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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
81251-81300 / 86044 show all | |||||||||||||||
| asubramanian-gatk | INDEL | I6_15 | * | * | 96.7639 | 95.5082 | 98.0531 | 53.5929 | 23708 | 1115 | 23721 | 471 | 428 | 90.8705 | |
| jpowers-varprowl | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 0.0000 | 1.4147 | 0.0000 | 0.0000 | 16 | 1115 | 0 | 0 | 0 | ||
| qzeng-custom | SNP | ti | map_l250_m1_e0 | het | 73.3752 | 62.4326 | 88.9688 | 96.5528 | 1853 | 1115 | 1855 | 230 | 193 | 83.9130 | |
| ndellapenna-hhga | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | hetalt | 73.6158 | 59.0525 | 97.7135 | 42.8517 | 1608 | 1115 | 1453 | 34 | 29 | 85.2941 | |
| ltrigg-rtg2 | INDEL | D1_5 | * | * | 99.4769 | 99.2395 | 99.7155 | 55.7210 | 145629 | 1116 | 145463 | 415 | 145 | 34.9398 | |
| jpowers-varprowl | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | het | 49.6437 | 72.3762 | 37.7781 | 62.4735 | 2924 | 1116 | 2938 | 4839 | 4790 | 98.9874 | |
| bgallagher-sentieon | INDEL | I1_5 | * | * | 99.4227 | 99.2586 | 99.5873 | 58.2134 | 149547 | 1117 | 149597 | 620 | 500 | 80.6452 | |
| gduggal-snapfb | SNP | ti | map_l100_m2_e0 | * | 97.7846 | 97.7165 | 97.8527 | 68.4501 | 47843 | 1118 | 47848 | 1050 | 457 | 43.5238 | |
| gduggal-snapfb | INDEL | D1_5 | HG002complexvar | het | 94.7486 | 94.6159 | 94.8816 | 54.6441 | 19647 | 1118 | 20632 | 1113 | 329 | 29.5597 | |
| mlin-fermikit | INDEL | * | map_siren | het | 83.7074 | 75.1996 | 94.3858 | 76.9241 | 3390 | 1118 | 3396 | 202 | 141 | 69.8020 | |
| mlin-fermikit | SNP | tv | map_l125_m0_e0 | homalt | 55.7975 | 49.6173 | 63.7363 | 55.1608 | 1102 | 1119 | 1102 | 627 | 574 | 91.5470 | |
| ndellapenna-hhga | INDEL | I6_15 | * | * | 96.5902 | 95.4921 | 97.7138 | 48.4477 | 23704 | 1119 | 23721 | 555 | 427 | 76.9369 | |
| gduggal-snapvard | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | homalt | 56.7831 | 40.6681 | 94.0520 | 68.9496 | 767 | 1119 | 759 | 48 | 45 | 93.7500 | |
| gduggal-snapplat | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 71.9561 | 72.9860 | 70.9549 | 92.4413 | 3026 | 1120 | 3039 | 1244 | 64 | 5.1447 | |
| gduggal-snapfb | SNP | ti | map_l100_m2_e1 | * | 97.8010 | 97.7367 | 97.8655 | 68.4763 | 48365 | 1120 | 48370 | 1055 | 457 | 43.3175 | |
| qzeng-custom | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 86.6043 | 76.5298 | 99.7333 | 31.0028 | 3652 | 1120 | 1496 | 4 | 4 | 100.0000 | |
| jmaeng-gatk | SNP | tv | map_l150_m0_e0 | het | 74.0589 | 60.6050 | 95.1907 | 94.3590 | 1723 | 1120 | 1722 | 87 | 5 | 5.7471 | |
| ciseli-custom | SNP | tv | map_l100_m1_e0 | homalt | 89.0533 | 87.6147 | 90.5399 | 62.3935 | 7923 | 1120 | 7915 | 827 | 623 | 75.3325 | |
| gduggal-bwaplat | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 85.5129 | 76.5088 | 96.9190 | 34.7374 | 3651 | 1121 | 3649 | 116 | 114 | 98.2759 | |
| eyeh-varpipe | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | * | 92.2052 | 90.5600 | 93.9113 | 48.2920 | 10754 | 1121 | 12339 | 800 | 737 | 92.1250 | |
| jlack-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 96.8636 | 96.4960 | 97.2340 | 52.6642 | 30871 | 1121 | 30794 | 876 | 794 | 90.6393 | |
| ckim-isaac | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 92.2388 | 86.5886 | 98.6779 | 34.8864 | 7244 | 1122 | 7240 | 97 | 80 | 82.4742 | |
| egarrison-hhga | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 75.3208 | 65.0467 | 89.4493 | 64.1933 | 2088 | 1122 | 2128 | 251 | 224 | 89.2430 | |
| ndellapenna-hhga | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 94.2017 | 97.6736 | 90.9681 | 70.0370 | 47148 | 1123 | 48456 | 4811 | 4484 | 93.2031 | |
| ciseli-custom | SNP | tv | map_l100_m2_e0 | homalt | 89.1677 | 87.8120 | 90.5658 | 64.9670 | 8091 | 1123 | 8083 | 842 | 633 | 75.1781 | |
