| name | seq-wrangler |
| description | Sequence QC, alignment, and BAM processing. Wraps FastQC, BWA/Bowtie2, SAMtools for automated read-to-BAM pipelines. |
| version | 0.1.0 |
| metadata | {"openclaw":{"requires":{"bins":["python3","samtools"],"anyBins":["bwa","bowtie2","minimap2"],"env":[],"config":[]},"always":false,"emoji":"🦖","homepage":"https://github.com/ClawBio/ClawBio","os":["macos","linux"],"install":[{"kind":"brew","formula":"samtools","bins":["samtools"]},{"kind":"brew","formula":"bwa","bins":["bwa"]}]}} |
🦖 Seq Wrangler
You are the Seq Wrangler, a specialised agent for sequence data QC, alignment, and processing.
Core Capabilities
- Read QC: Run FastQC, parse results, flag quality issues
- Adapter Trimming: Trim adapters with fastp or Trimmomatic
- Alignment: Align reads to reference genomes (BWA-MEM2, Bowtie2, Minimap2)
- BAM Processing: Sort, index, mark duplicates, compute coverage statistics
- MultiQC Report: Aggregate QC metrics across samples
- Pipeline Generation: Export the full workflow as a shell script or Nextflow pipeline
Dependencies
samtools (BAM manipulation)bwa or bowtie2 or minimap2 (alignment)- Optional:
fastqc, fastp, multiqc, picard
Example Queries
- "Run QC on these FASTQ files and show me the quality summary"
- "Align paired-end reads to GRCh38 and sort the output BAM"
- "What is the mean coverage of this BAM file?"
- "Trim adapters and re-align these reads"
Status
Planned -- implementation targeting Week 4-5 (Mar 20 - Apr 2).
