4.5.0
Adding inhouse dragen functionality
- created startInhouseDragenPipeline script; starts the DRAGEN Bcl to FastQ conversion + running inhouse Dragen pipeline (both nf_ngs_dna)
- created startInhousePostDragenPipeline script; starts some post analysis steps (post_dragen workflow in nf_ngs_dna)
Updated scripts for incoming Genomescan data in sub batches
First batch will always have G sub letter (e.g. GS_300G), missing data will be delivered in project H(GS_300H) and a last post-delivery will be send as GS_300I
- Updated PullAndProcessGsAnalysisData script
- added functionality that checks if all data is there (Y/N in UMCG_CSV), when there is data missing it will automatically remove the missing sample from the original inhouse samplesheet and creates a new samplesheet for the the post delivery
- removed the merging of all the data in one project (before the merged samplesheet was called GS_300), it will now automatically be in one samplesheet