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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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83651-83700 / 86044 show all | |||||||||||||||
| ciseli-custom | SNP | tv | map_l150_m1_e0 | * | 76.2235 | 70.9861 | 82.2954 | 80.7468 | 7746 | 3166 | 7744 | 1666 | 387 | 23.2293 | |
| ckim-isaac | SNP | tv | map_l125_m1_e0 | homalt | 62.9734 | 45.9727 | 99.9258 | 63.6902 | 2694 | 3166 | 2694 | 2 | 2 | 100.0000 | |
| jpowers-varprowl | SNP | ti | HG002complexvar | het | 99.4252 | 98.9938 | 99.8603 | 18.1914 | 311597 | 3167 | 311707 | 436 | 90 | 20.6422 | |
| gduggal-snapvard | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 0.0000 | 60.7906 | 0.0000 | 0.0000 | 4921 | 3174 | 0 | 0 | 0 | ||
| jli-custom | INDEL | * | * | * | 99.3675 | 99.0788 | 99.6580 | 57.6935 | 341368 | 3174 | 341213 | 1171 | 951 | 81.2126 | |
| gduggal-bwaplat | SNP | tv | map_l125_m2_e1 | homalt | 64.6312 | 47.7445 | 100.0000 | 81.7242 | 2900 | 3174 | 2900 | 0 | 0 | ||
| jmaeng-gatk | SNP | ti | map_l150_m1_e0 | homalt | 72.2900 | 56.6125 | 99.9759 | 78.8887 | 4148 | 3179 | 4148 | 1 | 1 | 100.0000 | |
| eyeh-varpipe | INDEL | D16_PLUS | * | * | 59.3408 | 53.1250 | 67.2039 | 51.2916 | 3604 | 3180 | 3586 | 1750 | 1709 | 97.6571 | |
| anovak-vg | SNP | * | map_l125_m2_e0 | homalt | 89.6412 | 81.6863 | 99.3125 | 67.9435 | 14193 | 3182 | 14013 | 97 | 81 | 83.5052 | |
| ckim-isaac | SNP | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 96.5147 | 94.2784 | 98.8597 | 54.0704 | 52448 | 3183 | 52797 | 609 | 355 | 58.2923 | |
| qzeng-custom | SNP | ti | map_l125_m1_e0 | homalt | 82.9138 | 71.1453 | 99.3472 | 63.5077 | 7858 | 3187 | 7762 | 51 | 50 | 98.0392 | |
| gduggal-bwaplat | INDEL | I1_5 | HG002compoundhet | hetalt | 83.2751 | 71.4771 | 99.7378 | 70.8280 | 7989 | 3188 | 7987 | 21 | 17 | 80.9524 | |
| jpowers-varprowl | INDEL | D6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 22.1585 | 18.8343 | 26.9076 | 54.2967 | 740 | 3189 | 737 | 2002 | 1995 | 99.6503 | |
| gduggal-snapvard | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 21.6505 | 12.3145 | 89.5161 | 61.9632 | 448 | 3190 | 333 | 39 | 39 | 100.0000 | |
| anovak-vg | SNP | * | map_l125_m2_e1 | homalt | 89.7095 | 81.8047 | 99.3055 | 67.9368 | 14342 | 3190 | 14156 | 99 | 83 | 83.8384 | |
| gduggal-bwaplat | INDEL | I1_5 | * | hetalt | 82.6726 | 71.4515 | 98.0748 | 76.8337 | 7999 | 3196 | 7998 | 157 | 152 | 96.8153 | |
| ckim-vqsr | SNP | ti | map_l125_m0_e0 | het | 75.6119 | 61.3095 | 98.6179 | 91.4278 | 5066 | 3197 | 5066 | 71 | 0 | 0.0000 | |
| ckim-isaac | SNP | tv | map_l150_m2_e0 | het | 71.5812 | 55.9018 | 99.4848 | 80.5969 | 4054 | 3198 | 4055 | 21 | 6 | 28.5714 | |
| ckim-gatk | SNP | ti | map_l150_m1_e0 | homalt | 72.0545 | 56.3396 | 99.9274 | 79.8232 | 4128 | 3199 | 4128 | 3 | 2 | 66.6667 | |
| ckim-isaac | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 92.5554 | 89.9881 | 95.2735 | 38.7245 | 28789 | 3203 | 28422 | 1410 | 1207 | 85.6028 | |
| ciseli-custom | INDEL | D16_PLUS | * | * | 59.6718 | 52.7860 | 68.6237 | 57.6195 | 3581 | 3203 | 3565 | 1630 | 1503 | 92.2086 | |
| anovak-vg | SNP | * | HG002compoundhet | het | 78.0560 | 77.3875 | 78.7362 | 46.6128 | 10972 | 3206 | 12323 | 3328 | 2553 | 76.7127 | |
| qzeng-custom | SNP | ti | map_l125_m2_e0 | homalt | 83.3237 | 71.7644 | 99.3217 | 66.9963 | 8151 | 3207 | 8054 | 55 | 54 | 98.1818 | |
| gduggal-snapplat | INDEL | D1_5 | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 92.8911 | 87.3497 | 99.1833 | 60.3693 | 22151 | 3208 | 22225 | 183 | 36 | 19.6721 | |
