Czech COVID-19 genomics portal

The German epigenome programme ‘DEEP’ is an interdisciplinary research network. Its goal is to generate data for biomedical interpretation of healthy and diseased cells. With this, DEEP will contribute to discover new functional epigenetic links useful for clinical diagnosis, therapy and health risk prevention. 

A Python framework for the analysis and visualization of trees.

The European Genome-phenome Archive (EGA) allows users to explore datasets from numerous genotype experiments, including case-control, population and family studies, that are supplied by a range of data providers. 

A comprehensive structural variant haplotype map of the Iberian population from high-coverage whole-genome sequencing

A specialized and medically-oriented database of published variations observed within the internal ribosome entry site (IRES) variants in hepatitis C virus.

IntOGen collects and analyses somatic mutations in thousands of tumor genomes to identify cancer driver genes.

The List of Prokaryotic names with Standing in Nomenclature (LPSN) provides comprehensive information on the nomenclature of prokaryotes and much more.

The Mass Centric Peptide Database contains the tryptic in silico digest of all known proteins in UniProt KB, stored in an efficient manner to be quickly searched.

dSysMap (Mapping of Human disease-related mutations at the systemic level) displays Human disease-related mutations on the structural interactome. Mapping of mutations on protein structures and on interaction interfaces allows you to visualize the region of the interactome that they affect and helps in rationalizing their mechanism of action.