Collaborators: Katharina Trunk
Create and activate a conda environment
cd rna_seq
conda create --name yeast_tfe --file env.txt
conda activate yeast_tfe
Make sure FASTQ files are in the ./fastq subdirectory.
Run snakemake
./run_snake.sh
This will trim adapters, perform quality control, download genome files, map reads to the reference and count reads per gene.
Once snakemake is finished, we suggest using RStudio. If this is done on a different machinge (I run RStudio on a laptop), some data need to be copied over (see ./get_data.sh and ./rsync_include.txt). Once in RStudio, start in the top project directory. The first step is to create environment using renv:
install.packages("renv")
renv::restore()
This will install all necessary packages. Run the targets pipeline.
targets::tar_make()
This will carry out all the calculations, create figures (some as targets, some in ./fig directory) and output TSV files in directory ./tab.