PrecisionFDA
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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 | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
41601-41650 / 86044 show all | |||||||||||||||
| ckim-isaac | INDEL | D1_5 | map_l100_m2_e1 | hetalt | 77.1930 | 66.6667 | 91.6667 | 89.2216 | 34 | 17 | 33 | 3 | 3 | 100.0000 | |
| gduggal-bwavard | INDEL | * | tech_badpromoters | * | 77.1889 | 76.3158 | 78.0822 | 58.7571 | 58 | 18 | 57 | 16 | 15 | 93.7500 | |
| eyeh-varpipe | INDEL | * | lowcmp_SimpleRepeat_diTR_11to50 | homalt | 77.1881 | 96.8041 | 64.1824 | 31.3791 | 10026 | 331 | 16242 | 9064 | 9022 | 99.5366 | |
| ndellapenna-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 77.1879 | 70.9467 | 84.6330 | 51.0225 | 9780 | 4005 | 9952 | 1807 | 1577 | 87.2717 | |
| egarrison-hhga | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_11to50 | * | 77.1877 | 70.6598 | 85.0445 | 46.2575 | 6683 | 2775 | 6784 | 1193 | 1020 | 85.4987 | |
| gduggal-snapfb | INDEL | D6_15 | map_l150_m0_e0 | het | 77.1875 | 65.0000 | 95.0000 | 85.9155 | 13 | 7 | 19 | 1 | 1 | 100.0000 | |
| gduggal-snapplat | INDEL | D1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | het | 77.1866 | 71.6422 | 83.6612 | 80.1878 | 23811 | 9425 | 27896 | 5448 | 1746 | 32.0485 | |
| ckim-isaac | SNP | tv | map_siren | homalt | 77.1855 | 62.8654 | 99.9539 | 50.4637 | 10838 | 6402 | 10838 | 5 | 5 | 100.0000 | |
| gduggal-snapfb | INDEL | I6_15 | HG002complexvar | het | 77.1850 | 70.0212 | 85.9817 | 41.0929 | 1649 | 706 | 2067 | 337 | 317 | 94.0653 | |
| eyeh-varpipe | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | * | 77.1843 | 73.4104 | 81.3673 | 37.5411 | 13404 | 4855 | 13616 | 3118 | 3097 | 99.3265 | |
| mlin-fermikit | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | hetalt | 77.1804 | 63.0915 | 99.3707 | 35.9250 | 8853 | 5179 | 9000 | 57 | 56 | 98.2456 | |
| anovak-vg | SNP | * | map_l125_m1_e0 | het | 77.1793 | 90.4691 | 67.2939 | 76.7918 | 25686 | 2706 | 25425 | 12357 | 2688 | 21.7529 | |
| gduggal-bwaplat | SNP | ti | map_l100_m2_e0 | homalt | 77.1723 | 62.8434 | 99.9652 | 71.1284 | 11506 | 6803 | 11495 | 4 | 4 | 100.0000 | |
| ckim-isaac | INDEL | * | map_l100_m1_e0 | homalt | 77.1685 | 63.0807 | 99.3582 | 75.2463 | 774 | 453 | 774 | 5 | 3 | 60.0000 | |
| ciseli-custom | SNP | * | map_l100_m0_e0 | het | 77.1628 | 71.2049 | 84.2088 | 78.9054 | 15099 | 6106 | 15086 | 2829 | 99 | 3.4995 | |
| mlin-fermikit | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | hetalt | 77.1546 | 63.0485 | 99.3919 | 33.0569 | 8678 | 5086 | 8826 | 54 | 53 | 98.1481 | |
