The Oxford Single Cell Biology Consortium
Lead Research Organisation:
University of Oxford
Department Name: Weatherall Inst of Molecular Medicine
Abstract
Limitations in our ability to study the biology of individual cells has historically been a major obstacle, inhibiting our understanding of some fundamental problems in biomedical research such as the onset of cancer, the immunological determination of 'self', and the ability to purify tissue-specific stem cells. Recent developments in the field of single cell genomics is now opening up unprecedented opportunities to uncover individual cell differences within such complex tissues. The objective of the proposed research is to establish a Centre of Single Cell Biology (CSCB) in Oxford that will take advantage of this pioneering technology in order to improve the diagnosis, stratification and treatment of a wide variety of human diseases. The CSCB will be coordinated by the Weatherall Institute of Molecular Medicine (WIMM) which has a long-standing technical and strategic expertise in single cell research. The capital development will be used to enhance single-cell research capabilities across the campus in a number of key areas:
Data analysis: Single cell genomics studies generate an enormous amount of data, with consequent challenges for the analysis and correct interpretation of these complex data sets. We propose to establish an entirely new research group devoted to the development of novel approaches for the statistical and computational analysis of single cell biology data and its application to medicine. This group will be located in new space to be developed at the WIMM, but jointly led by leading scientists across the campus. This new initiative will provide a clear pathway to integrate multidisciplinary, scientific and technical innovation in single cell biology research across the Oxford University Campus and to provide ground-breaking applications of this approach to medicine in the UK.
State of the art facilities: We will develop single cell biology research laboratories to allow practical access for research groups conducting these studies across the campus. These facilities will house cutting edge technology platforms and, importantly, will create "ultra clean" environments to carry out single cell experiments. This is necessary as very low levels of background "contamination" make the interpretation of single cell experiments challenging.
Projects: As a specific example of how this technology will be applied to address fundamental problems in human disease, the lead programme of research in the CSCB will be focused on inherited disorders of red blood cells. These disorders are amongst the most common of all human genetic diseases worldwide with an estimated 300,000 affected babies born each year and a total number of affected UK patients of ~16,000. Currently, severely affected individuals are treated with supportive care, including lifelong blood transfusion and treatment to prevent accumulation of iron in the body, which is costly, burdensome, and gives rise to serious, long-term clinical complications. Here we propose to "genetically repair" the damaged genes in the patient's own blood stem cells. Single cell biology will be central to this project: First, single cell genomic approaches will be used to identify the blood stem cells which are the best target for this therapy. Second, single-cell analysis will be used to assess the safety and efficiency of this approach. This programme, focussed on developing an entirely new approach to treating the haemoglobinopathies, has the potential to transform the treatment of all human genetic diseases that can be cured by stem cell transplantation. This is one example of many projects in development across the campus which will be greatly facilitated by the development of improved single cell research capabilities.
Oxford is in a very strong position to take a world-leading role in the up-and-coming area of Single Cell Biology and application of these technologies to important clinical and basic biology questions across the University and beyond.
Data analysis: Single cell genomics studies generate an enormous amount of data, with consequent challenges for the analysis and correct interpretation of these complex data sets. We propose to establish an entirely new research group devoted to the development of novel approaches for the statistical and computational analysis of single cell biology data and its application to medicine. This group will be located in new space to be developed at the WIMM, but jointly led by leading scientists across the campus. This new initiative will provide a clear pathway to integrate multidisciplinary, scientific and technical innovation in single cell biology research across the Oxford University Campus and to provide ground-breaking applications of this approach to medicine in the UK.
State of the art facilities: We will develop single cell biology research laboratories to allow practical access for research groups conducting these studies across the campus. These facilities will house cutting edge technology platforms and, importantly, will create "ultra clean" environments to carry out single cell experiments. This is necessary as very low levels of background "contamination" make the interpretation of single cell experiments challenging.
