Automatically updates terminal window title to reflect the current high-level task. Use at the start of every Claude Code session when the user provides their first prompt, and whenever the user switches to a distinctly new high-level task. Helps developers manage multiple Claude Code terminals by providing clear, at-a-glance identification of what each terminal is working on.
WHAT YOU BECOME
Perfect for these scenarios
Process VCF/BCF files to identify genetic variants in NGS data
Compute read coverage across genomic regions for QC or visualization
Convert between SAM, BAM, CRAM, VCF, BCF formats for compatibility
Extract specific genomic regions from large alignment files
MEASURED GAIN
Proven benefits and measurable impact
Reduce NGS data processing time with efficient BAM/VCF handling
Simplify workflows by eliminating external tool dependencies
Optimized performance for large-scale genomic datasets
WHAT YOU GET
Files, tags and the three-step install
Tip: Read the documentation and the code before first use, so you know what it does and which permissions it needs.
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