A rapid, cost-effective research services solution
Our customer-oriented team is experienced in a wide range of applications related to AgBiotech, Food and Nutrition, and Human Health. As a PacBio® certified service provider and one of the most capable genomics laboratories in North America, our genomics services offer you fast and accurate results using a unique combination of expertise and cutting-edge technologies from Illumina, Pacific Biosciences, Oxford Nanopore Technologies, 10x Genomics, and NanoString.
Nucleic Acid Extraction Services
- RNA and DNA extraction from optimized protocols
- From various sample types (Plant and animal tissues, Cells, Blood, Stool, Water, Soil, Bacteria, Yeast, AAV, FFPE, ..)
Genomics Services (available in short and long reads sequencing)
- Shotgun Metagenomic Sequencing (microbiome)
- Whole Genome Sequencing
- Whole Exome Sequencing
- Targeted Sequencing via PCR (16S, ITS, …) and Hybridization Capture
- AAV Sequencing
- Infinium microarrays (GDA, GSA, …)
- Axiom microarrays (SARS-CoV2, PMDA,…)
Transcriptomics Services
- RNA sequencing
- Single-cell RNA sequencing
- Full-length mRNA sequencing (Iso-Seq)
- Small-RNA sequencing
- Gene expression array (nCounter)
Epigenetics Services
- Whole Genome Methylation Sequencing (WGBS, RRBS)
- Targeted Methylation Sequencing
- Infinium methylation array (EpiC)
- Chromatin structure and accessibility (Hi-C, ATAC, CUT&RUN)
Microbiome Analysis: taxonomic & functional profiling
- Large range of samples (Gut, Plasma, Saliva, Urine, Soil, …)
- Metagenomics (ShotGun & HiFi)
- Metatranscriptomics
- 16S/ITS targeted sequencing
Blended Genome Exome (BGE) Sequencing
Strategic low-pass whole genome sequencing (4x) combined with targeted deep exome sequencing (30x) for comprehensive variant detection.
- Unbiased discovery of common and rare variants missed by exome-only or array methods
- Cost-effective alternative to deep WGS
- Enhanced variant calling and imputation accuracy with long read technology (PacBio)
Bioinformatics Services
- De novo and guided genome assembly
- Gene model and ncRNAs prediction and annotation
- Gene expression analysis
- Pathway and gene ontology analysis
- Chromatin and Methylation density analysis
- Microbiome analysis (taxonomic and functional profiling)
- Structural variants discovery and analysis (SNP, CNV,… )
- Custom analysis
