Sanger Human Cell Atlasing Project

NCT ID: NCT06497673

Last Updated: 2024-07-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

ENROLLING_BY_INVITATION

Total Enrollment

4000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2019-12-16

Study Completion Date

2029-11-07

Brief Summary

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"Cell Atlasing" refers to a novel strategy to characterise cells in tissues at the molecular level in a quantitative manner. The international Human Cell Atlas consortium brings together a community of biologists, clinicians, technologists, physicists, computational scientists, software engineers, and mathematicians to capitalise on drawing together leaders with various biological, technical and computational expertise. The project is based on the aim to define all human cell types in terms of their distinctive patterns of gene expression, physiological states, developmental trajectories, and location. This will pave the way to create a reference map of all human cells as a basis for understanding human health and diagnosing, monitoring, and treating disease.

Detailed Description

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Previous methods for quantifying molecular states of cells included microarray and standard RNA-seq analysis on a tissue section (RNA-seq is a technique to look at the activity of all the genes in a cell). These methods estimate the activity of any given gene by averaging the signal from millions of cells. Given the heterogeneity of cell populations (i.e.how uniform they are), measurement of the mean values of signals overlooks the internal interactions and differences within a cell population that may be crucial for maintaining normal tissue function and facilitating disease progression.

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

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Human Development Genetic Disease

Study Design

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Observational Model Type

OTHER

Study Time Perspective

OTHER

Interventions

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sample collection

New collected samples, as well as surplus surgical and diagnostic samples.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Samples are from the living and the deceased age 0 to 99+ from healthy and diseased individuals.
* All samples will have fully informed consent for use in research.

Exclusion Criteria

* Samples taken without consent for use in future research
* Samples taken from individuals without the capacity to consent to use in research
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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The Wellcome Sanger Institute

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Sarah Teichmann

Role: PRINCIPAL_INVESTIGATOR

Wellcome Sanger Institute

Locations

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Wellcome Sanger Institute

Cambridge, , United Kingdom

Site Status

Countries

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United Kingdom

Other Identifiers

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260474

Identifier Type: -

Identifier Source: org_study_id

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