With advancements in next-generation sequencing technology, whole genome re-sequencing (WGS) has become the most rapid and effective method to identify the genetic variations in individuals of the same species or between related species. The variation information such as single nucleotide polymorphism (SNP), insertion and deletion (InDel), copy number variation (CNV), and structural variation (SV) obtained through re-sequencing is used in population genetics research and genome-wide association studies (GWAS). These powerful tools are used to investigate the causes of diseases, to select plants and animals in agricultural breeding programs, and to identify common genetic variations among populations.
Advanced Analysis ‒ Population Genetics Research and GWAS analysis
Novogene Advantages
  • Scalable Sequencing Capacity 
  • Competitive Pricing
  • Extensive In-House Bioinformatics Expertise
Service Highlights
  • Comprehensive standard and advanced analysis pipeline
  • Customized analysis to meet your research needs
  • Best-in-class and widely recognized software
Novogene Powered Literature
* For Research Use Only. Exclusive for Clients in North and South America.

Novogene Corporation Inc.

8801 Folsom Blvd #290, Sacramento, CA 95826

916-252-0068-383     inquiry_us@novogene.com     en.novogene.com

Copyright©2011-2021 Novogene Corporation
All Rights Reserved. Information and specifications are subject to change at any time without notice.