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Onderzoeker

Elfride De Baere

  • Trefwoorden:medical genetics, transcriptomics, genomics, functional genomics, human molecular genetics, chromosome conformation capture, UMI-4C, 4C, cis-regulation, Xenopus, retina, Pore-C, clinical genomics, inherited blindness, gene therapy, cellular models, antisense oligonucleotide therapy, inherited retinal diseases, transcription factors, gene editing, enhanceropathies, Hi-C, gene regulation, 3D genome, induced pluripotent stem cells, CRISPR/Cas9, genetic eye diseases, animal models, enhancers, structural variants
  • Disciplines:Analyse van next-generation sequence data, Oogheelkunde, Klinische genetica en moleculaire diagnostiek, Medische epigenomics, Moleculaire diagnostiek, Medische genomics, Ontwikkelingsbiologie, Genetica, Medische transcriptomics, Bio-informatica van ziekten, Stamcelbiologie, Bio-informatica data-integratie en netwerkbiologie