Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
ENROLLING_BY_INVITATION
4000 participants
OBSERVATIONAL
2019-12-16
2029-11-07
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Functional Genomics of Rare Genetic Diseases: Realization of Innovative Tools With High Diagnostic Power
NCT04152876
Investigating the Role of Genetics in Disease Predisposition
NCT06584994
Genetic Markers and Biomarkers in Patients With Intellectual Disabilities of Genetic Origin
NCT05767203
Genetics of COVID-19 Susceptibility and Manifestations
NCT04371432
Gene Discovery Core, The Manton Center
NCT02743845
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The Sanger Human Cell Atlasing project will adopt various genomic approaches that will provide genome-wide information in a single experiment. This project aims to scale up the single cell genomics and high-throughput highly multiplex spatial gene expression profiling approaches. Coupled with powerful computational methods, this strategy will produce a comprehensive and systematic reference map of human cells, providing a fundamental blueprint of cell states for both basic biological research and clinical practice.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
OTHER
OTHER
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
sample collection
New collected samples, as well as surplus surgical and diagnostic samples.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* All samples will have fully informed consent for use in research.
Exclusion Criteria
* Samples taken from individuals without the capacity to consent to use in research
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
The Wellcome Sanger Institute
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Sarah Teichmann
Role: PRINCIPAL_INVESTIGATOR
Wellcome Sanger Institute
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Wellcome Sanger Institute
Cambridge, , United Kingdom
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
260474
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.