PrecisionFDA
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Explore HG002 comparison results
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| Entry | Type | Subtype | Subset | Genotype | F-score | Recall | Precision | Frac_NA | Truth TP | Truth FN | Query TP | Query FP | FP gt | % FP ma | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
2601-2650 / 86044 show all | |||||||||||||||
| anovak-vg | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 71.6357 | 72.7045 | 70.5979 | 41.7864 | 7530 | 2827 | 9069 | 3777 | 3029 | 80.1959 | |
| gduggal-snapfb | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 74.5911 | 64.9460 | 87.6005 | 39.3454 | 5234 | 2825 | 763 | 108 | 107 | 99.0741 | |
| gduggal-snapfb | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 74.5911 | 64.9460 | 87.6005 | 39.3454 | 5234 | 2825 | 763 | 108 | 107 | 99.0741 | |
| jpowers-varprowl | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 73.4486 | 61.1425 | 91.9567 | 37.2269 | 4431 | 2816 | 4413 | 386 | 340 | 88.0829 | |
| ckim-vqsr | SNP | tv | map_l100_m0_e0 | homalt | 42.2477 | 26.7811 | 100.0000 | 86.1726 | 1030 | 2816 | 1030 | 0 | 0 | ||
| egarrison-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 73.7836 | 58.7520 | 99.1512 | 28.6930 | 4011 | 2816 | 3738 | 32 | 26 | 81.2500 | |
| gduggal-snapplat | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 36.7443 | 23.6507 | 82.3171 | 53.0758 | 872 | 2815 | 810 | 174 | 64 | 36.7816 | |
| ghariani-varprowl | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 73.4052 | 61.1563 | 91.7896 | 37.5114 | 4432 | 2815 | 4416 | 395 | 339 | 85.8228 | |
| anovak-vg | SNP | ti | map_l150_m1_e0 | * | 79.4593 | 85.7346 | 74.0400 | 78.6204 | 16900 | 2812 | 16756 | 5875 | 1329 | 22.6213 | |
| anovak-vg | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 0.0000 | 20.2779 | 0.0000 | 0.0000 | 715 | 2811 | 0 | 0 | 0 | ||
| anovak-vg | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 0.0000 | 20.2779 | 0.0000 | 0.0000 | 715 | 2811 | 0 | 0 | 0 | ||
| anovak-vg | SNP | * | map_l125_m2_e1 | het | 77.5666 | 90.5162 | 67.8585 | 78.1432 | 26829 | 2811 | 26551 | 12576 | 2737 | 21.7637 | |
| ciseli-custom | SNP | * | map_l100_m2_e0 | homalt | 90.4763 | 89.7867 | 91.1766 | 62.8157 | 24712 | 2811 | 24604 | 2381 | 1867 | 78.4124 | |
| ciseli-custom | SNP | * | map_l250_m2_e1 | * | 69.2947 | 64.8053 | 74.4524 | 92.2088 | 5176 | 2811 | 5167 | 1773 | 350 | 19.7406 | |
| gduggal-bwaplat | INDEL | * | HG002complexvar | homalt | 93.8564 | 89.6215 | 98.5114 | 56.9159 | 24222 | 2805 | 24155 | 365 | 314 | 86.0274 | |
| anovak-vg | INDEL | I6_15 | HG002complexvar | * | 48.0486 | 41.4858 | 57.0779 | 45.2877 | 1988 | 2804 | 2008 | 1510 | 1270 | 84.1060 | |
| qzeng-custom | SNP | * | map_l150_m0_e0 | het | 75.9917 | 64.6851 | 92.0882 | 93.9068 | 5136 | 2804 | 5098 | 438 | 367 | 83.7900 | |
| gduggal-snapfb | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 77.3318 | 82.5652 | 72.7223 | 71.1326 | 13274 | 2803 | 12037 | 4515 | 1002 | 22.1927 | |
| gduggal-snapfb | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 77.3318 | 82.5652 | 72.7223 | 71.1326 | 13274 | 2803 | 12037 | 4515 | 1002 | 22.1927 | |
| ciseli-custom | SNP | * | map_l100_m1_e0 | homalt | 90.3629 | 89.6308 | 91.1071 | 60.1980 | 24203 | 2800 | 24096 | 2352 | 1848 | 78.5714 | |
| gduggal-snapvard | INDEL | D16_PLUS | * | het | 17.6734 | 11.3960 | 39.3474 | 71.0797 | 360 | 2799 | 410 | 632 | 372 | 58.8608 | |
| anovak-vg | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 77.4069 | 76.4295 | 78.4096 | 44.8000 | 9076 | 2799 | 9239 | 2544 | 1839 | 72.2877 | |
| eyeh-varpipe | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 63.5703 | 52.8321 | 79.7871 | 32.1688 | 3134 | 2798 | 11092 | 2810 | 2788 | 99.2171 | |
| gduggal-bwavard | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 78.2056 | 76.4379 | 80.0570 | 49.9353 | 9077 | 2798 | 8988 | 2239 | 1967 | 87.8517 | |
