LEARN MORE ABOUT EPIQUEST

Enter your name and email address below to receive more information about Zymo Research's EpiQuest™ Genomic Service.

EpiQuest Genomic Service

Single Base Resolution DNA Methylation Analysis

Genome-wide coverage: ~1,500,000 CpG Sites, >17,000 Gene Promoters, >21,500 CpG Islands!

Next-Gen bisulfite sequencing platforms for DNA methylation analysis

Streamlined workflows with comprehensive bioinformatic analysis

High quality publishable data delivery

Low DNA input (<500ng genomic DNA)

Applicable to a broad range of sample sources (human, mouse, rat, plant, etc.)

Customizable, rapid turnaround at an affordable cost


How does the EpiQuest™ Genomic Service work?

EpiQuest™ Genome-Wide Service expands upon the conventional RRBS (Reduced-Representation Bisulfite Sequencing) method to greatly increase sequence coverage. Genomic DNA is first digested by restriction endonuclease enzymes to produce fragments rich in CpG sites. These fragments are recovered, subject to bisulfite conversion, and sequenced to give single nucleotide resolution sequencing data. This provides a statistically significant representation of CpG dinucleotides throughout the genome.  Through the utilization of a multiple enzyme digestion and an optimized workflow (see below), the EpiQuest™ team at Zymo Research has been able to expand coverage to ≥ 75% of gene promoters and ≥ 80% of CpG islands (for human samples).

The EpiQuest™ Whole-Genome Service utilizes a streamlined library preparation and sophisticated alignment algorithms to deliver Whole Genome Bisulfite-Sequencing that covers > 75% of all the bases in the human genome at single-base resolution.


EpiQuest™ Genomic Service - Platform Details

For pricing information and a personalized quote please fill out a service inquiry form or call us at (949) 679-1190 or toll-free at (888) 882-9682.

Other EpiQuest™ services are now available including locus-specific validation via direct bisulfite sequencing,  and global 5mC and 5hmC quantitation by mass spectroscopy determination... please inquire.

Full Service

The Full Service package removes all complication from methylome sequencing - simply submit DNA samples and receive high-quality data from our comprehensive bioinformatic analysis. This package is recommended for customers without an extensive bioinformatics background.

Learn More


Basic Service

The Basic Service Package will provide Next-Gen sequencing data aligned to the reference genome using our proprietary pipeline and three UCSC genome browser tracks. This option is recommended for users well-versed in bioinformatics.

Learn More


Customized Service

EpiQuest™ service can be adapted to fit the needs of the investigator. There are many options for difficult samples, extra bioinformatic analysis, locus-specific validations, different organisms, and more.

Learn More