Studies

Testing biotx.ai's AI for wide data in Rare Diseases

Speciality area
Genomics and Rare Diseases

Study type
Data only

Researcher type
Commerical

Research lead
Marco Schmidt

BRIDGE- EDS (Ehlers-Danlos Syndrome)

Speciality area
Genomics and Rare Diseases

Study type
Data only

Researcher type
Non-commercial

Research lead
Heather Cordell

Genetic Links to Anxiety and Depression (GLAD) Study

Speciality area
Genomics and Rare Diseases, Mental Health

Study type
Data only

Researcher type
Non-commercial

Research lead
Gerome Breen

CGG trinucleotide short-tandem repeats in unexplained intellectual disability

Speciality area
Genomics and Rare Diseases

Study type
Data only

Researcher type
Non-commercial

Research lead
Dale Annear

Streamlining ethnicity/relatedness code

Speciality area
Genomics and Rare Diseases

Study type
Data only

Researcher type
Non-commercial

Research lead
Rachel Ong

To access and provide NIHR BioResource Rare Disease Genomes across all eligible disorders within the Genomics England Research Environment as an anonymised dataset alongside the 100,000 Genomes Project main programme data

Speciality area
Genomics and Rare Diseases

Study type
Data only

Researcher type
Non-commercial

Research lead
Mark Caulfield

Investigation of Omics in Chronic Widespread Pain

Speciality area
Genomics and Rare Diseases, Anaesthesia, Perioperative Medicine and Pain Management

Study type
Data only

Researcher type
Academic

Research lead
Frances Williams

Post-COVID-19 surveillance: To establish T cell assays for assessing T cell responses and identify individual and immunological factors that account for different disease outcomes

Speciality area
Infection

Study type
Samples and data

Researcher type
Non-commercial

Research lead
Dr Nyarie Sithole

Healthcare Worker T Cell Recall

Speciality area
Infection

Study type
Participant re-contact

Researcher type
Non-commercial

Research lead
Dr James Thaventhiran