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Exome sequencing

Exome sequencing (WES) is the process of sequencing the entire gene coding region of the human genome, which is approximately 3 nucleotides in size. Exons and untranslated regions (UTRs) only account for 1-2% of the human genome, but contain up to 85% of disease-related gene mutations. Under the same sequencing flux, exome sequencing has higher sequencing depth and coverage for the target region than whole genome resequencing. Therefore, this technology has high detection sensitivity for common and rare chromosomal variations occurring in the exon region. Its simplicity, economy, and efficiency have made it a popular technology in recent years.
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Service Advantages

Provide a comprehensive bioinformatics solution

Provide a comprehensive bioinformatics solution

01/03
Good uniformity of reads distribution improves sequencing preference

Good uniformity of reads distribution improves sequencing preference

02/03
Our independently developed genomic data analysis methods and algorithms provide advanced analysis for various genetic diseases and tumor directions

Our independently developed genomic data analysis methods and algorithms provide advanced analysis for various genetic diseases and tumor directions

03/03

Service Process

experimental design

experimental design

Library preparation

Library preparation

High throughput sequencing

High throughput sequencing

Bioinformatics analysis

Bioinformatics analysis

Delivery Results

If you have any other requirements, please send an email to order@gentlegen.com,We will serve you as soon as possible.

Mutation identification

Experimental result files

Sequencing raw data

Analyze data and analyze result files

Service&Support

Inquiry and ordering

Inquiry and ordering

Directly log in to GentleGen GBS Online Ordering System,Automatically obtain quotes and place orders; stay“Data Download”Download the corresponding service subscription form and send an email. We will provide you with a quotation as soon as possible.

Data Download

Data Download

Product manual download、order form

ordering information

ordering information

email:marketing@gentlegen.com Phone: 0512-67998818, ext. 8888

Sample Preparation

Nucleic acid ≥ 500g, concentration ≥ 10ng/μ l

Nucleic acid ≥ 500g, concentration ≥ 10ng/μ l

Application Direction

Conduct mutant related research

1/5

Characterizing the relationship between genotype and phenotype

2/5

Disease Research

Cancer, Mendelian diseases, complex diseases, population studies
3/5

Representing the level of the group

Characterize multiple low-frequency genotypes at the population level
4/5

Regional mutations

Discovering mutations in exon regions and exploring their relationship with genetic diseases, complex diseases, tumors, and other diseases
5/5

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