diff --git a/_reader/RNAseqWorkshop.pdf b/_reader/RNAseqWorkshop.pdf
index cb58970bab7087441631133a445aa8af56be043d..880d75f5b3142d42f261f281882ed0a52cba3ba8 100644
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diff --git a/_reader/sections/01_section_linux.tex b/_reader/sections/01_section_linux.tex
index a8d6ac681566b2f447f5a4b1e5cf2d01eda3bf55..1a849576bc82708907da7bd44cb7502fa23e56a3 100644
--- a/_reader/sections/01_section_linux.tex
+++ b/_reader/sections/01_section_linux.tex
@@ -390,7 +390,7 @@ of the course we'll use a second Docker container for
 this.
 
 \begin{itemize}
-\item acquire the \il{rstudio_docker.tar} file from sciebo or the ``Raumlaufwereke" folder (as before) 
+\item acquire the \il{rstudio_docker.tar} file from sciebo or the ``Raumlaufwerke" folder (as before) 
 \item on the \emph{host} machine, open a new terminal
 \item run the following
 \end{itemize}
@@ -435,7 +435,7 @@ library(ggplot2)
 
 Let's assume you have an Excel file and want to do something to it using R. First, always, always
 use tab-delimited text files to move from program to program, no matter which programs you use. Look at
-the small tab-delimited txt file in the \$HOME/rnaseq-workshop/\_WorkshopReader/intro\_scripts\_data called "example\_table.txt" 
+the small tab-delimited txt file in the \$HOME/rnaseq-workshop/\_reader/intro\_scripts\_data called "example\_table.txt" 
 using a text editor (e.g. `gedit') or LibreOffice Calc (which is just like Excel 
 except free, open source, and Linux compatible). Next we'll import this into R
 \begin{lstlisting}
diff --git a/_slides/slides01_housekeeping.pdf b/_slides/slides01_housekeeping.pdf
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diff --git a/_slides/slides03_experimental.pdf b/_slides/slides03_experimental.pdf
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diff --git a/_slides/slides04_quantification.pdf b/_slides/slides04_quantification.pdf
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