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An automated workflow for constructing maps of molecular mechanisms for given diseases. It streamlines querying gene-disease and variant-disease associations, calculating enrichment of disease maps and pathways, and combining enriched diagrams with text mining data into a single map, meant for the MINERVA Platform.

This project includes the generator scripts for generating the index files of the howto-cards and modules (handbook, qms, ...)

Fork from imp3 repo to use for NOMIS etc.

Code used for the analysis of the RNA-seq, ATAC-seq and ChIP-seq datasets produced in this study. Original fastq files deposited in https://ega-archive.org/, under the accession number EGAD00001009288.

Repository for all slides related to R3 courses.

Basic practice repository for git trainings

Basic practice repository for git trainings

Basic practice repository for git trainings

Basic practice repository for git trainings

Basic practice repository for git trainings

Basic practice repository for git trainings

Basic practice repository for git trainings

Basic practice repository for git trainings

Basic practice repository for git trainings

Basic practice repository for git trainings