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bio-consensus-sequences - Generate consensus FASTA sequences from VCF variants

Generates consensus FASTA sequences by applying VCF variants to a reference sequence using bcftools consensus.

Tags

Updated: 2026-09-24

Capabilities

Typical Inputs

Typical Outputs

What this skill does

  • Apply VCF variants to reference
  • Extract sample specific haplotypes
  • Encode IUPAC ambiguity codes
  • Mask low coverage regions
  • Generate coordinate chain files
  • Normalize VCF variant records

Inputs

  • Reference FASTA file
  • VCF variant file
  • BED mask file
  • BAM alignment file

Outputs

  • Consensus FASTA file
  • Coordinate chain file

Requirements

  • bcftools 1.19+
  • samtools 1.19+
  • bedtools 2.31+
  • minimap2 2.26+
  • BioPython 1.83+
  • cyvcf2

Source

  • Spec: SKILL.md

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bioinformatics
bcftools
vcf
fasta
consensus-sequence
genomics
Apply VCF variants to reference
Extract sample specific haplotypes
Encode IUPAC ambiguity codes
Mask low coverage regions
Reference FASTA file
VCF variant file
BED mask file
Consensus FASTA file
Coordinate chain file