Rare Diseases Package
Rare Diseases Package
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- Analysis by Medical Clinical-Grade Whole Genome Sequencing (WGS, 20.000+ genes)
- Personalized Rare Diseases Personalized Panel
- Raw data (BAM, FASTQ, VCF files)
- 1 Free update on current and newly discovered genetic associations
- Free logistics for sample collection
Our personalised rare diseases Whole Genome Sequencing test is based on Clinical Grade sequencing, providing a comprehensive analysis of genetic variants associated with rare and genetic disorders tailored to an individual’s specific genetic makeup.
This test is designed to identify rare and inherited genetic diseases that are difficult to diagnose using traditional methods.
Our test analyzes a broad range of genetic variants that are known to be associated with rare and genetic diseases, including neuromuscular disorders, inherited metabolic disorders, lysosomal storage disorders, and many others.
By examining a person’s unique genetic makeup, we can identify any variants that may be contributing to their symptoms or predisposing them to certain diseases.
In addition to the Personalized Rare Disease Panel, we offer optional analyses that can be included in your package to provide even more personalized information about an individual’s health.
These options include:
1. Pharmacogenomics Whole Genome SequencingPanel
This Panel provides personalized information about how the body processes medications. This analysis can help identify which medications may be more effective or cause adverse reactions, allowing healthcare providers to make more informed treatment decisions.
2. Wellness Whole Genome Sequencing Panel
This analysis includes Personalised Nutrigenetics, Fitness, Skincare and Wellness and Lifestyle panels and provides valuable information on how genetics may impact an individual's health and wellbeing, including personalized recommendations for diet, exercise, and skincare.
3. Full Genome Proactive screening analysis
Full Genome Proactive screening is based on whole genome sequencing, which includes all clinical panels. This report provides a comprehensive analysis of the genome and can identify genetic variants that increase risk for certain diseases, allowing individuals to take proactive steps to prevent or manage them.
Our clinical personalised whole genome sequencing test, along with our optional analyses, provides individuals and patients with the most comprehensive understanding of their genetic makeup and how it may impact their health.
As part of our service, we also provide the option for white-labelling and customisation of the package based on your needs. Contact us today to learn more about our test and the additional options available to you.