ucl cancer institute
paul o'gorman building
UCL logo

UCL Cancer Institute
Paul O'Gorman Building
72 Huntley Street
London WC1E 6BT

contact@cancer.ucl.ac.uk
Telephone: +44 (0)20 7679 6500

 

-Professor Stephan Beck

The laboratory has broad interests in the genomics of phenotypic plasticity in health and disease. In addition to polymorphisms and mutations, we study epigenetic changes such as DNA methylation and histone modifications that can modulate genome function under exogenous influence. Central to our research is the development an integrated systems approach - termed 'reverse phenotyping' - to screen genomes of common diseases as well as cancer for genetic, epigenetic and combinatorial variations. The ability to distinguish causal from consequential variations is one of the key challenges in biomedical research. Once fully established, 'reverse phenotyping' can be expected to significantly increase our ability to identify novel and, in particular, combinatorial variations causing or contributing to phenotypic plasticity and thus will provide new targets for translation into diagnostics and therapeutics. The laboratory offers state-of-the-art facilities and a stimulating environment for graduate and post-doctoral training.

 

The Cancer Methylome:
The Cancer Methylome Project aims to build a comprehensive profile of the human cancer methylome. The focus of this project is to provide a better understanding of how aberrant methylation affects the aetiology of cancer, and how we can use this information to identify novel diagnostic and prognostic markers or new therapeutic targets.
The Epigenomics of Common Disease:
Epigenetic factors, such as DNA methylation, are well established in the evolution of human cancer genomes; however the possible role they may play in other common diseases has not yet been elucidated. Epigenomics may add an extra dimension, upon identified susceptibility S.N.P.s & C.N.V.s, in the interplay between the environment and the genome in common diseases, and further aid in the understanding of the pathogenesis of these disorders.
High-throughput DNA methylation pipeline:
Methylated DNA immunoprecipitation (MeDIP) is a comprehensive but cumbrous technique to assess genome-wide DNA methylation profiles. This project aims to increase the throughput of the assay as part of an integrated analysis pipeline to ultimately aid the discovery of novel biomarkers for use in disease diagnostics and drug development.
BatCave:
BatCave is an integrated database designed for the storage and visualisation of data generated by the 'Batman' (Bayesian Tool for Methylation Analysis) analysis tool. The BatCave facilitates the integration of our work with publicly available datasets via the DAS (Distributed Annotation System) communication protocol.
ZooArray: Epigenetic Insights into Vertebrate Genomes:
Epigenetic modifications such as DNA methylation and post-translational modifications of histones play crucial roles in organizing chromatin structure, specifically at the non-coding regulatory regions which facilitates gene expression and regulates other cellular processes. The aim of this project is to elucidate the epigenetic states of the evolutionarily conserved genomic sequences in order to understand the importance of these modifications during vertebrate evolution.
NET BioBank:
Neuroendocrine Tumors (NETs) are a heterogeneous group of neoplasms which arise from the hormone-producing cells of the body’s nervous and endocrine systems. NETs affect 1/50 000 of the UK population. The project aims to carry out an integrated (epi)genomic analysis of the NET BioBank established at the Royal Free and UCL Hospitals to identify new biomarkers for translation into diagnostics and therapeutics
Statistical Cancer Genomics:
We develop advanced statistical methodology to enable a more meaningful interpretation of large scale multi-dimensional cancer genomic data. Specifically, we are applying tools from network theory, Bayesian statistics and machine learning to help address a variety of challenges in medical genomics and epigenomics, such as the characterisation of aberrant signalling pathway patterns in cancer, identification of cancer gene networks or the elucidation of the regulatory networks governing cancer stem cells.
Inflammatory Bowel Disease:
Inflammation is a key mechanism for maintaining immunological integrity. We aim to identify epigenetic factors contributing to Inflammatory Bowel Disease (IBD) by performing genome-wide screens in samples from IBD discordant monozygotic twins.
HEROIC:
The HEROIC Project provides a resource for functional studies into chromatin remodeling, mouse embryonic stem (ES) cell differentiation and regulation of the (epi)genome in general.
Human Epigenome Project:
Provides an epigenetic resource of genome-wide DNA methylation reference profiles in human tissues and cell lines.
The MHC Haplotype Project:
The MHC Haplotype Project provides genetic resources for association studies into inflammatory, autoimmune and infectious disease as well as forming a framework for population genetic studies.
The LRC Haplotype Project:
The LRC Haplotype Project provides genetic resources for association studies into inflammatory, autoimmune and infectious disease as well as forming a framework for population genetic studies.



 

Group Leader
Stephan Beck, PhD FMedSci
Prof. of Medical Genomics
UCL Cancer Institute
University College London
Paul O’Gorman Building
72 Huntley Street
London WC1E 6BT, UK
Tel: +44-20-7679-0964
s.beck@ucl.ac.uk

 

Research Projects

 

Group Members

 

Publications

 

Job Opportunities

 

Funded by: