EcTracker
EcTracker detects and characterizes ectopic gene expression and cell- or tissue-specific transcripts in single-cell RNA sequencing (scRNA-seq) datasets to support analysis of aberrant and context-specific transcriptional programs.
Key Features:
- CellEnrich: Identifies genes specifically enriched in particular cell types within scRNA-seq datasets.
- TissueEnrich: Detects tissue-specific gene expression patterns across sampled cells.
- Ectopic Expression Analysis: Identifies genes activated outside their normal regulatory contexts, including those arising from genomic alterations or pathological states.
- Regulon Analysis: Pinpoints transcription factors that regulate selected gene signatures and aids mapping of regulatory networks.
- Processing Speed and Add-on Modules: Implements rapid processing and supports modular add-on components to extend analytical functionality.
Scientific Applications:
- Analysis of genomic perturbations (CRISPRi): Detects ectopic and altered expression signatures resulting from CRISPR interference perturbations.
- Pathological state investigation: Identifies aberrant gene activation patterns associated with disease contexts.
- Reanalysis of developmental datasets: Reassesses datasets such as human embryonic stem cell differentiation into endoderm with SMAD2 knockout to resolve ambiguities in cellular identity and gene expression.
Methodology:
EcTracker leverages large-scale scRNA-seq data to perform integrative analyses that quantitatively assess cell- and tissue-specific transcripts, qualitatively identify ectopic expressions, and perform regulon analysis to map transcriptional regulatory networks.
Topics
Details
- Tool Type:
- library
- Operating Systems:
- Mac, Linux, Windows
- Programming Languages:
- R
- Added:
- 11/6/2021
- Last Updated:
- 11/6/2021
Operations
Publications
Gautam V, Mittal A, Kalra S, Mohanty SK, Gupta K, Rani K, Naidu S, Mishra T, Sengupta D, Ahuja G. EcTracker: Tracking and elucidating ectopic expression leveraging large-scale scRNA-seq studies. Briefings in Bioinformatics. 2021;22(6). doi:10.1093/bib/bbab237. PMID:34184038.