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Whole Genome Sequencing

Phronetik offers advanced Whole Genome Sequencing (WGS) services for disease research and population studies. Our WGS decodes an individual's entire DNA, revealing genetic variations crucial for understanding diseases and treatment efficacy.

For Disease Research


Our WGS service uncovers genetic insights for rare and common diseases, pinpointing mutations crucial for targeted therapies and diagnostics. Supporting research across oncology, neurodegenerative, cardiovascular, and infectious diseases, it advances personalized medicine with unprecedented detail.

For Population Research


Phronetik uses WGS in population studies to reveal genetic diversity and trait distribution across groups. This helps identify health disparities and genetic factors influencing disease prevalence, crucial for tailored public health interventions and policies.

Image by CDC

Key Features of our WGS Service


Comprehensive Coverage

Our commitment to eco-friendly design is central to our identity and strategy. Continuously enhancing our offerings and expanding our design and production capabilities defines our dedication. Contact us to discover more.


High Accuracy and Quality:

We use state-of-the-art sequencing technology to ensure high accuracy and quality in our data, enabling reliable identification of genetic variations.


Data Interpretation and Support

Beyond raw data, we offer expert interpretation and support, helping our clients understand the implications of their findings for research and clinical applications.


Ethical and Inclusive Research

Consistent with our mission, we emphasize diversity, equity, and inclusion in our studies, ensuring that our research benefits all populations.

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