PRECISION DRIVEN GENOMICS:
Redefining accuracy in healthcare.

At Genexfy, we specialize in genomics and bioinformatics services.

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Products / Services

Genomic Data Analysis

GeneXFY - Genomic Data Analysis

We utilize advanced genomic sequencing technologies and sophisticated bioinformatics tools to analyze genetic data and identify potential variants associated with rare diseases and oncology. Learn More

Variant interpretation

GeneXFY - Variant Interpretation

Our team of experts carefully analyze genomic variants to determine their clinical significance, helping healthcare professionals make informed decisions about diagnosis and treatment.
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Genomic Profiling

GeneXFY - Genomic profiling

By analyzing the genomic profile of patients, we assist healthcare providers in developing tailored treatment plans based on the specific genetic alterations driving their rare diseases or cancer. Learn More

Targeted therapies

GeneXFY - Targeted Therapies

We identify potential targeted therapies or clinical trials based on the genomic characteristics of the disease, enabling more effective and precise treatment options. Learn More

Technology

Our Octopus Owie™ Platform is a comprehensive and user-friendly solution for analyzing genetic variations in cancer, rare diseases, and preventive genomics.

Features

Octopus Owie™ covers a wide range of genetic variants, including single nucleotide variants (SNVs), insertions and deletions (indels), copy number variations (CNVs), and structural variations (SVs).

GeneXFY - Octopus owie - Key Features
GeneXFY - Our Services

Services

At Genexfy, we specialize in comprehensive genomic analysis and data-driven solutions, with a particular focus on rare diseases, oncology, and their association with genes.

Octopus Owie™ has a wide range of applications in cancer, rare disease, and preventive genomics research and practice. Some examples include:

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Cancer

Octopus Owie™ can be used to identify and annotate genetic variations that are associated with specific types of cancer, such as breast, lung, or ovarian cancer. This can provide insights into the underlying biology of cancer, and support the development of personalized and precision medicine approaches to diagnosis and treatment.

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Preventive genomics

Octopus Owie™ can be used to identify and annotate genetic variations that are associated with increased risk of common diseases, such as diabetes, cardiovascular disease, or Alzheimer's. This can support the development of preventive measures and interventions, such as lifestyle changes or pharmacological treatments, that can reduce the risk of these diseases.

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Rare Diseases

Octopus Owie™ can be used to identify and annotate genetic variations that are associated with rare diseases, such as cystic fibrosis, muscular dystrophy, or sickle cell disease.
This can provide a better understanding of the genetic basis of these diseases, and support the development of targeted therapies and diagnostic tests.

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Variant Interpretation

Our team of experts carefully analyzes genomic variants to determine their clinical significance, helping healthcare professionals make informed decisions about diagnosis and treatment. Genetic variant databases: We leverage comprehensive databases and resources to enhance the interpretation of genomic variants, increasing the accuracy and reliability of our findings.

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Octopus Owie™ is our flagship product, offering advanced genomic data analysis for a wide range of applications.

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