Genomics Analysis Services

Diverse genomics research solutions for translational and clinical studies

Genomics research supported by comprehensive analysis

Synexa’s dedicated genomics research team specialises in developing bespoke, precise, and robust assays that propel clinical research forward.

Our experienced team is well-versed in solving researchers’ most complex challenges, including those around single nucleotide polymorphism detection and quantification, larger-scale marker screening, targeted gene sequencing, as well as quantitative polymerase chain reaction (qPCR). With a strong focus on genomics analysis, we ensure that every step, from initial sample collection to final data interpretation, is handled with the utmost precision.

Synexa’s GCLP-accredited laboratories are supported by a broad range of technologies, with capabilities ranging from full sample management to comprehensive clinical sample analysis.

Synexa Genomics
Analysis Services

Although not limited to these, Synexa offers a wide range of specialised services, including comprehensive genomics research and precise genomics analysis.

Nucleic acid isolation from various matrices:

Buccal & skin swabs
Cell lysates
Extracellular vesicles
Saliva
Stool
Tissue biopsies
Urine
Whole blood

Gene expression analysis

mRNA expression
NanoString
qPCR and ddPCR
T-cell and B-cell receptor repertoire

Genotyping

Genotypic profiling
Single nucleotide polymorphism (SNP) detection

Sequencing

Microbiome profiling
Targeted DNA sequencing

Specialised pharmacogenomics

Bacteriophage therapy detection and quantification
Cell and gene therapy bioanalysis
ctDNA quantification
Persistence of Allogeneic Cell Therapy (IMPACT) dPCR
Viral shedding and biodistribution

Robust and Proven Platforms

Our technology platforms are robust, reliable and reputable in the clinical field and provide comprehensive and detailed data readouts for your application.