WASP

WASP processes and analyzes Drop-Seq-based single-cell RNA-seq (scRNA-seq) data from protocols such as ddSEQ and 10x Genomics to perform quality control, demultiplexing, reference alignment, and generation of gene expression matrices for downstream analyses.


Key Features:

  • Supported sequencing protocols: Supports Drop-Seq-based scRNA-seq datasets generated using ddSEQ and 10x Genomics protocols.
  • Raw read processing and quality control: Processes raw reads and produces initial quality control metrics.
  • Demultiplexing and reference alignment: Performs demultiplexing and aligns reads to a reference to enable assignment of reads to cells.
  • Gene expression matrix generation and metrics: Generates demultiplexed gene expression matrices accompanied by quality metrics.
  • Modular input handling: Accepts pre-processed gene expression matrices from external sources as well as matrices produced by its own processing steps.
  • Downstream analyses: Supports detection of differentially expressed genes, clustering of cellular populations, and graphical visualization of results.

Scientific Applications:

  • Cellular heterogeneity analysis: Enables identification and characterization of (sub-)cellular populations and cell-type specific expression patterns.
  • Domain-specific research: Applicable to developmental biology, oncology, immunology, and regenerative medicine for cell-resolved gene expression studies.

Methodology:

Initial quality control, demultiplexing, reference alignment, generation of demultiplexed gene expression matrices and quality metrics, handling of pre-processed matrices, detection of differentially expressed genes, clustering of cellular populations, and graphical visualization.

Topics

Details

License:
GPL-3.0
Tool Type:
workflow
Operating Systems:
Mac, Linux, Windows
Programming Languages:
R, Python
Added:
1/2/2022
Last Updated:
1/2/2022

Operations

Publications

Hoek A, Maibach K, Özmen E, Vazquez-Armendariz AI, Mengel JP, Hain T, Herold S, Goesmann A. WASP: a versatile, web-accessible single cell RNA-Seq processing platform. BMC Genomics. 2021;22(1). doi:10.1186/s12864-021-07469-6. PMID:33736596. PMCID:PMC7977290.

PMID: 33736596
PMCID: PMC7977290
Funding: - BMBF: FKZ 031A533 - DFG: KFO 309 P2/P5/P6/P7/P8/Z01, SFB-TR84 B/08, SFB1021 Z02

Documentation

Links