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This PhD project aims to uncover novel genetic contributors to ALS using whole genome sequencing (WGS). You will work with a unique biobank of 250 well-characterized ALS patients established in the Slachtova Lab and integrate genomic data with detailed clinical information. Your work will help reveal disease mechanisms and contribute to future precision medicine approaches for patients with ALS.
Job Responsibility
Analyse whole genome sequencing data from ALS patients
Identify known and novel genetic variants linked to ALS and explore genotype–phenotype relationships using clinical data
Work with large-scale genomic datasets using bioinformatics tools, collaborate with neurologists, geneticists, and other experts
Requirements
Master students
Doctoral candidate
PhD-holder
Curious, self-motivated person who enjoys learning new things
Likes working with large datasets, solving complex problems, and collaborating with others