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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
73301-73350 / 86044 show all | |||||||||||||||
| cchapple-custom | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 99.0130 | 99.6869 | 98.3480 | 64.2091 | 17513 | 55 | 17622 | 296 | 23 | 7.7703 | |
| gduggal-bwavard | SNP | tv | lowcmp_SimpleRepeat_homopolymer_6to10 | homalt | 99.0131 | 98.1219 | 99.9207 | 56.5287 | 3814 | 73 | 3779 | 3 | 2 | 66.6667 | |
| gduggal-snapvard | SNP | tv | lowcmp_SimpleRepeat_homopolymer_6to10 | homalt | 99.0133 | 98.1991 | 99.8412 | 55.4691 | 3817 | 70 | 3772 | 6 | 3 | 50.0000 | |
| dgrover-gatk | INDEL | * | segdup | het | 99.0133 | 99.2497 | 98.7780 | 95.2951 | 1455 | 11 | 1455 | 18 | 2 | 11.1111 | |
| rpoplin-dv42 | INDEL | D1_5 | map_siren | het | 99.0134 | 99.1217 | 98.9054 | 80.0820 | 2257 | 20 | 2259 | 25 | 7 | 28.0000 | |
| rpoplin-dv42 | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 99.0139 | 98.4069 | 99.6285 | 44.6543 | 10192 | 165 | 10191 | 38 | 37 | 97.3684 | |
| ltrigg-rtg2 | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 99.0140 | 98.1239 | 99.9205 | 31.1473 | 5021 | 96 | 5025 | 4 | 4 | 100.0000 | |
| astatham-gatk | INDEL | D6_15 | HG002complexvar | het | 99.0140 | 98.8462 | 99.1825 | 59.3945 | 3084 | 36 | 3033 | 25 | 19 | 76.0000 | |
| ltrigg-rtg1 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 99.0141 | 98.5968 | 99.4350 | 71.9122 | 2108 | 30 | 2112 | 12 | 2 | 16.6667 | |
| ckim-gatk | INDEL | D6_15 | HG002complexvar | het | 99.0142 | 98.9423 | 99.0862 | 59.4709 | 3087 | 33 | 3036 | 28 | 22 | 78.5714 | |
| raldana-dualsentieon | SNP | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 99.0144 | 98.4246 | 99.6113 | 60.1683 | 34861 | 558 | 34851 | 136 | 14 | 10.2941 | |
| raldana-dualsentieon | INDEL | * | lowcmp_SimpleRepeat_triTR_11to50 | hetalt | 99.0153 | 98.0498 | 100.0000 | 28.0159 | 905 | 18 | 907 | 0 | 0 | ||
| cchapple-custom | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 99.0153 | 100.0000 | 98.0498 | 71.9708 | 914 | 0 | 905 | 18 | 1 | 5.5556 | |
| ltrigg-rtg2 | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 99.0155 | 98.2173 | 99.8268 | 66.0394 | 1157 | 21 | 1153 | 2 | 1 | 50.0000 | |
| dgrover-gatk | SNP | tv | map_l150_m1_e0 | * | 99.0155 | 99.0927 | 98.9384 | 77.4338 | 10813 | 99 | 10811 | 116 | 24 | 20.6897 | |
| hfeng-pmm2 | SNP | tv | map_l125_m2_e0 | het | 99.0157 | 99.2434 | 98.7891 | 75.7772 | 10363 | 79 | 10361 | 127 | 11 | 8.6614 | |
| hfeng-pmm3 | INDEL | D1_5 | map_l100_m2_e1 | het | 99.0158 | 99.0536 | 98.9780 | 81.3490 | 1256 | 12 | 1259 | 13 | 2 | 15.3846 | |
| ltrigg-rtg1 | INDEL | * | * | * | 99.0160 | 98.3355 | 99.7061 | 56.0561 | 338806 | 5735 | 338554 | 998 | 454 | 45.4910 | |
| hfeng-pmm3 | SNP | * | map_l250_m2_e0 | * | 99.0163 | 98.9347 | 99.0981 | 88.6629 | 7801 | 84 | 7801 | 71 | 9 | 12.6761 | |
| ltrigg-rtg1 | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 99.0164 | 98.0519 | 100.0000 | 48.4429 | 453 | 9 | 447 | 0 | 0 | ||
| rpoplin-dv42 | INDEL | * | map_l125_m2_e0 | homalt | 99.0164 | 98.9515 | 99.0814 | 86.1076 | 755 | 8 | 755 | 7 | 6 | 85.7143 | |
| qzeng-custom | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 99.0167 | 99.6391 | 98.4019 | 66.3620 | 2485 | 9 | 2463 | 40 | 1 | 2.5000 | |
| bgallagher-sentieon | SNP | * | map_l125_m2_e1 | het | 99.0167 | 99.3893 | 98.6469 | 75.8815 | 29459 | 181 | 29453 | 404 | 55 | 13.6139 | |
| hfeng-pmm1 | SNP | ti | map_l125_m0_e0 | het | 99.0169 | 98.7414 | 99.2940 | 75.6362 | 8159 | 104 | 8157 | 58 | 15 | 25.8621 | |
