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SeqAnt | A web service to identify and annotate DNA sequence variations

Simplifies variant annotation and filtering. SeqAnt can annotate sequencing experiments on the scale of thousands of whole-genome samples and tens of millions of variants in a web browser, while also integrating the first natural-language search engine that enables filtering using English phrases. The software allows to find alleles of interest without significant computer science training, improves reproducibility, and reduces annotation and filtering costs for large experiments.

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SeqAnt classification

  • Animals
    • Homo sapiens

SeqAnt specifications

Unique identifier:
Alternative name:
Sequence Annotator(SeqAnt)
Restrictions to use:
GNU General Public License version 2.0
Registration required:
Sequence Annotator
Web user interface
Programming languages:
Javascript, Perl, PHP
Computer skills:


  • bystro

SeqAnt support


  • Thomas Wingo <>
  • Alex Kotlar <>

Additional information



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Department of Human Genetics, Emory University School of Medicine, Atlanta, GA, USA; Division of Neurology, Atlanta VA Medical Center, Atlanta, GA, USA; Department of Neurology, Emory University School of Medicine, Atlanta, GA, USA

Funding source(s)

Supported by the Molecules to Mankind program (a project of the Burroughs Wellcome Fund and the Laney Graduate School at Emory University), Veterans Health Administration (BX001820), National Institutes of Health (AG025688) and Amazon AWS Educate grants.

By using OMICtools you acknowledge that you have read and accepted the terms of the end user license agreement.