The Owie™ platform integrates advanced algorithms and computational methods with a user-friendly interface, enabling researchers, clinicians, and patients to easily and efficiently analyze large and complex datasets generated by high-throughput experiments, such as whole-genome or exome sequencing.
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Owie™
Owie™
Platform
A comprehensive and user-friendly solution for analyzing genetic variations in cancer, rare diseases, and preventive genomics.
Owie™ is available as a cloud-based solution, enabling users to access and analyze their data from anywhere, at any time, using a web browser. The platform will also soon be available as a local installation, providing users with the option to run the analysis on their own infrastructure, with full control over data storage and management.
Features
Comprehensive: 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).
Accurate: Owie™ uses state-of-the-art algorithms and databases to accurately and consistently identify and annotate genetic variants.
User-friendly: Owie™features a user-friendly interface that allows users to easily upload, visualize, and analyze their data, without requiring specialized training or expertise in bioinformatics.
Flexible: Owie™is highly customizable and can be tailored to the specific needs and goals of each user or project.
Secure: Owie™provides secure data storage and management, ensuring that users' data are kept confidential and protected.
Octopus Owie™ has a wide range of applications in cancer, rare disease, and preventive genomics research and practice. Some examples include:
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.
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.
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.
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.
Octopus Owie™ is our flagship product, offering advanced genomic data analysis for a wide range of applications.