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Related Concept Videos

RNA-seq03:21

RNA-seq

12.6K
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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Ribosome Profiling02:24

Ribosome Profiling

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Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique...
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Informatics for RNA Sequencing: A Web Resource for Analysis on the Cloud.

Malachi Griffith1, Jason R Walker2, Nicholas C Spies2

  • 1McDonnell Genome Institute, Washington University School of Medicine, St. Louis, Missouri, United States of America; Siteman Cancer Center, Washington University School of Medicine, St. Louis, Missouri, United States of America; Department of Genetics, Washington University School of Medicine, St. Louis, Missouri, United States of America.

Plos Computational Biology
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Summary

This guide introduces RNA sequencing (RNA-seq) molecular biology and bioinformatics. Open-access tutorials and pipelines cover RNA-seq analysis, from quality control to differential expression and splicing.

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Area of Science:

  • Molecular Biology
  • Bioinformatics
  • Genomics

Background:

  • Massively parallel RNA sequencing (RNA-seq) is a key technology for studying RNA.
  • Understanding RNA-seq requires knowledge of both molecular biology and computational analysis.
  • Existing resources for RNA-seq training are often fragmented or inaccessible.

Purpose of the Study:

  • To provide a comprehensive introduction to fundamental RNA-seq concepts.
  • To offer open-access tutorials covering the entire RNA-seq analysis workflow.
  • To make training resources, pipelines, and datasets readily available to researchers.

Main Methods:

  • Detailed explanation of RNA-seq molecular biology principles.
  • Introduction to essential bioinformatics concepts and tools for RNA-seq.
  • Development and provision of cloud-based tutorials and analysis pipelines.

Main Results:

  • Open-access tutorials are available covering cloud computing and tool installation.
  • Training materials include RNA-seq file formats, reference genomes, and annotation.
  • Methods for quality control, expression analysis, differential expression, and alternative splicing are detailed.

Conclusions:

  • Comprehensive RNA-seq training resources are now accessible.
  • The provided materials facilitate robust RNA-seq data analysis.
  • Researchers can utilize these resources for efficient transcriptomic studies.