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 | |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
2101-2150 / 86044 show all | |||||||||||||||
cchapple-custom | SNP | ti | map_siren | * | 98.4477 | 98.4784 | 98.4171 | 57.2072 | 98828 | 1527 | 98796 | 1589 | 367 | 23.0963 | |
ciseli-custom | INDEL | * | lowcmp_SimpleRepeat_triTR_11to50 | * | 76.5465 | 76.6078 | 76.4854 | 46.7535 | 5158 | 1575 | 5162 | 1587 | 1041 | 65.5955 | |
ciseli-custom | SNP | tv | map_l125_m2_e1 | het | 74.7394 | 68.6345 | 82.0365 | 81.7503 | 7243 | 3310 | 7243 | 1586 | 64 | 4.0353 | |
qzeng-custom | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 93.3965 | 91.9097 | 94.9321 | 59.4498 | 28867 | 2541 | 29709 | 1586 | 1202 | 75.7881 | |
qzeng-custom | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 93.3965 | 91.9097 | 94.9321 | 59.4498 | 28867 | 2541 | 29709 | 1586 | 1202 | 75.7881 | |
ndellapenna-hhga | INDEL | D6_15 | HG002compoundhet | het | 61.6175 | 85.1636 | 48.2714 | 46.2388 | 729 | 127 | 1480 | 1586 | 1544 | 97.3518 | |
cchapple-custom | SNP | ti | map_siren | het | 98.0329 | 98.5813 | 97.4906 | 61.4640 | 61497 | 885 | 61538 | 1584 | 362 | 22.8535 | |
jpowers-varprowl | SNP | * | map_siren | het | 98.0429 | 97.8328 | 98.2539 | 63.2948 | 89019 | 1972 | 89021 | 1582 | 312 | 19.7219 | |
gduggal-snapvard | INDEL | I6_15 | HG002complexvar | * | 55.8350 | 49.5825 | 63.8921 | 47.3893 | 2375 | 2415 | 2794 | 1579 | 1240 | 78.5307 | |
jlack-gatk | INDEL | * | * | homalt | 99.2685 | 99.7907 | 98.7518 | 57.7386 | 124910 | 262 | 124923 | 1579 | 1542 | 97.6567 | |
ghariani-varprowl | SNP | * | map_l100_m1_e0 | het | 97.8610 | 99.1424 | 96.6122 | 73.4449 | 44970 | 389 | 44973 | 1577 | 254 | 16.1065 | |
ckim-dragen | INDEL | * | HG002compoundhet | homalt | 46.1333 | 99.2711 | 30.0488 | 84.8211 | 681 | 5 | 677 | 1576 | 1573 | 99.8096 | |
gduggal-bwavard | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 38.7872 | 35.8879 | 42.1961 | 62.4776 | 1152 | 2058 | 1149 | 1574 | 1547 | 98.2846 | |
ghariani-varprowl | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | homalt | 81.5331 | 72.3481 | 93.3894 | 66.7128 | 22255 | 8506 | 22222 | 1573 | 1272 | 80.8646 | |
ciseli-custom | SNP | tv | map_l125_m2_e0 | het | 74.6164 | 68.4639 | 81.9839 | 81.7497 | 7149 | 3293 | 7149 | 1571 | 62 | 3.9465 | |
jpowers-varprowl | INDEL | I16_PLUS | * | * | 56.3839 | 48.9258 | 66.5246 | 59.4066 | 3120 | 3257 | 3122 | 1571 | 1564 | 99.5544 | |
gduggal-bwavard | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 48.6441 | 89.1553 | 33.4464 | 63.7189 | 781 | 95 | 789 | 1570 | 1544 | 98.3439 | |
ghariani-varprowl | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | * | 33.8478 | 32.4294 | 35.3960 | 74.1660 | 861 | 1794 | 858 | 1566 | 1515 | 96.7433 | |
gduggal-snapvard | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt51bp_gt95identity_merged | het | 71.6762 | 82.1328 | 63.5814 | 72.1033 | 1756 | 382 | 2734 | 1566 | 1053 | 67.2414 | |
ciseli-custom | SNP | ti | map_l100_m2_e1 | homalt | 91.1369 | 90.8132 | 91.4629 | 61.7425 | 16795 | 1699 | 16756 | 1564 | 1245 | 79.6036 | |
mlin-fermikit | SNP | ti | map_l100_m0_e0 | * | 60.1229 | 46.0705 | 86.5103 | 52.4193 | 10030 | 11741 | 10030 | 1564 | 1408 | 90.0256 | |
qzeng-custom | INDEL | D1_5 | * | het | 98.6409 | 98.8844 | 98.3986 | 58.7330 | 86597 | 977 | 96103 | 1564 | 1050 | 67.1355 | |
gduggal-bwaplat | INDEL | * | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 85.3226 | 75.6324 | 97.8608 | 79.5261 | 71434 | 23015 | 71409 | 1561 | 832 | 53.2992 | |
gduggal-bwavard | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | * | 31.9171 | 30.3578 | 33.6453 | 67.1740 | 806 | 1849 | 791 | 1560 | 1458 | 93.4615 | |
ciseli-custom | SNP | ti | lowcmp_AllRepeats_51to200bp_gt95identity_merged | * | 79.1047 | 96.5517 | 66.9981 | 74.4486 | 3136 | 112 | 3167 | 1560 | 81 | 5.1923 | |
