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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
80751-80800 / 86044 show all | |||||||||||||||
| gduggal-snapvard | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 1.5317 | 0.7843 | 32.5163 | 68.9024 | 12 | 1518 | 199 | 413 | 192 | 46.4891 | |
| gduggal-snapvard | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 1.5317 | 0.7843 | 32.5163 | 68.9024 | 12 | 1518 | 199 | 413 | 192 | 46.4891 | |
| gduggal-snapplat | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 86.9120 | 89.3082 | 84.6411 | 75.9718 | 2272 | 272 | 2276 | 413 | 12 | 2.9056 | |
| ghariani-varprowl | SNP | tv | segdup | het | 95.9597 | 99.4326 | 92.7212 | 94.3028 | 5257 | 30 | 5261 | 413 | 3 | 0.7264 | |
| cchapple-custom | INDEL | * | HG002complexvar | het | 98.8709 | 98.5307 | 99.2135 | 57.1695 | 45533 | 679 | 52101 | 413 | 306 | 74.0920 | |
| asubramanian-gatk | INDEL | D6_15 | HG002compoundhet | * | 94.5808 | 93.8213 | 95.3528 | 36.4670 | 8473 | 558 | 8474 | 413 | 394 | 95.3995 | |
| asubramanian-gatk | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 96.5878 | 96.0095 | 97.1732 | 53.9900 | 14195 | 590 | 14197 | 413 | 388 | 93.9467 | |
| ckim-dragen | INDEL | I1_5 | * | homalt | 99.5565 | 99.7948 | 99.3194 | 55.1956 | 60304 | 124 | 60271 | 413 | 409 | 99.0315 | |
| gduggal-snapfb | INDEL | * | HG002complexvar | hetalt | 65.6662 | 59.9081 | 72.6490 | 79.8155 | 2216 | 1483 | 1097 | 413 | 281 | 68.0387 | |
| jpowers-varprowl | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 57.9234 | 68.4909 | 50.1809 | 63.0076 | 413 | 190 | 416 | 413 | 407 | 98.5472 | |
| ltrigg-rtg1 | SNP | * | segdup | * | 99.0787 | 99.6188 | 98.5445 | 88.0967 | 27960 | 107 | 27963 | 413 | 51 | 12.3487 | |
| raldana-dualsentieon | SNP | ti | map_siren | het | 99.3661 | 99.3941 | 99.3382 | 55.1273 | 62004 | 378 | 61995 | 413 | 8 | 1.9371 | |
| raldana-dualsentieon | SNP | * | map_l125_m2_e1 | het | 98.7960 | 98.9845 | 98.6083 | 74.0672 | 29339 | 301 | 29333 | 414 | 4 | 0.9662 | |
| cchapple-custom | SNP | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 99.4715 | 99.6836 | 99.2603 | 56.9862 | 55455 | 176 | 55556 | 414 | 57 | 13.7681 | |
| gduggal-snapfb | SNP | * | map_l250_m2_e1 | * | 94.6649 | 94.5286 | 94.8016 | 89.9551 | 7550 | 437 | 7550 | 414 | 185 | 44.6860 | |
| mlin-fermikit | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 86.9863 | 88.6640 | 85.3710 | 87.2287 | 2409 | 308 | 2416 | 414 | 264 | 63.7681 | |
| mlin-fermikit | SNP | tv | map_l150_m0_e0 | * | 46.6065 | 33.3972 | 77.1018 | 65.0425 | 1394 | 2780 | 1394 | 414 | 356 | 85.9903 | |
| gduggal-bwafb | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 94.3584 | 92.3931 | 96.4091 | 46.0732 | 10239 | 843 | 11115 | 414 | 403 | 97.3430 | |
| eyeh-varpipe | INDEL | D1_5 | lowcmp_SimpleRepeat_quadTR_51to200 | homalt | 50.1159 | 99.4924 | 33.4936 | 34.9322 | 196 | 1 | 209 | 415 | 385 | 92.7711 | |
| gduggal-bwafb | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 82.4326 | 94.7547 | 72.9465 | 54.9486 | 1120 | 62 | 1119 | 415 | 412 | 99.2771 | |
| raldana-dualsentieon | SNP | * | map_l125_m1_e0 | * | 99.1433 | 99.2014 | 99.0854 | 69.5094 | 44965 | 362 | 44959 | 415 | 15 | 3.6145 | |
| anovak-vg | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 95.1588 | 93.9924 | 96.3545 | 65.5291 | 10858 | 694 | 10969 | 415 | 307 | 73.9759 | |
| anovak-vg | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 95.1588 | 93.9924 | 96.3545 | 65.5291 | 10858 | 694 | 10969 | 415 | 307 | 73.9759 | |
| bgallagher-sentieon | SNP | * | map_l125_m1_e0 | * | 99.2644 | 99.4418 | 99.0876 | 71.3529 | 45074 | 253 | 45068 | 415 | 70 | 16.8675 | |
