Skip to content
New issue

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

change messaging on publishing #465

Merged
merged 1 commit into from
Nov 18, 2024
Merged
Changes from all commits
Commits
File filter

Filter by extension

Filter by extension

Conversations
Failed to load comments.
Loading
Jump to
Jump to file
Failed to load files.
Loading
Diff view
Diff view
2 changes: 1 addition & 1 deletion docs/hello_nextflow/04_hello_genomics.md
Original file line number Diff line number Diff line change
Expand Up @@ -199,7 +199,7 @@ You should recognize all the pieces from what you learned in Part 1 & Part 2 of

!!! note

Even though the data files we're using here are very small, in genomics they can get very large, so we should get into the habit of using symbolic links rather than making actual copies of these files, unless there's a compelling reason to do so.
Even though the data files we're using here are very small, in genomics they can get very large. For the purposes of demonstration in the teaching environment, we're using the 'symlink' publishing mode to avoid unnecessary file copies. You shouldn't do this in your final workflows, since you'll lose results when you clean up your `work` directory.

This process is going to require us to pass in a file path via the `input_bam` input, so let's set that up next.

Expand Down
Loading