ciseli-custom | SNP | ti | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 53.2420 | 85.0543 | 38.7490 | 79.7595 | 939 | 165 | 985 | 1557 | 105 | 6.7437 | |
anovak-vg | SNP | ti | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 95.7089 | 96.7345 | 94.7048 | 54.9593 | 27046 | 913 | 27829 | 1556 | 769 | 49.4216 | |
gduggal-bwavard | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | het | 46.3721 | 79.4421 | 32.7422 | 66.7816 | 769 | 199 | 757 | 1555 | 1454 | 93.5048 | |
ciseli-custom | SNP | ti | map_l100_m2_e0 | homalt | 91.1050 | 90.7805 | 91.4319 | 61.7718 | 16621 | 1688 | 16583 | 1554 | 1237 | 79.6010 | |
ciseli-custom | SNP | tv | HG002compoundhet | homalt | 78.4375 | 94.1854 | 67.2014 | 50.7638 | 3191 | 197 | 3184 | 1554 | 424 | 27.2844 | |
ciseli-custom | SNP | tv | lowcmp_SimpleRepeat_diTR_11to50 | het | 76.8078 | 93.2966 | 65.2719 | 67.9320 | 2881 | 207 | 2917 | 1552 | 48 | 3.0928 | |
gduggal-snapplat | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | * | 31.1863 | 26.6694 | 37.5453 | 73.7371 | 643 | 1768 | 933 | 1552 | 633 | 40.7861 | |
gduggal-snapvard | INDEL | I6_15 | HG002complexvar | het | 67.8635 | 76.9851 | 60.6744 | 48.9450 | 1813 | 542 | 2393 | 1551 | 1213 | 78.2076 | |
anovak-vg | INDEL | D1_5 | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 76.9105 | 75.4795 | 78.3969 | 40.0251 | 5470 | 1777 | 5614 | 1547 | 1192 | 77.0524 | |
anovak-vg | INDEL | * | lowcmp_SimpleRepeat_quadTR_51to200 | * | 30.1806 | 24.9718 | 38.1353 | 46.7618 | 663 | 1992 | 953 | 1546 | 1250 | 80.8538 | |
ciseli-custom | INDEL | * | map_siren | * | 74.2881 | 71.4035 | 77.4156 | 83.7506 | 5291 | 2119 | 5296 | 1545 | 1017 | 65.8252 | |
jpowers-varprowl | INDEL | * | lowcmp_SimpleRepeat_triTR_11to50 | * | 73.0180 | 70.7114 | 75.4801 | 45.1896 | 4761 | 1972 | 4756 | 1545 | 1527 | 98.8350 | |
gduggal-snapfb | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 90.6005 | 89.5230 | 91.7043 | 43.8461 | 16346 | 1913 | 17079 | 1545 | 1043 | 67.5081 | |
jlack-gatk | INDEL | D1_5 | * | * | 99.0320 | 99.1134 | 98.9507 | 60.1218 | 145444 | 1301 | 145502 | 1543 | 552 | 35.7745 | |
jpowers-varprowl | SNP | tv | HG002compoundhet | * | 83.9956 | 84.7697 | 83.2355 | 57.3909 | 7564 | 1359 | 7661 | 1543 | 1144 | 74.1413 | |
ckim-gatk | SNP | * | map_siren | * | 94.1020 | 89.7981 | 98.8391 | 66.9681 | 131310 | 14918 | 131287 | 1542 | 125 | 8.1064 | |
ciseli-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | * | 46.8191 | 40.0480 | 56.3456 | 64.3182 | 2002 | 2997 | 1989 | 1541 | 1431 | 92.8618 | |
ciseli-custom | INDEL | D16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | * | 46.8191 | 40.0480 | 56.3456 | 64.3182 | 2002 | 2997 | 1989 | 1541 | 1431 | 92.8618 | |
gduggal-bwavard | SNP | tv | map_l100_m2_e1 | * | 95.9192 | 97.7930 | 94.1158 | 76.6728 | 24725 | 558 | 24632 | 1540 | 101 | 6.5584 | |
rpoplin-dv42 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331 | het | 96.3970 | 97.7723 | 95.0598 | 71.0826 | 29801 | 679 | 29633 | 1540 | 1434 | 93.1169 | |
rpoplin-dv42 | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_merged | het | 96.3970 | 97.7723 | 95.0598 | 71.0826 | 29801 | 679 | 29633 | 1540 | 1434 | 93.1169 | |
egarrison-hhga | INDEL | * | HG002complexvar | * | 97.4540 | 96.9352 | 97.9784 | 67.1267 | 74580 | 2358 | 74541 | 1538 | 1113 | 72.3667 | |
eyeh-varpipe | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | het | 92.5067 | 90.7170 | 94.3684 | 38.1735 | 14297 | 1463 | 25772 | 1538 | 1472 | 95.7087 | |
ciseli-custom | SNP | ti | map_l100_m1_e0 | homalt | 90.9965 | 90.6459 | 91.3498 | 59.1340 | 16280 | 1680 | 16242 | 1538 | 1227 | 79.7789 | |
ciseli-custom | SNP | tv | map_l125_m1_e0 | het | 74.2570 | 68.0229 | 81.7491 | 80.4845 | 6888 | 3238 | 6889 | 1538 | 57 | 3.7061 |