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Whole Genome Bisulfite Sequencing (WGBS) is a bisulfite sequencing method that enables the detection of DNA methylation at the whole-genome level. This encompasses the analysis of methylation at CpG sites and less common non-CpG sites, including CNG. The detection and quantification of methylation are of critical importance for the understanding of gene expression and other processes that are subjected to epigenetic regulation.
Applications

Construct genomic-scale DNA methylation profiles

Investigate for DNA methylation patterns in diseases

Explore the spatiotemporal-specific modification of genomic DNA methylation
Advantages

Unsurpassed data quality
It is our policy to provide single base resolution in our coverage area and a bisulfite conversion rate of at least 99%

Wide detection range
WGBS offers a comprehensive range of assays that facilitate the genome-wide detection of methylation sites

Professional team
We can provide assistance with the design of experiments and the interpretation of data from our team of experienced experts

Reliable and fast turnaround time
A dedicated project manager could be assigned, and the results would be provided within 30 business days of sample quality verification
Sample Requirements

Note: Sample amounts are provided for reference only. For detailed information, please contact us with your customized requests.

Our Comprehensive Service
At LC Sciences, we offer a genome-wide microRNA expression profiling service utilizing a microarray detection system that was developed specifically for microRNA detection. Send us your total RNA sample and we’ll perform all the necessary functions from sample QC through data analysis. We can perform microarray analysis on a single sample to create a simple expression profile or we can hybridize two samples to the same microarray for “dual sample” analysis. This is very useful whenever comparison of two samples is needed such as wildtype vs. mutant or samples treated in two different ways.
Our “Total RNA to Data” comprehensive service includes: Sample QC, Sample Preparation and Labeling, microRNA Detection (hybridization to a µParaflo® microfluidics chip), Array Scan and Data Extraction, and Full Data Analysis.
In about 2-3 weeks you will receive: original and processed scan images, array layout and a list of sequences, raw and processed data, a list of differentially expressed transcripts (dual sample arrays only), and a summary of the results.