Projects: As a specific example of how this technology will be applied to address fundamental problems in human disease, the lead programme of research in the CSCB will be focused on inherited disorders of red blood cells. These disorders are amongst the most common of all human genetic diseases worldwide with an estimated 300,000 affected babies born each year and a total number of affected UK patients of ~16,000. Currently, severely affected individuals are treated with supportive care, including lifelong blood transfusion and treatment to prevent accumulation of iron in the body, which is costly, burdensome, and gives rise to serious, long-term clinical complications. Here we propose to "genetically repair" the damaged genes in the patient's own blood stem cells. Single cell biology will be central to this project: First, single cell genomic approaches will be used to identify the blood stem cells which are the best target for this therapy. Second, single-cell analysis will be used to assess the safety and efficiency of this approach. This programme, focussed on developing an entirely new approach to treating the haemoglobinopathies, has the potential to transform the treatment of all human genetic diseases that can be cured by stem cell transplantation. This is one example of many projects in development across the campus which will be greatly facilitated by the development of improved single cell research capabilities.
Oxford is in a very strong position to take a world-leading role in the up-and-coming area of Single Cell Biology and application of these technologies to important clinical and basic biology questions across the University and beyond.
Technical Summary
We will establish a Centre of Single Cell Biology in Oxford that will improve the diagnosis, stratification and treatment of a wide variety of human diseases. The Centre will be coordinated from the Weatherall Institute of Molecular Medicine (WIMM), which has established technical and strategic expertise in single cell research, and will share experimental and analytical best practice with two linked experimental sites, at the Wellcome Trust Centre for Human Genetics (WTCHG) and the MRC Functional Genomics Unit (FGU). The Centre's lead project will use a combination of single cell genomic analysis and functional assays at the clonal level to refine current stem/progenitor/effector cell purification strategies for transplantation with the ultimate aim of developing entirely new approaches to therapy in blood diseases. This single cell expertise and platforms in haematopoiesis will be used as a paradigm to develop parallel cutting-edge translational programmes for other inherited and acquired human diseases (such as in Immunology, Cancer Biology and Neurology).
There are considerable computational and statistical challenges involved in state-of-the-art analysis and modelling of single cell data. To address these, the experimental single cell studies at the WIMM will interlink with the activities of the internationally renowned computational and statistical biologists from FGU and WTCHG. Specifically, we will establish an entirely new research group devoted to develop and apply novel approaches to the statistical and computational analysis of single cell biology and its application to medicine. This new initiative will provide a clear pathway to integrate multidisciplinary, scientific and technical innovation in single cell biology research across the Oxford University Campus and to provide ground-breaking applications of this approach to medicine in the UK.
There are considerable computational and statistical challenges involved in state-of-the-art analysis and modelling of single cell data. To address these, the experimental single cell studies at the WIMM will interlink with the activities of the internationally renowned computational and statistical biologists from FGU and WTCHG. Specifically, we will establish an entirely new research group devoted to develop and apply novel approaches to the statistical and computational analysis of single cell biology and its application to medicine. This new initiative will provide a clear pathway to integrate multidisciplinary, scientific and technical innovation in single cell biology research across the Oxford University Campus and to provide ground-breaking applications of this approach to medicine in the UK.
Planned Impact
This research will have a clear beneficial impact well beyond the immediate professional circle carrying out similar research. For example:
Academic Impact: As outlined in the academic beneficiaries statement, there is clear potential for academic impact in a number of key areas, including, but not limited to, computational analysis of complex single cell data sets, development of new techniques for single cell analysis, application of genomic engineering techniques for therapeutic use, understanding of ageing, understanding cell fate decisions and refining diagnosis and stratification of disease.
Beneficiaries in the commercial private sector: We have established a strategic partnership with Fluidigm, the world leader in microfluidic devices for single cell analysis. This partnership will include access to novel technology platforms and a dynamic and mutually beneficial sharing of information. Fluidigm will also co-sponsor our planned single-cell annual data analysis workshop, again, with clear potential for mutual benefit. This partnership will help to secure further inward investment and gain access to cutting-edge technologies.
