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Data vizualisation & manipulation
vlebars edited this page Apr 25, 2024
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To load a DESeq2 output file, click on the Browse... button on the top left corner and select the file you would like to analyse.

Once the file is loaded, the dataframe should now appear on the main page. With the panel on the left side (see next image), you can filter the table by several criteria:
- You can use the
Log2FoldChange Thresholdslider if you want to filter genes based on their differential expression level (By default all genes are kept). - In the same way, you can use the
padj Thresholdslider to filter genes that have a padj value above the chosen threshold (By default all genes are kept). -
DE typebuttons are to select which type of differential expression you want to see : "Both" shows down and up regulated genes (positive & negative Log2FoldChange), "Down" shows only down regulated genes (negative Log2FoldChange), and "Up" shows only up regulated genes (positive Log2FoldChange). - Two checkboxes allows you to filter if you want to see only protein coding genes & only known genes.

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Save current tablebutton on top of the table allows to save the dataframe with all the filters applied to it (sorting of rows are not saved however).
After loading the file, you can click on the Volcano Plot button
- It generates volcano plot. The data points displayed correspond with the filters applied on the side panel, like for the main table. You can see information about each point by hovering your mouse on it. It should update whenever you change your filters on the table.
