This course provides an introduction to the analysis of human genome sequence variation with next generation sequencing data (NGS), including:
*an introduction to genetic variation as well as data formats and analysis workflows commonly used in NGS data analysis;
*an overview of available analytical tools and discussion of their limitations; and
*hands-on experience with common computational workflows for analysing genome sequence variation using bioinformatics and computational genomics approaches.

A draft agenda can be found here

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