End-to-end Next Generation Sequencing for clinical, research and industrial genomics.
Sequencing has moved from a specialist research tool to a routine input for clinical decision-making, agricultural improvement and industrial microbiology. Our NGS services span sample preparation, library construction, sequencing on validated platforms and bioinformatics — delivered as a managed service so research and clinical teams can focus on biological questions, not infrastructure.
Unlock the complete genetic blueprint. WGS provides unparalleled resolution across both coding and non-coding regions, enabling the detection of structural variants, SNVs, and complex genomic rearrangements.
Population genetics, rare disease diagnostics, large-scale cohort studies.
Focus your sequencing budget on the ~2% of the genome that contains over 85% of known disease-causing variants. An efficient, cost-effective alternative to WGS for diagnostic applications.
Rare disease detection, clinical genetics, mutation analysis.
Map the dynamic transcriptome. From differential gene expression to novel splice variants, our RNA-Seq pipelines capture the functional state of your samples with precision.
Gene expression profiling, transcriptomics, biomarker discovery.
Profile complex microbial communities without the need for culturing. We offer both 16S/ITS amplicon sequencing for taxonomic profiling and shotgun metagenomics for functional insights.
Gut microbiome studies, environmental analysis, pathogen surveillance.
Achieve extreme depth of coverage over specific gene sets. Ideal for identifying rare somatic mutations in oncology or screening for inherited genetic disorders.
Oncology research, inherited disorders, pharmacogenomics.
Investigate gene regulation mechanisms beyond the primary sequence. We utilize advanced bisulfite and enzymatic conversion methods for precise DNA methylation profiling.
Epigenetics research, cancer studies, gene regulation analysis.
Cost-effective, high-throughput discovery of single nucleotide polymorphisms (SNPs) and structural variants across large-scale population cohorts.
Genetic screening, population studies, trait analysis.
A robust foundation for any sequencing project. We handle automated nucleic acid extraction, rigorous quality control, and library preparation tailored to your target platform.
DNA/RNA preparation, quality control, library generation.
Execute your runs on industry-leading short-read platforms (like Illumina NovaSeq). We guarantee data yield, quality scores, and deliver raw data securely.
High-throughput sequencing and genomic data generation.
Transform raw signals into actionable variant calls. Our automated pipelines handle demultiplexing, read alignment, and variant calling strictly adhering to GATK best practices.
Make sense of your genomic data. We provide clinical-grade variant annotation, prioritization, and interpretive reporting aligned with ACMG guidelines.
Require a non-standard approach? Our bioinformatics team builds bespoke pipelines for complex projects, including structural variant detection and advanced multi-omics integration.
Variant discovery for oncology, rare disease and reproductive health.
Trait mapping, marker-assisted selection and crop improvement.
Community profiling for ecology, public health and industrial microbiology.
Disease, breeding and conservation studies in domestic and wild species.
Variant–response associations to support personalised therapy and drug development.
DNA profiling and identity verification using high-resolution panels.
Configuration guidance, validation packs and pilot programs — tailored to your lab.