In the first part of this course you will learn to use a number of fundamental concepts and tools for genomic and metagenomic data, including:
- file formats, FastA, FastQ and SAM,
- sequence assembly (e.g. Velvet),
- short read alignment (Bowtie2 and Tablet),
- sequence preprocessing,
- sequence comparison and BLAST post-processing,
- genome browsers, MEGAN,
- taxonomic analysis of 16S data and
- functional analysis of metagenome data.
In the second part of the course you will use some of the introduced tools to perform a complete analysis of a mystery dataset.