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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
24451-24500 / 86044 show all | |||||||||||||||
| ckim-isaac | INDEL | * | HG002complexvar | * | 91.9300 | 88.4153 | 95.7357 | 48.5598 | 68025 | 8913 | 67037 | 2986 | 1352 | 45.2780 | |
| jpowers-varprowl | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 97.0066 | 99.5228 | 94.6144 | 77.5514 | 16894 | 81 | 16918 | 963 | 436 | 45.2752 | |
| jpowers-varprowl | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 97.0066 | 99.5228 | 94.6144 | 77.5514 | 16894 | 81 | 16918 | 963 | 436 | 45.2752 | |
| astatham-gatk | SNP | * | map_l125_m1_e0 | * | 91.2465 | 84.0779 | 99.7513 | 74.8310 | 38110 | 7217 | 38104 | 95 | 43 | 45.2632 | |
| astatham-gatk | SNP | * | map_l125_m2_e0 | * | 91.3143 | 84.1877 | 99.7590 | 76.2743 | 39335 | 7388 | 39329 | 95 | 43 | 45.2632 | |
| astatham-gatk | SNP | * | map_l125_m2_e1 | * | 91.3125 | 84.1829 | 99.7615 | 76.3148 | 39736 | 7466 | 39730 | 95 | 43 | 45.2632 | |
| gduggal-snapplat | INDEL | * | lowcmp_SimpleRepeat_triTR_11to50 | homalt | 59.8233 | 47.0725 | 82.0483 | 56.7574 | 1013 | 1139 | 1394 | 305 | 138 | 45.2459 | |
| gduggal-snapvard | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 96.3822 | 94.6628 | 98.1651 | 78.9575 | 2288 | 129 | 2247 | 42 | 19 | 45.2381 | |
| astatham-gatk | SNP | ti | map_l125_m1_e0 | het | 85.4533 | 74.7728 | 99.6933 | 79.6242 | 13658 | 4608 | 13654 | 42 | 19 | 45.2381 | |
| astatham-gatk | SNP | ti | map_l125_m2_e0 | het | 85.6054 | 75.0000 | 99.7041 | 80.6061 | 14157 | 4719 | 14153 | 42 | 19 | 45.2381 | |
| astatham-gatk | SNP | ti | map_l125_m2_e1 | het | 85.6126 | 75.0092 | 99.7074 | 80.6356 | 14317 | 4770 | 14313 | 42 | 19 | 45.2381 | |
| ciseli-custom | SNP | * | * | hetalt | 87.9067 | 82.2044 | 94.4591 | 39.6977 | 716 | 155 | 716 | 42 | 19 | 45.2381 | |
| ciseli-custom | SNP | tv | * | hetalt | 87.9067 | 82.2044 | 94.4591 | 39.6977 | 716 | 155 | 716 | 42 | 19 | 45.2381 | |
| ndellapenna-hhga | INDEL | * | map_l100_m1_e0 | * | 97.2875 | 96.9325 | 97.6451 | 97.5899 | 3476 | 110 | 3483 | 84 | 38 | 45.2381 | |
| jpowers-varprowl | SNP | tv | lowcmp_SimpleRepeat_triTR_11to50 | * | 98.2548 | 98.6087 | 97.9035 | 45.6956 | 3402 | 48 | 3409 | 73 | 33 | 45.2055 | |
| ltrigg-rtg1 | INDEL | D16_PLUS | * | het | 97.4370 | 95.9481 | 98.9728 | 64.1950 | 3031 | 128 | 2987 | 31 | 14 | 45.1613 | |
| mlin-fermikit | INDEL | D16_PLUS | map_siren | het | 71.4286 | 76.9231 | 66.6667 | 92.1980 | 60 | 18 | 62 | 31 | 14 | 45.1613 | |
| ndellapenna-hhga | SNP | * | map_l250_m2_e0 | het | 97.5992 | 95.8799 | 99.3814 | 87.8462 | 4980 | 214 | 4980 | 31 | 14 | 45.1613 | |
| egarrison-hhga | SNP | tv | map_l100_m0_e0 | * | 99.2887 | 98.8632 | 99.7179 | 67.1372 | 10958 | 126 | 10958 | 31 | 14 | 45.1613 | |
| anovak-vg | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 37.4335 | 27.0492 | 60.7595 | 65.3509 | 33 | 89 | 48 | 31 | 14 | 45.1613 | |
| ciseli-custom | INDEL | D1_5 | map_l125_m1_e0 | * | 76.7370 | 72.2426 | 81.8276 | 90.5347 | 786 | 302 | 788 | 175 | 79 | 45.1429 | |
| qzeng-custom | SNP | * | HG002complexvar | * | 99.1204 | 98.4430 | 99.8072 | 19.9398 | 742639 | 11746 | 723843 | 1398 | 631 | 45.1359 | |
| gduggal-snapvard | INDEL | D1_5 | map_siren | * | 89.9255 | 93.9643 | 86.2197 | 83.0558 | 3316 | 213 | 3729 | 596 | 269 | 45.1342 | |
| gduggal-snapplat | INDEL | D6_15 | HG002compoundhet | het | 18.8426 | 19.6262 | 18.1193 | 66.4873 | 168 | 688 | 79 | 357 | 161 | 45.0980 | |
| gduggal-bwavard | INDEL | C6_15 | HG002compoundhet | * | 0.0000 | 0.0000 | 27.1429 | 91.0026 | 0 | 0 | 19 | 51 | 23 | 45.0980 | |
