RCAT
RCAT extracts rhythmic components such as period, amplitude, and phase from time-series datasets to analyze circadian clock gene expression and dynamics measured by NGS, microarray, RNA-Seq, and real-time luminescence/fluorescence reporting systems.
Key Features:
- Rhythmic component extraction: Computes period, amplitude, and phase from time-series expression and protein-level data.
- Input data types: Accepts time-series data from next-generation sequencing (NGS), microarray, RNA-Seq, Lumicycle® luminometer real-time fluorescence/luminescence recordings, and synthetic datasets from CircaInSilico.
- Quality estimation: Reports relative amplitude error (RAE) as a criterion for result quality assessment.
- Output formats: Produces tabular and visual outputs and saves results as CSV files for downstream analysis.
- Benchmarking and robustness: Validated with synthetic genome biology data from CircaInSilico across varying collection intervals and amplitude ranges.
Scientific Applications:
- Microarray and RNA-Seq analysis: Identification of core clock genes with significant periodicity from Gene Expression Omnibus (GEO) liver tissue datasets.
- Real-time fluorescence/luminescence reporting: Computation of period, amplitude, and phase from Lumicycle® luminometer recording datasets to analyze dynamic circadian responses.
Methodology:
Extraction of rhythmic components from time-series datasets using statistical analysis, with benchmarking against synthetic data from CircaInSilico and application to experimental NGS, microarray/RNA-Seq, and Lumicycle® time-series data.
Topics
Details
- License:
- MIT
- Cost:
- Free of charge
- Tool Type:
- library
- Operating Systems:
- Windows
- Programming Languages:
- Python
- Added:
- 12/15/2021
- Last Updated:
- 12/15/2021
Operations
Publications
Liu Z, Meng M, Zhang S, Qiu H, Liu Z, Huang M. Rhythmic Component Analysis Tool (RCAT): A Precise, Efficient and User-Friendly Tool for Circadian Clock Genes Analysis. Interdisciplinary Sciences: Computational Life Sciences. 2021;14(1):269-278. doi:10.1007/s12539-021-00471-2. PMID:34374039.