Contribution to the nation's health: Our overarching goal is to accelerate the recent advances in single cell technologies though to patient benefit. There are a number of key areas where this might be achieved. First, improved understanding of complex tissues, for example, through refined stem cell purification strategies has clear potential to improve outcome of stem cell transplantation procedures, which are still associated with considerable morbidity and mortality. Second, the application of single cell genomic approaches to help accelerate the development of techniques to "genetically repair" inherited disorders of blood cells has clear potential to transform the application of single cell genomics into a major clinical research activity, with broad cross-disciplinary applicability. The concept of correcting inherited genetic abnormalities clearly has far reaching potential to contribute to improvement in the nation's health. Third, single cell genomics approaches will help to further develop and refine diagnostic and stratification approaches in human disease and thereby personalize patient management, for example though a deeper understanding of clonal complexity of tumour propagating cancer stem cells, and monitoring of these cells throughout the disease course and impact of therapy. Finally, single cell analysis offers the potential to provide unique insights into the ageing process at the single (stem) cell level, and how this affects tissue function and contributes to age-dependent disease (tissue degeneration, cancer).
Dissemination of knowledge: As outlined in the communication plan, the lead investigators have considerable experience of disseminating scientific research findings across academic peers and more broadly with the public, including schools, and also for inspiring young potential scientists. A number of specific initiatives will be developed to help disseminate research conducted by the Centre of Single Cell Biology, including a new website and an annual single cell workshop.
New processes: Techniques in single cell technology are likely to develop rapidly over the coming years. If funded, the Oxford Centre of Single Cell Biology will place the MRC at the forefront of these developments. As an example, the WIMM introduced the first Fluidigm C1 microfluidics platform in Europe in 2012. This new technology allows capture of single primary cells and the interrogation of RNA and DNA content by multiplex PCR or through whole transcriptome/genome analysis, all at the single cell level. This technology is now being introduced across a number of centres in the UK. We would anticipate that the Oxford Centre of Single Cell Biology would lead the way with similar groundbreaking technological advances in the future.
Academic Impact: As outlined in the academic beneficiaries statement, there is clear potential for academic impact in a number of key areas, including, but not limited to, computational analysis of complex single cell data sets, development of new techniques for single cell analysis, application of genomic engineering techniques for therapeutic use, understanding of ageing, understanding cell fate decisions and refining diagnosis and stratification of disease.
Beneficiaries in the commercial private sector: We have established a strategic partnership with Fluidigm, the world leader in microfluidic devices for single cell analysis. This partnership will include access to novel technology platforms and a dynamic and mutually beneficial sharing of information. Fluidigm will also co-sponsor our planned single-cell annual data analysis workshop, again, with clear potential for mutual benefit. This partnership will help to secure further inward investment and gain access to cutting-edge technologies.
Contribution to the nation's health: Our overarching goal is to accelerate the recent advances in single cell technologies though to patient benefit. There are a number of key areas where this might be achieved. First, improved understanding of complex tissues, for example, through refined stem cell purification strategies has clear potential to improve outcome of stem cell transplantation procedures, which are still associated with considerable morbidity and mortality. Second, the application of single cell genomic approaches to help accelerate the development of techniques to "genetically repair" inherited disorders of blood cells has clear potential to transform the application of single cell genomics into a major clinical research activity, with broad cross-disciplinary applicability. The concept of correcting inherited genetic abnormalities clearly has far reaching potential to contribute to improvement in the nation's health. Third, single cell genomics approaches will help to further develop and refine diagnostic and stratification approaches in human disease and thereby personalize patient management, for example though a deeper understanding of clonal complexity of tumour propagating cancer stem cells, and monitoring of these cells throughout the disease course and impact of therapy. Finally, single cell analysis offers the potential to provide unique insights into the ageing process at the single (stem) cell level, and how this affects tissue function and contributes to age-dependent disease (tissue degeneration, cancer).
Dissemination of knowledge: As outlined in the communication plan, the lead investigators have considerable experience of disseminating scientific research findings across academic peers and more broadly with the public, including schools, and also for inspiring young potential scientists. A number of specific initiatives will be developed to help disseminate research conducted by the Centre of Single Cell Biology, including a new website and an annual single cell workshop.
