Closed mistrm82 closed 6 months ago
A helpful slide deck: https://biohpc.cornell.edu/lab/doc/Variant_workshop_part1.pdf
sequencing depth considerations
Some content can also be taken from this old slide deck: https://github.com/hbctraining/In-depth-NGS-Data-Analysis-Course/blob/master/sessionVI/slides/Variant_Intro_rsk.pdf
cancer genomics: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5834793/
All advanced workshops begin with a markdown describing the technology. A bit of background on what it is and examples of its use. Also helpful would be considerations for when setting up a variant calling experiment
RNA-seq example and ChIP-seq example