Section 8 RSlyser
8.1 Interface
Input
Step 1
: Input a list of genomic regions with two columns. The 1st column contains genomic regions in the format ofchr:start-end
(based onGRCm38/mm10
), and the 2nd column for the significance information (p-values between 0 and 1).Step 2
: Use genomic proximity or enhancer-promoter datasets to identify linked genes.Step 3
andStep 4
: A subnetwork of highly-scored genes is identified from a gene network (Step 3
), with the desired number of genes in the resulting subnetwork (Step 4
). The significance (p-value) of observing the identified subnetwork by chance can also be estimated by a degree-preserving node permutation test.More Controls
: Use additional parameters to fine-tune the steps described above.SUBMIT
: click the SUBMIT button to execute the analysis.
Output
- Example Output includes interactive tables and high-quality figures for the resulting subnetwork. A summary of input data and the runtime (computed on the server side) is also provided for reference.

FIGURE 8.1: The interface of RSlyser
, including the Show/Hide Info
toggle button with the help information on how to use the interface.
8.2 Results
- Under the
Input: Region-Level Summary Data
tab,An interactive table
lists user-input summary data.

FIGURE 8.2: User-input summary data under the Input: Region-Level Summary Data
tab returned for exploration.
- Under the
Output: Linked Genes
tab,An interactive table
lists genes linked from the input genomic regions.

FIGURE 8.3: An interactive table listing genes linked from the input genomic regions under the Output: Linked Genes
tab.
- Under the
Output: Gene Subnetwork
tab,A network visualisation
of the identified subnetwork is provided, along withAn interactive table
for the subnetwork genes.

FIGURE 8.4: A network visualisation of the resulting subnetwork under the Output: Gene Subnetwork
tab, with genes/nodes color-coded by linked gene scores, which range from 1 to 10.