The future outlook for the programme is to build on current scientific and funding success with expansion of expertise in cell-atlasing approaches, spatial genomics and computational approaches and use of cell-atlasing technologies to understand in vitro systems such as IPSCs and organoids. This will be coupled with increasing focus on using cell-atlasing to understand disease.
The Cellular Genetic’s Programme jointly lead the “Human Cell Atlas” (HCA) global consortium alongside the Broad Institute, with Sarah Teichmann as co-lead and co-founder, together with Aviv Regev (MIT/Broad). The HCA vision is to create comprehensive reference maps of all human cells—the fundamental units of life—as a basis for both understanding human health and diagnosing, monitoring, and treating disease.
The “resolution revolution” in genomics has enabled the study of single cells, so-called “single cell genomics”, such that we can now sequence millions of individual cells in unprecedented detail. On a similar scale to the Human Genome Project, the Human Cell Atlas aims to create a 3D ‘Google map’ of the 37 trillion cells of the human body which will allow scientists to zoom into organs, tissues and cells to reveal the location and gene activity patterns of each cell type.
The Human Cell Atlas was launched in London in 2016 with a kick-off meeting attended by an interdisciplinary community of biomedical experts, genomics technologists and computational biologists at an international meeting to discuss how to create a Human Cell Atlas. Three years later, the global Human Cell Atlas initiative has over 1,500 researchers from more than 60 countries and has achieved success in fundamental areas of basic and translational research including oncology, immunology, respiratory disease, human development and reproductive biology.
We seek to explore the vast cellular diversity in the human brain using large-scale spatial transcriptomics, imaging and functional screens.
Connecting human development and disease
Our research sits at the interface of cancer genomics and single cell transcriptomics. Our aim is to unravel the identity and ...
Cellular Genetics Informatics
Our team provides efficient access to cutting-edge analysis methods, environments and pipelines for Cellular Genetics programme, which leads and is involved ...
Single-cell multi-omics tissue mapping and organoid-based disease modeling
We work on a range of tissues and employ multiple cutting-edge tools such as CRISPR perturbation and organoid modeling.
Our research is focused on understanding what type of immune cells live within different organs in humans, and how the special ...
Cellular Genetics Programme
The team’s research applies disruptive cutting-edge techniques to study the genomics of immune cell populations at single-cell resolution and uses ...
Quantitative models of gene expression
The Hemberg group is interested in developing quantitative models of gene expression. Our approach is theoretical and we strive to develop ...
Human Cell Atlas Group
We are undertaking research to develop, optimise and assess the performance of key enabling experimental and computational technologies that will underly ...
Single cell genomics
John Marioni's group develop computational and statistical tools to exploit high-throughput genomics data to understand the regulation of gene expression ...
Stegle and Theis Group
Cellular Genetics Programme
We aim to leverage machine learning in the context of single cell genomics to provide a true model-based understanding of the ...
Gene expression genomics
We use cutting edge single cell genomics technologies and computational methods to understand genes, proteins and cells in human health and ...
The Trynka group combines experimental and computational approaches to study how genetics control the immune system and predispose individuals to autoimmune ...
The Vento Lab uses genomics and computational tools to reconstruct immune environments. The main areas of focus are: Immunogenomics - Immune responses ...
Epigenetic mechanisms in health and disease
Adrian's group is investigating "The function of long non-coding RNAs originating at CpG island promoters" and "The effects of ...
The Bradley laboratory is a multi-disciplinary environment with a number of parallel research themes. One of our core disciplines is the ...
Genomics of gene regulation
Gene expression involves the transformation of genetic information encoded in DNA sequence into a gene product, such as a protein. Regulation ...
The Vallier laboratory studies the basic mechanisms controlling differentiation of human pluripotent cells into pancreas, lung, gut and liver cells.
Related International Fellows and Honorary Faculty
Dr Annettee Nakimuli
Annettee Nakimuli is a leading maternal health researcher based in Uganda, focused primarily on investigating the aetiology, treatment, prevention and long ...
Cellular Genetics Portals
Open-access data portals
The Cellular Genetics Programme is committed to making cell atlasing data analysis and visualisation tools available to the scientific community
Cellular Genetics Software
Open access tools
Computational tools developed by the research groups and scientific teams of the Cellular Genetics Programme
Related news and blogs
21 Jan 2021
Developmental origins of eczema and psoriasis discovered
Skin Cell Atlas points to new drug targets for inflammatory diseases
15 Dec 2020
Ten artists to create artworks for global research project mapping the human body
Human Cell Atlas explored through art science collaboration