RMDisease V2.0 an updated database of genetic variants that affect RNA modifications with disease and trait implication
The following options are available:
Input Data: Standard VCF file of a specific species.
Genome Assembly: Genome assembly selected for analysis. (default: Human/hg19)
Modification Type: Modification type selected for analysis. (default: m6A)
Association Level: The association level (AL) between genetic variant and RNA modification site, AL ranges from 0 to 1 with 1 indicating the greatest impact of the variant on modification status. Users can tune this value. (default: 0.4)
E-mail Address: A notification will be sent to the Email when your job is finished.