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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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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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functional evolution 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
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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
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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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dependents can obtain a degree TUITION FREE A generous retirement plan and so much more! Salary Grade: T23 Learn more about the “T” salary structure here: https://careers.temple.edu/sites/careers/files
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BAP-2026-481 Is the Job related to staff position within a Research Infrastructure? No Offer Description Inactivation of the Prolyl Endopeptidase-Like (PREPL) gene on chromosome 2p21 causes a recessive