Related Experiment Video
Updated: Dec 27, 2025

10:36
Rare Event Detection Using Error-corrected DNA and RNA Sequencing
Published on: August 3, 2018
12.5K
Rapid Detection of Nocardia by Next-Generation Sequencing
Shan-Shan Weng1, Han-Yue Zhang1, Jing-Wen Ai1
1Department of Infectious Diseases, Huashan Hospital of Fudan University, Shanghai, China.
Frontiers in Cellular and Infection Microbiology
|March 6, 2020
Summary
Next-generation sequencing (NGS) improves Nocardia detection and diagnosis time for nocardiosis. A specific read count cutoff aids in differentiating disease cases.
Area of Science:
- Medical Microbiology
- Infectious Diseases
- Diagnostic Technologies
Background:
- Nocardiosis is a challenging bacterial infection requiring accurate and timely diagnosis.
- Traditional culture methods for Nocardia spp. can be slow and have limitations in detection rates.
Purpose of the Study:
- To evaluate the efficacy of next-generation sequencing (NGS) compared to culture for diagnosing Nocardia infections.
- To identify potential diagnostic criteria using NGS data for clinical application.
Main Methods:
- Retrospective review of nocardiosis cases diagnosed between 2014-2018.
- Comparison of culture and NGS methods for Nocardia spp. detection.
- Analysis of NGS-specific read counts in patients with and without nocardiosis.
Main Results:
- NGS demonstrated a higher detection rate for Nocardia spp. compared to culture.
- NGS significantly reduced the turnaround time for Nocardia diagnosis.
- A cutoff value based on the ranking of Nocardia-specific reads among the top two showed potential for clinical diagnosis.
Conclusions:
- NGS is a promising method for rapid and accurate diagnosis of nocardiosis.
- NGS offers advantages over traditional culture in terms of speed and sensitivity.
- Further validation of NGS-based criteria could enhance clinical decision-making for nocardiosis.
Related Concept Videos
Next-generation Sequencing
97.3K
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....
97.3K
RNA-seq
11.6K
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...
11.6K

