The areas of the genome that encode functional proteins are called exons. Whole exome sequencing (WES) is a next-generation sequencing (NGS) technique that allows for the efficient and cost-effective sequencing of the exome, which comprises the protein-coding regions of the genome. It provides valuable information about variations and mutations, which can be potential contributors to the aging process or age-related diseases. At CD BioSciences, our bioinformatics team provides one-stop technical services for your exome sequencing project.
CD BioSciences has developed a state-of-the-art WES platform that combines advanced sequencing technologies with robust bioinformatics analysis pipelines. Our comprehensive approach encompasses targeted capture, library preparation, sequencing, and data analysis, enabling us to provide our clients with accurate and detailed information on the genetic variations present in the exome.
Identification of genetic variants in aging
Utilizing WES, we can identify rare or common genetic variants that are associated with aging-related traits, including age-related diseases, longevity, or age-associated phenotypes.
Discovery of novel genes in aging
By examining the entire exome, we offer the service of discovering unknown genes that may be involved in the aging process.
Samples | DNA contents |
Fresh and frozen samples | ≥ 0.6 μg DNA |
FFPE samples | ≥ 0.8 μg DNA |
We offer a range of services for whole exome sequencing in aging research. Our workflow follows a standardized protocol that ensures reproducibility and data quality.
Fig. 1 Technical routes for whole exome sequencing.
Data Analysis Services | Details |
Genetic variations identification and annotation | We prioritize and annotate the identified variants based on their functional consequences and relevance to aging using databases. |
Pathway analysis | We perform pathway analysis to understand the biological processes and pathways associated with aging. |
CD BioSciences follows rigorous quality control measures throughout the entire workflow of WES to ensure the accuracy and reproducibility of the sequencing results. If you are interested in our services, please feel free to contact us or make an online inquiry.
All of our services and products are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.