The Centre for Genetic Epidemiology (CGE) within Institute for Clinical Epidemiology and Applied Biometry is looking for researchers with expertise from diverse backgrounds such as genetic epidemiology, statistical genetics, mathematics, Machine learning/artificial intelligence, and bioinformatics. CGE has a long-standing experience in studying the genetic architecture of complex diseases including neurodegenerative diseases using state-of-the-art approaches such as exome/genome sequencing, Mendelian randomization, machine learning, artificial intelligence, deep learning, etc. We seek to unravel the role of common and rare variants in Parkinson’s disease by utilizing a variety of genetic epidemiological approaches. A variety of techniques including next-generation sequencing, machine learning, Bayesian approaches, and the use of standard statistical-genetics packages such as PLINK, SKAT, and meta-analytical approaches will be applied to understand the genetic etiology of PD. CGE is leading large-scale international projects funded by various organizations such as DFG and Michael J Fox Foundation, USA.
CGE is a part of multinational consortia and has access to high-quality next-generation sequencing data. We are developing a comprehensive database for Parkinson’s disease, and as such we are looking for interesting candidates to join our team.
Postion 1 (Statistical Genetics), 3 years, full time:
The candidate should have experience in conducting genome-wide association studies, and next-generation sequencing analyses such as whole genome sequencing and transcriptomics (single cell and bulk RNA sequencing). It is expected that a candidate will supervise graduate students. This position will require extensive engagement with partners nationally and internationally, thus flexibility and strong interpersonal skills are required to lead a multinational project. In addition, the candidate will lead monthly virtual meetings, prepare minutes, and will also be involved in project management. The previous publication track record in the above-mentioned approaches will be required.
The candidate will lead the ongoing GWAS analyses and will play an important role in analyzing ongoing whole-genome sequencing analysis. The candidate should have expert-level knowledge of R. Advanced knowledge of statistical-genetics approaches and programming languages such as GWAS analyses, copy number variation, Mendelian randomization, and Python is required. The track record in the above-mentioned approaches will be considered an asset during selection.
Additional skills in machine learning, and programming languages such as C++, and Java and database management with MySQL will be an asset, but not mandatory. Knowledge of cloud computing will be an asset. Prior working experience in neurodegenerative disease is not mandatory. The position will provide valuable experience to the candidate and will offer a chance to lead their projects. The position will require communication with research groups around the globe. Strong personal communication skills will be required to coordinate projects with various labs around the globe. The position will be for three years, and further extension will be possible depending upon the performance and availability of funds.
Position 2 (Data analyst), 3 years, full-time:
We are looking for a full-time data analyst who will be involved in epidemiological, sociodemographic, and clinical data curation, harmonization, integration, and analysis. In addition, the candidate will be involved in building a clinical glossary from electronic Case Report Forms (eCRFs). The candidate will be responsible for the deployment and maintenance of the data and computing platform. The candidate will work closely with other team members on the design and implementation of statistical, ML/AI analysis workflows and visualization tools.
We are seeking a candidate with a doctoral degree in computational biology, bioinformatics, or related fields, with an interest in biomedical informatics and transla