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privefl avatar privefl commented on September 7, 2024

There are many ways you can do that:

  • combine the bed files with PLINK (I think I talk about that in another issue here).
  • compute 22 predictions (one for each chr) and sum them.
  • you can also maybe directly compute the scores from bed files using PLINK (maybe using all 22 chromosomes at once with first point) or using bigsnpr::bed_prodVec() and combining all 22 scores.

from paper-ldpred2.

lizlitkowski avatar lizlitkowski commented on September 7, 2024

Thanks for the options! I had already tried the PLINK option but I was having trouble merging the files because the variant names seem to have fallen away after I used vcftools to extract my list of SNPs. I was trying to avoid the second option but I know that one will work. Thanks again.

from paper-ldpred2.

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