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 3andStep 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 Datatab,An interactive tablelists 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 Genestab,An interactive tablelists 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 Subnetworktab,A network visualisationof the identified subnetwork is provided, along withAn interactive tablefor 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.