This is more long term but it would be nice to have a script that finds incorrect variant formats early, so we can avoid trying to annotate them. That way we can also immediately get back to centers about issues with the format that's been delivered. Could be a separate command within genome-nexus-annotation-pipeline or a script part of this repo
This is more long term but it would be nice to have a script that finds incorrect variant formats early, so we can avoid trying to annotate them. That way we can also immediately get back to centers about issues with the format that's been delivered. Could be a separate command within genome-nexus-annotation-pipeline or a script part of this repo