Gene Marker Detection

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Gene Marker Detection

Gene Marker Detection & Analysis Capabilities

Genome-wide Association Studies (GWAS)
By analyzing genetic variations across the entire genome in populations with and without a particular trait we can identify associations between specific genetic markers and traits, helping uncover the genetic basis of diseases.
Polymerase Chain Reaction (PCR) and DNA Sequencing
Using PCR against specific DNA regions we can detect mutations or variations in targeted genes associated with diseases, aiding in diagnostics and personalized medicine.
Single Nucleotide Polymorphism (SNP) Analysis
To understand genetic predispositions, study population genetics, and develop markers for disease susceptibility or drug response we can use variations at a single nucleotide level to identify SNPs associated with traits.
Expression Profiling (Transcriptomics)
Gene markers associated with diseases can be identified by studying gene regulation, and understanding variations in gene expression levels of genes in a tissue or cell.
CRISPR-Cas9 Genome Editing
Using CRISPR technology to introduce or edit specific genetic markers can be used to investigate gene function by creating or modifying markers, potentially offering therapeutic interventions for genetic disorders.
Bioinformatics and Data Mining
Large-scale genomic data using computational tools and algorithms can discover patterns and relationships within genomic data, facilitating the identification of potential gene markers associated with diseases or traits.
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WORK PROCESS

How genix.ai process & works.

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Sample Preparation & Sequencing

Collect biological samples and perform DNA sequencing to generate high-quality raw genomic data.

Data Processing & Quality Control

Align sequencing reads to a reference genome, remove duplicates, and perform quality filtering to ensure reliable downstream analysis.

Variant Detection & Gene Marker Identification

Detect genetic variants (SNVs, Indels, CNVs) and identify specific gene markers associated with diseases or traits.

Interpretation & Clinical Reporting

Analyze the clinical relevance of identified markers, generate comprehensive reports, and provide actionable insights for patient care.

Ready to unlock the power of your DNA?

Your health story starts with a single saliva sample.

Frequently Ask Questions

1. What is included in the Genix DNA Report?
The Genix DNA Report offers a comprehensive view of your genetic makeup, covering key aspects of your health and wellness. It includes insights into your general well-being (like immunity and metabolism), athletic performance traits, genomic-based nutrition recommendations, skin health, and allergy predispositions. Additionally, it assesses your genetic risk for common cancers, identifies rare or hereditary disorders, and provides valuable data for reproductive and family planning decisions. All sections are presented in a user-friendly format with actionable recommendations.
2. How do I provide my DNA sample?
You will receive a saliva collection kit. Just follow the instructions and send it back to our lab.
  • Avoid eating, drinking, smoking, or chewing gum for 30–45 minutes before collection.
  • Spit into the provided funnel until it reaches the marked level.
  • Secure the sample with the stabilizing cap and return it using the prepaid return envelope. No blood, needles, or complicated tools are involved — just a quick, painless saliva sample.
3. Is the saliva collection process safe and easy?
Yes, the entire process is designed to be safe, hygienic, and hassle-free. The saliva kit meets international collection standards and includes clear, step-by-step instructions. Anyone can complete the collection independently at home in just a few minutes, making it accessible for both adults and children (above 2 years, with supervision).
4.How long does it take to get my report?
From the moment your sample reaches our certified lab, it typically takes 10 to 14 business days for processing, sequencing, and report generation. You will be notified via email and app notifications once your personalized report is ready to view.
5. How accurate is the analysis?
We use next-generation sequencing (NGS) and AI-powered genomic interpretation pipelines that are validated against international benchmarks. Our bioinformatics platform delivers insights with over 99.9% accuracy. Additionally, our content is curated and reviewed by certified clinical geneticists to ensure scientific and medical validity.
6. Is my genetic data safe and private?
Absolutely. At Genix.ai, privacy is our highest priority. Your genetic data is:
  • Encrypted at every stage (storage, transfer, and access)
  • Stored in HIPAA-compliant, secure cloud environments
  • You can also request complete deletion of your data at any time from within your Genix app.
7. Can I understand the report without a science background?
Yes, the report is written in simple, easy-to-understand language and includes intuitive visuals like charts and color-coded risk levels. Each section offers clear summaries, followed by optional detailed breakdowns for those who want to dive deeper. For further support, we offer in-app consultations with a certified genetic counselor to walk you through your results.
8. Will I receive diet or fitness recommendations?
Yes. Your DNA influences how your body metabolizes nutrients, builds muscle, responds to different diets, and recovers from exercise. Based on your genetic profile, you’ll receive personalized nutrition tips, recommended macronutrient balance, supplement advice, and fitness plans suited to your body type (endurance vs. power training potential, recovery time, etc.).
9. Can this test predict cancer or rare diseases?
The Genix DNA report does not diagnose diseases but instead evaluates your genetic predisposition to certain conditions based on known biomarkers and clinical evidence. For example, we assess your risk for BRCA-related breast and ovarian cancer, Lynch syndrome, or mitochondrial disorders. These insights empower you to seek preventive screening or lifestyle changes and discuss proactive care with a healthcare provider.
10. Is this test suitable for children?
Yes, children aged 2 years and older can take the test. Early access to genetic insights can help parents make informed decisions about nutrition, physical development, allergy management, and even emotional well-being. However, we recommend discussing sensitive results (e.g., disease risk) with a healthcare professional to ensure appropriate interpretation and action.
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Genix.ai is an AI-powered clinical platform using NGS and imaging to detect biomarkers early, enabling clinicians to deliver cost-effective, personalized treatments for rare pediatric conditions, cancer care, and infectious diseases.

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