Fix indentation of snippet

galaxyproject · Mar 8, 2024 · 2c4cb06 · 2c4cb06
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diff --git a/faqs/galaxy/analysis_troubleshooting.md b/faqs/galaxy/analysis_troubleshooting.md
@@ -33,10 +33,8 @@ When something goes wrong in Galaxy, there are a number of things you can do to
 
 5. **Ask for help!**
    - Where?
-    {% if include.sc %} -
-     - In the [Single cell user community](https://matrix.to/#/#Galaxy-Training-Network_galaxy-single-cell:gitter.im)
-     {% endif %}
-     - In the [GTN Matrix Channel](https://gitter.im/Galaxy-Training-Network/Lobby)
+     {% if include.sc %}- In the [Single cell user community](https://matrix.to/#/#Galaxy-Training-Network_galaxy-single-cell:gitter.im)
+     {% endif %}- In the [GTN Matrix Channel](https://gitter.im/Galaxy-Training-Network/Lobby)
      - In the [Galaxy Matrix Channel](https://gitter.im/galaxyproject/Lobby)
      - Browse the [Galaxy Help Forum](https://help.galaxyproject.org/) to see if others have encountered the same problem before (or post your question).
    - When asking for help, it is useful to [share a link to your history]({% link faqs/galaxy/histories_sharing.md %})
diff --git a/topics/single-cell/index.md b/topics/single-cell/index.md
@@ -3,7 +3,7 @@ layout: topic
 topic_name: single-cell
 ---
 
-{% snippet faqs/galaxy/analysis_troubleshooting.md %}
+{% snippet faqs/galaxy/analysis_troubleshooting.md sc=true %}
 
 ## Want to explore analysis beyond our tutorials?
 

diff --git a/topics/single-cell/tutorials/scrna-case_alevin-combine-datasets/tutorial.md b/topics/single-cell/tutorials/scrna-case_alevin-combine-datasets/tutorial.md
@@ -126,7 +126,7 @@ REMEMBER TO ADD THE CODE FOR SNIPPETS BACK IN
 
 {% snippet topics/single-cell/faqs/single_cell_omics.md %}
 
-{% snippet faqs/galaxy/analysis_troubleshooting.md %}
+{% snippet faqs/galaxy/analysis_troubleshooting.md sc=true %}
 
 ## Concatenating objects
 

diff --git a/topics/single-cell/tutorials/scrna-case_alevin/tutorial.md b/topics/single-cell/tutorials/scrna-case_alevin/tutorial.md
@@ -145,7 +145,7 @@ Additionally, to map your reads, you will need a transcriptome to align against
 
 {% snippet topics/single-cell/faqs/single_cell_omics.md %}
 
-{% snippet faqs/galaxy/analysis_troubleshooting.md %}
+{% snippet faqs/galaxy/analysis_troubleshooting.md sc=true %}
 
 ## Generate a transcript to gene map
 

diff --git a/topics/single-cell/tutorials/scrna-case_basic-pipeline/tutorial.md b/topics/single-cell/tutorials/scrna-case_basic-pipeline/tutorial.md
@@ -118,7 +118,7 @@ You can also pull the data from publicly available [Single Cell Expression Atlas
 
 {% snippet topics/single-cell/faqs/single_cell_omics.md %}
 
-{% snippet faqs/galaxy/analysis_troubleshooting.md %}
+{% snippet faqs/galaxy/analysis_troubleshooting.md sc=true %}
 
 # Filtering
 

diff --git a/topics/single-cell/tutorials/scrna-case_trajectories/tutorial.md b/topics/single-cell/tutorials/scrna-case_trajectories/tutorial.md
@@ -64,7 +64,7 @@ We will use the same sample from the previous three tutorials, which contains la
 
 {% snippet topics/single-cell/faqs/single_cell_omics.md %}
 
-{% snippet faqs/galaxy/analysis_troubleshooting.md %}
+{% snippet faqs/galaxy/analysis_troubleshooting.md sc=true %}
 
 # Prepare datasets