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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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Related Experiment Video

Updated: Nov 6, 2025

Integration of Wet and Dry Bench Processes Optimizes Targeted Next-generation Sequencing of Low-quality and Low-quantity Tumor Biopsies
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Integration of Wet and Dry Bench Processes Optimizes Targeted Next-generation Sequencing of Low-quality and Low-quantity Tumor Biopsies

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NGScloud2: optimized bioinformatic analysis using Amazon Web Services.

Fernando Mora-Márquez1, José Luis Vázquez-Poletti2, Unai López de Heredia1

  • 1GI Sistemas Naturales e Historia Forestal, Dpto. Sistemas y Recursos Naturales, ETSI Montes, Forestal y del Medio Natural, Universidad Politécnica de Madrid, Madrid, Spain.

Peerj
|May 7, 2021
PubMed
Summary
This summary is machine-generated.

NGScloud2 is an updated bioinformatic system for cloud-based RNA sequencing analysis, offering cost savings and expanded tools for various genomic applications. It provides accessible infrastructure for complex data analysis.

Keywords:
AWSBioinformaticsCloud computingFunctional annotationNext generation sequencingTranscriptomics

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • NGScloud was an early cloud-based system for de novo RNAseq analysis of non-model species.
  • Rapid advancements in cloud computing and bioinformatics tools rendered NGScloud obsolete.
  • NGScloud2 has been developed to address these limitations and provide an updated solution.

Purpose of the Study:

  • To present NGScloud2, an enhanced bioinformatic system for cloud-based genomic data analysis.
  • To enable efficient and cost-effective analysis of various next-generation sequencing data types.
  • To provide accessible cloud computing infrastructure for researchers lacking specialized hardware.

Main Methods:

  • NGScloud2 leverages cloud computing infrastructure, specifically Amazon Web Services (AWS), with optimized instance types and spot instance capabilities for cost savings.
  • The system incorporates updated and common applications for de novo RNAseq analysis.
  • It includes tools for reference-based RNAseq, RADseq, and functional annotation workflows.

Main Results:

  • NGScloud2 successfully processed pipelines for de novo RNAseq, reference-based RNAseq, RADseq, and functional annotation using real experimental data.
  • Workflow performance estimates and optimization tips are provided.
  • A qualitative comparison with the Galaxy framework is presented.

Conclusions:

  • NGScloud2 offers an enhanced and expanded platform for cloud-based genomic data analysis, improving upon its predecessor.
  • The system optimizes access to large-scale computing resources, making advanced bioinformatic tools accessible to a wider range of users.
  • Code and companion utilities are publicly available to facilitate adoption and downstream analysis.