AI-Powered Genomic Analysis for Precision Medicine
From Raw Variants to Actionable Answers
DNA GTx’s D-KRYPT® is a cutting-edge, AI-powered platform that delivers a fully integrated pipeline for both hereditary and somatic genomic analysis. Purpose-built to transform complex sequencing data into clinically actionable insights, D-KRYPT® enables the identification of pathogenic variants across exomes, whole genomes, and targeted panels. By applying rigorous prioritization frameworks aligned with AMP and ACMG guidelines, the platform ensures the highest standards of clinical relevance in cancer genomics.
Beyond variant detection, D-KRYPT® supports familial mutation tracking through trio sample analysis, enhancing the understanding of inherited risk. It also provides intuitive visualization of gene fusions identified in hybrid sequencing panels, empowering clinicians with clear, interpretable results. Together, these capabilities advance precision oncology and enable truly personalized patient care.
What Makes Us Unique?
Data Uploading
- Secure and fast upload of FASTQ, BAM or VCF files
Variant Calling and Annotation
- Comprehensive analysis of multi-omics datasets for deeper biological and clinical insights
- High sensitivity detection of variants, even at low coverage or ≥1% variant allele frequency
- Flexible pipelines supporting single-sample and multi-sample (trio) workflows for rare variant discovery
- Simplified trio analysis to streamline familial mutation tracking
- Clear QC reporting that highlights the most relevant quality metrics and findings
- Dedicated expert support from our team at every stage of the process
Prioritization and Filtering
- Advanced database filtering options to streamline variant prioritization
- Intuitive, user-friendly interface for effortless navigation and analysis
- Unified access to all databases in a single platform
- Customizable filter presets for quick reuse and consistent workflows
Variant Interpretation
- Intuitive, dynamic, and user-friendly interface
- Classification of variants based on risk factor and drug response
Reporting
- Patient report generation based on ACMG/AMP guidelines
- Upload templates and create custom reports as per user request
Unlock the Power of AI-Driven Genomics with D-KRYPT®
Experience how D-KRYPT® turns complex genomic data into clear, actionable insights.
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