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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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Genomics02:02

Genomics

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Genomics is the science of genomes: it is the study of all the genetic material of an organism. In humans, the genome consists of information carried in 23 pairs of chromosomes in the nucleus, as well as mitochondrial DNA. In genomics, both coding and non-coding DNA is sequenced and analyzed. Genomics allows a better understanding of all living things, their evolution, and their diversity. It has a myriad of uses: for example, to build phylogenetic trees, to improve productivity and...
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Next-generation Sequencing03:00

Next-generation Sequencing

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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
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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.
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Genome Annotation and Assembly03:36

Genome Annotation and Assembly

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The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.
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Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
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Related Experiment Video

Updated: Feb 21, 2026

Transcriptomic Analysis of C. elegans RNA Sequencing Data Through the Tuxedo Suite on the Galaxy Project
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Transcriptomic Analysis of C. elegans RNA Sequencing Data Through the Tuxedo Suite on the Galaxy Project

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Viewing RNA-seq data on the entire human genome.

Eric M Weitz1, Lorena Pantano2, Jingzhi Zhu3

  • 1National Center for Biotechnology Information, U.S. National Library of Medicine, Bethesda, MD, 20894, USA.

F1000Research
|October 6, 2017
PubMed
Summary

RNA-Seq Viewer is a new web tool for visualizing genome-wide expression data from NCBI databases. This application prototype allows researchers to easily explore RNA sequencing data from SRA and GEO.

Keywords:
RNA-seqideogramjavascriptnext generation sequencing

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Area of Science:

  • Bioinformatics
  • Genomics
  • Computational Biology

Background:

  • Accessing and visualizing large-scale RNA sequencing data from public repositories like NCBI's Sequence Read Archive (SRA) and Gene Expression Omnibus (GEO) can be challenging for researchers.
  • There is a need for user-friendly tools to facilitate the exploration of genome-wide expression patterns.

Purpose of the Study:

  • To develop and present RNA-Seq Viewer, a novel web application for visualizing genome-wide expression data.
  • To enable researchers to easily access and interpret expression data from SRA and GEO.

Main Methods:

  • A web application prototype was developed during a three-day hackathon.
  • The backend data pipeline was built and deployed on Amazon Web Services (AWS) EC2 instances.
  • Source code was made publicly available on GitHub.

Main Results:

  • RNA-Seq Viewer provides a platform for visualizing genome-wide expression data.
  • The application integrates data from NCBI's SRA and GEO databases.
  • A functional prototype was successfully developed and deployed.

Conclusions:

  • RNA-Seq Viewer offers a valuable resource for researchers studying gene expression.
  • The tool simplifies the process of exploring large-scale transcriptomic datasets.
  • The open-source nature of the code encourages community development and adoption.