| Table of Contents | ||
|---|---|---|
|
...
In the ‘2.Setup’ section, you downloaded 3 nfcore/sarek runs to H:/workshop/sarek/runs. These represent sarek variant calling results from the 3 exercises run in session 2:
...
SNPeff creates its own variant analysis reports (html reports) for each sample, which can be seen here:
H:/workshop/sarek/runs/run2_trio/results/reports/snpeff/haplotypecaller
We’ll be creating our of reports, with some additional functional information, using R.
...
Click ‘Knit’ to generate the report. It will ask you to name the file and ask where to save the file. Call it ‘test’ and save it in H:/workshop
...
You will see it generates the test html report.
...
In RStudio, select ‘File’ → “Open File”
Browse to H:/workshop/sarek/runs/run3_liver
Select the ‘modify.R’ file and click ‘Open’.
Open the ‘function_report.Rmd’ file in the same way (it’s in the same location as modify.R)
...
This sets the working directory you want to run the analysis from. This needs to be the same directory where you ran your sarek script from, i.e. where the sarek ‘results’ directory is.
IMPORTANT: while the modify'R script can be run from anywhere, you'll need to copy the function_report.Rmd script to this working directory, because that R markdown script calls to subdirectories from its location.
Line 69: maingroup <- "C1"
...