STCRDab

OAS

A diverse database of cleaned, annotated, and translated unpaired and paired antibody sequences.

CoV-AbDab

the Coronavirus Antibody Database (CoV-AbDab) is a database containing the oV-AbDab contains data on over published and patented antibodies and nanobodies known to bind to at least one betacoronavirus ...

Therapeutic Structural Antibody Database

The Therapeutic Structural Antibody Database tracks all antibody- and nanobody-related therapeutics recognized by the World Health Organisation (WHO), and identifies any corresponding structures in th ...

OPTIC

Orthologous and Paralogous Transcripts in Clades

Priority index

A Comprehensive Resource for Genetic Targets in Immune-Mediated Disease

Long Covid Phenotype Ontology

Oxford-RCGP RSC Long COVID-19 (LC) Phenotype Ontology

COVID-19 Surveillance Ontology

The COVID-19 Surveillance Ontology is an application ontology used to support SARS-CoV-2 (severe acute respiratory syndrome coronavirus 2) surveillance in primary care. The ontology facilitates monit ...

ChemBio Hub

The ChemBio Hub vision is to provide the tools that will make it easier for Oxford University scientists to connect with colleagues to improve their research, to satisfy funders that the data they hav ...

GWAS Diagram Browser

SIFTS

Structure Integration with Function, Taxonomy and Sequences

MitoMiner

MitoMiner is an integrated data warehouse of mammalian localisation evidence, phenotypes and diseases. This data has been integrated to allow the creation of sophisticated data mining queries spanning ...

PhenoScanner

Database of human genotype-phenotype associations.

BloodExpress

Database of Gene Expression in Mouse Haematopoiesis

CoGenT++

Complete Genome Tracking database

MoKCa

Mutations of Kinases in Cancer

coliBASE

A database for E. coli, Salmonella and Shigella

PepSeeker

Peptide identification and ion information from proteome experiments

PIPs

Predicted human protein-protein interactions

UK Biobank

UK Biobank is a large-scale biomedical database and research resource that provides researchers access to detailed longitudinal phenotype, medical and genetic data from 500,000 volunteer participants. ...