plink 软件中 --allow-no-sex 参数的作用
--allow-no-sex:在进行关联分析时,缺失性别信息时,仍然进行分析。
001、缺失性别信息, 同时不使用改参数时:
root@DESKTOP-1N42TVH:/home/test3# ls clean.bed clean.bim clean.fam root@DESKTOP-1N42TVH:/home/test3# head -n 5 clean.fam Line105 Line105 0 0 0 108.668751356079 Line174 Line174 0 0 0 112.071538795501 Line154 Line154 0 0 0 92.6270391416653 Line107 Line107 0 0 0 108.668751356079 Line148 Line148 0 0 0 82.9047893147477 root@DESKTOP-1N42TVH:/home/test3# plink --bfile clean --allow-extra-chr --linear --out result PLINK v1.90b6.26 64-bit (2 Apr 2022) www.cog-genomics.org/plink/1.9/ (C) 2005-2022 Shaun Purcell, Christopher Chang GNU General Public License v3 Logging to result.log. Options in effect: --allow-extra-chr --bfile clean --linear --out result 16007 MB RAM detected; reserving 8003 MB for main workspace. 38375 variants loaded from .bim file. 176 people (0 males, 0 females, 176 ambiguous) loaded from .fam. Ambiguous sex IDs written to result.nosex . 176 phenotype values loaded from .fam. Warning: Ignoring phenotypes of missing-sex samples. If you don't want those phenotypes to be ignored, use the --allow-no-sex flag. Using 1 thread (no multithreaded calculations invoked). Before main variant filters, 176 founders and 0 nonfounders present. Calculating allele frequencies... done. Total genotyping rate is 0.931314. 38375 variants and 176 people pass filters and QC. Note: No phenotypes present. Warning: Skipping --linear since # variables >= # samples. root@DESKTOP-1N42TVH:/home/test3# ls clean.bed clean.bim clean.fam result.log result.nosex
002、增加该参数
root@DESKTOP-1N42TVH:/home/test3# ls clean.bed clean.bim clean.fam root@DESKTOP-1N42TVH:/home/test3# plink --bfile clean --allow-extra-chr --linear --allow-no-sex --out result PLINK v1.90b6.26 64-bit (2 Apr 2022) www.cog-genomics.org/plink/1.9/ (C) 2005-2022 Shaun Purcell, Christopher Chang GNU General Public License v3 Logging to result.log. Options in effect: --allow-extra-chr --allow-no-sex --bfile clean --linear --out result 16007 MB RAM detected; reserving 8003 MB for main workspace. 38375 variants loaded from .bim file. 176 people (0 males, 0 females, 176 ambiguous) loaded from .fam. Ambiguous sex IDs written to result.nosex . 176 phenotype values loaded from .fam. Using 1 thread (no multithreaded calculations invoked). Before main variant filters, 176 founders and 0 nonfounders present. Calculating allele frequencies... done. Total genotyping rate is 0.931314. 38375 variants and 176 people pass filters and QC. Phenotype data is quantitative. Writing linear model association results to result.assoc.linear ... done. root@DESKTOP-1N42TVH:/home/test3# ls clean.bed clean.bim clean.fam result.assoc.linear result.log result.nosex root@DESKTOP-1N42TVH:/home/test3# head -n 5 result.assoc.linear CHR SNP BP A1 TEST NMISS BETA STAT P 1 1:11923 11923 A ADD 170 0.8928 0.3621 0.7178 1 1:12127 12127 A ADD 159 -1.618 -0.6809 0.4969 1 1:41890 41890 C ADD 166 -4.173 -5.688 5.755e-08 1 1:129602 129602 C ADD 165 -2.79 -1.791 0.07518
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