Open jbloom opened 3 years ago
@dbacsik, you made a correction to the sample indices in this commit a4cca72f304. But that was to the now deleted data/experiments_config.yml
, not to config.yaml
where configuration now lives.
Where those changes designed to fix this issue or some other problem? In any case, you should make these same changes to where the experimental configuration currently lives in config.yaml
. But how about wait until we get new_refactor_pipeline
merged in main
first, and then you can do this as separate pull request? (So hold on just a bit.)
These are two different errors.
The ones I fixed in commit a4cca72 were simple typos. I will repeat these corrections in config.yml
later.
The issue started here (#43) references a bigger problem, which is that the barcode sequencing samples were mis-labelled with the wrong indices when the sequencing was submitted. This will need to be remedied by either:
For the time being, I am going to leave this pilot branch alone. As this issue describes, the FASTQ files are manually demuxed in the project folder, rather than on the sequencing server, because I needed to correct the sample-index pairs.
The bulk progeny production pilot experiment is analyzed on the progeny_pilot_v2 branch. This pilot has served its purpose for now, but may be referenced as we build out the viral barcode analysis. Please do not delete this branch.
@dbacsik, I'm re-opening this issue. Everytime you close an issue (unless we decide that it really doesn't matter at all), that should be associated with a pull request into main
that addresses the issue.
As far as I can tell, we still don't have a pull request into main
that addresses the issue here (correct specification of these data), so this issue should stay open. I think your proposed solution of providing specifications to FASTQs that are manually de-multiplexed correctly is probably fine, but there isn't any pull request to master
that provides any of these specifications so this issue should stay open.
Roger that!
@dbacsik says: