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of nanofabricated sample supports and tracking algorithms for 5D electron diffraction (5DED). EMAT is one of the leading electron microscopy centers in the world and has a vast expertise in both fundamental and
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, Belgium ) and Dr. An-Sofie Schoonjans (Pediatric Neurology Department UZA) are seeking a highly motivated PhD student to work on clinical data analyses and multi-omics approaches in the rare genetic
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, genomics, computational and systems biology. Charcot-Marie-Tooth disease (CMT) represents the most common genetic disorder of the peripheral nervous system. Patients experience progressive distal muscle
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to neurodegenerative diseases of the central and peripheral nervous system, with an emphasis on understanding the genetic etiology and developing diagnostics and treatment methods for these diseases. Approaches range
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towards CRC. The presence of genetic differences, including single nucleotide polymorphisms (SNPs), in mucin genes can give rise to a large repertoire of structurally diverse mRNA isoforms via alternative
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, biochemistry, genomics, bacterial genetics and bioinformatics. You can work both independently as well as in an international team You can plan and perform laboratory experiments accurately You have strong
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are highly polymorphic and gene polymorphisms affecting mucin gene expression have been reported to influence susceptibility towards CRC. The presence of genetic differences, including single nucleotide