Closed Tman3 closed 6 years ago
I don't have such function currently.
But you can call snpgdsGDS2BED()
with a set of selected SNPs to create a BED file, and then call snpgdsBED2GDS()
to import the genotypes.
Hello! I am actually trying to do the same thing as Tman3 (so a function would definitely be great!) Unfortunately, I tried to do what was suggested (convert selected SNPs to BED file, and then import the genotypes) but got this error:
Converting from GDS to PLINK binary PED: Working space: NUM samples, 6826 NUM SNPs Error in if ((opt$autosome.start == 1) & (opt$autosome.end == 22)) { : missing value where TRUE/FALSE needed
The command I used:
snpset <- snpgdsLDpruning(genofile, ld.threshold=0.2, autosome.only = FALSE) snpset.id <- unlist(snpset) snpgdsGDS2BED(genofile, "bed.fn", snp.id=snpset.id) ^^ Error here.
I can't seem to find much about resolving this error. Have you seen it before, and do you have any suggestions moving forward?
Thanks!
See the function snpgdsCreateGenoSet()
in the package SNPRelate.
I have provided such function in the package.
I performed PCA analysis on a vcf file after being LD-pruned in SNPRelate. Would like to determine whether I could output such GDS file from SNPRelate so I could use it as input for SNPhylo. My goal is to use the same LD-pruned GDS file or the revised list of SNPs in the SNPhylo analysis. Your advice is appreciated.