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RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
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High-throughput Identification of Gene Regulatory Sequences Using Next-generation Sequencing of Circular Chromosome Conformation Capture 4C-seq
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Basic4Cseq: an R/Bioconductor package for analyzing 4C-seq data.

Carolin Walter1, Daniel Schuetzmann1, Frank Rosenbauer1

  • 1Institute of Medical Informatics, University of Münster, 48149 Münster, Germany, and Institute of Molecular Tumorbiology, University of Münster, 48149 Münster, Germany.

Bioinformatics (Oxford, England)
|August 1, 2014
PubMed
Summary
This summary is machine-generated.

Basic4Cseq is a new R/Bioconductor package for analyzing 4C-seq data, offering filtering, quality control, and visualization of genomic interactions. It simplifies the processing of 4C-seq (Circular Chromosome Conformation Capture sequencing) data from raw reads to insightful visualizations.

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Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • 4C-seq (Circular Chromosome Conformation Capture sequencing) is a powerful technique for studying genome-wide interactions.
  • Analyzing 4C-seq data involves complex steps from raw reads to interpretable results.
  • Existing tools may lack comprehensive functionalities for basic filtering, analysis, and visualization.

Purpose of the Study:

  • To introduce Basic4Cseq, an R/Bioconductor package designed for the comprehensive analysis of 4C-seq data.
  • To provide users with essential tools for filtering, quality control, and visualization of 4C-seq experimental results.
  • To facilitate the near-cis visualization of genomic interactions derived from 4C-seq experiments.

Main Methods:

  • The package processes aligned 4C-seq raw data in Binary Alignment/Map (BAM) format.
  • It maps short reads to a virtual fragment library, including functions to create these libraries.
  • Includes optional filters for invalid reads and 4C-seq fragments, alongside basic quality controls.

Main Results:

  • Basic4Cseq enables the creation of virtual fragment libraries with detailed genomic information.
  • The package offers filtering capabilities for BAM files and 4C-seq fragments to refine data quality.
  • Visualizations include coverage plots and multi-scale contact profiles for data in the vicinity of the viewpoint.

Conclusions:

  • Basic4Cseq provides a user-friendly and efficient R/Bioconductor package for 4C-seq data analysis.
  • The package supports the entire workflow from raw data processing to advanced visualization.
  • Export options for Wig and CSV files allow for further analysis and integration with other bioinformatics tools.