Analyzing patient history and NGS data.
Downloading data from platform server.
Filtration of variants based on different criteria.
Classification of variants based on ACMG and AMP guidelines.
Interpreting genetic data (somatic and germline) according to cancer types.
Using data from different literature, research to recommend finding and therapies and summarize results for oncologist
Critical curation of literature and specific gene panels
Preparing report.
Develop and implement bioinformatics pipelines to make reports more effortlessly.
Collaborate with team to integrate findings.
Maintain databases and software for genomic analysis.
Maintain internal variant databases and update knowledge on new variants.
Checking variants in IGV files for checking reportability
Contribute to research projects and publications in clinical genomics.