Uncover the Whole Genome, Not Just a Part

Whole Genome Sequencing (WGS) is a comprehensive method that determines the complete DNA sequence of an organism’s genome. Unlike targeted approaches such as WES, WGS captures both coding and non-coding regions, providing an unbiased view of genetic variation across the entire genome.

Using next-generation sequencing (NGS), millions of DNA fragments are sequenced and aligned to a reference genome. Bioinformatics analysis is then used to identify a wide range of variants, including single nucleotide variants (SNVs), insertions and deletions (indels), copy number variations (CNVs), and structural changes.

This broad coverage makes WGS valuable for applications such as rare disease research, cancer genomics, and population studies, while also allowing data to be reanalysed as new insights emerge.

State-of-the-Art Technology

Industry-leading Sequencer

Our NGS services are powered by the AVITI System, delivering high-quality data with exceptional accuracy and efficiency. This advanced platform enables us to generate reliable genomic data across a wide range of applications, from whole genome to targeted sequencing.

Applications

Rare and Undiagnosed Diseases

Identify genetic causes in patients with complex or unexplained clinical presentations.

Inherited Disorders

Detect pathogenic variants associated with hereditary conditions and support family risk assessment.

Support early diagnosis in critically ill infants and children with suspected genetic conditions.

Pediatric and Neonatal Diagnostics

Oncology Support

Enable comprehensive genomic profiling to inform diagnosis, prognosis, and potential therapeutic strategies.

More in our brochure

Find out more about our WGS service.

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