Sanger Human Cell Atlasing Project
NCT06497673 · Status: ENROLLING_BY_INVITATION · Type: OBSERVATIONAL · Enrollment: 4000
Last updated 2024-07-12
Summary
"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.
Conditions
- Human Development
- Genetic Disease
Interventions
- OTHER
-
sample collection
New collected samples, as well as surplus surgical and diagnostic samples.
Sponsors & Collaborators
-
The Wellcome Sanger Institute
lead OTHER
Principal Investigators
-
Sarah Teichmann · Wellcome Sanger Institute
Eligibility
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2019-12-16
- Primary Completion
- 2029-11-07
- Completion
- 2029-11-07
Countries
- United Kingdom
Study Locations
More Related Trials
-
Next Generation to Identify Genetic Causes of Disease in Patients Participating in NICHD Clinical Protocols
NCT01375543 ·Status: COMPLETED
-
The Healthy Elderly Longevity Cohort
NCT01004133 ·Status: RECRUITING
-
BioGene Bank Cohort Study for Approved Research Requests
NCT02550171 ·Status: COMPLETED
-
Study of Clinical and Molecular Manifestations of Genetic Disorders
NCT00001466 ·Status: COMPLETED
-
Biomarkers in Neurodegenerative Diseases
NCT04055532 ·Status: WITHDRAWN
-
Identification of New FTLD Genes
NCT02363062 ·Status: UNKNOWN
-
Control Cohort CTRL COH
NCT05370079 ·Status: RECRUITING ·Phase: NA
-
Collection and Storage of Human Biospecimens for Research Into Rare Diseases and Medical Conditions
NCT02365376 ·Status: UNKNOWN
-
Clinical and Molecular Studies in Families With Inherited Eye Disease
NCT02771236 ·Status: RECRUITING
-
PROGENI (Parkinson's Research: The Organized Genetics Initiative) Family Study of LRRK2 (Leucine-rich Repeat Kinase 2)
NCT01536821 ·Status: COMPLETED
-
NIEHS Repository of Stored Biological Samples for Future Use
NCT05666739 ·Status: RECRUITING
-
Developing a Pipeline to Employ RNA-Seq as a Complementary Diagnostic Tool in Rare Diseases
NCT05996731 ·Status: RECRUITING ·Phase: NA
-
Uncovering Genes Behind Cartilage Tumors and Vascular Anomalies Using Genomic Sequencing
NCT06749366 ·Status: RECRUITING
-
Observational Study of Advanced Data Analytics in Genetic Conditions
NCT05657405 ·Status: RECRUITING
-
Molecular Genetic Study of Mayer-Rokitansky-Kuster-Hauser Syndrome
NCT02967822 ·Status: RECRUITING
-
Study of Heritable Connective Tissue Disorders
NCT00001641 ·Status: COMPLETED
-
Drivers of Hypoxia-induced Angiogenesis in Tumor Development
NCT03979833 ·Status: UNKNOWN
-
Newborn Sequencing Screening in China
NCT05476640 ·Status: NOT_YET_RECRUITING
-
Integrative Sequencing In Germline and Hereditary Tumours
NCT03857594 ·Status: ACTIVE_NOT_RECRUITING
-
Use of Population Descriptors in Human Genetic Research
NCT00767702 ·Status: COMPLETED
-
Personalized Genomic Research
NCT01294345 ·Status: COMPLETED
-
Adult Patients With Undiagnosed Conditions and Their Responses to Clinically Uncertain Results From Exome Sequencing
NCT03605004 ·Status: COMPLETED
-
Genome Medical Sequencing for Gene Discovery
NCT01087320 ·Status: RECRUITING
-
Transcriptomic Approach for the Identification and Prioritization of Genome Variants in Neurodevelopmental Disorders With Malformation
NCT06762678 ·Status: NOT_YET_RECRUITING ·Phase: NA
-
Identification and Characterization of Monogenic Diabetes
NCT01481623 ·Status: COMPLETED ·Phase: NA