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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
19851-19900 / 86044 show all | |||||||||||||||
mlin-fermikit | SNP | tv | lowcmp_SimpleRepeat_triTR_11to50 | * | 98.1542 | 97.8551 | 98.4553 | 37.1727 | 3376 | 74 | 3378 | 53 | 35 | 66.0377 | |
ckim-gatk | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 96.2770 | 99.0654 | 93.6413 | 86.2049 | 1802 | 17 | 1561 | 106 | 70 | 66.0377 | |
ckim-gatk | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 96.2770 | 99.0654 | 93.6413 | 86.2049 | 1802 | 17 | 1561 | 106 | 70 | 66.0377 | |
gduggal-snapvard | INDEL | D6_15 | map_l125_m2_e1 | het | 77.2841 | 88.7324 | 68.4524 | 86.1272 | 63 | 8 | 115 | 53 | 35 | 66.0377 | |
ghariani-varprowl | SNP | * | map_l100_m2_e1 | homalt | 99.3161 | 99.0071 | 99.6271 | 64.4501 | 27520 | 276 | 27520 | 103 | 68 | 66.0194 | |
rpoplin-dv42 | SNP | * | map_l250_m2_e0 | * | 98.3456 | 98.0089 | 98.6847 | 88.0100 | 7728 | 157 | 7728 | 103 | 68 | 66.0194 | |
cchapple-custom | SNP | tv | HG002compoundhet | het | 98.8352 | 98.5020 | 99.1705 | 51.5239 | 4603 | 70 | 5978 | 50 | 33 | 66.0000 | |
ciseli-custom | INDEL | * | map_l100_m2_e0 | * | 70.8083 | 66.3417 | 75.9196 | 88.0680 | 2450 | 1243 | 2456 | 779 | 514 | 65.9820 | |
jpowers-varprowl | INDEL | D1_5 | map_l100_m2_e1 | * | 93.6537 | 92.4703 | 94.8677 | 84.4955 | 1793 | 146 | 1793 | 97 | 64 | 65.9794 | |
rpoplin-dv42 | SNP | tv | map_l250_m2_e0 | * | 97.9798 | 97.6058 | 98.3566 | 87.5544 | 2813 | 69 | 2813 | 47 | 31 | 65.9574 | |
ghariani-varprowl | INDEL | D1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 98.0582 | 99.4990 | 96.6586 | 57.2289 | 14696 | 74 | 14695 | 508 | 335 | 65.9449 | |
gduggal-bwavard | SNP | tv | HG002complexvar | het | 98.2582 | 97.4538 | 99.0760 | 23.1907 | 146896 | 3838 | 144431 | 1347 | 888 | 65.9243 | |
asubramanian-gatk | INDEL | D1_5 | * | * | 99.2637 | 98.9281 | 99.6016 | 61.0980 | 145172 | 1573 | 145253 | 581 | 383 | 65.9208 | |
ckim-dragen | INDEL | * | * | * | 99.1359 | 99.1574 | 99.1143 | 60.3466 | 341639 | 2903 | 341303 | 3050 | 2010 | 65.9016 | |
rpoplin-dv42 | SNP | ti | map_l100_m0_e0 | * | 99.1759 | 98.9481 | 99.4047 | 66.3363 | 21542 | 229 | 21539 | 129 | 85 | 65.8915 | |
asubramanian-gatk | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | * | 97.2439 | 97.3027 | 97.1852 | 57.6417 | 35605 | 987 | 38256 | 1108 | 730 | 65.8845 | |
ckim-isaac | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 92.1912 | 88.4459 | 96.2678 | 41.3787 | 3261 | 426 | 3250 | 126 | 83 | 65.8730 | |
eyeh-varpipe | INDEL | I1_5 | map_l100_m1_e0 | het | 97.0283 | 97.4260 | 96.6338 | 80.2465 | 757 | 20 | 1177 | 41 | 27 | 65.8537 | |
qzeng-custom | INDEL | D1_5 | map_l100_m2_e1 | het | 89.9622 | 84.0694 | 96.7434 | 89.9976 | 1066 | 202 | 1218 | 41 | 27 | 65.8537 | |
jlack-gatk | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 98.3350 | 98.3733 | 98.2966 | 76.2904 | 2419 | 40 | 2366 | 41 | 27 | 65.8537 | |
gduggal-snapplat | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 65.7127 | 54.1731 | 83.4992 | 45.7734 | 1058 | 895 | 1007 | 199 | 131 | 65.8291 | |
ciseli-custom | INDEL | * | map_siren | * | 74.2881 | 71.4035 | 77.4156 | 83.7506 | 5291 | 2119 | 5296 | 1545 | 1017 | 65.8252 | |
egarrison-hhga | INDEL | * | lowcmp_SimpleRepeat_diTR_51to200 | homalt | 82.8877 | 86.3510 | 79.6915 | 44.5869 | 310 | 49 | 310 | 79 | 52 | 65.8228 | |
anovak-vg | INDEL | D1_5 | segdup | * | 91.5860 | 90.4805 | 92.7189 | 94.7590 | 998 | 105 | 1006 | 79 | 52 | 65.8228 | |
egarrison-hhga | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 83.1419 | 76.6600 | 90.8213 | 72.4184 | 381 | 116 | 376 | 38 | 25 | 65.7895 | |