| anovak-vg | INDEL | D6_15 | lowcmp_SimpleRepeat_quadTR_51to200 | * | 27.0890 | 20.6844 | 39.2387 | 39.7707 | 272 | 1043 | 268 | 415 | 363 | 87.4699 | |
| qzeng-custom | SNP | ti | map_l150_m2_e0 | het | 80.5235 | 69.5753 | 95.5605 | 89.8900 | 8962 | 3919 | 8933 | 415 | 349 | 84.0964 | |
| qzeng-custom | SNP | ti | map_l150_m2_e1 | het | 80.5961 | 69.6581 | 95.6089 | 89.9144 | 9066 | 3949 | 9036 | 415 | 349 | 84.0964 | |
| ltrigg-rtg2 | INDEL | D1_5 | * | * | 99.4769 | 99.2395 | 99.7155 | 55.7210 | 145629 | 1116 | 145463 | 415 | 145 | 34.9398 | |
| ndellapenna-hhga | SNP | * | * | homalt | 99.9243 | 99.8838 | 99.9648 | 18.1151 | 1178790 | 1371 | 1178818 | 415 | 332 | 80.0000 | |
| jmaeng-gatk | INDEL | D6_15 | * | * | 97.9970 | 97.6008 | 98.3964 | 55.6203 | 25466 | 626 | 25465 | 415 | 366 | 88.1928 | |
| gduggal-snapplat | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | * | 42.7404 | 30.1771 | 73.2258 | 61.7378 | 1176 | 2721 | 1135 | 415 | 63 | 15.1807 | |
| gduggal-snapvard | INDEL | D1_5 | map_l100_m1_e0 | * | 88.9711 | 94.4264 | 84.1118 | 85.2613 | 1745 | 103 | 2197 | 415 | 169 | 40.7229 | |
| gduggal-snapvard | INDEL | D1_5 | map_l100_m2_e1 | het | 87.6002 | 97.6341 | 79.4365 | 87.6420 | 1238 | 30 | 1607 | 416 | 161 | 38.7019 | |
| ckim-gatk | SNP | ti | map_l125_m2_e0 | het | 89.0209 | 81.9824 | 97.3815 | 86.6933 | 15475 | 3401 | 15471 | 416 | 41 | 9.8558 | |
| ckim-dragen | INDEL | I6_15 | * | homalt | 96.6294 | 99.7115 | 93.7321 | 54.6498 | 6221 | 18 | 6221 | 416 | 414 | 99.5192 | |
| ciseli-custom | INDEL | I16_PLUS | HG002compoundhet | homalt | 0.9434 | 33.3333 | 0.4785 | 52.5000 | 1 | 2 | 2 | 416 | 387 | 93.0288 | |
| jlack-gatk | SNP | tv | map_l250_m2_e0 | * | 92.0635 | 97.6058 | 87.1168 | 93.0345 | 2813 | 69 | 2813 | 416 | 24 | 5.7692 | |
| jpowers-varprowl | SNP | tv | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 97.9095 | 98.1671 | 97.6533 | 71.1033 | 17246 | 322 | 17311 | 416 | 17 | 4.0865 | |
| ltrigg-rtg1 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 97.1631 | 95.7743 | 98.5927 | 68.0014 | 29192 | 1288 | 29144 | 416 | 97 | 23.3173 | |
| ltrigg-rtg1 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 97.1631 | 95.7743 | 98.5927 | 68.0014 | 29192 | 1288 | 29144 | 416 | 97 | 23.3173 | |
| asubramanian-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 97.3524 | 99.2470 | 95.5288 | 54.1878 | 8303 | 63 | 8888 | 416 | 317 | 76.2019 | |
| astatham-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 98.2925 | 98.9506 | 97.6432 | 71.0801 | 17632 | 187 | 17235 | 416 | 367 | 88.2212 | |
| ckim-gatk | SNP | ti | map_l125_m2_e1 | het | 89.1406 | 82.1659 | 97.4093 | 86.6958 | 15683 | 3404 | 15679 | 417 | 41 | 9.8321 | |
| ghariani-varprowl | SNP | ti | map_l125_m0_e0 | * | 97.4197 | 98.0724 | 96.7757 | 78.9680 | 12516 | 246 | 12516 | 417 | 104 | 24.9400 | |
| ghariani-varprowl | INDEL | * | map_l100_m1_e0 | het | 90.5454 | 98.1655 | 84.0230 | 89.3321 | 2194 | 41 | 2193 | 417 | 195 | 46.7626 | |
| gduggal-bwaplat | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 85.9444 | 77.0743 | 97.1216 | 57.5074 | 14073 | 4186 | 14070 | 417 | 292 | 70.0240 | |
| rpoplin-dv42 | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 94.6815 | 98.3806 | 91.2505 | 66.8429 | 4374 | 72 | 4349 | 417 | 409 | 98.0815 | |
| ckim-isaac | SNP | ti | * | het | 98.7325 | 97.5284 | 99.9667 | 15.6908 | 1250214 | 31683 | 1250525 | 417 | 31 | 7.4341 | |
| jlack-gatk | INDEL | I1_5 | HG002compoundhet | homalt | 60.9506 | 99.3921 | 43.9516 | 87.9475 | 327 | 2 | 327 | 417 | 414 | 99.2806 | |
| jlack-gatk | SNP | tv | map_l250_m2_e1 | * | 92.1359 | 97.6337 | 87.2243 | 93.0989 | 2847 | 69 | 2847 | 417 | 24 | 5.7554 | |