Genome Browser VCF+tabix Track Format
Filtering of VCF Files
VCF‐Server: A web‐based visualization tool for high‐throughput variant data mining and management - Jiang - 2019 - Molecular Genetics & Genomic Medicine - Wiley Online Library
A spectrum of free software tools for processing the VCF variant call format: vcflib, bio-vcf, cyvcf2, hts-nim and slivar | PLOS Computational Biology
Learning the VCF format
MoMI-G tools — MoMI-G 1.0.0 documentation
Formato Variant Call - Wikipedia, la enciclopedia libre
GitHub - OpenGenomics/vcf-tools
vcftools
VIVA (VIsualization of VAriants): A VCF File Visualization Tool | Scientific Reports
problems with vcftools merge command - usegalaxy.org support - Galaxy Community Help
A spectrum of free software tools for processing the VCF variant call format: vcflib, bio-vcf, cyvcf2, hts-nim and slivar | PLOS Computational Biology
Scaling Genomic Workflows with Spark SQL BGEN and VCF Readers | Databricks Blog
VIVA (VIsualization of VAriants): A VCF File Visualization Tool | Scientific Reports
Open-source tools for working with GWAS-VCF | Download Scientific Diagram
The Variant Call Format (VCF): A Standard Format for Representing and Processing Genetic Variation Callsets Derived from Next-Generation Sequencing Data | PDF | Single Nucleotide Polymorphism | Genetics
VCF.filter | BockLab
VCFTools 1.0 Download (Free trial) - vcftools.exe
VCF Format – NGS Analysis
vcftools installation in Centos 7.4 - YouTube
VCF Plotein · GenoCat.tools
How to Combine/Merge multiple vCard (VCF) files into One File?
modules/vcftools
Haploid mode by jydu · Pull Request #69 · vcftools/vcftools · GitHub
VCFTools Download: A simple to use application that enables you to quickly modify vCards fields, then convert them to CSV files or XLS/XLSX spreadsheets
Working with VCF Files
How to Install VCFTOOLS in any LINUX system by building from source - YouTube
vCard Splitter & Merger - Split & Merge VCF Files and Contacts
