Related Experiment Video
Updated: May 18, 2026

Next Generation Sequencing for the Detection of Actionable Mutations in Solid and Liquid Tumors
Published on: September 20, 2016
Application of next-generation sequencing in clinical oncology to advance personalized treatment of cancer
Yan-Fang Guan1, Gai-Rui Li, Rong-Jiao Wang
1Shenzhen Clinical Molecular Diagnostic Engineering Laboratory, BGI-Shenzhen, Shenzhen, Guangdong, People's Republic of China.
Abstract:
With the development and improvement of new sequencing technology, next-generation sequencing (NGS) has been applied increasingly in cancer genomics research over the past decade. More recently, NGS has been adopted in clinical oncology to advance personalized treatment of cancer. NGS is used to identify novel and rare cancer mutations, detect familial cancer mutation carriers, and provide molecular rationale for appropriate targeted therapy. Compared to traditional sequencing, NGS holds many advantages, such as the ability to fully sequence all types of mutations for a large number of genes (hundreds to thousands) in a single test at a relatively low cost. However, significant challenges, particularly with respect to the requirement for simpler assays, more flexible throughput, shorter turnaround time, and most importantly, easier data analysis and interpretation, will have to be overcome to translate NGS to the bedside of cancer patients. Overall, continuous dedication to apply NGS in clinical oncology practice will enable us to be one step closer to personalized medicine.
Insights
Next-generation sequencing (NGS) advances cancer genomics and personalized medicine by identifying mutations for targeted therapy. Challenges in data analysis and interpretation must be addressed for widespread clinical adoption.
Area of Science:
- Oncology
- Genomics
- Bioinformatics
Background:
- Next-generation sequencing (NGS) has become a vital tool in cancer genomics research.
- Its application is expanding in clinical oncology for personalized cancer treatment.
Purpose of the Study:
- To review the role and impact of NGS in cancer genomics and clinical oncology.
- To highlight the advantages and challenges of implementing NGS in cancer care.
Main Methods:
- Review of current applications of NGS in cancer research and clinical practice.
- Analysis of NGS capabilities in mutation detection and targeted therapy selection.
Main Results:
- NGS enables comprehensive sequencing of numerous cancer genes, identifying mutations and carriers for personalized therapies.
- It offers advantages over traditional methods in cost and scope of genetic analysis.
Conclusions:
- NGS is crucial for advancing personalized cancer medicine through precise mutation identification.
- Overcoming challenges in assay simplicity, throughput, turnaround time, and data interpretation is essential for clinical integration.
More Related Videos
13:24Integration of Wet and Dry Bench Processes Optimizes Targeted Next-generation Sequencing of Low-quality and Low-quantity Tumor Biopsies
Published on: April 11, 2016
05:17Detection of Targetable Alterations in Non-small Cell Lung Cancer using Next-generation Sequencing
Published on: October 10, 2025
Related Concept Videos
Next-generation Sequencing
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features.
Combination Therapies and Personalized Medicine
The combination of the drug acetazolamide and sulforaphane is a good example of combination therapy to treat cancer. The cells in the interior of a large tumor often die due to the hypoxic and...
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
Cancer
Pharmacogenomics: Identification of New Drug Targets