Reliable NGS Services for Your Next Discovery

Designed for technology partners, core labs, and service labs, our hassle-free NGS Foundry simplifies complex research, making your aspirations attainable.

Flexibility, Expertise, and Innovation

Accelerate your next breakthrough with our expert team and cutting-edge technology.

Advancing your critical research requires precise, reliable sequencing, but managing complex NGS can be a hurdle. Our NGS foundry provides the expert support and advanced technology you need to drive science forward.

Transparent Pricing and Scheduling

Easy Transition to CAP/CLIA/NYS

Adjacent Services Available

*Note: Pricing will vary based on requested turnaround time

The Power of Parallel Sequencing

Whole Genome Sequencing (WGS)

Comprehensive sequencing of an organism’s entire DNA, including all genes, regulatory regions, and non-coding sequences. This approach provides the most complete genetic information and is ideal for identifying structural variants, copy number variations, and mutations across the entire genome.

Whole Exome Sequencing (WES)

WES focuses specifically on sequencing the exome, the protein-coding regions of the genome, which contain the majority of known disease-causing mutations. This cost-effective approach efficiently identifies genetic variants linked to various conditions, making it ideal for clinical diagnostics and research into rare diseases.

Single-Cell Analysis

This service enables the study of individual cells, providing unprecedented resolution into cellular heterogeneity within a sample. By analyzing genetic or gene expression profiles cell by cell, it uncovers unique insights that are masked in traditional bulk sequencing methods.

Spatial Analysis

Access multiple cutting-edge technologies driven by the power of SBS chemistry, including our in house GeoMx platform. GeoMx Spatial Analysis combines high-throughput sequencing with spatial information, allowing researchers to precisely profile RNA and protein expression within specific regions of tissue samples. This technology reveals how molecular features vary across different cell types and tissue compartments, providing crucial context for biological processes.

RNA Sequencing

RNA-Seq quantifies and characterizes the RNA molecules (transcriptome) present in a sample, providing a dynamic view of gene activity. This service is essential for understanding gene expression levels, identifying novel transcripts, and studying alternative splicing patterns under various conditions.

Bioinformatic Analysis

Following sequencing, our bioinformatic analysis service transforms raw data into meaningful biological insights. Utilizing advanced computational tools and statistical methods, we process, align, and interpret complex genomic data to identify key findings and support research objectives.