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Fully Funded PhD Position: Decoding Chromosome 1 Risk in AMD Using Stem Cell–Derived Retinal Models Host: Newcastle University (UNEW), UK Consortium: MSCA Innovative Training Network Pandora Start date
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contamination, or cytogenetics. • Familiarity with next-generation sequencing data or genomic variant analysis. • Familiarity with cytogenetic nomenclature or chromosome-level genomic data. • Experience using
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and multi-omic datasets; integrating genomic findings with clinical phenotypes; and supporting functional studies to evaluate relevant genes and variants associated with chromosome 9p disorders
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of Pathology. Laboratory testing includes but is not limited to chromosome analysis, chromosomal microarray and Fluorescent In-Situ Hybridization (FISH). Position includes opportunity for advancement
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. • Implement analysis and visualization workflows for repeat expansions, chromosome and cytogenetic findings, FISH results, whole-genome sequencing variants, and copy-number variants from genomic arrays
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numerical simulations to understand molecular mechanisms of epigenetic regulation by the Polycomb and Trithorax group proteins. Project description Chromosomal rearrangements of the human MLL1 gene
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. Thorough knowledge of theories and principles of human genetics, including knowledge of cell cycle, meiosis and mitosis; knowledge of chromosomal aberrations and associated clinical features; knowledge
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including chromosome analysis, FISH, chromosomal microarray, MLPA, and DNA and RNA sequencing. The successful candidate should possess strong interpersonal skills and experience with lab operations. They will
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of protein-coding genes, alternative splicing, long noncoding RNAs, microRNAs, and sex chromosomes across organs and species, as well as their phenotypic implications. We currently offer a range of possible
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, and sex chromosomes across organs and species, as well as their phenotypic implications. We currently offer a range of possible projects addressing the evolution of gene expression and its regulatory