AI Diagnostic Tool

Accelerating Precision Medicine with Intelligent Genomic Interpretation

At Alstronix Technologies, we combine cutting-edge genomics with the power of artificial intelligence to deliver faster, smarter, and more accurate diagnostics. Our AI-Powered Genomic Diagnostics solution transforms raw sequencing data into clinically actionable insights, helping healthcare providers make confident decisions in real time.

What Makes It AI-Powered?

Our proprietary AI engine integrates:

·       Variant classification algorithms

·       Genotype-phenotype correlation models

·       Natural language processing (NLP) to mine scientific literature

·       Machine learning to rank disease-causing variants

·       Clinical knowledge graphs for contextual interpretation

The result? High-quality interpretations that improve speed, accuracy, and scalability in genomics diagnostics.

Features at a Glance

Automated Variant Prioritization

·       ACMG/AMP guidelines embedded in AI workflows

·       Pathogenicity scoring and evidence aggregation

·       Population-specific allele frequency filtering (including Indian genomes)

·       Multi-omic integration (genomic, phenotypic, pharmacogenomic)

Clinical Report Generation

·       AI-assisted drafting and QC

·       Support for custom clinical workflows

·       Integration with EHRs and LIMS

·       Clear visualization of gene-disease links, inheritance patterns, and treatment implications

 Continuous Learning System

·       Real-time updates from ClinVar, OMIM, gnomAD, HGMD, and literature

·       Learns from previous case outcomes and user feedback

·       Suggests new gene-disease associations as knowledge grows

 Applications

·       Rare and undiagnosed diseases

·       Pediatric and neonatal genetic disorders

·       Oncology (tumor sequencing and liquid biopsy)

·       Carrier screening and prenatal diagnostics

·       Pharmacogenomics integration

 Benefits

·        Reduce Time-to-Diagnosis: Get results in hours, not weeks

·        Improve Diagnostic Yield: Identify previously missed or novel variants

·        Lower Interpretation Burden: Automate 80–90% of variant curation

·        Connect Genotype to Phenotype: Enhanced diagnostic accuracy using HPO and clinical notes

 Tech Ecosystem & Integration

·       Modular and API-friendly platform

·       Cloud and on-premise deployment options

·       Supports industry-standard formats (VCF, BAM, JSON, HL7, FHIR)

·       Scalable from single lab to national networks

Built for Indian Healthcare, Backed by Global Science

Our AI tools are trained on both international datasets and India-specific genetic backgrounds, ensuring relevance and reliability for South Asian populations.

Make Diagnostics Smarter, Faster, and More Scalable

Whether you're a diagnostic lab, hospital, or research institute, Alstronix helps you integrate AI-driven precision genomics into your workflow—with full support from data to decision.