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Cloud-native genomic dataframes and batch computing

A framework for state-of-the-art pre-trained bio foundation models on genomics and transcriptomics modalities.

tools for reading, writing, merging, and remapping SNPs

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.

Re-implementation of the CADA phenotype-based prioritization algorithm

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.

VCF Operations vCommunity Management Pack

vembrane filters VCF records using python expressions

Flexible Trio DNV detection on existing VCFs.

A Python utility to merge and deduplicate VCF (vCard) contact files.

Structural variant toolkit for VCFs

Highly Open Workflow for Annotation & Ranking toward genomic variant Discovery

Tiny Python script that reads all contacts from a CardDAV addressbook and inserts them into Asterisk's CID lookup database

Tools for parsing .vcf addressbook/contacts files

A lightweight Windows x64 GUI app that fliters a vcf file to contain only coding regions and adds coding sequence identifier information

Powerful statistics for VCF files

VMware Cloud Foundation on AWS with Elastic Volumes Service integration

VMware VCP, VVF, and VCF certification study materials and preparation resources