This repository made for certification course BIOINFORMATICS FOR BIOLOGISTS: ANALYSING AND INTERPRETING GENOMICS DATASETS by WELLCOME CONNECTING SCIENCE.

In this cousre i learned about:

• Next Generation Sequencing and its significance in genomics,
• the installation of widely-used bioinformatics tools,
• the use of different file formats
• Linux commands for sequence quality control, mapping, and variant calling.
• The analysis was also performed using the workflow management system Nextflow and applied to viralrecon, an existing bioinformatics pipeline.
• Downstream analysis included RStudio data visualization of variants obtained from genomic data sample.