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Annotation, Visualization and Impact Analysis

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Analysis of Genomic Variations with AVIA

AVIA Cascade Filtering Request

In this tool, you can set up a variant data reduction method by filtering mutations in the 1000 Genomes Project, HapMap, CGI Populations, dbSNP or removing variants using user specified SIFT/Polyphen2 cutoffs. Then you can annotate the remaining variants using AVIA.   Please read our FAQ or Tutorials for detailed information.If you do not have any data to start with, click on the button below labeled 'Sample BED data' for a self guided tutorial.

Section I. Input Data (Required)

A field with an asterisk (*) before it is a required field.

Name your submission (optional):If name exists, AVIA will add timestamp
  (?)
-- or --
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*Input format:
*Organism and build
*E-mail address:
You will be notified by email when the process is complete
*Confirm E-mail address:

Section II. Cascade Filtering Parameters

1) Select Filter database:

Section III. Annotation and Visualization Parameters

By clicking this box, I am verifying that I have read the full disclaimer and I fully understand that the information provided for me by AVIA is for research purposes only. The ABCC, FNLCR, and the NIH or any of the linked websites do not approve use of this information for diagnostic purposes.