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Related Concept Videos

RNA-seq03:21

RNA-seq

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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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Analyzing Multifactorial RNA-Seq Experiments with DiCoExpress
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DaMiRseq-an R/Bioconductor package for data mining of RNA-Seq data: normalization, feature selection and

Mattia Chiesa1, Gualtiero I Colombo1, Luca Piacentini1

  • 1Immunology and Functional Genomics Unit, Centro Cardiologico Monzino, IRCCS, 20138 Milan, Italy.

Bioinformatics (Oxford, England)
|December 14, 2017
PubMed
Summary
This summary is machine-generated.

DaMiRseq provides a robust R framework for analyzing high-dimensional RNA-Seq data. This tool effectively reduces noise and bias, enabling accurate biomarker discovery and classification for transcriptome profiling.

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • High-throughput transcriptome profiling using RNA-Seq is crucial for differential gene expression analysis and biomarker discovery.
  • Analyzing high-dimensional genomic data presents significant computational challenges.

Purpose of the Study:

  • To introduce DaMiRseq, a flexible R package designed for systematic analysis of RNA-Seq data.
  • To provide a framework for noise reduction, feature selection, and accurate classification in high-dimensional genomic datasets.

Main Methods:

  • DaMiRseq utilizes an organized framework to preprocess and analyze RNA-Seq data.
  • The package incorporates methods for noise and bias removal.
  • Feature selection algorithms are employed to identify the most informative genomic features.

Main Results:

  • DaMiRseq facilitates efficient noise and bias reduction in transcriptome data.
  • The framework enables accurate classification of samples based on genomic features.
  • It supports effective biomarker discovery from high-dimensional RNA-Seq datasets.

Conclusions:

  • DaMiRseq offers a powerful and convenient solution for analyzing complex RNA-Seq data.
  • The package enhances the utility of RNA-Seq for biomarker discovery and classification.
  • It is a valuable tool for researchers working with high-throughput genomic data.