New processes: Techniques in single cell technology are likely to develop rapidly over the coming years. If funded, the Oxford Centre of Single Cell Biology will place the MRC at the forefront of these developments. As an example, the WIMM introduced the first Fluidigm C1 microfluidics platform in Europe in 2012. This new technology allows capture of single primary cells and the interrogation of RNA and DNA content by multiplex PCR or through whole transcriptome/genome analysis, all at the single cell level. This technology is now being introduced across a number of centres in the UK. We would anticipate that the Oxford Centre of Single Cell Biology would lead the way with similar groundbreaking technological advances in the future.
Publications
Ashley N
(2019)
Cellular polarity modulates drug resistance in primary colorectal cancers via orientation of the multidrug resistance protein ABCB1.
in The Journal of pathology
Aulicino A
(2018)
Invasive Salmonella exploits divergent immune evasion strategies in infected and bystander dendritic cell subsets
in Nature Communications
Blobel GA
(2021)
Testing the super-enhancer concept.
in Nature reviews. Genetics
Blohmke CJ
(2019)
Diagnostic host gene signature for distinguishing enteric fever from other febrile diseases.
in EMBO molecular medicine
Buono M
(2016)
A dynamic niche provides Kit ligand in a stage-specific manner to the earliest thymocyte progenitors.
in Nature cell biology
Campbell KR
(2016)
Order Under Uncertainty: Robust Differential Expression Analysis Using Probabilistic Models for Pseudotime Inference.
in PLoS computational biology
Carrelha J
(2018)
Hierarchically related lineage-restricted fates of multipotent haematopoietic stem cells.
in Nature
Corridoni D
(2020)
Single-cell atlas of colonic CD8+ T cells in ulcerative colitis.
in Nature medicine
Corridoni D
(2020)
Single-cell atlas of colonic CD8+ T cells in ulcerative colitis
in Nature Medicine
Drissen R
(2019)
Identification of two distinct pathways of human myelopoiesis.
in Science immunology
Drissen R
(2016)
Hematopoietic Lineage Diversification, Simplified.
in Cell stem cell
Drissen R
(2016)
Distinct myeloid progenitor-differentiation pathways identified through single-cell RNA sequencing
in Nature Immunology
Farmer D
(2021)
The developing mouse coronal suture at single-cell resolution
in Nature Communications
Fawkner-Corbett D
(2021)
Spatiotemporal analysis of human intestinal development at single-cell resolution.
in Cell
Francis H
(2020)
Scalable In Vitro Production of Defined Mouse Erythroblasts
Fraser E
(2021)
Multi-Modal Characterization of Monocytes in Idiopathic Pulmonary Fibrosis Reveals a Primed Type I Interferon Immune Phenotype
in Frontiers in Immunology
Fritzsche M
(2015)
CalQuo: automated, simultaneous single-cell and population-level quantification of global intracellular Ca2+ responses.
in Scientific reports
Giustacchini A
(2017)
Single-cell transcriptomics uncovers distinct molecular signatures of stem cells in chronic myeloid leukemia.
in Nature medicine
Graf T
(2019)
Transcription Factor Stoichiometry Drives Cell Fate: Single-Cell Proteomics to the Rescue.
in Cell stem cell
Grover A
(2016)
Single-cell RNA sequencing reveals molecular and functional platelet bias of aged haematopoietic stem cells.
in Nature communications
Handel AE
(2016)
Assessing similarity to primary tissue and cortical layer identity in induced pluripotent stem cell-derived cortical neurons through single-cell transcriptomics.
in Human molecular genetics
Harland LTG
(2021)
The T-box transcription factor Eomesodermin governs haemogenic competence of yolk sac mesodermal progenitors.
in Nature cell biology
Harland LTG
(2021)
Publisher Correction: The T-box transcription factor Eomesodermin governs haemogenic competence of yolk sac mesodermal progenitors.
in Nature cell biology
Harrison CN
(2022)
Phase III MANIFEST-2: pelabresib + ruxolitinib vs placebo + ruxolitinib in JAK inhibitor treatment-naive myelofibrosis.
