Ok. PRSice seems more convenient for me at this stage. So, In order to calculate the PRS in my test data, can I simply provide, GWAS base data, target data with these options, -bar-levels <p-value threshold> --no-full --fastscore? I cannot provide phenotype file because my independent sample comprised of 3 different phenotypic categories and I simply need to calculate the PRS at the specific threshold for specific individuals. I donot need bar plot and models with R2. Thanks
Hi
I am trying to calculate PRS in test sample after getting best SNPs from PRSice 2 with highest R2 My target data is in the form of bed,bim, fam for 22 chromosomes, I want to use plink for specific p-value threshold in this scenario,
plink2 \
--bfile T2test3 \ ## For one chromosome only
--score T2baseNoBMI.uniq.txt 2 4 6 header \
--q-score-range range_list SNP.pvalue \
--extract EUR.valid.snp \
--out EUR
This is working for just a single chromosome, I want to perform my analysis considering all autosomes and need a final final file with IIDs and their corresponding PRS based on all chromosome SNP information,
Please help
Thanks
1 answer
You will need to combine the genotype file. Not sure if --score works with --bmerge. You can have a try.
Alternatively, as you are already using PRSice, do
--bar-levels <p-value threshold> --no-full --fastscore and you should in theory get the PRS at the specific p-value threshold
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