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Related Concept Videos

RNA-seq03:21

RNA-seq

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 microarray-based...
Next-generation Sequencing03:00

Next-generation Sequencing

The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features.

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Related Experiment Video

Updated: May 23, 2026

Leveraging CyVerse Resources for De Novo Comparative Transcriptomics of Underserved (Non-model) Organisms
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Eoulsan: a cloud computing-based framework facilitating high throughput sequencing analyses.

Laurent Jourdren1, Maria Bernard, Marie-Agnès Dillies

  • 1École normale supérieure, Institut de Biologie de l'ENS, INSERM U1024, Paris, France. eoulsan@biologie.ens.fr

Bioinformatics (Oxford, England)
|April 12, 2012
PubMed
Summary
This summary is machine-generated.

We created Eoulsan, a scalable framework for analyzing high-throughput sequencing data. It automates sample analysis on cloud computing clusters, with costs and running times scaling linearly with data size and resources.

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • High-throughput sequencing generates massive datasets requiring efficient analysis.
  • Existing frameworks may lack scalability or ease of use for cloud environments.

Purpose of the Study:

  • To develop a modular and scalable framework for automated high-throughput sequencing data analysis.
  • To enable users to easily set up cloud computing clusters for genomic data processing.

Main Methods:

  • Developed Eoulsan, a framework based on the Hadoop MapReduce algorithm.
  • Implemented in Java and supported on Linux systems.
  • Tested on Amazon Web Services cloud infrastructure.

Main Results:

  • Eoulsan demonstrated modularity and scalability for high-throughput sequencing data analysis.
  • Cloud computation cost scaled linearly with the number of instances.
  • Running time scaled linearly with increasing data amounts.

Conclusions:

  • Eoulsan provides an efficient and cost-effective solution for large-scale genomic data analysis.
  • The framework facilitates automated analysis pipelines in cloud environments.
  • Its linear scalability ensures performance with growing datasets.