Not exact matches
The researchers developed an easy - to - use toolkit, which can be used to integrate the
different layers of «
omics»
data from the BXD mouse population.
Set up to overcome the siloing, fragmentation and inaccessibility of datasets from
different projects, it links
omics data with phenotypic
data and information in registries and biobanks at both an individual ‐ patient and whole ‐ cohort level to enable researchers to analyse their own
data and gain a complete view of their disease and patient population of interest.
To help researchers study rare diseases, RD - Connect links
different data types -
omics (e.g. genomics), clinical information, patient registries and biobanks - into a common resource.