| gduggal-bwavard | INDEL | D16_PLUS | map_l100_m2_e1 | * | 55.1438 | 57.7320 | 52.7778 | 93.1122 | 56 | 41 | 57 | 51 | 23 | 45.0980 | |
| ciseli-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 72.5469 | 76.4799 | 68.9986 | 69.9494 | 23308 | 7168 | 24351 | 10941 | 4932 | 45.0781 | |
| ciseli-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 72.5469 | 76.4799 | 68.9986 | 69.9494 | 23308 | 7168 | 24351 | 10941 | 4932 | 45.0781 | |
| eyeh-varpipe | SNP | tv | HG002compoundhet | homalt | 96.9051 | 99.4687 | 94.4704 | 53.4614 | 3370 | 18 | 1213 | 71 | 32 | 45.0704 | |
| egarrison-hhga | SNP | ti | map_l100_m2_e0 | * | 99.5647 | 99.2770 | 99.8541 | 64.5210 | 48607 | 354 | 48608 | 71 | 32 | 45.0704 | |
| ndellapenna-hhga | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 94.3116 | 95.7208 | 92.9434 | 47.3511 | 8008 | 358 | 8008 | 608 | 274 | 45.0658 | |
| qzeng-custom | INDEL | I6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 92.5975 | 97.2222 | 88.3929 | 44.7887 | 210 | 6 | 693 | 91 | 41 | 45.0549 | |
| ciseli-custom | INDEL | D1_5 | map_l125_m2_e0 | * | 76.8250 | 72.2660 | 81.9980 | 90.9083 | 826 | 317 | 829 | 182 | 82 | 45.0549 | |
| gduggal-snapfb | SNP | * | map_l250_m2_e0 | * | 94.6894 | 94.5212 | 94.8581 | 89.8978 | 7453 | 432 | 7453 | 404 | 182 | 45.0495 | |
| jmaeng-gatk | SNP | ti | HG002complexvar | * | 99.5813 | 99.1995 | 99.9661 | 17.9457 | 504366 | 4070 | 504306 | 171 | 77 | 45.0292 | |
| gduggal-snapplat | SNP | tv | map_siren | het | 96.1131 | 95.9558 | 96.2709 | 75.9094 | 27452 | 1157 | 27468 | 1064 | 479 | 45.0188 | |
| gduggal-snapfb | INDEL | D1_5 | * | hetalt | 84.1984 | 78.0771 | 91.3611 | 79.2100 | 7999 | 2246 | 3289 | 311 | 140 | 45.0161 | |
| qzeng-custom | INDEL | I1_5 | map_l125_m2_e0 | het | 77.9993 | 65.7948 | 95.7627 | 93.1215 | 327 | 170 | 452 | 20 | 9 | 45.0000 | |
| qzeng-custom | INDEL | I1_5 | map_l125_m2_e1 | het | 78.2603 | 66.1417 | 95.8159 | 93.1509 | 336 | 172 | 458 | 20 | 9 | 45.0000 | |
| ndellapenna-hhga | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 97.4344 | 96.9479 | 97.9258 | 61.8911 | 3780 | 119 | 3777 | 80 | 36 | 45.0000 | |
| ndellapenna-hhga | INDEL | I1_5 | lowcmp_SimpleRepeat_triTR_11to50 | * | 97.9476 | 97.8095 | 98.0861 | 56.9959 | 1027 | 23 | 1025 | 20 | 9 | 45.0000 | |
| ndellapenna-hhga | SNP | * | map_l100_m2_e1 | * | 99.3413 | 98.8761 | 99.8109 | 63.7314 | 73897 | 840 | 73899 | 140 | 63 | 45.0000 | |
| ltrigg-rtg2 | INDEL | I6_15 | HG002complexvar | het | 98.2137 | 97.4098 | 99.0310 | 49.5355 | 2294 | 61 | 2044 | 20 | 9 | 45.0000 | |
| rpoplin-dv42 | SNP | tv | map_l100_m0_e0 | * | 98.7643 | 98.7911 | 98.7375 | 67.3276 | 10950 | 134 | 10949 | 140 | 63 | 45.0000 | |
| egarrison-hhga | SNP | tv | map_l125_m0_e0 | * | 99.1050 | 98.5221 | 99.6948 | 73.4104 | 6533 | 98 | 6533 | 20 | 9 | 45.0000 | |
| egarrison-hhga | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 96.1650 | 95.9220 | 96.4093 | 67.7662 | 541 | 23 | 537 | 20 | 9 | 45.0000 | |
| ckim-isaac | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 70.9431 | 59.3496 | 88.1657 | 78.6885 | 146 | 100 | 149 | 20 | 9 | 45.0000 | |
| asubramanian-gatk | INDEL | * | map_siren | homalt | 97.0575 | 94.9906 | 99.2163 | 82.1825 | 2522 | 133 | 2532 | 20 | 9 | 45.0000 | |
| jlack-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | * | 99.5173 | 99.5860 | 99.4487 | 75.8037 | 3608 | 15 | 3608 | 20 | 9 | 45.0000 | |
| jlack-gatk | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 98.6913 | 98.9198 | 98.4639 | 87.5787 | 1282 | 14 | 1282 | 20 | 9 | 45.0000 | |