bcftools merge: Merge multiple VCF/BCF files from non-overlapping sample sets to create one multi-sample file

Metadata

Links

• bio.tools: BCFtools

EDAM Operations

• Data handling
• Variant calling

EDAM Topics

• GWAS study
• Genetic variation
• Genotyping experiment
• DNA polymorphism

Observed Tool Versions

Within GTN tutorials

1.10

• UseGalaxy.eu ⭐️
• UseGalaxy.fr ⭐️
• UseGalaxy.org (Main) ⭐️
• UseGalaxy.org.au ⭐️
• GalaxyTrakr
• UseGalaxy.be
• UseGalaxy.no

Relevant Tutorials

• Variant Analysis / Trio Analysis using Synthetic Datasets from RD-Connect GPAP