We are seeking to appoint a new Bioinformatician to perform cutting-edge research into genome regulation and identification of novel therapeutic targets for rare disease.
You will be motivated by the power of genomics to inform rare disease diagnosis and excited by the promise of genome-targeted therapies for the treatment of rare disease. You will lead analysis of large-scale 'omics datasets, including genomic sequencing (e.g. Genomics England and UK Biobank), RNA-sequencing, and ribosome profiling data to develop new insights, uncover novel rare disease diagnoses, and identify new therapeutic targets.
You will join the Computational Rare Disease Genomics Team, who collectively use computational genomics to understand mechanisms underlying rare human disease to enhance diagnosis and treatment. We have a highly collaborative, open-science approach. We have a strong commitment within the group to both personal and professional development, and you will be encouraged to develop your own ideas, attend scientific seminars and conferences, and build your research profile. This project represents an exciting opportunity to work in a highly collaborative research environment, interfacing with the new MRC centre of research excellence in Therapeutic Genomics.
You will be responsible for performing detailed analysis of large genomic datasets, including data processing, statistical analyses, interpretation and presentation. Where appropriate, you will develop novel analytical and statistical approaches. You will take responsibility for day-to-day management and development of the research project, keep up-to-date with the scientific literature relevant to the role and project, write research articles and project reports, and give seminars/research talks to disseminate your research findings
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