in Future oncology (London, England)
Hentges LD
(2022)
LanceOtron: a deep learning peak caller for genome sequencing experiments.
in Bioinformatics (Oxford, England)
Higgs DR
(2020)
Enhancer-promoter interactions and transcription.
in Nature genetics
Higgs DR
(2021)
Author Correction: Enhancer-promoter interactions and transcription.
in Nature genetics
Jeziorska DM
(2022)
On-microscope staging of live cells reveals changes in the dynamics of transcriptional bursting during differentiation.
in Nature communications
Karamitros D
(2015)
Geminin deletion increases the number of fetal hematopoietic stem cells by affecting the expression of key transcription factors.
in Development (Cambridge, England)
Karamitros D
(2018)
Single-cell analysis reveals the continuum of human lympho-myeloid progenitor cells.
in Nature immunology
Kinchen J
(2018)
Structural Remodeling of the Human Colonic Mesenchyme in Inflammatory Bowel Disease.
in Cell
Loughran SJ
(2017)
Mbd3/NuRD controls lymphoid cell fate and inhibits tumorigenesis by repressing a B cell transcriptional program.
in The Journal of experimental medicine
Louka E
(2021)
Heterogeneous disease-propagating stem cells in juvenile myelomonocytic leukemia.
in The Journal of experimental medicine
Luis T
(2016)
Embryonic thymopoiesis is initiated by an immune-restricted lympho-myeloid progenitor independently of notch signaling
in Experimental Hematology
Luis TC
(2016)
Initial seeding of the embryonic thymus by immune-restricted lympho-myeloid progenitors.
in Nature immunology
Lukoseviciute M
(2018)
From Pioneer to Repressor: Bimodal foxd3 Activity Dynamically Remodels Neural Crest Regulatory Landscape In Vivo.
in Developmental cell
Marie R
(2018)
Single-molecule DNA-mapping and whole-genome sequencing of individual cells
in Proceedings of the National Academy of Sciences
Mascarenhas J
(2022)
A randomized phase 3 trial of interferon-a vs hydroxyurea in polycythemia vera and essential thrombocythemia.
in Blood
McCarthy DJ
(2017)
Scater: pre-processing, quality control, normalization and visualization of single-cell RNA-seq data in R.
in Bioinformatics (Oxford, England)
Mead AJ
(2017)
Niche-mediated depletion of the normal hematopoietic stem cell reservoir by Flt3-ITD-induced myeloproliferation.
in The Journal of experimental medicine
Mead AJ
(2022)
A retrospective real-world study of the current treatment pathways for myelofibrosis in the United Kingdom: the REALISM UK study.
in Therapeutic advances in hematology
Merryweather-Clarke AT
(2018)
Does osteogenic potential of clonal human bone marrow mesenchymal stem/stromal cells correlate with their vascular supportive ability?
in Stem cell research & therapy
Description | BRC3 Haematology and Stem Cell |
Amount | £4,602,645 (GBP) |
Funding ID | BRC3 |
Organisation | National Institute for Health Research |
Department | NIHR Biomedical Research Centre |
Sector | Public |
Country | United Kingdom |
Start | 03/2017 |
End | 03/2022 |
Description | CRUK Senior Cancer Research Fellowship |
Amount | £2,426,011 (GBP) |
Organisation | Hub at the MRC/CRUK/BHF Clinical Trial Service Unit |
Sector | Academic/University |
Country | United Kingdom |
Start | 03/2019 |
End | 05/2025 |
Description | Capital Prioritisation for MRC Units and Institutes |
Amount | £300,000 (GBP) |
Organisation | Medical Research Council (MRC) |
Sector | Public |
Country | United Kingdom |
Start | 03/2018 |
End | 04/2019 |
Description | Clinical Research Training Fellowship (Nicholas Fordham): The Role of EZH2 mutation in paediatric myelodysplasia |
Amount | £276,500 (GBP) |
Organisation | The Kay Kendall Leukaemia Fund |
Sector | Academic/University |
