ChIP-Sequencing
ChIP-Sequencing (ChIP-Seq) is widely used to analyze protein interaction with DNA. We have extensive experience supporting partners across the world with their ChIP-Seq research needs. Tell us about your project, our experts are here to help.
ChIP Sequencing Introduction
ChIP-Sequencing is widely used to analyze protein interaction with DNA. It combines chromatin immunoprecipitation (ChIP) with massively parallel DNA sequencing to identify binding sites of DNA-associated proteins, and can be used to precisely map global binding sites for any protein of interest. ChIP sequencing offers higher resolution and more precise and abundant information in comparison to array-based ChIP-chip approaches.
In addition to clean data output, BGI offers a range of standard, advanced and customized bioinformatics pipelines for your ChIP-Seq analysis project. We have particular expertise in the correlation analysis of RNA-Seq differential expression genes and ChIP-Seq peak related genes. Contact us for a no obligation discussion with our project experts.
Wide detection range: genome wide protein DNA interaction studies
Cost-effective: less data required for identifying the binding sites in the genome
Low input DNA: as low as 5ng ChIP-ed DNA for human samples
ChIP-Sequencing-BGI Service Overview
Sample Requirements
• Mass:≥10 ng
• Concentration:≥1 ng/μL
• Volume：15 μL
Sequencing Standards
• 50 bp Single-end sequencing reads
• Standard output 20 million reads per sample
• Available data storage and bioinformatics applications
• Cloud-based data storage and delivery system
Key Service Details
• Typical 25 working days from sample QC acceptance to filtered raw data availability
ChIP Sequencing Technology
BGI Genomics' ChIP Sequencing services are typically executed with proprietary DNBSEQ™ sequencing technology platforms, for great sequencing data at some of the lowest costs in the industry. DNBSEQ™ offers advantages in terms of lower amplification error rates and much lower duplication rates. In addition, studies have shown the lower index hopping rate in DNBSEQ™ platforms.
Contact us with any general enquiries or questions for our sequencing experts, we are here to help.
Access Further Sequencing Resources
We care for your samples from the start through to the result reporting. Highly experienced laboratory professionals follow strict quality procedures to ensure the integrity of your results. Access more sequencing resources below for full access to our range of educational resources and sample guides.
