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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
24351-24400 / 86044 show all | |||||||||||||||
ciseli-custom | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 80.7504 | 86.1111 | 76.0181 | 63.2280 | 496 | 80 | 504 | 159 | 37 | 23.2704 | |
anovak-vg | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 0.0000 | 18.7595 | 0.0000 | 0.0000 | 496 | 2148 | 0 | 0 | 0 | ||
astatham-gatk | INDEL | * | map_l150_m0_e0 | * | 96.2251 | 96.4981 | 95.9538 | 92.9541 | 496 | 18 | 498 | 21 | 4 | 19.0476 | |
bgallagher-sentieon | INDEL | D6_15 | map_siren | * | 97.5395 | 97.4460 | 97.6331 | 85.2014 | 496 | 13 | 495 | 12 | 2 | 16.6667 | |
asubramanian-gatk | INDEL | I1_5 | map_l100_m2_e0 | homalt | 96.4050 | 93.4087 | 99.6000 | 83.0048 | 496 | 35 | 498 | 2 | 2 | 100.0000 | |
jmaeng-gatk | INDEL | I1_5 | map_l150_m1_e0 | * | 96.8834 | 98.0237 | 95.7692 | 92.4077 | 496 | 10 | 498 | 22 | 3 | 13.6364 | |
ghariani-varprowl | INDEL | I1_5 | map_l150_m2_e0 | * | 93.8505 | 95.5684 | 92.1933 | 92.5267 | 496 | 23 | 496 | 42 | 11 | 26.1905 | |
hfeng-pmm1 | INDEL | * | map_l150_m0_e0 | * | 97.1639 | 96.4981 | 97.8389 | 90.4125 | 496 | 18 | 498 | 11 | 4 | 36.3636 | |
dgrover-gatk | INDEL | D6_15 | map_siren | * | 97.7320 | 97.4460 | 98.0198 | 85.5879 | 496 | 13 | 495 | 10 | 2 | 20.0000 | |
eyeh-varpipe | INDEL | * | map_l150_m0_e0 | * | 96.3994 | 96.4981 | 96.3009 | 96.8271 | 496 | 18 | 781 | 30 | 19 | 63.3333 | |
ckim-vqsr | INDEL | D1_5 | map_l150_m2_e1 | het | 94.6619 | 95.0192 | 94.3074 | 93.7699 | 496 | 26 | 497 | 30 | 3 | 10.0000 | |
ckim-vqsr | INDEL | I1_5 | map_l150_m2_e0 | * | 96.5943 | 95.5684 | 97.6424 | 93.2903 | 496 | 23 | 497 | 12 | 2 | 16.6667 | |
astatham-gatk | INDEL | I1_5 | map_l150_m2_e0 | * | 96.8719 | 95.3757 | 98.4158 | 90.8249 | 495 | 24 | 497 | 8 | 2 | 25.0000 | |
hfeng-pmm1 | INDEL | D6_15 | map_siren | * | 98.1160 | 97.2495 | 98.9980 | 81.6071 | 495 | 14 | 494 | 5 | 1 | 20.0000 | |
gduggal-bwavard | INDEL | I1_5 | map_l100_m1_e0 | homalt | 97.3420 | 95.5598 | 99.1919 | 72.4388 | 495 | 23 | 491 | 4 | 2 | 50.0000 | |
gduggal-bwafb | INDEL | I1_5 | map_l150_m2_e0 | * | 96.7742 | 95.3757 | 98.2143 | 89.7789 | 495 | 24 | 495 | 9 | 2 | 22.2222 | |
ltrigg-rtg2 | INDEL | D1_5 | map_l150_m2_e0 | het | 97.7334 | 96.3035 | 99.2063 | 80.3967 | 495 | 19 | 500 | 4 | 0 | 0.0000 | |
ndellapenna-hhga | INDEL | * | lowcmp_SimpleRepeat_homopolymer_6to10 | hetalt | 95.1923 | 92.5234 | 98.0198 | 73.2238 | 495 | 40 | 495 | 10 | 10 | 100.0000 | |
ltrigg-rtg2 | SNP | tv | map_l250_m0_e0 | het | 92.6096 | 86.5385 | 99.5968 | 76.3020 | 495 | 77 | 494 | 2 | 0 | 0.0000 | |
ciseli-custom | INDEL | D1_5 | HG002compoundhet | hetalt | 0.0000 | 4.8453 | 0.0000 | 0.0000 | 495 | 9721 | 0 | 0 | 0 | ||
ciseli-custom | INDEL | I1_5 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 74.3243 | 87.7660 | 64.4531 | 60.5344 | 495 | 69 | 495 | 273 | 223 | 81.6850 | |
ckim-gatk | INDEL | D6_15 | map_siren | * | 97.2468 | 97.2495 | 97.2441 | 86.7501 | 495 | 14 | 494 | 14 | 2 | 14.2857 | |
gduggal-snapvard | INDEL | D6_15 | HG002complexvar | hetalt | 0.0000 | 48.8648 | 0.0000 | 0.0000 | 495 | 518 | 0 | 0 | 0 | ||
gduggal-snapvard | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | het | 71.3852 | 85.9375 | 61.0476 | 58.4323 | 495 | 81 | 641 | 409 | 297 | 72.6161 | |
ghariani-varprowl | INDEL | D16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 67.3943 | 54.1667 | 89.1697 | 75.4215 | 494 | 418 | 494 | 60 | 57 | 95.0000 | |
