Entering edit mode
6.7 years ago
bha
▴
80
I got 1000 genomes data which is in vcf format. All chromosomes (1 to 22) are in separate files. Is there any way to combine all 22 chromosomes in a single file? My final task is to prune that single file based on MAF and LD. I tried in PLINK (first convert everything in PLINK and tried to merge, but ends up with multi-position variants error, because there are some multiallelics ) . is anyone come across this issue? Any advice please?
bcftools merge
may be better. Documentation here.Is vcf-tools out of date ?
bcftool concat
will be more appropriate?