PrecisionFDA
Truth Challenge
Engage and improve DNA test results with our community challenges
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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
5101-5150 / 86044 show all | |||||||||||||||
dgrover-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | homalt | 98.8527 | 99.9044 | 97.8230 | 55.8586 | 8358 | 8 | 8358 | 186 | 184 | 98.9247 | |
gduggal-bwavard | INDEL | * | map_l100_m1_e0 | het | 89.9219 | 98.1208 | 82.9876 | 89.4070 | 2193 | 42 | 2200 | 451 | 184 | 40.7982 | |
jmaeng-gatk | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 99.0283 | 99.8745 | 98.1963 | 46.0818 | 10344 | 13 | 10344 | 190 | 184 | 96.8421 | |
gduggal-snapplat | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 87.6106 | 86.8839 | 88.3495 | 88.3802 | 17011 | 2568 | 17070 | 2251 | 184 | 8.1741 | |
gduggal-snapplat | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 87.6106 | 86.8839 | 88.3495 | 88.3802 | 17011 | 2568 | 17070 | 2251 | 184 | 8.1741 | |
gduggal-snapvard | INDEL | I1_5 | map_siren | * | 90.0863 | 91.7138 | 88.5156 | 83.2677 | 2756 | 249 | 2898 | 376 | 184 | 48.9362 | |
gduggal-snapvard | SNP | * | map_l125_m0_e0 | het | 87.4804 | 96.0281 | 80.3301 | 84.3236 | 12161 | 503 | 12023 | 2944 | 184 | 6.2500 | |
ghariani-varprowl | SNP | ti | map_l100_m1_e0 | * | 98.6066 | 98.9944 | 98.2219 | 68.9891 | 47449 | 482 | 47451 | 859 | 183 | 21.3038 | |
ghariani-varprowl | SNP | tv | map_siren | * | 98.2281 | 99.2140 | 97.2616 | 65.3754 | 45569 | 361 | 45570 | 1283 | 183 | 14.2634 | |
gduggal-snapfb | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 69.2577 | 84.5629 | 58.6437 | 58.1740 | 1364 | 249 | 1937 | 1366 | 183 | 13.3968 | |
gduggal-bwafb | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 81.6794 | 97.9405 | 70.0491 | 45.2509 | 428 | 9 | 428 | 183 | 183 | 100.0000 | |
gduggal-bwavard | SNP | * | map_l125_m2_e1 | * | 95.7732 | 97.6865 | 93.9333 | 79.9451 | 46110 | 1092 | 45506 | 2939 | 183 | 6.2266 | |
cchapple-custom | SNP | tv | map_siren | * | 97.8668 | 98.4651 | 97.2758 | 62.3550 | 45225 | 705 | 45206 | 1266 | 183 | 14.4550 | |
bgallagher-sentieon | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | homalt | 92.2288 | 98.9002 | 86.4006 | 59.8278 | 1169 | 13 | 1169 | 184 | 183 | 99.4565 | |
anovak-vg | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 73.2802 | 81.7861 | 66.3768 | 81.5483 | 696 | 155 | 916 | 464 | 182 | 39.2241 | |
bgallagher-sentieon | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 97.4461 | 99.1228 | 95.8251 | 69.1792 | 4407 | 39 | 4361 | 190 | 182 | 95.7895 | |
gduggal-bwavard | SNP | * | lowcmp_SimpleRepeat_diTR_11to50 | * | 95.4182 | 95.3879 | 95.4484 | 71.2860 | 9245 | 447 | 9143 | 436 | 182 | 41.7431 | |
gduggal-bwavard | SNP | * | map_l125_m2_e0 | * | 95.7523 | 97.6821 | 93.8973 | 79.8955 | 45640 | 1083 | 45051 | 2928 | 182 | 6.2159 | |
gduggal-bwaplat | INDEL | * | HG002compoundhet | het | 66.0619 | 55.5447 | 81.4921 | 84.3450 | 2274 | 1820 | 2272 | 516 | 182 | 35.2713 | |
gduggal-bwafb | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 95.6219 | 95.5496 | 95.6944 | 76.1461 | 29757 | 1386 | 29827 | 1342 | 182 | 13.5618 | |
gduggal-bwafb | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 95.6219 | 95.5496 | 95.6944 | 76.1461 | 29757 | 1386 | 29827 | 1342 | 182 | 13.5618 | |
gduggal-bwafb | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 68.9517 | 64.3204 | 74.3017 | 60.0892 | 530 | 294 | 532 | 184 | 182 | 98.9130 | |
gduggal-snapfb | SNP | * | map_l250_m2_e0 | * | 94.6894 | 94.5212 | 94.8581 | 89.8978 | 7453 | 432 | 7453 | 404 | 182 | 45.0495 | |
gduggal-snapfb | SNP | tv | * | homalt | 99.5195 | 99.7842 | 99.2562 | 25.9790 | 376309 | 814 | 376328 | 2820 | 182 | 6.4539 | |
gduggal-snapplat | INDEL | D6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 57.7611 | 43.8153 | 84.7293 | 69.3664 | 1594 | 2044 | 1487 | 268 | 182 | 67.9104 | |