ghariani-varprowl | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 51.7650 | 93.7381 | 35.7550 | 67.8055 | 494 | 33 | 502 | 902 | 894 | 99.1131 | |
gduggal-snapfb | INDEL | D1_5 | map_l150_m2_e0 | het | 94.7138 | 96.1089 | 93.3586 | 86.7121 | 494 | 20 | 492 | 35 | 5 | 14.2857 | |
mlin-fermikit | INDEL | D1_5 | map_l100_m2_e1 | homalt | 79.7254 | 79.6774 | 79.7735 | 78.1084 | 494 | 126 | 493 | 125 | 119 | 95.2000 | |
ndellapenna-hhga | INDEL | * | map_l150_m0_e0 | * | 96.5844 | 96.1089 | 97.0646 | 99.2093 | 494 | 20 | 496 | 15 | 5 | 33.3333 | |
hfeng-pmm1 | INDEL | D1_5 | map_l150_m2_e0 | het | 97.5340 | 96.1089 | 99.0020 | 86.1869 | 494 | 20 | 496 | 5 | 0 | 0.0000 | |
hfeng-pmm2 | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_51to200 | * | 81.2500 | 70.8752 | 95.1830 | 49.0677 | 494 | 203 | 494 | 25 | 23 | 92.0000 | |
astatham-gatk | INDEL | D1_5 | map_l150_m2_e1 | het | 95.2826 | 94.6360 | 95.9381 | 90.5225 | 494 | 28 | 496 | 21 | 3 | 14.2857 | |
astatham-gatk | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 98.6028 | 97.4359 | 99.7980 | 86.4421 | 494 | 13 | 494 | 1 | 1 | 100.0000 | |
eyeh-varpipe | INDEL | I1_5 | map_l125_m2_e1 | het | 97.2633 | 97.2441 | 97.2826 | 84.5216 | 494 | 14 | 716 | 20 | 12 | 60.0000 | |
ckim-dragen | INDEL | D6_15 | map_siren | * | 97.6267 | 97.0530 | 98.2072 | 86.4726 | 494 | 15 | 493 | 9 | 2 | 22.2222 | |
rpoplin-dv42 | INDEL | I1_5 | map_l150_m1_e0 | * | 98.2131 | 97.6285 | 98.8048 | 88.8071 | 494 | 12 | 496 | 6 | 2 | 33.3333 | |
raldana-dualsentieon | INDEL | I1_5 | map_l125_m2_e1 | het | 97.5364 | 97.2441 | 97.8304 | 85.6618 | 494 | 14 | 496 | 11 | 0 | 0.0000 | |
astatham-gatk | INDEL | D6_15 | map_siren | * | 97.2363 | 96.8566 | 97.6190 | 85.4503 | 493 | 16 | 492 | 12 | 2 | 16.6667 | |
ltrigg-rtg2 | INDEL | I16_PLUS | lowcmp_AllRepeats_lt51bp_gt95identity_merged | hetalt | 90.9728 | 84.5626 | 98.4344 | 65.7965 | 493 | 90 | 503 | 8 | 8 | 100.0000 | |
qzeng-custom | INDEL | * | lowcmp_SimpleRepeat_homopolymer_6to10 | hetalt | 95.8196 | 92.1495 | 99.7942 | 70.9504 | 493 | 42 | 485 | 1 | 0 | 0.0000 | |
ltrigg-rtg2 | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | homalt | 98.6000 | 97.2387 | 100.0000 | 79.3163 | 493 | 14 | 478 | 0 | 0 | ||
qzeng-custom | INDEL | D1_5 | map_l100_m1_e0 | homalt | 90.3416 | 83.2770 | 98.7159 | 78.5468 | 493 | 99 | 615 | 8 | 8 | 100.0000 | |
ckim-vqsr | INDEL | D6_15 | map_siren | * | 97.3325 | 96.8566 | 97.8131 | 86.8634 | 493 | 16 | 492 | 11 | 2 | 18.1818 | |
egarrison-hhga | INDEL | * | lowcmp_SimpleRepeat_homopolymer_6to10 | hetalt | 94.9922 | 92.1495 | 98.0159 | 72.8155 | 493 | 42 | 494 | 10 | 10 | 100.0000 | |
ckim-isaac | SNP | tv | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | homalt | 96.7615 | 93.9048 | 99.7976 | 61.1635 | 493 | 32 | 493 | 1 | 0 | 0.0000 | |
eyeh-varpipe | INDEL | * | map_l100_m0_e0 | homalt | 96.1789 | 96.8566 | 95.5107 | 86.4425 | 493 | 16 | 851 | 40 | 34 | 85.0000 | |
gduggal-snapvard | INDEL | I1_5 | map_l150_m2_e0 | * | 89.7214 | 94.9904 | 85.0062 | 90.8896 | 493 | 26 | 686 | 121 | 44 | 36.3636 | |
hfeng-pmm3 | INDEL | D6_15 | map_siren | * | 98.1089 | 96.8566 | 99.3939 | 82.2134 | 493 | 16 | 492 | 3 | 0 | 0.0000 | |
hfeng-pmm1 | INDEL | I1_5 | map_l150_m1_e0 | * | 98.0147 | 97.4308 | 98.6056 | 88.2104 | 493 | 13 | 495 | 7 | 2 | 28.5714 | |
ciseli-custom | INDEL | D1_5 | map_l150_m1_e0 | * | 74.0933 | 68.7587 | 80.3252 | 92.6268 | 493 | 224 | 494 | 121 | 55 | 45.4545 |