
Scientist Position in Rare Skeletal Diseases Research
1 day ago
We are seeking a highly motivated scientist to join our research group focused on rare skeletal diseases. Our team uses cutting-edge methodologies, including whole-genome sequencing and RNA-sequencing, to identify disease-causing gene defects.
The successful candidate will work closely with molecular biologists, physicians, and bioinformaticians to actively participate in national and international collaborative research projects.
About the Project- We aim to recruit a postdoctoral researcher with a strong background in clinical genetics and bioinformatics.
- The project focuses on identifying new genetic causes for skeletal disorders with osteoporosis and abnormal mineral homeostasis.
- The study includes patients and families who suffer from these rare diseases.
We offer a creative and inspiring environment with wide-ranging expertise and interests. Our research is conducted in collaboration with other members of the team, emphasizing personal suitability.
Required Skills and QualificationsTo be eligible for this position, you must have a PhD or a foreign degree deemed equivalent to a Swedish PhD. Prior experience with a variety of genetic methods, such as exome and whole-genome sequencing data analysis, Sanger sequencing, and transcriptome analysis, is advantageous.
You should also have familiarity with high-performance computing environments, Linux, Python, R scripting, or other programming languages. Experience with variant interpretation and classification using the American College of Medical Genetics and Genomics (ACMG) guidelines would be beneficial.
BenefitsAs a member of our team, you will enjoy a competitive salary package and access to cutting-edge research facilities.
In addition, you will have opportunities to develop your skills and knowledge through professional development programs and collaborations with renowned researchers.
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