The Clinical NGS Data Analysis Nordic Workshop 2019 is dedicated to analysis of the data as well as the clinical interpretation of variants.
The Clinical NGS Data Analysis Nordic Workshop 2019 covers topics such as:
- The generation of the bam- and vcf- files that will be used in the subsequent filtering for variants
- Acquisition of sequencing data
- Variants will be evaluated using various databases and prediction tools to establish potential pathogenic variants
The Clinical NGS Data Analysis Nordic Workshop 2019 brings together:
- Researchers and students
- NGS users
- NHS & Private Labs
- Bioinformaticians
- CRO’s
- Biotech Companies
- Bioinformatics
- Service Providers and everyone interested in NGS
- Computational biology
- Biomarkers
- Data interpretation
- Data analysis
- Genetics
- DNA sequencing
- NGS data storage
- Infectious and inherited diseases
- Molecular and cell biology and molecular diagnostics
- Informatics