Country | United Kingdom |
Start | 03/2017 |
End | 03/2020 |
Description | ELSTAR Small Scale |
Amount | £7,980 (GBP) |
Organisation | Elstar Therapeutics Inc. |
Sector | Private |
Country | United States |
Start | 01/2018 |
End | 12/2018 |
Description | ELSTAR: Large Scale |
Amount | £777,818 (GBP) |
Organisation | Elstar Therapeutics Inc. |
Sector | Private |
Country | United States |
Start | 01/2019 |
End | 01/2022 |
Description | Exploring mechanisms of enhancer action in erythropoiesis |
Amount | £250,000 (GBP) |
Funding ID | 209181 |
Organisation | Sir Henry Dale Fellowships |
Sector | Charity/Non Profit |
Country | United Kingdom |
Start | 03/2018 |
End | 03/2022 |
Description | Genome and Transcriptome analysis of patients with rare stem and Myeloid disorders |
Amount | £65,000 (GBP) |
Organisation | University of Oxford |
Department | John Fell Fund |
Sector | Academic/University |
Country | United Kingdom |
Start | 06/2017 |
End | 06/2019 |
Description | Identification and therapeutic targeting of the abnormal bone marrow stromal cells underlying bone marrow fibrosis in myelofibrosis |
Amount | £216,000 (GBP) |
Organisation | The Kay Kendall Leukaemia Fund |
Sector | Academic/University |
Country | United Kingdom |
Start | 11/2018 |
End | 10/2021 |
Description | Impact of Leukaemia-Associated Loss of Function of Epigenetic Regulators on Distinct Haematopoietic Stem Cells (Co-applicant with Sten Eirik Jacobsen) |
Amount | £266 (GBP) |
Organisation | The Kay Kendall Leukaemia Fund |
Sector | Academic/University |
Country | United Kingdom |
Start | 01/2017 |
End | 12/2019 |
Description | LAB282 Large Scale Award |
Amount | £499,817 (GBP) |
Organisation | LAB 282 |
Sector | Charity/Non Profit |
Start | 01/2019 |
End | 06/2020 |
Description | MRC CRI: The Oxford Single Cell Biology Consortium (co-investigator) |
Amount | £4,975,434 (GBP) |
Funding ID | MR/M00919X/1 |
Organisation | Medical Research Council (MRC) |
Sector | Public |
Country | United Kingdom |
Start | 03/2015 |
End | 04/2016 |
Description | MRC Discovery Award (co-investigator) |
Amount | £1,000,000 (GBP) |
Organisation | Medical Research Council (MRC) |
Sector | Public |
Country | United Kingdom |
Start | 03/2016 |
End | 04/2019 |
Description | MRC Discovery Award - Identification and characterisation of cellular targets for genome editing of foetal haematopoietic stem/progenitor cells |
Amount | £56,000 (GBP) |
Organisation | Medical Research Council (MRC) |
Sector | Public |
Country | United Kingdom |
Start | 08/2016 |
End | 08/2017 |
Description | MRC Proximity to discovery Industry Engagement Fund |
Amount | £10,000 (GBP) |
Organisation | Medical Research Council (MRC) |
Sector | Public |
Country | United Kingdom |
Start | 02/2016 |
End | 07/2016 |
Description | Measuring DNA damage in Single Cells Using a Novel High Throughput Genomic Assay |
Amount | £15,000 (GBP) |
Organisation | University of Oxford |
Department | John Fell Fund |
Sector | Academic/University |
Country | United Kingdom |
Start | 03/2017 |
End | 03/2018 |
Description | Megakaryocytes as novel cellular targets for myelofibrosis, a severe bone marrow disorder |
Amount | £54,166 (GBP) |
Organisation | LAB 282 |
Sector | Charity/Non Profit |
Start | 02/2018 |
End | 09/2018 |
Description | Molecular Haematology Unit Affiliate Programme |
Amount | £500,000 (GBP) |
Organisation | Medical Research Council (MRC) |
Sector | Public |
Country | United Kingdom |
Start | 03/2022 |
End | 03/2027 |
Description | Oxford Cancer Research Centre |
Amount | £11,000,000 (GBP) |
Organisation | Cancer Research UK |
Sector | Charity/Non Profit |
Country | United Kingdom |
Start | 03/2022 |
End | 04/2027 |
