Human Whole Genome Sequencing

Human whole genome Whole genome of animals and plants CycloneSEQ

Your location： Home· Service·Whole Genome Sequencing·Human whole genome

Whole Genome Sequencing (WGS) of humans involves sequencing the entire genome of different individuals or populations. Through sequence alignment, a large number of SNPs, insertion/deletion sites, structure variation and copy number variation sites can be identified. This comprehensive exploration of genetic variations at the DNA level provides crucial information for identifying disease-causing and susceptibility genes, as well as studying pathogenesis and genetic mechanisms.

Advantage 01

Rolling circle amplification constructs DNB sequencing library, PCR-free resequencing detects InDels more accurately. No worries about index hopping. Low duplication rate without manual intervention.

Advantage 02

DNBSEQ-T20 has ultra-high throughput, short cycles, and high cost-effectiveness.

Applications

Crowd Database Construction

Cohort Research

Health Plan

Drug Development

Complex Disease Research

Tumor Research

Technical procedure

Sample Detection

Library Construction

Sequencing

Data Quality Control

Bioinformatics Analysis

case analysis

ChinaMAP发布最大规模中国人群全基因组测序和表型研究成果

Research background

Research Strategy

Finding

代谢性疾病，包括2型糖尿病和肥胖症，是全球范围内日益严重的公共卫生问题，它们由不同的亚型组成，需要特定的诊断和治疗方法。理解这些疾病的遗传结构对于个体风险评估、预防和治疗至关重要。目前，通过大规模队列的全面遗传分析，可以系统地发现新的标志物和治疗靶点。群体基因组学的研究有助于深化我们对代谢性状和疾病遗传基础的理解，而全基因组关联研究（GWAS）和群体基因组测序项目进一步构建了与代谢性状相关的变异知识体系。