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Updated
Jan 10, 2026 - Python
✂️ Cut and manage snippets of code easily with Snippy, your tool for quick access to reusable code blocks and streamlined workflows.
VarFish: comprehensive DNA variant analysis for diagnostics and research
VCF Generator Lite is a lightweight tool that quickly converts name and phone number lists into VCF files for batch import to mobile contacts.
vembrane filters VCF records using python expressions
Tools for parsing .vcf addressbook/contacts files
VMware Cloud Foundation architecture designs and deployment patterns
VMware VCP, VVF, and VCF certification study materials and preparation resources
VMware Cloud Foundation on AWS with Elastic Volumes Service integration
A species-agnostic BioSaaS platform that creates automated, natural-language clinical/functional reports and 3D protein visualizations from raw genomic data (FASTA/VCF/plain DNA sequence) using a modular, async pipeline.
Python tools for proteogenomics analysis toolkit
A collection of software to work with genomic variants
A Python utility to merge and deduplicate VCF (vCard) contact files.
Re-implementation of the CADA phenotype-based prioritization algorithm
A framework for state-of-the-art pre-trained bio foundation models on genomics and transcriptomics modalities.
Download public databases for VarFish
tools for reading, writing, merging, and remapping SNPs
VCF Operations vCommunity Management Pack
Flexible Trio DNV detection on existing VCFs.
Add a description, image, and links to the vcf topic page so that developers can more easily learn about it.
To associate your repository with the vcf topic, visit your repo's landing page and select "manage topics."