Summary
The aim of this deliverable is to share the information currently collected for UM patients and samples across the reference centres, in order to agree on a common minimal set of data that should be available for all UM samples. This precedes the harmonisation efforts among centres which is absolutely necessary to build the common virtual biobank.
The common minimal set will be represented by an Excel file with one column per field to be included in the database, and an attached report with description of the work.
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