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Update tutorial.md #5602
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@@ -63,10 +63,10 @@ In this tutorial will use the following datasets: | |||
## [A] Marker Genes: | |||
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We'll start with two input datasets of marker genes (Study sets): | |||
* **Marker genes per cell cluster:** This dataset lists the genes that are significantly different in each cell cluster. | |||
* **Marker genes per condition (wt and ko):** This dataset lists the genes that are significantly different between the wild-type (wt) and knockout (ko) conditions. | |||
* **Marker genes per cell cluster:** This dataset lists the genes that are differentially enriched different in each cell cluster. |
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* **Marker genes per cell cluster:** This dataset lists the genes that are differentially enriched different in each cell cluster. | |
* **Marker genes per cell cluster:** This dataset lists the genes that are differentially enriched in each cell cluster. |
@@ -134,7 +134,7 @@ To perform GO enrichment analysis on each cell cluster individually, we need to | |||
> 1. {% tool [Split file](toolshed.g2.bx.psu.edu/repos/bgruening/split_file_on_column/tp_split_on_column/0.4) %} with the following parameters: | |||
> - {% icon param-file %} *"File to select"*: `Markers_cluster` (Input dataset) | |||
> - *"on column"*: `c1` | |||
> - *"Include the header in all splitted files?"*: `Yes` | |||
> - *"Include the header in all split files?"*: `Yes` |
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> - *"Include the header in all split files?"*: `Yes` | |
> - *"Include the header in all splitted files?"*: `Yes` |
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Unfortunately, the tool itself says 'splitted', so we have to make sure the tutorial text matches the tool text in the Graphical User Interface / Galaxy interface, otherwise people can get confused.
Some great catches here, thanks! Check the suggestions above and commit or change, and we should be able to review and merge this! |
TODO: