Key Offerings at CodonDx
Reproductive Genetics
Understanding genetic risk factors is crucial for determining a couple's reproductive health when planning to start a family.
Oncology Genetics
CodonDx offers a variety of cancer genomics testing to help solve the most urgent need to profile tumours for targeted treatment.
Neurogenetics
Predictive genomics services help patients anticipate response to a variety of medications and the risk of disease development.
Cardiovascular Genetics
Comprehensive study of the genetic basis of cardiovascular diseases including DCM, HCM, Brugada, LQTS, Marfan, Noonan syndrome, and others.
Cytogenetics & Microarray
Genome-wide detection of chromosomal abnormalities, copy-number variations, and regions of homozygosity.
Pharmacogenomics
Test identifies genetic variations that affect drug response, allowing clinicians to personalise treatments based on genetic profiles.
Thalassaemia Syndromes & Familial Disorders
Makes a molecular diagnosis of alpha and beta thalassaemia syndromes along with haemoglobinopathies.
Immunogenetics / HLA Genotyping
Identifies genetic variants that dysregulate normal immune pathways, leading to immune disorders and HLA-associated diseases.
Endocrine Genetics
Study genetic variations that affect hormone production and regulation, leading to more personalised and effective treatment management.
Whole Exome Sequencing
Provides insight into the protein-coding regions of the genome, approximately 34 million bases of the 3 billion bases in the human genome.
Predictive Genomics
Predictive genomics services help patients and individuals anticipate response to a variety of medications and the risk of disease development.
Consumer Genetics
Direct-to-consumer genetic testing and personal genomic services available without the direct involvement of a healthcare provider.
Genetic Diagnostic Services You Can Trust
For Aneuploidies
Constitutional cytogenetic analysis for reproductive partners.
Mutation Confirmation
Familial mutation testing and orthogonal confirmation of variants.
Paternity Testing
Non-legal paternity and sibship testing for immigration and peace of mind.
For Genetic Diagnostics
Paired- and single-end sequencing for diagnostics and research.
Genome-wide Copy Number Variations
Detects CNVs and ROH linked to anomalies and genetic syndromes.
Spectrometry-based Genotyping
High-throughput mass-spectrometry genotyping of SNPs and mutations.
Absolute Quantification
Sensitive detection of rare variants and copy-number changes.
Personalised Dermatology
Genetic mapping of skin traits to support personalised treatment.
Trusted by clinicians, researchers, and patients across the region
CodonDx has redefined excellence in genetic diagnostics. Their reports are clinically robust and remarkably clear — bridging the gap between complex variant interpretation and real-world decision-making.
Their Preimplantation Genetic Testing helped clarify a complex case and provided valuable, actionable insights. The turnaround time was rapid, and the genetic counselling support was outstanding.
The team explained my genetic results in a way I could understand. I felt supported and informed throughout the entire process.
