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Related Concept Videos

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.
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...
Genomics02:02

Genomics

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...
RACE - Rapid Amplification of cDNA Ends02:35

RACE - Rapid Amplification of cDNA Ends

Rapid Amplification of cDNA Ends, or RACE, is one of the most effective methods to obtain a full-length cDNA from an mRNA sequence between a known internal region to the unknown sequence at the 5’ or 3’ end. The unknown region is cloned in the cDNA by a gene-specific primer that binds the known end, and a hybrid primer that attaches a predefined anchor sequence to the unknown end of the cDNA. The sequence in between is amplified by PCR with an anchor primer and a gene-specific primer.
Since the...
Sanger Sequencing01:57

Sanger Sequencing

DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
Hybridoma Technology01:31

Hybridoma Technology

Hybridoma technology is used for the large-scale production of monoclonal antibodies. Monoclonal antibodies bind to only a single antigenic determinant or epitope. Such antibodies are used in research, diagnostics, and disease therapy. The hybridoma technology established in 1975 by Georges Köhler and Cesar Milstein was awarded the Nobel Prize in Medicine in 1984 for revolutionizing research and therapy.
Hybridoma Selection
Commonly used fusion techniques — electroporation, polyethylene glycol...

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Leveraging CyVerse Resources for De Novo Comparative Transcriptomics of Underserved (Non-model) Organisms
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CloVR: a virtual machine for automated and portable sequence analysis from the desktop using cloud computing.

Samuel V Angiuoli1, Malcolm Matalka, Aaron Gussman

  • 1Institute for Genome Sciences (IGS), University of Maryland School of Medicine, Baltimore, Maryland, USA. angiuoli@umiacs.umd.edu

BMC Bioinformatics
|September 1, 2011
PubMed
Summary
This summary is machine-generated.

Cloud Virtual Resource (CloVR) is a desktop application simplifying automated sequence analysis for microbial genomics. This portable virtual machine (VM) enables push-button analysis on local or cloud resources, making complex bioinformatics accessible.

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Next-generation sequencing (NGS) necessitates user-friendly, portable, and scalable bioinformatics tools.
  • Cloud computing offers on-demand infrastructure for high-throughput data analysis.

Purpose of the Study:

  • To introduce Cloud Virtual Resource (CloVR), a desktop application for automated sequence analysis.
  • To enable efficient utilization of local and cloud computing resources for bioinformatics workflows.

Main Methods:

  • CloVR is a portable virtual machine (VM) providing automated analysis pipelines for microbial genomics (16S, whole genome, metagenome).
  • The VM runs on personal computers with minimal installation, leveraging local resources.
  • CloVR supports remote cloud computing for enhanced performance in large-scale processing.

Main Results:

  • CloVR facilitates automated, push-button sequence analysis.
  • Demonstrated successful automatic processing of NGS data on multiple cloud platforms.
  • The VM integrates local and cloud resources for scalable bioinformatics.

Conclusions:

  • CloVR reduces the complexity of implementing advanced bioinformatics protocols.
  • The architecture supports both local and cloud-based high-throughput data processing.
  • Lowers the barrier to entry for complex genomic data analysis.