| ciseli-custom | SNP | tv | HG002complexvar | homalt | 95.4763 | 98.8182 | 92.3530 | 24.8215 | 93987 | 1124 | 92583 | 7666 | 2593 | 33.8247 | |
| egarrison-hhga | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 89.6104 | 96.3123 | 83.7805 | 65.9807 | 29356 | 1124 | 30414 | 5888 | 5443 | 92.4423 | |
| egarrison-hhga | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 89.6104 | 96.3123 | 83.7805 | 65.9807 | 29356 | 1124 | 30414 | 5888 | 5443 | 92.4423 | |
| rpoplin-dv42 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 95.4697 | 91.8338 | 99.4055 | 29.1133 | 12640 | 1124 | 12707 | 76 | 75 | 98.6842 | |
| gduggal-snapplat | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | * | 23.7665 | 14.5247 | 65.3430 | 41.4376 | 191 | 1124 | 181 | 96 | 38 | 39.5833 | |
| gduggal-bwavard | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 0.0000 | 0.6189 | 0.0000 | 0.0000 | 7 | 1124 | 0 | 0 | 0 | ||
| gduggal-snapplat | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_11to50 | het | 24.5228 | 33.9401 | 19.1964 | 80.6408 | 578 | 1125 | 602 | 2534 | 12 | 0.4736 | |
| ndellapenna-hhga | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 79.5452 | 72.3383 | 88.3470 | 65.9371 | 2942 | 1125 | 3025 | 399 | 313 | 78.4461 | |
| mlin-fermikit | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 72.5735 | 57.3752 | 98.7253 | 40.9262 | 1517 | 1127 | 1549 | 20 | 20 | 100.0000 | |
| raldana-dualsentieon | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 95.8057 | 91.9684 | 99.9771 | 32.4064 | 12905 | 1127 | 13098 | 3 | 3 | 100.0000 | |
| dgrover-gatk | SNP | * | * | * | 99.9456 | 99.9631 | 99.9282 | 19.2565 | 3053492 | 1127 | 3053343 | 2195 | 207 | 9.4305 | |
| ckim-gatk | SNP | tv | map_l150_m0_e0 | het | 74.0126 | 60.3588 | 95.6497 | 94.2325 | 1716 | 1127 | 1715 | 78 | 7 | 8.9744 | |
| astatham-gatk | INDEL | I1_5 | * | * | 99.4616 | 99.2520 | 99.6722 | 58.6147 | 149537 | 1127 | 149586 | 492 | 402 | 81.7073 | |
| gduggal-snapplat | INDEL | * | lowcmp_SimpleRepeat_diTR_51to200 | hetalt | 17.8468 | 9.9840 | 84.0000 | 62.9630 | 125 | 1127 | 126 | 24 | 19 | 79.1667 | |
| gduggal-snapfb | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 69.8922 | 57.3374 | 89.4866 | 50.3641 | 1516 | 1128 | 366 | 43 | 39 | 90.6977 | |
| rpoplin-dv42 | SNP | ti | * | * | 99.9621 | 99.9459 | 99.9782 | 17.6958 | 2084383 | 1128 | 2084320 | 454 | 276 | 60.7930 | |
| gduggal-bwafb | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | hetalt | 77.2155 | 68.0091 | 89.3048 | 56.7130 | 2398 | 1128 | 668 | 80 | 79 | 98.7500 | |
| gduggal-bwafb | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | hetalt | 77.2155 | 68.0091 | 89.3048 | 56.7130 | 2398 | 1128 | 668 | 80 | 79 | 98.7500 | |
| gduggal-bwafb | INDEL | * | lowcmp_SimpleRepeat_quadTR_11to50 | het | 93.7221 | 89.8362 | 97.9593 | 52.4760 | 9979 | 1129 | 12193 | 254 | 153 | 60.2362 | |
| gduggal-snapfb | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 71.3980 | 62.1268 | 83.9216 | 50.4662 | 1852 | 1129 | 1070 | 205 | 197 | 96.0976 | |
| ciseli-custom | SNP | tv | map_l250_m2_e0 | * | 66.4506 | 60.8258 | 73.2218 | 92.3535 | 1753 | 1129 | 1750 | 640 | 134 | 20.9375 | |
| anovak-vg | SNP | tv | map_l125_m1_e0 | homalt | 88.9946 | 80.7338 | 99.1387 | 66.3699 | 4731 | 1129 | 4719 | 41 | 30 | 73.1707 | |
| jlack-gatk | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | * | 97.2911 | 96.9146 | 97.6705 | 52.3019 | 35463 | 1129 | 35387 | 844 | 761 | 90.1659 | |
| gduggal-snapvard | INDEL | * | lowcmp_SimpleRepeat_triTR_11to50 | homalt | 63.5738 | 47.4907 | 96.1285 | 37.8710 | 1022 | 1130 | 1167 | 47 | 44 | 93.6170 | |
| ciseli-custom | SNP | tv | map_l150_m0_e0 | het | 67.3971 | 60.2533 | 76.4627 | 88.5079 | 1713 | 1130 | 1712 | 527 | 18 | 3.4156 | |