Whole Genome Sequencing (WGS) provides a complete map of an organism’s DNA. With this service, entire genome can be sequenced to determine genetic variants that may be associated to disease or other phenotypic traits. WGS can be used for de-novo assembly when the genome of interest is poorly annotated.
Epigenomics refer to a range of technics used to analyze the chemical modifications and interactions between DNA and proteins to better understand the molecular mechanisms underlying complex diseases and identify potential targets for therapeutic intervention.
Targeted Sequencing is a technique allowing to focus on specific regions of interest in the genome. Our service is ideal for identifying genetic variants that are associated with specific diseases or traits.
RNA Sequencing is a powerful tool for studying gene expression and identifying novel transcripts. Our service provides a complete transcriptome, for the identification of genes that are differentially expressed under different conditions.
Our labs are equipped with the latest and most innovative technologies dedicated to Next-Generation Sequencing, leading to a swift sample analysis and reduced analytical cost.
Output range
Run time
Maximum reads per run
Maximum read lenght
* Possibility to generate contiguous long-read sequences of 5-7 kb with some reads > 10 kb
We use the latest sequencing technology and only the highest quality reagents and equipment to ensure that our clients’ receive the most accurate and reliable results.
Our team has extensive experience in sequencing and omic data analysis and is dedicated to provide a tailored solution and extensive support throughout our clients’ projects.
Understanding that time is critical when it comes to research projects, we strive to provide fast turnaround times without compromising on quality.
Understanding the uniqueness of every research project, we offer omics solutions tailored to our clients’ specific needs and research goals, from sample preparation to data analysis.