Human whole genome resequencing

Whole Genome Sequencing (WGS) is the use of high-throughput sequencing platforms to perform whole genome sequencing on different individuals or populations of humans, utilizing bioinformatics methods to obtain whole genome sequences and comprehensively explore genetic variations at the DNA level, including significant structural variations. The sequencing cycle is short, the data coverage is uniform, and it can be used for detecting copy number and structural variations, fusion gene detection, virus integration site detection, and non coding region mutation detection. To screen the pathogenic and susceptible genes of diseases, study the pathogenesis and genetic mechanisms, and provide important information on human evolution and population genetics.

Service Advantages

High quality: Stable output of high-quality sequencing data, multi-layer sample quality control to ensure data quality

01/05

Wide detection range: detecting high-precision and sensitive variation information across the entire genome

02/05

Detecting genetic diversity: comprehensively exploring various genetic variations, especially some large structural variations

03/05

Uniform coverage: Effective data coverage is uniform and can detect virus integrated genomic regions

04/05

Rich experience in sample processing, involving various experimental samples such as tissues, cells, whole blood, serum, plasma, FFPE, etc

05/05

Service Process

experimental design

nucleic acid extraction

library construction

High throughput sequencing

Bioinformatics analysis

Delivery Results

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raw data

analysis report

Service&Support

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.