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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
11101-11150 / 86044 show all | |||||||||||||||
| ghariani-varprowl | SNP | tv | map_l100_m2_e0 | * | 97.8210 | 98.9893 | 96.6799 | 73.9056 | 24780 | 253 | 24781 | 851 | 137 | 16.0987 | |
| gduggal-snapvard | SNP | * | lowcmp_SimpleRepeat_quadTR_11to50 | het | 88.9438 | 97.7871 | 81.5673 | 65.0094 | 11180 | 253 | 11085 | 2505 | 89 | 3.5529 | |
| gduggal-snapplat | INDEL | I6_15 | map_siren | * | 27.1540 | 17.0492 | 66.6667 | 90.7063 | 52 | 253 | 50 | 25 | 2 | 8.0000 | |
| gduggal-snapvard | SNP | tv | lowcmp_SimpleRepeat_diTR_11to50 | * | 90.2938 | 94.7900 | 86.2049 | 78.5292 | 4603 | 253 | 4568 | 731 | 64 | 8.7551 | |
| gduggal-snapvard | SNP | tv | map_l125_m1_e0 | het | 90.5242 | 97.5015 | 84.4788 | 81.5577 | 9873 | 253 | 9846 | 1809 | 112 | 6.1913 | |
| ghariani-varprowl | INDEL | D6_15 | * | het | 73.5164 | 97.8175 | 58.8869 | 57.8444 | 11339 | 253 | 11364 | 7934 | 7830 | 98.6892 | |
| ghariani-varprowl | SNP | * | map_l125_m2_e1 | homalt | 99.1110 | 98.5626 | 99.6655 | 70.0625 | 17280 | 252 | 17280 | 58 | 39 | 67.2414 | |
| gduggal-snapplat | INDEL | I1_5 | map_siren | homalt | 85.7005 | 79.2079 | 93.3526 | 86.1508 | 960 | 252 | 969 | 69 | 6 | 8.6957 | |
| ckim-isaac | INDEL | I16_PLUS | HG002complexvar | hetalt | 38.7208 | 24.7761 | 88.5714 | 62.2302 | 83 | 252 | 93 | 12 | 10 | 83.3333 | |
| egarrison-hhga | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 96.4687 | 96.5227 | 96.4148 | 36.9062 | 6995 | 252 | 6992 | 260 | 103 | 39.6154 | |
| jpowers-varprowl | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 57.4755 | 62.1622 | 53.4460 | 78.1472 | 414 | 252 | 411 | 358 | 355 | 99.1620 | |
| jpowers-varprowl | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 57.4755 | 62.1622 | 53.4460 | 78.1472 | 414 | 252 | 411 | 358 | 355 | 99.1620 | |
| jpowers-varprowl | SNP | ti | map_l250_m2_e1 | * | 95.5153 | 95.0355 | 96.0000 | 91.5044 | 4824 | 252 | 4824 | 201 | 59 | 29.3532 | |
| anovak-vg | INDEL | D16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 74.0703 | 72.3684 | 75.8542 | 64.2217 | 660 | 252 | 666 | 212 | 139 | 65.5660 | |
| asubramanian-gatk | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | hetalt | 96.5522 | 94.7192 | 98.4575 | 25.9492 | 4520 | 252 | 4532 | 71 | 69 | 97.1831 | |
| asubramanian-gatk | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 97.2696 | 97.9874 | 96.5623 | 64.0273 | 12269 | 252 | 13595 | 484 | 266 | 54.9587 | |
| mlin-fermikit | INDEL | I6_15 | * | homalt | 94.2236 | 95.9609 | 92.5481 | 47.3706 | 5987 | 252 | 6011 | 484 | 481 | 99.3802 | |
| ltrigg-rtg2 | SNP | ti | map_l250_m2_e1 | * | 97.3857 | 95.0355 | 99.8552 | 81.2214 | 4824 | 252 | 4827 | 7 | 4 | 57.1429 | |
| ltrigg-rtg2 | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 98.3352 | 97.2892 | 99.4041 | 71.1873 | 9044 | 252 | 9174 | 55 | 55 | 100.0000 | |
| eyeh-varpipe | SNP | * | HG002complexvar | homalt | 99.9303 | 99.9127 | 99.9480 | 18.2871 | 288323 | 252 | 263218 | 137 | 103 | 75.1825 | |
| gduggal-bwaplat | INDEL | * | map_l150_m2_e1 | homalt | 65.5738 | 48.7805 | 100.0000 | 94.1449 | 240 | 252 | 240 | 0 | 0 | ||
| gduggal-bwaplat | INDEL | I1_5 | map_l150_m2_e1 | * | 68.8039 | 52.5424 | 99.6429 | 96.3688 | 279 | 252 | 279 | 1 | 0 | 0.0000 | |
| raldana-dualsentieon | SNP | * | map_l100_m0_e0 | het | 98.7044 | 98.8116 | 98.5974 | 70.4890 | 20953 | 252 | 20949 | 298 | 3 | 1.0067 | |
| raldana-dualsentieon | SNP | * | map_l150_m1_e0 | het | 98.5115 | 98.6954 | 98.3283 | 76.6149 | 19064 | 252 | 19058 | 324 | 3 | 0.9259 | |
| raldana-dualsentieon | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_51to200 | hetalt | 83.1099 | 71.1009 | 100.0000 | 26.0069 | 620 | 252 | 643 | 0 | 0 | ||
