Be capable of navigating a Linux operating system and TACC's Lonestar system in particular
Understand common workflows and tools for NGS analysis:
- "Re-sequencing" - comparing raw sequence data to a reference genome, calling variants, and annotating variants DNA sequencing data
- RNA-seq - quantifying gene expression and determining splice variation from RNA-seq data
- de novo genome assembly and annotation

Understand the broadest definition of "biomedical/biological informatics" and where this course fits in
Learn and practice essential Linux concepts and commands, including where to get more help & information
Learn and practice working with TACC systems (Lonestar in particular)

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