At Alstronix Technologies, we combine the power of artificial intelligence,
population-specific genomics, and clinical insight to drive faster, smarter,
and more inclusive healthcare solutions.
We build cutting-edge tools and platforms that decode the human genome — with
a focus on real-time diagnostics, personalized medicine, and the unique genetic
landscape of India.
We specialize in Rapid Whole Genome Sequencing (rWGS),
optimized for urgent clinical settings like NICUs and ICUs. Our pipelines are
built to reduce diagnosis time from weeks to hours — delivering answers when
they matter most.
·
Real-time variant calling
·
Neonatal & rare disease support
·
AI-enhanced interpretation
Our flagship Variant Intelligence Engine uses machine
learning to analyze, score, and prioritize variants across millions of data
points. It empowers geneticists and labs to focus on what matters.
·
Deep learning models
·
Clinical database integration
·
Population-specific prioritization
We’re building tools that reflect India’s rich genetic mosaic,
creating regional reference genomes and enabling population-scale
analysis for better diagnostic accuracy.
·
Ancestry & ethnicity profiling
·
Population genomics visualizations
·
Indian-focused allele frequencies
Through our Pharmacogenomics Toolkit, we connect genetic
variation to drug response — helping doctors make personalized treatment
decisions and reduce adverse drug reactions.
·
AI-driven gene-drug matching
·
Risk allele detection
·
Dose optimization by genotype
Every platform we create is designed to be scalable, affordable,
and clinically actionable — whether you're a research
institution, hospital, startup, or government program.
·
Secure cloud deployment
·
Custom APIs and data privacy
·
Multi-omics integration
We work with:
· Leading
hospitals and diagnostic labs
· Academic
researchers and public health agencies
· Biotech
startups and pharma companies
· Government and nonprofit health programs
Let’s advance precision healthcare — together.
