This option provides drug prioritization prediction with limited number of genes. Please select the mutated genes in the given table of signature genes.

This module is better than Option 1 in terms of performaces of models. This option requires a list of Hugo names of all the mutated genes of a genome. User may submit by pasting the list of upload the file with list.

This module uses the converted Variant Calling Format (VCF) file of genome sequencing. Since the VCF files are large in size, the user has to convert the VCF file to ANNOVAR input file and then upload it to server. The performances of models in this option is same as option2.

This module has same performace as option2 and uses the raw sequencing file in the form of Variant Calling Format (VCF). User has to submit the VCF file, which is well accepted format for variant information storage.