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genomic PhD Projects, Programs & Scholarships

We have 153 genomic PhD Projects, Programs & Scholarships

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We have 153 genomic PhD Projects, Programs & Scholarships

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Determining the role of genomic instability in the response of leukaemias to chemotherapies

Treatment of leukaemia remains a significant challenge primarily due to disease recurrence. Gene mutations present at diagnosis inform clinical risk stratification and type of treatment, while the accumulation of additional genetic lesions accompanies progression of leukaemia. Read more

Enhanced variant interpretation for the discovery of mechanisms underpinning Ophthalmic genomic disorders

This project will utilize large genomic sequencing datasets from the 100,000 genomes project and the UK BioBank to understand how genomic variation impacts the development and function of cells vital for correct vision. Read more

Exploring evolutionary change through genomic sequencing of museum specimens

Next-generation sequencing has made it possible to sequence the genomes of museum specimens dating back several hundred years. In this project you will generate genomic data from museum specimens of birds, principally great tits. Read more

The genomic basis of obligate ant/plant symbioses

I am seeking a highly motivated PhD student to join this exciting project on the genomics of mutualism dependence using ant/plant symbioses as model systems. Read more

3D genome folding and its role in DNA-based processes

The organization of genomic DNA into chromatin fibres and nucleosomes and their regulation by histone modifications is well understood, as is the relevance of these mechanisms for gene regulation. Read more

Obtaining a genetic Diagnostic Yield via assessment of in-utero Scan findings prior to the introduction of SEquencing retrospectivelY (ODYSSEY) – a cohort study

  Research Group: Centre for Public Health
*Application closing date has been extended from 24 to 31 January 2022*. With the introduction of novel genomic technologies it is now possible to significantly shorten the diagnostic odyssey that children with rare disease and their parents endure. Read more

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