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researchers investigating the molecular and biophysical mechanisms underlying genome function and regulation. Areas of interest include, but are not limited to: Chromatin and chromosome architecture and their
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the organization of DNA and its relation to the dynamic 3D-structured chromosomes. The student will form a part of our new NEST initiative funded by the Wallenberg AI, Autonomous Systems and Software Program (WASP
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and regulation. Areas of interest include, but are not limited to: Chromatin and chromosome architecture and their mechanistic roles in gene regulation RNA processing, modification, localisation, and
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to:•Chromatin and chromosome architecture and their mechanistic roles in gene regulation•RNA processing, modification, localisation, and decay•Genome stability and repair pathways•Mechanisms of transcriptional
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. In-depth knowledge of DNA methylation and X-chromosome biology. Merits: Experience working in a highly international and multicultural team. Excellent communication and scientific presentation skills
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Hirszfeld Institute of Immunology and Experimental Therapy Polish Academy of Sciences | Poland | about 2 months ago
, identification of chromosomal rearrangements and haplotypes, as well as direct assessment of DNA methylation. In parallel, bioinformatics analyses will be conducted, including data quality control, alignment
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the role of aneuploidy, or chromosome copy number changes, in cancer-related processes. We are looking to hire a computational biologist who will work closely with other scientists in the Sheltzer Lab to aid
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diseased neural circuits. We pursue a multi-disciplinary approach integrating data across biological scales in the brain, including molecular Chromosome-Conformation-Capture sequencing technologies, single
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circuits. We pursue a multi-disciplinary approach integrating data across biological scales in the brain, including molecular Chromosome-Conformation-Capture sequencing technologies, single-cell imaging
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for evaluating and improving early intervention services for children under five with cerebral palsy, chromosome abnormalities, and rare genetic disorders. The project is led by Dr Benjamin T. Sharpe, Senior