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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
79051-79100 / 86044 show all | |||||||||||||||
| anovak-vg | INDEL | I1_5 | map_l150_m2_e1 | * | 59.8471 | 62.1469 | 57.7114 | 90.7116 | 330 | 201 | 348 | 255 | 162 | 63.5294 | |
| jpowers-varprowl | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 56.6114 | 42.2485 | 85.7701 | 63.4733 | 1537 | 2101 | 1537 | 255 | 235 | 92.1569 | |
| gduggal-bwafb | SNP | tv | map_l125_m1_e0 | * | 98.6420 | 98.8699 | 98.4152 | 72.8937 | 15835 | 181 | 15835 | 255 | 50 | 19.6078 | |
| eyeh-varpipe | SNP | ti | map_l150_m2_e1 | het | 98.7627 | 99.5083 | 98.0281 | 80.5176 | 12951 | 64 | 12677 | 255 | 11 | 4.3137 | |
| qzeng-custom | SNP | tv | lowcmp_SimpleRepeat_quadTR_11to50 | het | 97.1050 | 99.5095 | 94.8139 | 49.1046 | 4666 | 23 | 4662 | 255 | 3 | 1.1765 | |
| mlin-fermikit | SNP | tv | map_l250_m2_e1 | homalt | 50.9001 | 43.3404 | 61.6541 | 74.8392 | 410 | 536 | 410 | 255 | 239 | 93.7255 | |
| hfeng-pmm2 | SNP | * | map_l100_m0_e0 | het | 99.0069 | 99.2124 | 98.8022 | 73.2241 | 21038 | 167 | 21034 | 255 | 23 | 9.0196 | |
| jmaeng-gatk | SNP | tv | map_l150_m2_e0 | het | 83.9830 | 74.9448 | 95.5001 | 91.0642 | 5435 | 1817 | 5433 | 256 | 6 | 2.3438 | |
| ghariani-varprowl | INDEL | I6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 73.6289 | 89.6552 | 62.4633 | 66.7479 | 416 | 48 | 426 | 256 | 253 | 98.8281 | |
| ghariani-varprowl | SNP | ti | map_l250_m2_e1 | * | 96.1939 | 97.3404 | 95.0741 | 91.3522 | 4941 | 135 | 4941 | 256 | 54 | 21.0938 | |
| gduggal-snapplat | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 73.6501 | 74.6171 | 72.7079 | 81.2886 | 682 | 232 | 682 | 256 | 1 | 0.3906 | |
| ckim-gatk | INDEL | * | lowcmp_SimpleRepeat_diTR_51to200 | * | 85.8873 | 84.9119 | 86.8852 | 57.3613 | 1784 | 317 | 1696 | 256 | 250 | 97.6562 | |
| ckim-isaac | INDEL | D1_5 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 83.4407 | 85.5319 | 81.4493 | 59.0504 | 1206 | 204 | 1124 | 256 | 208 | 81.2500 | |
| dgrover-gatk | INDEL | * | lowcmp_SimpleRepeat_diTR_51to200 | * | 85.9977 | 85.1023 | 86.9121 | 57.7994 | 1788 | 313 | 1700 | 256 | 250 | 97.6562 | |
| anovak-vg | INDEL | I16_PLUS | HG002compoundhet | * | 11.6860 | 7.0929 | 33.1593 | 41.3476 | 152 | 1991 | 127 | 256 | 126 | 49.2188 | |
| asubramanian-gatk | INDEL | I1_5 | * | homalt | 99.5606 | 99.5449 | 99.5763 | 55.0778 | 60153 | 275 | 60163 | 256 | 247 | 96.4844 | |
| gduggal-snapfb | INDEL | * | map_siren | het | 93.3260 | 92.3026 | 94.3724 | 79.8904 | 4161 | 347 | 4293 | 256 | 57 | 22.2656 | |
| gduggal-bwavard | SNP | tv | map_l250_m0_e0 | * | 83.6982 | 96.2092 | 74.0666 | 94.7166 | 736 | 29 | 734 | 257 | 5 | 1.9455 | |
| eyeh-varpipe | INDEL | I6_15 | lowcmp_SimpleRepeat_triTR_11to50 | * | 66.9909 | 56.2201 | 82.8667 | 28.6733 | 235 | 183 | 1243 | 257 | 257 | 100.0000 | |
| ckim-vqsr | SNP | ti | map_siren | het | 91.0834 | 83.9713 | 99.5117 | 71.3937 | 52383 | 9999 | 52376 | 257 | 20 | 7.7821 | |
| egarrison-hhga | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.7965 | 98.4954 | 99.0994 | 71.1241 | 28280 | 432 | 28279 | 257 | 56 | 21.7899 | |
| egarrison-hhga | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.7965 | 98.4954 | 99.0994 | 71.1241 | 28280 | 432 | 28279 | 257 | 56 | 21.7899 | |
| gduggal-snapplat | SNP | ti | map_l250_m2_e1 | het | 88.7384 | 85.9654 | 91.6963 | 94.7638 | 2836 | 463 | 2838 | 257 | 134 | 52.1401 | |
| ghariani-varprowl | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 60.1899 | 90.0452 | 45.2026 | 89.8966 | 199 | 22 | 212 | 257 | 21 | 8.1712 | |
