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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
3151-3200 / 86044 show all | |||||||||||||||
gduggal-bwafb | SNP | * | HG002complexvar | het | 99.7664 | 99.7319 | 99.8010 | 20.1804 | 464252 | 1248 | 464384 | 926 | 324 | 34.9892 | |
astatham-gatk | INDEL | * | * | homalt | 99.5755 | 99.8874 | 99.2657 | 58.8575 | 125031 | 141 | 125041 | 925 | 908 | 98.1622 | |
qzeng-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 94.0704 | 96.0794 | 92.1437 | 38.7632 | 8038 | 328 | 10849 | 925 | 888 | 96.0000 | |
mlin-fermikit | SNP | * | map_l150_m0_e0 | * | 47.5288 | 33.5688 | 81.3658 | 64.0159 | 4039 | 7993 | 4039 | 925 | 818 | 88.4324 | |
mlin-fermikit | SNP | ti | HG002compoundhet | * | 93.7043 | 92.8195 | 94.6061 | 36.5228 | 16223 | 1255 | 16224 | 925 | 739 | 79.8919 | |
jpowers-varprowl | SNP | ti | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 97.7595 | 98.7696 | 96.7698 | 62.5065 | 27615 | 344 | 27711 | 925 | 281 | 30.3784 | |
ckim-gatk | INDEL | * | * | homalt | 99.5712 | 99.8778 | 99.2664 | 58.9388 | 125019 | 153 | 125032 | 924 | 905 | 97.9437 | |
jpowers-varprowl | SNP | ti | map_siren | * | 98.7281 | 98.3847 | 99.0739 | 58.8371 | 98734 | 1621 | 98737 | 923 | 255 | 27.6273 | |
ckim-isaac | INDEL | D1_5 | HG002compoundhet | * | 88.8135 | 85.9501 | 91.8743 | 43.5269 | 10516 | 1719 | 10436 | 923 | 829 | 89.8158 | |
gduggal-snapvard | INDEL | * | map_l100_m2_e1 | het | 84.8243 | 94.1101 | 77.2064 | 88.4817 | 2205 | 138 | 3123 | 922 | 425 | 46.0954 | |
ghariani-varprowl | INDEL | D6_15 | HG002complexvar | het | 84.7743 | 95.1923 | 76.4117 | 58.8552 | 2970 | 150 | 2977 | 919 | 877 | 95.4298 | |
ndellapenna-hhga | INDEL | * | HG002complexvar | het | 97.4850 | 96.9835 | 97.9917 | 54.0711 | 44818 | 1394 | 44840 | 919 | 671 | 73.0141 | |
ckim-vqsr | INDEL | * | * | homalt | 99.5675 | 99.8658 | 99.2711 | 58.9429 | 125004 | 168 | 125017 | 918 | 901 | 98.1481 | |
anovak-vg | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 56.9297 | 50.5845 | 65.0951 | 55.0427 | 1601 | 1564 | 1712 | 918 | 650 | 70.8061 | |
gduggal-snapfb | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 78.8680 | 83.9810 | 74.3417 | 54.2249 | 2658 | 507 | 2654 | 916 | 914 | 99.7817 | |
gduggal-snapfb | SNP | tv | lowcmp_SimpleRepeat_diTR_51to200 | * | 4.1580 | 76.9231 | 2.1368 | 79.9012 | 20 | 6 | 20 | 916 | 7 | 0.7642 | |
gduggal-snapfb | SNP | ti | lowcmp_SimpleRepeat_quadTR_51to200 | het | 10.6178 | 83.3333 | 5.6701 | 81.1174 | 55 | 11 | 55 | 915 | 8 | 0.8743 | |
astatham-gatk | INDEL | * | * | het | 99.5127 | 99.4973 | 99.5281 | 60.7701 | 193157 | 976 | 192779 | 914 | 573 | 62.6915 | |
mlin-fermikit | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 96.9772 | 98.0684 | 95.9100 | 75.5337 | 21476 | 423 | 21433 | 914 | 898 | 98.2495 | |
qzeng-custom | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 94.3405 | 95.3885 | 93.3153 | 37.1067 | 6371 | 308 | 12759 | 914 | 716 | 78.3370 | |
eyeh-varpipe | SNP | * | map_l125_m1_e0 | het | 98.1718 | 99.6126 | 96.7721 | 75.4925 | 28282 | 110 | 27402 | 914 | 28 | 3.0635 | |
dgrover-gatk | INDEL | * | * | homalt | 99.5819 | 99.8906 | 99.2752 | 59.0938 | 125035 | 137 | 125045 | 913 | 890 | 97.4808 | |
jlack-gatk | SNP | * | map_l250_m2_e1 | * | 93.5343 | 97.8966 | 89.5442 | 92.9358 | 7819 | 168 | 7819 | 913 | 69 | 7.5575 | |
jmaeng-gatk | SNP | ti | map_siren | het | 96.0962 | 93.8396 | 98.4641 | 69.3151 | 58539 | 3843 | 58530 | 913 | 76 | 8.3242 | |
ckim-isaac | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 89.9895 | 86.0506 | 94.3064 | 43.1744 | 15206 | 2465 | 15106 | 912 | 765 | 83.8816 | |
