SvAnna
======

Efficient and accurate pathogenicity prediction for coding and regulatory structural variants
in long-read genome sequencing.

SvAnna performs phenotype-driven prioritization of structural variants in VCF files,
focusing specifically on long-read WGS analysis of germline variants.


.. toctree::
   :maxdepth: 2
   :caption: Contents:

   quickstart
   setup
   running
   outputformats
   examples


.. enhancers