This site is now read-only. You can find our new documentation site and support forum for posting questions here.
Be sure to read our welcome blog!
Is there a way to merge VCF files and not have duplicate entries. It seems to be able to merge SNPs onto the same line and show two alternate alleles, but INDELS are also placed as another entry even if they have an identical CHR POS. This is really a minor problem but would help my downstream analysis in R if there is an option to deal with this. Thanks for your time.