| ckim-dragen | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 99.0173 | 98.5075 | 99.5324 | 77.0540 | 1518 | 23 | 1490 | 7 | 3 | 42.8571 | |
| ltrigg-rtg1 | INDEL | * | map_l100_m0_e0 | homalt | 99.0173 | 99.2141 | 98.8212 | 82.1404 | 505 | 4 | 503 | 6 | 3 | 50.0000 | |
| dgrover-gatk | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 99.0176 | 98.6372 | 99.4008 | 77.5553 | 1520 | 21 | 1493 | 9 | 3 | 33.3333 | |
| eyeh-varpipe | INDEL | I1_5 | map_l150_m2_e0 | homalt | 99.0179 | 99.5025 | 98.5380 | 88.0795 | 200 | 1 | 337 | 5 | 5 | 100.0000 | |
| hfeng-pmm3 | SNP | ti | map_l150_m0_e0 | het | 99.0183 | 98.9602 | 99.0764 | 81.1323 | 5044 | 53 | 5042 | 47 | 2 | 4.2553 | |
| ltrigg-rtg2 | SNP | ti | map_l125_m2_e1 | * | 99.0186 | 98.1877 | 99.8636 | 61.5506 | 30015 | 554 | 30018 | 41 | 10 | 24.3902 | |
| ltrigg-rtg2 | SNP | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 99.0190 | 98.1121 | 99.9429 | 58.3888 | 1715 | 33 | 1750 | 1 | 1 | 100.0000 | |
| ltrigg-rtg1 | SNP | ti | map_l100_m1_e0 | het | 99.0192 | 98.2900 | 99.7593 | 54.6205 | 29430 | 512 | 29432 | 71 | 7 | 9.8592 | |
| hfeng-pmm3 | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 99.0193 | 98.0576 | 100.0000 | 32.2402 | 1464 | 29 | 1467 | 0 | 0 | ||
| gduggal-bwafb | SNP | ti | segdup | * | 99.0195 | 99.5086 | 98.5352 | 91.2837 | 19441 | 96 | 19441 | 289 | 16 | 5.5363 | |
| jli-custom | INDEL | I6_15 | HG002complexvar | homalt | 99.0196 | 99.8353 | 98.2172 | 53.8692 | 1212 | 2 | 1212 | 22 | 22 | 100.0000 | |
| ltrigg-rtg1 | SNP | ti | map_l100_m2_e0 | het | 99.0198 | 98.3084 | 99.7416 | 57.0120 | 30104 | 518 | 30106 | 78 | 7 | 8.9744 | |
| ckim-vqsr | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 99.0199 | 98.6449 | 99.3978 | 76.9388 | 6333 | 87 | 6272 | 38 | 24 | 63.1579 | |
| ckim-vqsr | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 99.0199 | 98.6449 | 99.3978 | 76.9388 | 6333 | 87 | 6272 | 38 | 24 | 63.1579 | |
| hfeng-pmm1 | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | het | 99.0203 | 98.2985 | 99.7527 | 60.4577 | 10919 | 189 | 10893 | 27 | 9 | 33.3333 | |
| ltrigg-rtg1 | INDEL | * | map_l100_m2_e1 | homalt | 99.0206 | 98.5948 | 99.4501 | 82.2479 | 1263 | 18 | 1266 | 7 | 4 | 57.1429 | |
| hfeng-pmm3 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 99.0206 | 99.3362 | 98.7071 | 54.3318 | 3741 | 25 | 3741 | 49 | 45 | 91.8367 | |
| hfeng-pmm3 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 99.0206 | 99.3362 | 98.7071 | 54.3318 | 3741 | 25 | 3741 | 49 | 45 | 91.8367 | |
| eyeh-varpipe | SNP | ti | map_l250_m2_e1 | * | 99.0209 | 99.4484 | 98.5971 | 90.5779 | 5048 | 28 | 4990 | 71 | 6 | 8.4507 | |
| hfeng-pmm1 | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 99.0211 | 98.0611 | 100.0000 | 42.7615 | 2630 | 52 | 2649 | 0 | 0 | ||
| hfeng-pmm1 | INDEL | * | segdup | * | 99.0215 | 98.9437 | 99.0995 | 94.0294 | 2529 | 27 | 2531 | 23 | 4 | 17.3913 | |
| bgallagher-sentieon | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 99.0215 | 98.2585 | 99.7963 | 32.1198 | 1467 | 26 | 1470 | 3 | 3 | 100.0000 | |
| hfeng-pmm3 | SNP | tv | map_l125_m0_e0 | het | 99.0220 | 98.9321 | 99.1120 | 76.4302 | 4354 | 47 | 4353 | 39 | 3 | 7.6923 | |
| egarrison-hhga | SNP | tv | map_l150_m1_e0 | het | 99.0220 | 98.3876 | 99.6646 | 73.3388 | 6834 | 112 | 6834 | 23 | 9 | 39.1304 | |
| gduggal-bwavard | SNP | tv | func_cds | * | 99.0223 | 98.5358 | 99.5136 | 36.8583 | 4307 | 64 | 4296 | 21 | 9 | 42.8571 | |
| ckim-dragen | SNP | ti | map_siren | * | 99.0224 | 99.5177 | 98.5321 | 56.8522 | 99871 | 484 | 99880 | 1488 | 162 | 10.8871 | |