| raldana-dualsentieon | INDEL | I6_15 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 95.7931 | 91.9551 | 99.9655 | 41.6230 | 2869 | 251 | 2898 | 1 | 1 | 100.0000 | |
| dgrover-gatk | SNP | ti | map_l100_m1_e0 | * | 99.5344 | 99.4763 | 99.5926 | 66.0277 | 47680 | 251 | 47673 | 195 | 49 | 25.1282 | |
| hfeng-pmm1 | SNP | * | map_l150_m2_e1 | het | 99.1153 | 98.7674 | 99.4657 | 76.0302 | 20112 | 251 | 20106 | 108 | 27 | 25.0000 | |
| gduggal-snapplat | INDEL | * | HG002compoundhet | homalt | 27.3298 | 63.4111 | 17.4185 | 67.5742 | 435 | 251 | 668 | 3167 | 2730 | 86.2015 | |
| ghariani-varprowl | SNP | * | map_l125_m2_e0 | homalt | 99.1058 | 98.5554 | 99.6624 | 70.0500 | 17124 | 251 | 17124 | 58 | 39 | 67.2414 | |
| ghariani-varprowl | SNP | tv | map_l100_m1_e0 | * | 97.8612 | 98.9756 | 96.7717 | 72.1277 | 24250 | 251 | 24251 | 809 | 135 | 16.6873 | |
| ltrigg-rtg2 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 98.5176 | 97.3637 | 99.6992 | 42.0335 | 9270 | 251 | 9282 | 28 | 26 | 92.8571 | |
| ckim-dragen | INDEL | * | HG002complexvar | het | 99.6184 | 99.4569 | 99.7805 | 57.4574 | 45961 | 251 | 45458 | 100 | 50 | 50.0000 | |
| cchapple-custom | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 93.3139 | 89.5894 | 97.3615 | 44.5095 | 2160 | 251 | 2214 | 60 | 45 | 75.0000 | |
| qzeng-custom | INDEL | * | HG002compoundhet | het | 90.0667 | 93.8691 | 86.5604 | 55.7571 | 3843 | 251 | 30091 | 4672 | 2782 | 59.5462 | |
| qzeng-custom | INDEL | * | lowcmp_SimpleRepeat_homopolymer_6to10 | * | 98.9022 | 99.1118 | 98.6934 | 54.7879 | 28009 | 251 | 51137 | 677 | 94 | 13.8848 | |
| qzeng-custom | INDEL | * | map_l150_m2_e0 | het | 81.2179 | 72.2958 | 92.6521 | 95.0610 | 655 | 251 | 807 | 64 | 30 | 46.8750 | |
| ndellapenna-hhga | SNP | tv | map_l100_m1_e0 | het | 99.0304 | 98.3784 | 99.6911 | 62.9947 | 15167 | 250 | 15167 | 47 | 17 | 36.1702 | |
| ndellapenna-hhga | SNP | tv | map_l100_m2_e0 | het | 99.0369 | 98.4154 | 99.6662 | 64.6823 | 15527 | 250 | 15527 | 52 | 17 | 32.6923 | |
| qzeng-custom | INDEL | * | map_l100_m0_e0 | het | 81.4136 | 75.5142 | 88.3128 | 92.9110 | 771 | 250 | 1005 | 133 | 30 | 22.5564 | |
| mlin-fermikit | INDEL | I1_5 | HG002compoundhet | het | 38.7440 | 70.5882 | 26.6993 | 68.3093 | 600 | 250 | 546 | 1499 | 1487 | 99.1995 | |
| mlin-fermikit | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 96.0492 | 94.1010 | 98.0798 | 79.0164 | 3988 | 250 | 3984 | 78 | 11 | 14.1026 | |
| ndellapenna-hhga | INDEL | D1_5 | HG002compoundhet | het | 53.2922 | 85.5324 | 38.7035 | 48.7795 | 1478 | 250 | 2006 | 3177 | 3125 | 98.3632 | |
| ltrigg-rtg2 | INDEL | D16_PLUS | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 93.0557 | 88.2519 | 98.4127 | 61.7176 | 1878 | 250 | 1860 | 30 | 25 | 83.3333 | |
| ltrigg-rtg2 | SNP | ti | map_l250_m2_e0 | * | 97.3703 | 95.0080 | 99.8532 | 81.1041 | 4758 | 250 | 4761 | 7 | 4 | 57.1429 | |
| mlin-fermikit | INDEL | D16_PLUS | lowcmp_SimpleRepeat_diTR_11to50 | * | 87.3444 | 86.0491 | 88.6792 | 69.8967 | 1542 | 250 | 1551 | 198 | 185 | 93.4343 | |
| egarrison-hhga | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_51to200 | hetalt | 65.6565 | 49.0835 | 99.1266 | 31.0241 | 241 | 250 | 227 | 2 | 1 | 50.0000 | |
| astatham-gatk | SNP | ti | segdup | het | 98.8338 | 97.9219 | 99.7628 | 90.8470 | 11780 | 250 | 11778 | 28 | 2 | 7.1429 | |
| raldana-dualsentieon | SNP | ti | map_l125_m2_e0 | * | 99.1246 | 99.1738 | 99.0754 | 71.0207 | 30008 | 250 | 30004 | 280 | 11 | 3.9286 | |
| raldana-dualsentieon | SNP | ti | map_l125_m2_e1 | * | 99.1254 | 99.1822 | 99.0686 | 71.0811 | 30319 | 250 | 30315 | 285 | 11 | 3.8597 | |