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consensus-sequences

Maintainer FreedomIntelligence · Last updated April 1, 2026

consensus-sequences.

OpenClawNanoClawAnalysisReproductionconsensus-sequencesopenclaw medical skillsadditional scientific toolsconsensus

Original source

FreedomIntelligence/OpenClaw-Medical-Skills

https://github.com/FreedomIntelligence/OpenClaw-Medical-Skills/tree/main/skills/consensus-sequences

Maintainer
FreedomIntelligence
License
MIT
Last updated
April 1, 2026

Skill Snapshot

Key Details From SKILL.md

2 min

Key Notes

  • Apply variants to reference FASTA using bcftools consensus.
  • samtools depth input.bam | awk '$3<10 {print $1"\t"$2-1"\t"$2}' > low_coverage.bed.

Source Doc

Excerpt From SKILL.md

Haplotype Options

OptionDescription
-H 1First haplotype
-H 2Second haplotype
-H AApply all ALT alleles
-H RApply REF alleles where heterozygous
-IApply IUPAC ambiguity codes (separate flag)

IUPAC Codes for Heterozygous Sites

Heterozygous sites encoded with IUPAC ambiguity codes:

  • A/G → R
  • C/T → Y
  • A/C → M
  • G/T → K
  • A/T → W
  • C/G → S

Mark Low Coverage as N

Using a mask BED file:

Use cases

  • Use consensus-sequences in research workflows aligned with this subject area.
  • Follow the upstream documentation for the full working procedure.

Not for

  • Do not rely on this catalog entry alone for installation or maintenance details.

Upstream Related Skills

  • variant-calling - Generate VCF for consensus
  • filtering-best-practices - Filter variants before consensus
  • variant-normalization - Normalize indels first
  • alignment-files/reference-operations - Reference manipulation

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