Description | Proximity to Discovery Industry Engagement |
Amount | £10,000 (GBP) |
Organisation | Medical Research Council (MRC) |
Sector | Public |
Country | United Kingdom |
Start | 02/2016 |
End | 07/2016 |
Description | Rosetrees Trust |
Amount | £40,000 (GBP) |
Organisation | Rosetrees Trust |
Sector | Charity/Non Profit |
Country | United Kingdom |
Start | 01/2015 |
End | 01/2017 |
Description | The Oxford Single Cell Biology Consortium |
Amount | £4,975,434 (GBP) |
Funding ID | MR/M00919X/1 |
Organisation | Medical Research Council (MRC) |
Sector | Public |
Country | United Kingdom |
Start | 03/2015 |
End | 09/2016 |
Description | The Oxford Single Cell Biology Consortium |
Amount | £399,179 (GBP) |
Funding ID | MR/M00919X/1 |
Organisation | University of Oxford |
Department | John Fell Fund |
Sector | Academic/University |
Country | United Kingdom |
Start | 04/2016 |
End | 03/2019 |
Description | The single cell immunological landscape of Juvenile Myelomonocytic Leukaemia |
Amount | £12,000 (GBP) |
Organisation | University of Oxford |
Sector | Academic/University |
Country | United Kingdom |
Start | 06/2018 |
End | 07/2019 |
Description | The single cell immunological landscape of Juvenile Myelomonocytic Leukaemia |
Amount | £36,000 (GBP) |
Organisation | University of Oxford |
Sector | Academic/University |
Country | United Kingdom |
Start | 06/2018 |
End | 07/2019 |
Description | Tracking the origins of post-transplant myelofibrosis relapse at single cell level |
Amount | £240,000 (GBP) |
Organisation | Hub at the MRC/CRUK/BHF Clinical Trial Service Unit |
Sector | Academic/University |
Country | United Kingdom |
Start | 03/2018 |
End | 03/2021 |
Description | Unravelling signatures of clonal response, resistance and evolution of high-risk essential thrombocythaemia at single-cell resolution |
Amount | £261,848 (GBP) |
Funding ID | MR/S001190/1 |
Organisation | Medical Research Council (MRC) |
Sector | Public |
Country | United Kingdom |
Start | 08/2018 |
End | 08/2021 |
Description | Wellcome Trust Postdoctoral Research Training Fellowship for Clinician |
Amount | £248,107 (GBP) |
Organisation | Wellcome Trust |
Department | Wellcome Trust Research Training Fellowship |
Sector | Charity/Non Profit |
Country | United Kingdom |
Start | 07/2016 |
End | 07/2019 |
Description | Enhancing tumour specific immune responses for the treatment of ovarian cancer |
Organisation | University of Oxford |
Country | United Kingdom |
Sector | Academic/University |
PI Contribution | Access to ovarian cancer biology and computational work |
Collaborator Contribution | Immunology expertise and cancer antigene prediction. |
Impact | The Ovarian Cancer Action (OCA) international grand challenge award Publication by Cancer Cell in Feb 2020: " The Repertoire of Serous Ovarian Cancer Non-genetic Heterogeneity Revealed by Single-Cell Sequencing of Normal Fallopian Tube Epithelial Cells" |
Start Year | 2016 |
Description | Molecular Haematology Unit seminar |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | Local |
Primary Audience | Postgraduate students |
Results and Impact | A talk regarding the work on single-cell systems biology carried out by the company to date. This sparked a good debate between the presenter and the audience. |
Year(s) Of Engagement Activity | 2016,2017,2018,2019 |
Description | Science Career Seminar |
Form Of Engagement Activity | A talk or presentation |
Part Of Official Scheme? | No |
Geographic Reach | Regional |
Primary Audience | Postgraduate students |
Results and Impact | A career talk to students and post-docs involving working in the USA |
Year(s) Of Engagement Activity | 2016 |