ndellapenna-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | homalt | 96.0365 | 96.2201 | 95.8537 | 59.0186 | 8044 | 316 | 8045 | 348 | 182 | 52.2989 | |
ndellapenna-hhga | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | homalt | 96.0365 | 96.2201 | 95.8537 | 59.0186 | 8044 | 316 | 8045 | 348 | 182 | 52.2989 | |
mlin-fermikit | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | het | 89.8601 | 93.0301 | 86.8990 | 65.5793 | 1268 | 95 | 1247 | 188 | 182 | 96.8085 | |
ckim-vqsr | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 95.5725 | 99.1852 | 92.2138 | 66.1587 | 2191 | 18 | 2191 | 185 | 182 | 98.3784 | |
ckim-isaac | INDEL | D16_PLUS | HG002compoundhet | het | 48.4816 | 76.0494 | 35.5828 | 39.9632 | 308 | 97 | 116 | 210 | 182 | 86.6667 | |
ckim-isaac | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 85.3420 | 79.4704 | 92.1504 | 48.6116 | 2551 | 659 | 2524 | 215 | 182 | 84.6512 | |
eyeh-varpipe | INDEL | * | map_l100_m2_e0 | * | 94.5816 | 93.6637 | 95.5178 | 92.5332 | 3459 | 234 | 4944 | 232 | 182 | 78.4483 | |
ciseli-custom | INDEL | * | map_l150_m1_e0 | * | 65.1609 | 58.8939 | 72.9205 | 92.7722 | 788 | 550 | 789 | 293 | 182 | 62.1160 | |
ckim-dragen | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 95.3176 | 99.5904 | 91.3963 | 41.9328 | 1945 | 8 | 1944 | 183 | 182 | 99.4536 | |
ckim-gatk | INDEL | D6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 93.7734 | 92.6190 | 94.9569 | 54.7101 | 3639 | 290 | 3634 | 193 | 182 | 94.3005 | |
cchapple-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 97.7128 | 97.1052 | 98.3282 | 43.4107 | 3757 | 112 | 11704 | 199 | 182 | 91.4573 | |
ciseli-custom | INDEL | I6_15 | lowcmp_SimpleRepeat_diTR_11to50 | * | 19.2271 | 11.7330 | 53.2189 | 75.6912 | 283 | 2129 | 248 | 218 | 182 | 83.4862 | |
jmaeng-gatk | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 97.3197 | 98.8079 | 95.8756 | 69.0152 | 4393 | 53 | 4347 | 187 | 182 | 97.3262 | |
jmaeng-gatk | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 97.9856 | 97.6629 | 98.3105 | 52.2428 | 10823 | 259 | 10823 | 186 | 181 | 97.3118 | |
gduggal-bwafb | INDEL | D16_PLUS | HG002compoundhet | homalt | 6.1901 | 87.5000 | 3.2086 | 48.1994 | 7 | 1 | 6 | 181 | 181 | 100.0000 | |
eyeh-varpipe | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 22.2368 | 13.7681 | 57.7726 | 41.9919 | 57 | 357 | 249 | 182 | 181 | 99.4505 | |
eyeh-varpipe | INDEL | I1_5 | lowcmp_SimpleRepeat_quadTR_51to200 | homalt | 0.0000 | 0.0000 | 21.0909 | 34.8341 | 0 | 1 | 58 | 217 | 181 | 83.4101 | |
gduggal-bwaplat | SNP | ti | HG002compoundhet | het | 83.6361 | 90.0158 | 78.1008 | 46.8217 | 8556 | 949 | 8677 | 2433 | 181 | 7.4394 | |
bgallagher-sentieon | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 97.1583 | 99.0954 | 95.2956 | 68.4624 | 3834 | 35 | 3788 | 187 | 181 | 96.7914 | |
astatham-gatk | INDEL | D6_15 | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 93.9904 | 93.0008 | 95.0013 | 54.6571 | 3654 | 275 | 3649 | 192 | 181 | 94.2708 | |
astatham-gatk | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | * | 97.8931 | 97.7585 | 98.0280 | 45.2710 | 9246 | 212 | 9246 | 186 | 181 | 97.3118 | |
astatham-gatk | INDEL | * | lowcmp_AllRepeats_51to200bp_gt95identity_merged | homalt | 95.5706 | 99.1399 | 92.2494 | 66.0177 | 2190 | 19 | 2190 | 184 | 181 | 98.3696 | |
astatham-gatk | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 99.0520 | 99.8745 | 98.2429 | 45.7715 | 10344 | 13 | 10344 | 185 | 181 | 97.8378 | |
gduggal-snapvard | SNP | ti | HG002complexvar | homalt | 98.1979 | 96.6107 | 99.8382 | 17.7966 | 186907 | 6557 | 182591 | 296 | 181 | 61.1486 | |
gduggal-snapfb | SNP | ti | map_l150_m0_e0 | * | 94.8381 | 94.0720 | 95.6168 | 81.0969 | 7395 | 466 | 7395 | 339 | 181 | 53.3923 |