Press Release:
Press Release:
Designed for technology partners, core labs, and service labs, our hassle-free NGS Foundry simplifies complex research, making your aspirations attainable.
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.
*Note: Pricing will vary based on requested turnaround time
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.
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.
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.
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-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.
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.
MiSeq
MiSeq
25 Million reads
25 Samples x Panel
2 Exomes
1 Human Genome
NextSeq
NextSeq550
400 Million Reads
~50-100+ samples x Targeted Panel
12-15 Exomes
1 Human Genome
NovaSeq X Plus
NovaSeq X Series
52 Billion reads
4,000-8,000 Samples x Panel
1,000 Exomes
88 Human Genome
Competitive pricing by run and by lane available
Rapid Quote Turnaround
Same Day Local Pickup
Sample to Data in 1 Week
Begin sequencing your customer-prepared libraries today. Fill out a form, and a project manager will be in touch shortly
