User Guide:

Get the somatic mutation profile in the specific clinical parameter that user choose and get the p-values from Fisher's exact test in the selected clinical parameter.

• Gene: Select gene input format (Gene symbol,Gene Accession,NCBI Gene ID) and enter your gene of interest. You can enter multiple, separated by Comma.(Limit 10).
• Cancer selection: Select Cancer by clicking on the one you are in interest. It can also be selected multiple.
• Clinical Parameter: Select the clincial parameter.
• Data Type: Select the data type for somatic mutation analysis. Somatic mutations can be detected using either DNA-seq or RNA-seq alone, or by combining the results from both sequencing datasets, referred to as "DNA-seq + RNA-seq".