Whole Genome Bisulfite Sequencing

DNA methylation at the C5 position of cytosine plays a crucial role in gene expression and chromatin remodeling. Perturbations in methylation patterns are associated with tumorigenesis, neurodegenerative diseases and neurological disorders. Bioinformatic analysis of methylomes is widely used in various research areas, including studies on gene regulation, cell differentiation, embryogenesis, aging, occurrence and development of disease, phenotypic diversity and evolution in plants and animals.

Category:

Novogene provides whole genome bisulfite sequencing (WGBS) to efficiently identify methylated cytosines on a genome-wide scale with a single nucleotide resolution. The deep reach of the methylome is imperative for understanding gene expression and multiple biological processes that are subject to epigenetic regulation.

Applications

  • Novogene delivers high-quality data and publication-ready analysis results of WGBS services, to faciliate research including:
  • Profiling methylation patterns at CG, CHG and CHH sites with single nucleotide resolution
  • Identifying differentially methylated sites associated with experimental treatments or sample conditions
  • Understanding mechanisms of cell differentiation or tissue development on the basis of methylation profiles
  • Early diagnosis of diseases and cancers through the detection of DNA hypermethylation or hypomethylation

Benefits

  • Hundreds of projects have been successfully completed with highly professional, publication-quality data output and bioinformatics analysis.
  • Ultra-low input DNA and high bisulfite conversion rate are available in methylation library preparation.
  • Industry-standard software (such as Bismark) and mature in-house pipelines are used for mapping and comprehensive bioinformatics analysis.
  • Customized association analysis can explore correlations between methylation and gene expression.

Specifications: DNA Sample Requirements

Sample Type Required Amount Purity
Genomic DNA ≥ 200 ng A260/280=1.8-2.0

Specifications: Sequencing and Analysis

Platform Type Illumina NovaSeq 6000
Read Length Paired-end 150 bp
Sequencing Depth ≥ 30× coverage for the species with reference genome
Standard Data Analysis   Data Quality Control

  mCs detection, methylation level calculation

  Methylation level and frequency distribution

  Differentially Methylated Site (DMS) detection

  Differentially Methylated Regions (DMRs), Differentially Methylated Promoter (DMPs) detection and annotation

  Function enrichment of DMR-associated genes and DMP-associated genes

  Visualization of BS seq data

  Comparative analysis (among samples)

Project Workflow

Novogene provides high-quality products and expert services throughout the entire project workflow. Every step is carefully designed and executed to meet rigorous scientific standards, ensuring exceptional research outcomes. To guarantee the accuracy and reliability of sequencing data, stringent quality control (QC) measures are implemented at each stage of the process. The workflow encompasses key steps such as sample preparation and quantification, library preparation, library quality control, sequencing, and bioinformatics analysis.

Whole Genome Bisulfite Sequencing

GeneSmart tự hào là đơn vị tiên phòng đầu tiên tại Việt Nam cung cấp giải pháp:

1. Giải trình tự tế bào đơn (SINGLE-CELL SEQUENCING);

2. Chuẩn bị mẫu tự động (AUTOMATED LIQUID HANDLING);

3. Xét nghiệm và chẩn đoán bệnh nhiễm (DIAGNOSIS OF INFECTIOUS DISEASE);

4. Sinh chiết lỏng (LIQUID BIOPSY)

5. Giải phẫu bệnh sinh học phân tử (MOLECULAR PATHOLOGY)

6. Nghiên cứu ung thư (CANCER RESEARCH)

7. Nghiên cứu miễn dịch (IMMUNOLOGY)

8. Khoa học hình sự (FORENSIC)

9. Trữ mẫu sinh học (Ngân hàng sinh học, BIOBANKING)

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