bwa

Use BWA for aligning sequencing reads to a reference genome for variant calling pipelines. Use when mapping short-read Illumina data to reference genomes for variant calling pipelines.

$ Instalar

git clone https://github.com/benchflow-ai/skillsbench /tmp/skillsbench && cp -r /tmp/skillsbench/shared_workspace/dna-variant-calling/environment/skills/bwa ~/.claude/skills/skillsbench

// tip: Run this command in your terminal to install the skill