Entering edit mode
4.7 years ago
Hello,
Is there a recommended workflow to cross-reference a list of genomic regions (say a bed file of H3K27Ac ChIP-seq peaks) against GWAS SNPs?
The output I am hoping for is basically, to assess all the genomic co-ordinates in my bed file and see which ones overlap a SNP, and whether that SNP is also a GWAS hit.
Thank you.