| gduggal-bwafb | SNP | ti | * | * | 99.8083 | 99.8659 | 99.7507 | 20.3177 | 2082722 | 2796 | 2082858 | 5206 | 495 | 9.5083 | |
| gduggal-bwafb | INDEL | * | HG002complexvar | het | 96.3773 | 93.9496 | 98.9337 | 53.9146 | 43416 | 2796 | 46670 | 503 | 367 | 72.9622 | |
| gduggal-bwaplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | homalt | 85.2919 | 75.6705 | 97.7165 | 64.9393 | 8690 | 2794 | 8687 | 203 | 174 | 85.7143 | |
| ckim-isaac | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 91.0850 | 84.6196 | 98.6202 | 51.6582 | 15372 | 2794 | 15367 | 215 | 153 | 71.1628 | |
| ckim-isaac | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 91.0850 | 84.6196 | 98.6202 | 51.6582 | 15372 | 2794 | 15367 | 215 | 153 | 71.1628 | |
| anovak-vg | SNP | * | map_l125_m2_e0 | het | 77.4707 | 90.4768 | 67.7339 | 78.1138 | 26526 | 2792 | 26255 | 12507 | 2731 | 21.8358 | |
| gduggal-bwavard | INDEL | I16_PLUS | * | * | 58.4101 | 56.2490 | 60.7439 | 65.3100 | 3587 | 2790 | 3593 | 2322 | 1708 | 73.5573 | |
| ndellapenna-hhga | SNP | ti | * | het | 99.8668 | 99.7824 | 99.9512 | 16.9483 | 1279102 | 2789 | 1279103 | 624 | 83 | 13.3013 | |
| qzeng-custom | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 91.6276 | 91.2822 | 91.9757 | 41.4101 | 29203 | 2789 | 47992 | 4187 | 3097 | 73.9670 | |
| ckim-isaac | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 94.2166 | 90.2898 | 98.5006 | 65.6575 | 25924 | 2788 | 26146 | 398 | 31 | 7.7889 | |
| ckim-isaac | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 94.2166 | 90.2898 | 98.5006 | 65.6575 | 25924 | 2788 | 26146 | 398 | 31 | 7.7889 | |
| mlin-fermikit | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | * | 90.5721 | 88.6430 | 92.5871 | 36.0947 | 21753 | 2787 | 21720 | 1739 | 1695 | 97.4698 | |
| ciseli-custom | SNP | * | map_l250_m2_e0 | * | 69.1818 | 64.6798 | 74.3575 | 92.1767 | 5100 | 2785 | 5092 | 1756 | 343 | 19.5330 | |
| ciseli-custom | INDEL | * | HG002compoundhet | het | 30.5417 | 31.9071 | 29.2883 | 74.6335 | 1305 | 2785 | 2889 | 6975 | 4438 | 63.6272 | |
| ghariani-varprowl | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 29.6692 | 20.3322 | 54.8638 | 69.9063 | 710 | 2782 | 705 | 580 | 561 | 96.7241 | |
| ckim-isaac | INDEL | D1_5 | HG002complexvar | * | 94.1980 | 91.4993 | 97.0606 | 47.3235 | 29934 | 2781 | 29752 | 901 | 456 | 50.6104 | |
| mlin-fermikit | SNP | tv | map_l150_m0_e0 | * | 46.6065 | 33.3972 | 77.1018 | 65.0425 | 1394 | 2780 | 1394 | 414 | 356 | 85.9903 | |
| gduggal-bwaplat | SNP | ti | map_l125_m0_e0 | homalt | 55.1813 | 38.1207 | 99.8832 | 84.5557 | 1712 | 2779 | 1710 | 2 | 2 | 100.0000 | |
| gduggal-bwaplat | SNP | ti | map_l150_m0_e0 | het | 62.3303 | 45.4974 | 98.9334 | 94.9642 | 2319 | 2778 | 2319 | 25 | 10 | 40.0000 | |
| ndellapenna-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | hetalt | 74.2193 | 59.3086 | 99.1453 | 28.8754 | 4049 | 2778 | 3712 | 32 | 27 | 84.3750 | |
| gduggal-snapfb | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | het | 86.5531 | 82.3858 | 91.1644 | 45.8288 | 12984 | 2776 | 21554 | 2089 | 859 | 41.1202 | |
| gduggal-bwavard | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 29.6006 | 20.5326 | 53.0130 | 62.9452 | 717 | 2775 | 695 | 616 | 592 | 96.1039 | |
| egarrison-hhga | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | * | 77.1877 | 70.6598 | 85.0445 | 46.2575 | 6683 | 2775 | 6784 | 1193 | 1020 | 85.4987 | |
| jlack-gatk | INDEL | * | HG002compoundhet | * | 91.0082 | 90.7410 | 91.2769 | 62.3551 | 27186 | 2774 | 27070 | 2587 | 2465 | 95.2841 | |
| ghariani-varprowl | INDEL | D16_PLUS | * | * | 61.7015 | 59.1244 | 64.5135 | 70.3568 | 4011 | 2773 | 4025 | 2214 | 2123 | 95.8898 | |
| ghariani-varprowl | INDEL | * | * | het | 89.6326 | 98.5731 | 82.1789 | 64.2989 | 191361 | 2770 | 191449 | 41517 | 38150 | 91.8901 | |