eyeh-varpipe | INDEL | C6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 0.0000 | 0.0000 | 38.7097 | 93.8796 | 0 | 0 | 24 | 38 | 25 | 65.7895 | |
cchapple-custom | INDEL | D1_5 | * | * | 99.4223 | 99.1584 | 99.6877 | 55.8052 | 145510 | 1235 | 145535 | 456 | 300 | 65.7895 | |
qzeng-custom | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 96.0217 | 94.2549 | 97.8560 | 49.0716 | 3675 | 224 | 8535 | 187 | 123 | 65.7754 | |
mlin-fermikit | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 88.0789 | 89.7382 | 86.4799 | 86.3258 | 2125 | 243 | 2130 | 333 | 219 | 65.7658 | |
ciseli-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 72.4338 | 76.9090 | 68.4508 | 62.7083 | 2518 | 756 | 2788 | 1285 | 845 | 65.7588 | |
gduggal-bwavard | SNP | * | HG002complexvar | het | 98.2730 | 97.3044 | 99.2610 | 20.1947 | 452952 | 12548 | 441659 | 3288 | 2162 | 65.7543 | |
gduggal-bwavard | SNP | * | HG002complexvar | * | 98.3118 | 97.1354 | 99.5171 | 19.6107 | 732775 | 21610 | 712182 | 3456 | 2272 | 65.7407 | |
anovak-vg | INDEL | I6_15 | map_siren | * | 52.3607 | 48.1967 | 57.3123 | 74.7000 | 147 | 158 | 145 | 108 | 71 | 65.7407 | |
mlin-fermikit | SNP | * | lowcmp_SimpleRepeat_diTR_11to50 | * | 96.0726 | 96.5229 | 95.6265 | 68.5165 | 9355 | 337 | 9380 | 429 | 282 | 65.7343 | |
ndellapenna-hhga | INDEL | * | lowcmp_SimpleRepeat_homopolymer_6to10 | het | 99.4473 | 99.1113 | 99.7856 | 56.2027 | 16283 | 146 | 16290 | 35 | 23 | 65.7143 | |
rpoplin-dv42 | SNP | ti | map_siren | * | 99.6562 | 99.5227 | 99.7902 | 53.3616 | 99876 | 479 | 99868 | 210 | 138 | 65.7143 | |
eyeh-varpipe | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 93.8809 | 89.9476 | 98.1740 | 49.0700 | 7552 | 844 | 7527 | 140 | 92 | 65.7143 | |
gduggal-snapplat | SNP | * | map_siren | homalt | 97.4154 | 95.0214 | 99.9332 | 54.3867 | 52410 | 2746 | 52361 | 35 | 23 | 65.7143 | |
eyeh-varpipe | INDEL | * | map_l100_m2_e1 | het | 96.0818 | 95.5186 | 96.6518 | 82.4853 | 2238 | 105 | 3031 | 105 | 69 | 65.7143 | |
ckim-isaac | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_51to200bp_gt95identity_merged | * | 91.7822 | 88.7139 | 95.0704 | 56.7337 | 676 | 86 | 675 | 35 | 23 | 65.7143 | |
egarrison-hhga | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 94.0522 | 92.1444 | 96.0407 | 70.6215 | 868 | 74 | 849 | 35 | 23 | 65.7143 | |
jmaeng-gatk | SNP | ti | * | homalt | 99.6264 | 99.2642 | 99.9912 | 16.0789 | 797129 | 5909 | 797120 | 70 | 46 | 65.7143 | |
hfeng-pmm3 | INDEL | D1_5 | * | * | 99.5137 | 99.1441 | 99.8861 | 56.7122 | 145489 | 1256 | 145542 | 166 | 109 | 65.6627 | |
gduggal-bwavard | SNP | tv | * | homalt | 99.4965 | 99.0327 | 99.9647 | 19.0358 | 373475 | 3648 | 371220 | 131 | 86 | 65.6489 | |
qzeng-custom | INDEL | I1_5 | * | * | 97.7958 | 96.8327 | 98.7782 | 55.3353 | 145892 | 4772 | 145850 | 1804 | 1184 | 65.6319 | |
qzeng-custom | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 99.7317 | 99.7821 | 99.6812 | 62.4851 | 10075 | 22 | 10007 | 32 | 21 | 65.6250 | |
mlin-fermikit | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 77.7614 | 75.7576 | 79.8742 | 91.5962 | 125 | 40 | 127 | 32 | 21 | 65.6250 | |
hfeng-pmm2 | INDEL | D1_5 | HG002complexvar | * | 99.1842 | 98.4778 | 99.9009 | 57.1533 | 32217 | 498 | 32268 | 32 | 21 | 65.6250 | |
gduggal-snapplat | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 37.3854 | 26.5403 | 63.2184 | 72.2930 | 56 | 155 | 55 | 32 | 21 | 65.6250 | |
ciseli-custom | INDEL | * | lowcmp_SimpleRepeat_triTR_11to50 | * | 76.5465 | 76.6078 | 76.4854 | 46.7535 | 5158 | 1575 | 5162 | 1587 | 1041 | 65.5955 |