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Whole Genome Sequencing Data Analysis (WGS)



Description

Whole Genome Sequencing (WGS) is the use of high-throughput sequencing technology to sequence the whole genome of individuals or groups to find sequence or structural variation and other information. For species with known genomes, genome sequencing is carried out on different individuals (such as patients and normal individuals) or different tissues of an individual (such as diseased tissues and normal tissues). Differences between individuals or between tissues and cells can be found at the overall level. Through this method, we can find a large number of variation information such as Single nucleotide Variants (SNV) Insertion Deletion (Indel), Structural Variation (SV) and Copy Number Variation (CNV), so as to find the pathogenic genes and mutations of the disease, analyze the pathogenesis of the disease, population genetic mechanism and obtain population genetic characteristics.



Applications

Whole genome sequencing analysis can be used for the following research, but it is not limited to the following research:

  • Single gene inherited disease;
  • Complex disease;
  • Cancer Research;
  • Mutation site;
  • DNA Testing;
  • Group research;

Turnaround Time

Depending on the number of samples and the quality and size of the sample data.


Objectifs

We can mine the genetic variation at the DNA level based on the whole genome sequencing data by virtue of the excellent bioinformation analysis technology. Our unique skills in data analysis can meet customers' personalized data analysis needs and provide you with comprehensive data analysis results.

  • Data quality control, remove joint contamination and low quality data;
  • Align to reference genome sequence, statistical sequencing depth and coverage;
  • SNP / InDel / SV / CNV detection, annotation and statistics;
  • Circos diagram display of genome variation;


Importante Note

In addition, we can tailor the content of whole-genome biological information analysis according to your specific project needs. BBL provides general analysis and customized analysis of whole genome sequencing data analysis. Experienced teams of scientists, researchers, and technicians, we provide fast turnaround, high-quality data reports at competitive prices for worldwide customers. Customers can contact our employees directly and we will respond promptly. If you are interested in our services, please contact us for more detailed information.

Data Analysis Workflow