AnyVLM |version|
!!!!!!!!!!!!!!!!
**AnyVLM** is an off-the-shelf solution for adding local aggregate-level variant information to a `Variant-Level Matching (VLM) network `_. It provides a REST API service that integrates with GA4GH standards for genomic data exchange.
AnyVLM enables genomic research organizations to:
- **Ingest VCF files** containing variant and allele frequency data
- **Register variants** using the GA4GH Variant Representation Specification (VRS) via AnyVar
- **Store cohort allele frequencies** (CAF) with zygosity-stratified counts
- **Serve VLM protocol-compliant responses** with Beacon handover capabilities
This service is designed for rare disease variant frequency tracking in genomic research networks such as `GREGoR `_.
If you're setting up AnyVLM for the first time, begin with the :doc:`Getting Started guide `, which covers different installation options. To learn how to use AnyVLM as a service, see :doc:`Usage `. For further assistance, please refer to :doc:`Getting Help `.
.. toctree::
:maxdepth: 2
:caption: Contents
:hidden:
Getting Started
Features
Usage
Configuration
API Reference
Getting Help
Changelog
Contributing
Project Roadmap
License