Related Experiment Video
Updated: Aug 8, 2025

09:36
Unbiased Deep Sequencing of RNA Viruses from Clinical Samples
Published on: July 2, 2016
17.1K
Agnostic Sequencing for Detection of Viral Pathogens
Nick P G Gauthier1, Samuel D Chorlton2, Mel Krajden3,4
1Department of Microbiology and Immunology, University of British Columbia, Vancouver, British Columbia, Canada.
Clinical Microbiology Reviews
|February 27, 2023
Summary
Viral metagenomics offers an agnostic approach to infectious disease diagnostics, sequencing all nucleic acids without prior pathogen knowledge. This review explores its potential for rapid outbreak response and clinical adoption challenges.
Area of Science:
- Microbiology
- Genomics
- Infectious Disease Diagnostics
Background:
- Next-generation sequencing (NGS) has advanced microbial genome analysis and diagnostics.
- Current targeted assays (PCR, NGS) require prior pathogen knowledge, missing novel or unknown threats.
- Public health crises highlight the need for rapid, agnostic diagnostic tools for emerging viral pathogens.
Purpose of the Study:
- To review advancements in metagenomic viral sequencing performance.
- To discuss current clinical applications of viral metagenomics.
- To identify challenges hindering widespread adoption in clinical laboratories.
Main Methods:
- Review of recent literature on viral metagenomics.
- Analysis of performance improvements in metagenomic sequencing.
- Examination of current clinical laboratory applications and challenges.
Main Results:
- Metagenomic techniques offer an untargeted approach, detecting all nucleic acids.
- Viral metagenomics is established in research but underutilized in clinical diagnostics.
- Improvements in sequencing performance are noted, but adoption barriers persist.
Conclusions:
- Viral metagenomics holds significant promise for rapid, agnostic detection of emerging viral pathogens.
- Overcoming challenges is crucial for integrating viral metagenomics into routine clinical diagnostics.
- Further development is needed to fully realize the potential of metagenomic diagnostics in public health.
Related Concept Videos
Sanger Sequencing
755.6K
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...
755.6K
RNA-seq
10.2K
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...
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
10.2K
Next-generation Sequencing
91.9K
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....
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
91.9K

