Genomics Services Lab

Sequencing Services

Our team is here to support you with an extensive range of cost-effective and innovative sequencing services, from whole genome re-sequencing to genetic analysis, helping you meet your specific scientific goals.

As part of our comprehensive genomics services offering, our team provides a complete assembly and analysis service, including DNA and RNA extraction and high-quality library preparation, using state-of-the-art next-generation sequencing platforms.

We will work with you to develop the best approach to obtain the data you need at the level of detail and quality you require, and help you analyze and interpret in the context of your study.

Take advantage of our expertise with our wide range of sequencing services:

Whole Genome Re-Sequencing

Whole genome resequencing compares your unknown genome to a known reference genome to help identify mutations such as single nucleotide polymorphisms (SNP), insertion deletions (InDel), structure variations (SV) and copy number variations (CNV).

De Novo Sequencing

De novo sequencing can help you to determine an unknown/unreferenced genome, or identify complex organisms and structural variants, by assembling small overlapping pieces of DNA into contigs or scaffolds to form a complete sequence.

Low-pass Whole Genome Sequencing

Low-pass or shallow whole genome sequencing offers a cost-effective method to alternative genome sequencing approaches, with greater opportunity to increase throughput giving you more data, greater statistical power, and more accurate variant calling.

Target Region Sequencing

Target region sequencing offers higher coverage for a specific subset of genes or region of interest. Compared to whole genome sequencing, target region sequencing provides greater sensitivity and specificity when looking to identify rare variants.

Exome Sequencing

Sequencing protein-coding regions of the genome can help to accurately identify phenotypic variants that may be associated with disease characteristics specific to your study. A more cost-effective approach compared to whole genome sequencing, exome sequencing offers greater coverage and faster analysis times.


Find out how we can help you meet your sequencing goals

With extensive expertise in AgBiotech, Food and Nutrition, and Human Health, our team can help you find the sequencing services you need.

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"Eremid provides the support we need to make a global impact in our large immunogenomic oncology clinical studies. The team’s expertise and flexibility from assay design to data delivery is helping us achieve our vision – an ideal research partner." Geoffrey Erickson, Immunis AI, MI USA — Senior Vice President, Corporate Development
"Working with Eremid has been a pleasure. We received excellent data with a very fast turnaround and appreciated the attentive and helpful project management!" Steve Watkins, BCD Biosciences, CA USA — CEO
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