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genomic-medicine-sweden / tomte

A nextflow pipeline for analysing expression and splicing in RNA seq data from rare disease patient
MIT License
12 stars 3 forks source link

Add hgnc id to research output in DROP #130

Open Lucpen opened 5 months ago

Lucpen commented 5 months ago

Description of feature

Add hgnc id to research output in DROP

Jakob37 commented 2 months ago

This would be valuable also for us in Lund! Looking into loading Tomte runs into Scout now. It worked after adding this manually.