What problem does it solve?
It turns a complex amplicon sequencing pipeline into a validated, reproducible run plan so you can process marker-gene data without guessing flags or looking up release-specific options.
Core Features & Use Cases
- Run the nf-core/ampliseq workflow for 16S, ITS, CO1, 18S, and other amplicon studies.
- Support paired-end Illumina, single-end Illumina, PacBio, and IonTorrent inputs, with optional primer trimming, quality filtering, taxonomic assignment, phylogenetic placement, and downstream diversity analysis.
- Use it to process a microbiome samplesheet, generate abundance tables and reports, or rerun a pinned release with the exact parameter set required by that version.
Quick Start
Ask the ampliseq skill to analyze your samplesheet, choose the desired pipeline version and profile, and produce a validated command for the output directory you want.