| ghariani-varprowl | INDEL | D16_PLUS | HG002complexvar | het | 84.6320 | 90.1536 | 79.7478 | 64.8768 | 998 | 109 | 1012 | 257 | 243 | 94.5525 | |
| hfeng-pmm2 | SNP | * | map_l150_m2_e0 | het | 98.9416 | 99.1556 | 98.7286 | 79.5932 | 19963 | 170 | 19957 | 257 | 23 | 8.9494 | |
| jlack-gatk | INDEL | D1_5 | HG002compoundhet | homalt | 69.2124 | 99.6564 | 53.0165 | 77.8632 | 290 | 1 | 290 | 257 | 257 | 100.0000 | |
| jlack-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 98.2945 | 99.6172 | 97.0064 | 59.6494 | 8328 | 32 | 8328 | 257 | 256 | 99.6109 | |
| jlack-gatk | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 98.2945 | 99.6172 | 97.0064 | 59.6494 | 8328 | 32 | 8328 | 257 | 256 | 99.6109 | |
| jmaeng-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 98.1507 | 99.0803 | 97.2383 | 83.3124 | 9049 | 84 | 9049 | 257 | 10 | 3.8911 | |
| jmaeng-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 98.1507 | 99.0803 | 97.2383 | 83.3124 | 9049 | 84 | 9049 | 257 | 10 | 3.8911 | |
| jmaeng-gatk | SNP | tv | map_l150_m2_e0 | * | 79.9418 | 68.0934 | 96.7823 | 89.5425 | 7732 | 3623 | 7730 | 257 | 7 | 2.7237 | |
| jmaeng-gatk | SNP | tv | segdup | * | 98.1687 | 99.3085 | 97.0548 | 94.6921 | 8473 | 59 | 8469 | 257 | 8 | 3.1128 | |
| jmaeng-gatk | SNP | * | HG002complexvar | * | 99.5566 | 99.1508 | 99.9656 | 19.5091 | 747975 | 6406 | 747823 | 257 | 106 | 41.2451 | |
| cchapple-custom | INDEL | D6_15 | * | het | 98.5018 | 98.2488 | 98.7561 | 48.6146 | 11389 | 203 | 20403 | 257 | 215 | 83.6576 | |
| mlin-fermikit | INDEL | D6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 79.1842 | 93.5216 | 68.6585 | 57.6883 | 563 | 39 | 563 | 257 | 251 | 97.6654 | |
| mlin-fermikit | SNP | ti | segdup | * | 98.0976 | 97.5329 | 98.6689 | 85.0585 | 19055 | 482 | 19051 | 257 | 86 | 33.4630 | |
| ndellapenna-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 95.0800 | 95.1730 | 94.9873 | 39.7320 | 4870 | 247 | 4870 | 257 | 123 | 47.8599 | |
| ndellapenna-hhga | SNP | ti | * | homalt | 99.9286 | 99.8893 | 99.9678 | 16.7330 | 802149 | 889 | 802170 | 258 | 209 | 81.0078 | |
| ndellapenna-hhga | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 98.8647 | 98.5647 | 99.1665 | 69.0402 | 30696 | 447 | 30695 | 258 | 94 | 36.4341 | |
| ndellapenna-hhga | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 98.8647 | 98.5647 | 99.1665 | 69.0402 | 30696 | 447 | 30695 | 258 | 94 | 36.4341 | |
| mlin-fermikit | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 86.4854 | 99.1784 | 76.6727 | 86.8957 | 845 | 7 | 848 | 258 | 212 | 82.1705 | |
| raldana-dualsentieon | INDEL | * | lowcmp_SimpleRepeat_diTR_51to200 | * | 82.1683 | 78.7720 | 85.8708 | 53.3827 | 1655 | 446 | 1568 | 258 | 253 | 98.0620 | |
| ghariani-varprowl | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | homalt | 73.1437 | 60.1120 | 93.3897 | 54.7163 | 3650 | 2422 | 3645 | 258 | 193 | 74.8062 | |
| gduggal-snapfb | SNP | ti | lowcmp_SimpleRepeat_triTR_11to50 | * | 96.6308 | 99.6416 | 93.7966 | 43.2141 | 3892 | 14 | 3901 | 258 | 11 | 4.2636 | |
| gduggal-snapplat | INDEL | D1_5 | map_siren | het | 85.7607 | 82.4769 | 89.3168 | 89.6940 | 1878 | 399 | 2157 | 258 | 42 | 16.2791 | |
| ghariani-varprowl | INDEL | I1_5 | map_siren | * | 92.4494 | 93.3444 | 91.5714 | 83.4764 | 2805 | 200 | 2803 | 258 | 121 | 46.8992 | |
| gduggal-snapplat | SNP | ti | map_l250_m2_e0 | * | 88.7392 | 83.8658 | 94.2139 | 93.6830 | 4200 | 808 | 4201 | 258 | 136 | 52.7132 | |
| eyeh-varpipe | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 98.1071 | 97.0183 | 99.2207 | 69.5547 | 32245 | 991 | 32847 | 258 | 171 | 66.2791 | |
| eyeh-varpipe | INDEL | I1_5 | HG002compoundhet | het | 74.0633 | 83.6471 | 66.4499 | 67.5390 | 711 | 139 | 511 | 258 | 225 | 87.2093 | |