Our unique ability to uncover causal and mechanistic connections between biology and disease sets us apart. We have deep genomic science expertise and we collaborate with top clinical experts across many diseases.
Our global team of scientists comprises over 80 experts in molecular biology, population genomics, oncology, neurology, computational biology, systems biology, clinical genetics, artificial intelligence and machine learning.
Our laboratories located in Boston, USA and Dublin, Ireland, operate to the highest international accreditation standards (CAP/CLIA, ISO).
Our comprehensive range of services covers everything from sample processing, biobanking, nucleic acid extraction, QC and genotyping, to next generation sequencing techniques, methylation profiling and data delivery. The work processes are supported by a dedicated team of scientists, an integrated laboratory information management system (LIMS) and full automation to ensure high-quality research and research services.
High-quality purification of DNA and RNA from multiple sample types
Precipitation based genomic DNA extraction from blood and saliva
Magnetic bead-based RNA extraction from PAX gene blood tubes
Magnetic bead-based DNA, RNA and miRNA extraction from tissue
Advanced systems ensure quality inputs for superior outcomes
Spectrophotometric UV absorbance, quality and fluorescence-based concentration analysis
Automated DNA & RNA fragment analysis of size, concentration and integrity
Smear, Fragment Analysis and quality control for NGS Library Preparation
Automated processes deliver higher quality while decreasing time and effort
LIMS integrated automated liquid handling enables fully traceable, scalable (1-96 samples) automated library preparation including QC and library pooling
Infinium Global Screening Assay v3.0 library and chip loading
Scalability without sacrificing data quality or reproducibility in genetic analysis assays, from high-throughput genotyping to DNA methylation analysis
Innovative array scanner that supports rapid, sensitive, and accurate imaging of Illumina BeadChips for exceptional genetic analysis results
Multi-ethnic genome-wide content, curated clinical research variants, and quality control (QC) markers for precision medicine research
Interrogates over 850,000 methylation sites quantitatively across the genome at single-nucleotide resolution
Solutions to accommodate a wide variety of NGS methods
Rapidly and efficient generation of Single Cell Gene Expression v3.1 Library for single cell RNA sequencing analysis
Scalable throughput and flexibility for virtually any sequencing method, genome, and scale of project.
Scalable throughput and flexibility for virtually any sequencing method, genome, and scale of project
Fast turnaround for sequencing applications such as TruSight™ Oncology 500 Assay and Single cell RNA sequencing
Flexible benchtop sequencing and analysis device designed to run and analyze up to five experiments concurrently
Low-throughput benchtop system that delivers gold-standard Sanger sequencing technology and fragment analysis
