- The following options are available:
- Input Data: A list of human genetic variants. (VCF format, see example below)
- Genome Assembly: Currently supports human (assembly:hg19) only.
- Window: If selected 40, the 81 bp genomic ranges centered on variants will be extracted for screening.
- Statistical Significance: 0.01 or 0.05
- E-mail Address: A notification will be sent to the Email when your job is finished.
- Note: The web server is currently not supporting submitting job through iPhone & iPad.
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