nanostring
nanostring performs automated, reproducible, and scalable processing and analysis of NanoString nCounter data for targeted quantification of gene expression across up to approximately 800 genes.
Key Features:
- Comprehensive analysis workflow: Includes quality control, data normalization, expression visualization, annotation with additional metadata, and preparation of input files for differential gene expression analysis.
- Batch processing: Processes multiple samples consistently to support high-throughput analyses.
- Reproducibility and scalability: Implemented as a Nextflow pipeline to enable reproducible and scalable execution across computing infrastructures.
- Portability and environment support: Supports Docker, Singularity, Podman, and Conda environments for deployment across diverse platforms.
- Open-source extensibility: Distributed as open-source code permitting extension and customization.
- Quality metrics reporting: Generates detailed quality metrics for all stages of the analysis.
Scientific Applications:
- Targeted gene expression profiling with NanoString nCounter: Quantification and analysis of expression for up to approximately 800 genes from nCounter assay data.
- Differential gene expression analysis: Produces normalized and annotated inputs suitable for downstream differential gene expression workflows.
Methodology:
Performs quality control, data normalization, expression visualization, annotation with additional metadata, and preparation of input files for differential gene expression analysis; implemented in the Nextflow workflow language and supports Docker, Singularity, Podman, and Conda.
Topics
Details
- Cost:
- Free of charge
- Tool Type:
- workflow
- Operating Systems:
- Mac, Linux, Windows
- Added:
- 5/18/2024
- Last Updated:
- 11/24/2024
Operations
Data Inputs & Outputs
Differential gene expression profiling
Publications
Peltzer A, Mohr C, Stadermann KB, Zwick M, Schmid R. nf-core/nanostring: a pipeline for reproducible NanoString nCounter analysis. Bioinformatics. 2024;40(1). doi:10.1093/bioinformatics/btae019. PMID:38212989. PMCID:PMC10805338.