DELPHI
Simplified Genomic Analysis
The Genomic Oracle of Delphos (Delphi) is an advanced tool that enables rapid annotation and report generation from VCF files, efficiently and accurately.
Key Features
Fast Analysis
The speed at which genomic data can be analyzed is critical for timely decision-making in both clinical and research settings. Our platform processes whole genomes with optimized algorithms, delivering results in less than an hour. This rapid analysis reduces wait times and accelerates the diagnostic process, allowing clinicians and researchers to act swiftly on genetic insights.
Omics Knowledge Base
Integrated information from more than 100 omics data sources, creating a rich, interconnected knowledge ecosystem that spans genomics, transcriptomics, proteomics, and metabolomics. We offer secure integration of your proprietary databases and private data sources, maintaining strict data privacy and access controls while enriching your analysis with organization-specific knowledge.
Timely Data
Our automated system ensures your genetic analyses remain up to date with the most recent discoveries. Both our omics knowledge base and patient reports update dynamically as new research emerges. This means users will never miss critical updates.
Disease-Specific Analysis
We optimize our analysis pipeline for specific diseases, starting with hereditary cancer. By incorporating disease-specific genetic patterns and clinical guidelines, we deliver deeper, more accurate insights tailored to each condition's unique characteristics.
True Personalization
We go beyond surface-level customization by offering genuine, end-to-end personalization that adapts to your specific requirements. Unlike one-size-fits-all solutions, our platform allows you to tailor every aspect of the analysis process. We understand that each use case has unique challenges and objectives, which is why we've built a flexible system that can be precisely configured to match your needs.
Intuitive Interface
Our user interface is designed with simplicity and efficiency in mind. Even users with minimal technical background can navigate the platform with ease. From uploading VCF files to viewing detailed reports, the interface ensures a smooth, streamlined experience, enhancing productivity and ensuring that essential data is always at your fingertips.
Genomic Report Process
Genetic reports play a crucial role in diagnosing and treating various diseases. Genomics provides deep insights into genetic variations that can have a significant impact on human health. Genome studies allow for the identification of genetic mutations, some of which are directly related to specific disorders.
Our optimized process ensures that every step, from the VCF file to the final report delivery, is efficient, precise, and rapid, facilitating informed clinical decision-making.
DNA Sequencing
The process begins with DNA sequencing, generating comprehensive genomic data. This foundational step captures the complete genetic makeup, providing the raw data necessary for subsequent analysis.
Data Interpretation
After the relevant genomic mutations are identified and saved into a VCF file, our advanced algorithms come into play, interpreting the genomic data and the VCF (Variant Call Format) files. This process involves identifying genetic variants and understanding their potential impact on health.
Automated Reporting
We generate automated reports that translate complex genomic data into actionable insights. These reports provide clear and precise information tailored to each individual's genetic profile.
Clinical Insights
The reports offer clinicians precise tools for informed decision-making. By delivering rapid and accurate genetic information, we enhance the ability to diagnose and treat various conditions effectively.
