Hello,I am glad that my last question was answered by you
and,now,i have other questions and hope to get your help
Is there a one-to-one correspondence between the result file after using the genind2hierfstat to convert the adegenet::genind file and the genepop file I input? and my code as follows:
_x <- read.genepop("maf0.05.recode.p.snps.gen",ncode = 2L)
basic.stats(x)
genet.dist(x)
head(genind2hierfstat(x)[,1:10])
b <- genind2hierfstat(x)_
so what i want to know is whether the loci of maf0.05.recode.p.snps.gen and b is one - to - one?
i want to extract the loci of b that fst > 0.01 ,and convert it to vcf file , how can i achieve this goal?
Or i want to use these loci perform PCA,can you give me some clues?
sorry about these clueless questions ,i am a really freshman in R and bioinformatics.
so i am waiting for your reply!
Hello,I am glad that my last question was answered by you and,now,i have other questions and hope to get your help
so what i want to know is whether the loci of maf0.05.recode.p.snps.gen and b is one - to - one?
sorry about these clueless questions ,i am a really freshman in R and bioinformatics. so i am waiting for your reply!