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Molecular Biology (genomic) PhD Projects, Programmes & Scholarships

We have 66 Molecular Biology (genomic) PhD Projects, Programmes & Scholarships

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We have 66 Molecular Biology (genomic) PhD Projects, Programmes & Scholarships

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Conservation management of the Isle of Wight red squirrel population

The Evolutionary Significant Unit (ESU) concept was developed to provide a rational basis for prioritizing conservation effort. it defines unique population(s) that have evolved independently (Ryder, 1986). Read more

A Multi-Omics approach to understanding cardiovascular risk in patients with End-Stage Kidney Disease

Background. End-stage Kidney failure, also known as End-Stage Kidney Disease (ESKD), is the final, irreversible stage of chronic kidney disease (CKD), where kidney function has worsened to the point that the kidneys can no longer function independently. 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

Epi-Genomic and Epi-Transcriptomic Aberrations in Breast Cancer Brain Metastasis

A SFI funded PhD position is available within the Department of Surgery, Royal College of Surgeons, Dublin, Ireland for a highly motivated person with an upper second or first class honours degree or Masters degree in clinical biology or a related subject. Read more

The Mechanisms of Epigenetic Regulation in Ageing and Age-Related Neurodegeneration

We are seeking a bright, talented, and highly motivated PhD student to lead a project investigating basic mechanisms of epigenetic regulation and their involvement in ageing and age-related neurodegeneration. Read more

Self funded BMS Project: Understanding the population dynamics of haematopoietic stem cells during gene therapy for sickle cell disease

Applications accepted for PhD Only. Background. This project builds on the recent discovery that whole genome sequencing approaches in blood stem and progenitor cells can be used to estimate the number of actively contributing blood stem cells in humans (Lee-Six et al., Nature 2018). Read more

De Novo Mutations and Human Disease

De novo mutations (DNMs) are a significant contributor to human disease, affecting ~1:300 new births. We study the mechanisms by which these spontaneous mutations arise in the first instance, concentrating on the tissue where most originate, the human testis. Read more

De Novo Mutations and Human Disease

De novo mutations (DNMs) are a significant contributor to human disease, affecting ~1:300 new births. We study the mechanisms by which these spontaneous mutations arise in the first instance, concentrating on the tissue where most originate, the human testis. Read more

Building the skull - normal and abnormal development

Using a combination of patient samples and mouse models, we study the causes and developmental origins of skull malformation. The work ranges from screening human DNA for new mutations, to use of genome editing and single cell transcriptomics to model the developmental causes of these malformations in mice. Read more

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