This repository has been archived by the owner on May 18, 2018. It is now read-only.
Now able to handle reference/vcf files that all have chr chromosome pfx #1
Add this suggestion to a batch that can be applied as a single commit.
This suggestion is invalid because no changes were made to the code.
Suggestions cannot be applied while the pull request is closed.
Suggestions cannot be applied while viewing a subset of changes.
Only one suggestion per line can be applied in a batch.
Add this suggestion to a batch that can be applied as a single commit.
Applying suggestions on deleted lines is not supported.
You must change the existing code in this line in order to create a valid suggestion.
Outdated suggestions cannot be applied.
This suggestion has been applied or marked resolved.
Suggestions cannot be applied from pending reviews.
Suggestions cannot be applied on multi-line comments.
Suggestions cannot be applied while the pull request is queued to merge.
Suggestion cannot be applied right now. Please check back later.
Small change. Rather than specifically forcing a lookup of
'chr'+str(chr_no)
uses the user-suppliedchr_prefix
to handle the case where the reference, vcf files, bam file all share the same label for the chromosome (chr20
for example).