| ckim-vqsr | SNP | tv | map_l150_m1_e0 | het | 77.1500 | 63.6050 | 98.0249 | 91.7841 | 4418 | 2528 | 4417 | 89 | 0 | 0.0000 | |
| anovak-vg | INDEL | D6_15 | map_siren | het | 77.1497 | 77.5000 | 76.8025 | 78.9021 | 217 | 63 | 245 | 74 | 50 | 67.5676 | |
| ckim-vqsr | SNP | * | map_l100_m2_e1 | * | 77.1389 | 63.0879 | 99.2421 | 83.6761 | 47150 | 27587 | 47142 | 360 | 16 | 4.4444 | |
| gduggal-snapvard | INDEL | I1_5 | lowcmp_AllRepeats_lt51bp_gt95identity_merged | * | 77.1368 | 72.0532 | 82.9923 | 72.5173 | 11223 | 4353 | 45225 | 9268 | 7975 | 86.0488 | |
| ckim-gatk | SNP | * | map_l125_m2_e0 | homalt | 77.1330 | 62.8029 | 99.9359 | 76.3243 | 10912 | 6463 | 10912 | 7 | 4 | 57.1429 | |
| gduggal-snapvard | SNP | * | HG002compoundhet | het | 77.1322 | 83.8682 | 71.3978 | 57.2411 | 11890 | 2287 | 13270 | 5316 | 2307 | 43.3973 | |
| eyeh-varpipe | INDEL | I6_15 | map_l150_m1_e0 | * | 77.1296 | 68.0000 | 89.0909 | 85.2151 | 17 | 8 | 49 | 6 | 5 | 83.3333 | |
| gduggal-bwafb | INDEL | D1_5 | map_l100_m2_e1 | hetalt | 77.1285 | 64.7059 | 95.4545 | 93.7143 | 33 | 18 | 21 | 1 | 1 | 100.0000 | |
| eyeh-varpipe | INDEL | I6_15 | map_l125_m2_e0 | * | 77.1277 | 67.9245 | 89.2157 | 81.4208 | 36 | 17 | 91 | 11 | 9 | 81.8182 | |
| eyeh-varpipe | INDEL | I6_15 | map_l125_m2_e1 | * | 77.1277 | 67.9245 | 89.2157 | 81.6876 | 36 | 17 | 91 | 11 | 9 | 81.8182 | |
| gduggal-snapfb | INDEL | D6_15 | map_l100_m1_e0 | * | 77.1252 | 65.1163 | 94.5652 | 81.3576 | 168 | 90 | 174 | 10 | 9 | 90.0000 | |
| gduggal-bwaplat | INDEL | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_all_gt95identity_merged | het | 77.1235 | 65.2618 | 94.2549 | 80.4969 | 11629 | 6190 | 11632 | 709 | 196 | 27.6446 | |
| egarrison-hhga | INDEL | D6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 77.1234 | 70.6347 | 84.9247 | 50.6689 | 9737 | 4048 | 9864 | 1751 | 1570 | 89.6630 | |
| anovak-vg | INDEL | * | map_siren | homalt | 77.1234 | 89.6798 | 67.6512 | 75.5300 | 2381 | 274 | 2405 | 1150 | 1080 | 93.9130 | |
| egarrison-hhga | INDEL | D1_5 | lowcmp_SimpleRepeat_triTR_11to50 | hetalt | 77.1180 | 63.2035 | 98.8889 | 37.9310 | 292 | 170 | 267 | 3 | 3 | 100.0000 | |
| anovak-vg | SNP | * | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt51bp_gt95identity_merged | het | 77.1176 | 83.8177 | 71.4094 | 81.9321 | 1269 | 245 | 1596 | 639 | 277 | 43.3490 | |
| gduggal-snapvard | INDEL | D1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRgt6_lt101bp_gt95identity_merged | * | 77.1166 | 84.3061 | 71.0570 | 69.6058 | 1300 | 242 | 2131 | 868 | 620 | 71.4286 | |
