We read every piece of feedback, and take your input very seriously.
To see all available qualifiers, see our documentation.
Have a question about this project? Sign up for a free GitHub account to open an issue and contact its maintainers and the community.
By clicking “Sign up for GitHub”, you agree to our terms of service and privacy statement. We’ll occasionally send you account related emails.
Already on GitHub? Sign in to your account
Does this work for hg38 or is it tied to hg19/grch37?
The text was updated successfully, but these errors were encountered:
This only works with GRCh37, but the script will check the MAF and error out if a different reference genome is specified
Sorry, something went wrong.
Do you want to see what I changed to allow more variants to be used or do you think you can guess based on my description?
No branches or pull requests
Does this work for hg38 or is it tied to hg19/grch37?
The text was updated successfully, but these errors were encountered: