seqplots
seqplots visualizes signal profiles and heatmaps from high-throughput sequencing (HTS) datasets to examine chromatin function and gene expression.
Key Features:
- Rapid Visualization Generation: Produces profile plots and heatmaps showing average signal or stacked rows of signal coverage over specified genomic features such as promoters and gene bodies.
- Support for HTS Assays: Handles signal data from ChIP-seq, RNA-seq, DNase-seq, and MNase-seq experiments for comparative visualization.
- Comprehensive File Format Support: Accepts major genomic file formats as input to ensure compatibility with diverse sequencing datasets.
- Motif Density Calculation: Calculates and plots user-defined motif density profiles derived from reference genomes.
- Advanced Plot Customization: Provides configurable parameters for profile plots and heatmaps to tailor visual output.
- Batch Processing Capabilities: Supports batch generation of multiple plots for large-scale analysis.
- Integration with R/Bioconductor: Offers an R/Bioconductor package for integration into R-based bioinformatics workflows.
Scientific Applications:
- Chromatin Modification and Factor Binding Analysis: Visualizes ChIP-seq signal distributions to assess chromatin modifications and transcription factor binding across genomic regions.
- Gene Expression Studies: Visualizes RNA-seq signal to evaluate gene expression changes and regulatory patterns.
- Chromatin Structure Assays: Visualizes DNase-seq and MNase-seq data to examine chromatin accessibility and nucleosome positioning.
Methodology:
Organizes heatmaps using clustering algorithms and computes user-defined motif density profiles from reference genomes.
Topics
Collections
Details
- License:
- GPL-3.0
- Tool Type:
- command-line tool, library
- Operating Systems:
- Linux, Windows, Mac
- Programming Languages:
- R
- Added:
- 1/17/2017
- Last Updated:
- 12/10/2018
Operations
Publications
Stempor P, Ahringer J. SeqPlots - Interactive software for exploratory data analyses, pattern discovery and visualization in genomics. Wellcome Open Research. 2016;1:14. doi:10.12688/wellcomeopenres.10004.1. PMID:27918597. PMCID:PMC5133382.
Funding: - Wellcome Trust: 101863