| ciseli-custom | INDEL | D6_15 | * | het | 77.1133 | 84.3154 | 71.0447 | 55.4839 | 9773 | 1818 | 10153 | 4138 | 1402 | 33.8811 | |
| mlin-fermikit | INDEL | I6_15 | lowcmp_SimpleRepeat_quadTR_11to50 | hetalt | 77.1048 | 63.8066 | 97.4057 | 47.3945 | 409 | 232 | 413 | 11 | 11 | 100.0000 | |
| gduggal-bwaplat | INDEL | I16_PLUS | HG002complexvar | hetalt | 77.0889 | 63.2836 | 98.5981 | 68.1548 | 212 | 123 | 211 | 3 | 3 | 100.0000 | |
| gduggal-bwavard | INDEL | I16_PLUS | segdup | * | 77.0833 | 78.7234 | 75.5102 | 94.6389 | 37 | 10 | 37 | 12 | 6 | 50.0000 | |
| ckim-gatk | SNP | ti | map_l125_m0_e0 | * | 77.0822 | 63.5950 | 97.8298 | 88.5344 | 8116 | 4646 | 8114 | 180 | 23 | 12.7778 | |
| mlin-fermikit | INDEL | * | map_l100_m2_e0 | homalt | 77.0808 | 73.9096 | 80.5363 | 81.0585 | 932 | 329 | 931 | 225 | 197 | 87.5556 | |
| ckim-gatk | SNP | ti | map_l125_m1_e0 | homalt | 77.0788 | 62.7343 | 99.9279 | 73.7914 | 6929 | 4116 | 6929 | 5 | 4 | 80.0000 | |
| qzeng-custom | INDEL | I16_PLUS | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | * | 77.0774 | 70.4225 | 85.1214 | 55.3497 | 350 | 147 | 1087 | 190 | 150 | 78.9474 | |
| gduggal-bwafb | INDEL | I6_15 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_lt101bp_gt95identity_merged | het | 77.0749 | 65.9030 | 92.8079 | 55.0487 | 489 | 253 | 942 | 73 | 69 | 94.5205 | |
| gduggal-snapplat | INDEL | I1_5 | HG002complexvar | * | 77.0714 | 71.7352 | 83.2654 | 65.6966 | 23933 | 9430 | 24301 | 4884 | 375 | 7.6781 | |
| ckim-isaac | INDEL | I1_5 | map_l125_m2_e0 | homalt | 77.0609 | 63.0499 | 99.0783 | 80.6250 | 215 | 126 | 215 | 2 | 0 | 0.0000 | |
| ndellapenna-hhga | INDEL | D6_15 | lowcmp_SimpleRepeat_diTR_51to200 | homalt | 77.0538 | 84.4720 | 70.8333 | 31.6726 | 136 | 25 | 136 | 56 | 35 | 62.5000 | |
| gduggal-snapplat | INDEL | I1_5 | * | * | 77.0401 | 71.8692 | 83.0128 | 69.8058 | 108281 | 42383 | 109381 | 22383 | 1242 | 5.5489 | |
| gduggal-bwaplat | INDEL | D1_5 | map_l125_m1_e0 | * | 77.0354 | 63.0515 | 98.9899 | 94.0592 | 686 | 402 | 686 | 7 | 1 | 14.2857 | |
| gduggal-bwaplat | INDEL | D1_5 | map_l100_m0_e0 | het | 77.0340 | 63.2826 | 98.4211 | 94.5205 | 374 | 217 | 374 | 6 | 1 | 16.6667 | |
| ghariani-varprowl | INDEL | D6_15 | lowcmp_SimpleRepeat_homopolymer_gt10 | het | 77.0340 | 78.5714 | 75.5556 | 99.4804 | 33 | 9 | 34 | 11 | 6 | 54.5455 | |
| eyeh-varpipe | INDEL | I1_5 | lowcmp_Human_Full_Genome_TRDB_hg19_150331_TRlt7_51to200bp_gt95identity_merged | het | 77.0302 | 66.6667 | 91.2088 | 61.5222 | 192 | 96 | 332 | 32 | 14 | 43.7500 | |