| gduggal-snapplat | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 0.0000 | 0.0000 | 0.0000 | 0 | 3210 | 0 | 0 | 0 | |||
| gduggal-snapfb | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 0.0000 | 0.0000 | 0.0000 | 0 | 3210 | 0 | 0 | 0 | |||
| gduggal-snapvard | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 0.0000 | 60.7121 | 0.0000 | 0.0000 | 4962 | 3211 | 0 | 0 | 0 | ||
| qzeng-custom | SNP | ti | map_l125_m2_e1 | homalt | 83.4603 | 71.9759 | 99.3054 | 66.9858 | 8247 | 3211 | 8149 | 57 | 56 | 98.2456 | |
| gduggal-snapplat | INDEL | D6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 28.5833 | 18.1471 | 67.2691 | 61.6333 | 713 | 3216 | 670 | 326 | 173 | 53.0675 | |
| asubramanian-gatk | SNP | tv | map_l150_m1_e0 | homalt | 31.2233 | 18.4997 | 100.0000 | 92.4835 | 730 | 3216 | 730 | 0 | 0 | ||
| jmaeng-gatk | SNP | ti | map_l150_m2_e0 | homalt | 73.2296 | 57.7731 | 99.9773 | 80.4374 | 4400 | 3216 | 4400 | 1 | 1 | 100.0000 | |
| astatham-gatk | SNP | ti | map_l150_m2_e0 | * | 91.3750 | 84.3165 | 99.7232 | 79.9461 | 17295 | 3217 | 17291 | 48 | 27 | 56.2500 | |
| ckim-isaac | SNP | tv | map_l125_m0_e0 | * | 67.9069 | 51.4704 | 99.7662 | 76.9939 | 3413 | 3218 | 3413 | 8 | 1 | 12.5000 | |
| ckim-isaac | SNP | tv | map_l125_m2_e0 | homalt | 63.4373 | 46.4683 | 99.9285 | 67.7501 | 2796 | 3221 | 2796 | 2 | 2 | 100.0000 | |
| anovak-vg | SNP | * | map_l125_m0_e0 | * | 79.0837 | 83.3789 | 75.2094 | 80.8664 | 16163 | 3222 | 15982 | 5268 | 1460 | 27.7145 | |
| ckim-isaac | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 92.6629 | 89.7351 | 95.7882 | 48.3290 | 28184 | 3224 | 28110 | 1236 | 977 | 79.0453 | |
| ckim-isaac | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 92.6629 | 89.7351 | 95.7882 | 48.3290 | 28184 | 3224 | 28110 | 1236 | 977 | 79.0453 | |
| ckim-vqsr | SNP | tv | map_l125_m1_e0 | het | 80.4152 | 68.0822 | 98.2049 | 89.2490 | 6894 | 3232 | 6893 | 126 | 1 | 0.7937 | |
| ckim-vqsr | INDEL | * | * | * | 99.2541 | 99.0614 | 99.4476 | 60.7768 | 341308 | 3234 | 341167 | 1895 | 1532 | 80.8443 | |
| gduggal-bwavard | SNP | ti | HG002compoundhet | * | 84.8363 | 81.4967 | 88.4613 | 41.1291 | 14244 | 3234 | 14298 | 1865 | 1554 | 83.3244 | |
| ckim-gatk | SNP | ti | map_l150_m2_e0 | homalt | 73.0167 | 57.5236 | 99.9316 | 81.2297 | 4381 | 3235 | 4381 | 3 | 2 | 66.6667 | |
| ciseli-custom | INDEL | * | HG002complexvar | homalt | 81.7869 | 88.0268 | 76.3731 | 56.3608 | 23791 | 3236 | 23555 | 7287 | 5323 | 73.0479 | |
| ckim-isaac | SNP | tv | map_l150_m2_e1 | het | 71.6314 | 55.9608 | 99.4920 | 80.5897 | 4112 | 3236 | 4113 | 21 | 6 | 28.5714 | |
| jmaeng-gatk | SNP | tv | map_l100_m0_e0 | * | 81.7650 | 70.7957 | 96.7567 | 85.8314 | 7847 | 3237 | 7846 | 263 | 11 | 4.1825 | |
| jmaeng-gatk | SNP | ti | map_l150_m2_e1 | homalt | 73.3394 | 57.9098 | 99.9776 | 80.4132 | 4455 | 3238 | 4455 | 1 | 1 | 100.0000 | |
| ciseli-custom | SNP | tv | map_l125_m1_e0 | het | 74.2570 | 68.0229 | 81.7491 | 80.4845 | 6888 | 3238 | 6889 | 1538 | 57 | 3.7061 | |
| ciseli-custom | SNP | tv | map_l150_m2_e0 | * | 76.6548 | 71.4839 | 82.6322 | 82.1021 | 8117 | 3238 | 8112 | 1705 | 399 | 23.4018 | |
| gduggal-snapvard | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 60.1668 | 61.4104 | 58.9725 | 57.4072 | 5164 | 3245 | 7289 | 5071 | 4386 | 86.4918 | |
| anovak-vg | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 0.0000 | 30.1700 | 0.0000 | 0.0000 | 1402 | 3245 | 0 | 0 | 0 | ||
| ckim-isaac | SNP | tv | map_l125_m2_e1 | homalt | 63.5067 | 46.5426 | 99.9293 | 67.7423 | 2827 | 3247 | 2827 | 2 | 2 | 100.0000 | |