We are looking for someone who has experience in the following areas;
- Bench marking genome analysis pipelines
- Performing computational analyses for a range of projects
- Monitoring quality of WGS data
- Carrying out alignment and variant calling
Ideally:
- Strong programming skills (Python, R)
- Experience with full cycle of analysing NGS data from sequencing
- Post-doctoral experience with Rare Diseases or genetics
- PhD (or equivalent experience) in Bioinformatics, Systems Biology or Genetics
- Experience handling large data sets and setting pipelines
- Strong understanding of inherited disease and human genetics
- Solid knowledge of family based analysis and knowledge of association testing
- Practical knowledge and understanding of statistics
