.7005 | 91.2387 | 67.6609 | 95.5856 | 302 | 29 | 431 | 206 | 49 | 23.7864 | |
gduggal-snapvard | INDEL | C1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 0.0000 | 0.0000 | 9.2511 | 83.1727 | 0 | 0 | 21 | 206 | 16 | 7.7670 | |
gduggal-snapplat | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_51to200 | * | 11.3424 | 10.7807 | 11.9658 | 93.0543 | 29 | 240 | 28 | 206 | 15 | 7.2816 | |
ghariani-varprowl | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 98.4008 | 99.8073 | 97.0334 | 44.7618 | 6732 | 13 | 6738 | 206 | 131 | 63.5922 | |
mlin-fermikit | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 87.1624 | 85.4630 | 88.9307 | 63.9481 | 1652 | 281 | 1655 | 206 | 205 | 99.5146 | |
gduggal-bwaplat | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 85.2828 | 75.9897 | 97.1657 | 76.5450 | 7064 | 2232 | 7062 | 206 | 204 | 99.0291 | |
gduggal-bwavard | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 96.3194 | 97.8377 | 94.8474 | 67.7840 | 3846 | 85 | 3792 | 206 | 24 | 11.6505 | |
gduggal-bwaplat | SNP | * | segdup | * | 98.6033 | 97.9585 | 99.2566 | 93.9219 | 27494 | 573 | 27505 | 206 | 20 | 9.7087 | |
gduggal-bwaplat | SNP | ti | map_l100_m1_e0 | * | 83.2803 | 71.6572 | 99.4040 | 79.8206 | 34346 | 13585 | 34357 | 206 | 64 | 31.0680 | |
gduggal-bwafb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 87.8267 | 81.6103 | 95.0682 | 57.7013 | 13633 | 3072 | 3971 | 206 | 202 | 98.0583 | |
gduggal-bwafb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 87.8267 | 81.6103 | 95.0682 | 57.7013 | 13633 | 3072 | 3971 | 206 | 202 | 98.0583 | |
gduggal-bwafb | SNP | tv | map_l100_m0_e0 | * | 98.4300 | 98.7008 | 98.1606 | 72.2063 | 10940 | 144 | 10940 | 205 | 38 | 18.5366 | |
gduggal-bwaplat | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 85.5433 | 76.2190 | 97.4669 | 52.9093 | 7894 | 2463 | 7888 | 205 | 168 | 81.9512 | |
eyeh-varpipe | INDEL | D16_PLUS | HG002complexvar | homalt | 44.7304 | 49.8270 | 40.5797 | 45.3249 | 144 | 145 | 140 | 205 | 205 | 100.0000 | |
gduggal-bwavard | INDEL | * | map_l150_m1_e0 | het | 88.6308 | 98.5965 | 80.4948 | 92.7959 | 843 | 12 | 846 | 205 | 44 | 21.4634 | |
gduggal-bwavard | INDEL | C1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 0.0000 | 0.0000 | 45.6233 | 95.4980 | 0 | 1 | 172 | 205 | 16 | 7.8049 | |
gduggal-bwavard | INDEL | C1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 0.0000 | 0.0000 | 41.7614 | 95.5004 | 0 | 1 | 147 | 205 | 16 | 7.8049 | |
gduggal-bwavard | INDEL | C1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 0.0000 | 0.0000 | 45.6233 | 95.4980 | 0 | 1 | 172 | 205 | 16 | 7.8049 | |
gduggal-bwavard | INDEL | C1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 0.0000 | 0.0000 | 41.7614 | 95.5004 | 0 | 1 | 147 | 205 | 16 | 7.8049 | |
jmaeng-gatk | SNP | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 99.5601 | 99.6979 | 99.4226 | 63.8015 | 35312 | 107 | 35301 | 205 | 16 | 7.8049 | |
jlack-gatk | INDEL | * | map_l125_m2_e1 | * | 94.6989 | 98.2022 | 91.4369 | 90.8050 | 2185 | 40 | 2189 | 205 | 14 | 6.8293 | |
hfeng-pmm2 | SNP | ti | map_l100_m2_e0 | het | 99.3370 | 99.3436 | 99.3305 | 69.0739 | 30421 | 201 | 30414 | 205 | 16 | 7.8049 | |
ckim-gatk | SNP | * | HG002complexvar | het | 99.7401 | 99.5255 | 99.9558 | 19.1024 | 463288 | 2209 | 463160 | 205 | 69 | 33.6585 | |
bgallagher-sentieon | SNP | * | map_l150_m0_e0 | * | 98.7085 | 99.1107 | 98.3096 | 80.7877 | 11925 | 107 | 11922 | 205 | 30 | 14.6341 | |
gduggal-snapfb | SNP | * | lowcmp_SimpleRepeat_diTR_51to200 | homalt | 11.9658 | 93.3333 | 6.3927 | 89.8892 | 14 | 1 | 14 | 205 | 4 | 1.9512 | |
gduggal-snapfb | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 71.3980 | 62.1268 | 83.9216 | 50.4662 | 1852 | 1129 | 1070 | 205 | 197 | 96.0976 | |
gduggal-snapvard | INDEL | I6_15 | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 63.6275 | 87.0968 | 50.1217 | 72.1733 | 54 | 8 | 206 | 205 | 170 | 82.9268 | |
raldana-dualsentieon | SNP | ti | map_l100_m0_e0 | het | 98.6534 | 98.7699 | 98.5371 | 69.8191 | 13811 | 172 | 13808 | 205 | 2 | 0.9756 | |
jmaeng-gatk | INDEL | D6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 92.9102 | 91.2700 | 94.6103 | 54.6326 | 3586 | 343 | 3581 | 204 | 197 | 96.5686 | |
jpowers-varprowl | SNP | tv | map_l150_m0_e0 | het | 93.9990 | 95.0405 | 92.9800 | 87.0071 | 2702 | 141 | 2702 | 204 | 53 | 25.9804 | |
eyeh-varpipe | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 54.4885 | 52.9412 | 56.1290 | 51.1555 | 261 | 232 | 261 | 204 | 201 | 98.5294 | |
gduggal-bwavard | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 96.2853 | 97.2759 | 95.3147 | 68.9687 | 4178 | 117 | 4150 | 204 | 19 | 9.3137 | |
gduggal-bwavard | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 94.9992 | 97.3939 | 92.7195 | 74.6356 | 2616 | 70 | 2598 | 204 | 19 | 9.3137 | |
egarrison-hhga | INDEL | D1_5 | HG002complexvar | homalt | 98.5958 | 99.1036 | 98.0931 | 56.9237 | 10503 | 95 | 10494 | 204 | 148 | 72.5490 | |
hfeng-pmm3 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 98.0454 | 96.7804 | 99.3438 | 49.5652 | 30962 | 1030 | 30885 | 204 | 187 | 91.6667 | |
gduggal-snapvard | INDEL | * | map_l250_m2_e1 | het | 72.6943 | 94.7867 | 58.9537 | 96.0937 | 200 | 11 | 293 | 204 | 47 | 23.0392 | |
ghariani-varprowl | INDEL | * | map_l100_m0_e0 | het | 89.7886 | 97.7473 | 83.0283 | 91.0144 | 998 | 23 | 998 | 204 | 61 | 29.9020 | |
qzeng-custom | INDEL | I6_15 | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 58.1718 | 93.5484 | 42.2096 | 64.5582 | 58 | 4 | 149 | 204 | 8 | 3.9216 |