Key Offerings at CodonDx
Reproductive Genetics
Understanding the genetic risk factors is crucial for determining a couple's reproductive health when they are 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 a targeted treatment.
Neurogenetics
Predictive genomics services helps patients and individuals anticipate response to variety of medications and the risk of disease developement.
Cardiovascular Genetics
Comprehensive study of the genetic basis of cardiovascular diseases including DCM, HCM, Brugada, LQTS, Marfan, Noonan syndrome, and others.
Cytogenetics & Microarray
Understanding the gentic risk factors is crucial for determining a couple's reproductive health when they are planning to start a family.
Pharmacogenomics
Test identifies genetic variations that affect drug response allowing clinicians to personalise treatments based on their genetic profiles
Thalassaemia Syndromes & Familial Disorders
Makes a molecular diagnosis of Alpha and beta thalassaemia syndromes with haemoglobinpathies.
Immunogenetics /HLA Genotyping
Identifies genetic variants that dysregulate the normal immune pathways leading to immune disorders and HLA associated diseases.
Endocrine Genetics
Study the genetic variations that affect hormone production and regulation, leading to more personalized and effective treatments. management
Whole Exome Sequencing
Provides insight into the protein-coding regions of the genome, which is made up of approximately 34 million bases – of the total 3 billion bases in the human genome.
Predictive Genomics
Predictive genomics services helps patients and individuals anticipate response to variety of medications and the risk of disease developement.
Consumer Genetics
Direct-to-cosumer genetic tesing and personal genomic services are available withouth the direct involvement of a health care 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 & research.
Genome-wide Copy Number Variations
Detects CNVs and ROH linked to anomalies & 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 worldwide