ckim-isaac | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 89.9895 | 86.0506 | 94.3064 | 43.1744 | 15206 | 2465 | 15106 | 912 | 765 | 83.8816 | |
ghariani-varprowl | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 70.0058 | 58.6077 | 86.9078 | 48.1851 | 6070 | 4287 | 6054 | 912 | 765 | 83.8816 | |
eyeh-varpipe | SNP | ti | map_siren | * | 99.4355 | 99.7967 | 99.0768 | 57.9702 | 100151 | 204 | 97874 | 912 | 55 | 6.0307 | |
ckim-dragen | SNP | ti | map_l100_m1_e0 | het | 98.1230 | 99.2485 | 97.0227 | 71.3768 | 29717 | 225 | 29720 | 912 | 87 | 9.5395 | |
ciseli-custom | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 81.5701 | 97.8381 | 69.9407 | 68.1937 | 2127 | 47 | 2122 | 912 | 19 | 2.0833 | |
ciseli-custom | SNP | ti | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 95.3321 | 99.2576 | 91.7054 | 59.1877 | 10027 | 75 | 10072 | 911 | 306 | 33.5895 | |
ciseli-custom | INDEL | D16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 62.4926 | 91.1184 | 47.5533 | 63.3312 | 831 | 81 | 826 | 911 | 847 | 92.9748 | |
gduggal-snapvard | INDEL | * | map_l100_m1_e0 | * | 85.9341 | 89.2080 | 82.8920 | 85.9643 | 3199 | 387 | 4414 | 911 | 427 | 46.8716 | |
qzeng-custom | SNP | * | HG002complexvar | het | 99.0563 | 98.3261 | 99.7975 | 19.7489 | 457708 | 7792 | 449025 | 911 | 250 | 27.4424 | |
eyeh-varpipe | SNP | ti | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 97.1889 | 99.5294 | 94.9560 | 60.6805 | 17767 | 84 | 17150 | 911 | 86 | 9.4402 | |
gduggal-snapfb | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 66.3492 | 99.1247 | 49.8623 | 65.6965 | 906 | 8 | 905 | 910 | 5 | 0.5495 | |
gduggal-snapfb | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 79.3964 | 87.2325 | 72.8520 | 53.8546 | 2446 | 358 | 2442 | 910 | 909 | 99.8901 | |
ciseli-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | het | 84.2619 | 97.2450 | 74.3373 | 66.4617 | 2612 | 74 | 2636 | 910 | 12 | 1.3187 | |
ghariani-varprowl | INDEL | I6_15 | HG002complexvar | * | 71.5536 | 66.2145 | 77.8293 | 58.1077 | 3173 | 1619 | 3191 | 909 | 871 | 95.8196 | |
gduggal-snapvard | INDEL | * | map_l100_m2_e0 | het | 85.0151 | 94.3650 | 77.3510 | 88.3503 | 2177 | 130 | 3101 | 908 | 421 | 46.3656 | |
gduggal-snapplat | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 52.3943 | 37.9325 | 84.6777 | 63.9143 | 5229 | 8556 | 5018 | 908 | 475 | 52.3128 | |
ciseli-custom | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 95.2928 | 99.2077 | 91.6751 | 67.8866 | 10017 | 80 | 9999 | 908 | 277 | 30.5066 | |
mlin-fermikit | SNP | tv | map_l150_m1_e0 | homalt | 59.5283 | 52.1287 | 69.3761 | 55.9108 | 2057 | 1889 | 2057 | 908 | 841 | 92.6211 | |
jlack-gatk | SNP | * | map_l250_m2_e0 | * | 93.5078 | 97.9074 | 89.4865 | 92.8768 | 7720 | 165 | 7720 | 907 | 67 | 7.3870 | |
jlack-gatk | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 98.6377 | 99.1486 | 98.1322 | 75.2542 | 47860 | 411 | 47652 | 907 | 540 | 59.5369 | |
ckim-vqsr | INDEL | * | * | het | 99.5204 | 99.5086 | 99.5323 | 62.3713 | 193179 | 954 | 192796 | 906 | 561 | 61.9205 | |
ciseli-custom | SNP | ti | map_l150_m0_e0 | het | 72.0997 | 66.3920 | 78.8811 | 87.9805 | 3384 | 1713 | 3384 | 906 | 29 | 3.2009 | |
jpowers-varprowl | INDEL | D6_15 | HG002complexvar | het | 82.3223 | 90.1603 | 75.7381 | 57.2412 | 2813 | 307 | 2822 | 904 | 873 | 96.5708 | |
jmaeng-gatk | INDEL | * | HG002compoundhet | homalt | 60.0968 | 99.5627 | 43.0372 | 84.8886 | 683 | 3 | 683 | 904 | 898 | 99.3363 | |
gduggal-snapfb | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | * | 81.2248 | 74.4026 | 89.4244 | 27.1457 | 7037 | 2421 | 7644 | 904 | 893 | 98.7832 |