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3.8 years ago
MAPK
★
2.1k
Hi All,
I am having issues with plink as it is not able to detect pheno file( $METADATA
as shown below) and I was wondering if someone has solution. Thanks!
[AN@AN 03-PLINK-QC-files]$ head $METADATA
FID IID SEX STATUS WXS
10R_R48 10R_R48_11 2 2 2
10R_R48 10R_R48_1 2 2 1
10R_R54 10R_R54_10 2 1 2
This is the command I am trying to run:
plink1.9 --bfile ${BFILE} --pheno ${METADATA} --pheno-name WXS --test-missing --allow-no-sex --out ${BFILE}-missing-WXS
This is the log I am getting which says 0 phenotype values present after --pheno.
which obviously means it's not reading my phenotype file. Is there anything I am missing here?
PLINK v1.90b6.4 64-bit (7 Aug 2018) www.cog-genomics.org/plink/1.9/
(C) 2005-2018 Shaun Purcell, Christopher Chang GNU General Public License v3
Logging to FASe_3894_WXS_SNPS_INDELS-hwe-geno0.05-mind0.1-missing-WXS.log.
Options in effect:
--allow-no-sex
--bfile FASe_3894_WXS_SNPS_INDELS-hwe-geno0.05-mind0.1
--memory 100000
--out FASe_3894_WXS_SNPS_INDELS-hwe-geno0.05-mind0.1-missing-WXS
--pheno Final_Pheno_FASe_3894.txt
--pheno-name WXS
--test-missing
--threads 12
773748 MB RAM detected; reserving 100000 MB for main workspace.
2901689 variants loaded from .bim file.
3892 people (0 males, 0 females, 3892 ambiguous) loaded from .fam.
Ambiguous sex IDs written to
FASe_3894_WXS_SNPS_INDELS-hwe-geno0.05-mind0.1-missing-WXS.nosex .
0 phenotype values present after --pheno.
Using 1 thread (no multithreaded calculations invoked).
Before main variant filters, 3892 founders and 0 nonfounders present.
Calculating allele frequencies... done.
Total genotyping rate is 0.996216.
2901689 variants and 3892 people pass filters and QC.
Note: No phenotypes present.
Warning: Skipping --test-missing since at least one case and one control is
required.
Hi, Thanks for your comment. I think that makes sense. How do I add actual FID in my BFILE? Right now, I have IID and FID same in .fam.
This is the command I used to create BFILE. How do I add actual FID instead of
--double-id
?plink1.9 --vcf ${VCF} --double-id --keep-allele-order --make-bed --out ${BFILE}