TECHBIO - AI - DECODING BIOLOGICAL DATA
Semantic Web Tech builds AI-powered data and knowledge infrastructure at the intersection of technology and biology.
We turn complex biological data into connected knowledge systems that power clinical decisions, research discovery, and life-changing outcomes
— in one of the fastest growing markets in global healthcare
THE PROBLEM WE SOLVE
The cost of sequencing a human genome has fallen 99.9% in two decades. NGS testing is now routine in hospitals across the world.
Yet the ability to interpret what that data means — clinically, accurately, at speed — has not kept pace.
Labs are overwhelmed. Clinicians lack the tools to act. And patients wait.
The bottleneck is interpretation. The gap is intelligence.
Behind every unresolved variant is a patient still waiting for an answer.
WHO ARE WE
We are a team of genomics scientists, bioinformaticians, data scientists, and AI engineers who share a single conviction: that the most important unsolved problems in medicine are not biological. They are intelligence problems.
Biology generates more data than it has ever been able to act on. The gap is not in sequencing, imaging, or discovery, it is in the infrastructure to reason through what that data means, connect it to knowledge, and surface answers that clinicians and researchers can act on with confidence.
We started Semantic Web Tech to close that gap. Not with another machine learning model that pattern matches historical data but with a reasoning engine that understands biological relationships, context, and consequence.
That engine powers SemGenome, our clinical genomics platform. And it is built to power much more.
WHAT WE DO
Get your Genomics Labs the analysis tool to deliver precise and effective clinical decision
with the SemGenome Genomics Decision Support platform. Integrate EHR, LIMS and your own knowledge sources for a seamless sample to report experience.
KromaBio is a curated collection of knowledge graphs built from vast biological sources unifying structured and unstructured data into a context-aware semantic knowledge graph that can be repurposed to enable pharma and clinical teams uncover relationships, generate insights, and accelerate advancements in genomics, drug discovery, and personalized medicine.
indiVAR-KB is a growing knowledgebase of genetic variants in the Indian population, aggregated from diverse sources using advanced knowledge representation - available as standalone, open access for single variant search, providing latest variant annotations aligned with ACMG/AMP/ClinGen guidelines.
HOW WE SEE AI
In genomic medicine, an AI recommendation is only as good as the reasoning behind it.
We don’t build black boxes. We build systems that clinicians can trace, verify, and trust — because in this field, explainability isn’t a feature. It’s a clinical requirement.
Transparent, Traceable AI — built to support your clinical judgement, not replace it.
Every variant prioritisation SemGenome produces is traceable to its source — the biological relationship, the database reference, the reasoning path. No recommendation without a reason. No reason without a citation.
Our AI is grounded in established biological knowledge — curated ontologies, peer-reviewed databases, validated clinical evidence. We augment human scientific judgement. We do not replace it.
Every decision SemGenome supports can be reviewed, challenged, and overridden by the clinician. The human is always in the loop. Always in control. AI advises. The clinician decides.
Responsible AI is not a policy we added after building the platform. It is a design principle embedded from day one — in our knowledge graph architecture, our annotation methodology, and our clinical workflow integration.
WHERE WE ARE TODAY
SemGenome is not a prototype waiting for its first customer. It is a live platform — deployed, integrated, and processing real patient cases in clinical and research environments today.
We are early. And we are already inside the lab
SemGenome underwent a pilot validation with datasets from leading genomics research organisations including Centre for Cellular and Molecular Biology and Centre for DNA Fingerprinting and Diagnostics.
SemGenome is live — integrated into real diagnostic workflows, processing patient cases, and delivering variant intelligence that clinicians act on.
As more cases flow through SemGenome, every case deepens the knowledge graph and the platform is enriched.
BACKED BY
Semantic Web Tech has been supported by Incubators and Investors in this journey through Angel Investment, Government Investments (SISFS, NIDHI SSS, TIDE 2.0).
The indiVAR-KB project was selected as part of the Karnataka Elevate 2023.
SemGenome was pilot tested and validated with data from our partners CCMB and CDFD.
The Indigenomes from IGIB is integrated within the SemGenome platform.
THE MISSION AND THE TEAM
MISSION - To bridge the gap between biological data and clinical action through AI that understands biology—democratizing intelligence across genomics and life sciences.
We are a team of genomics scientists, bioinformaticians, data scientists, and AI engineers who combine scientific rigour with technology execution — a team that understands both the biology and the technology that can power the next innovation
A team that has lived the problem — and is building the solution
GET IN TOUCH
Whether you are a clinician looking to transform your genomics workflow, a researcher seeking intelligent variant analysis, or an organisation looking to partner with one of TechBio’s growing platforms — we want to hear from you.
Discover how SemGenome can transform your genomic data into confident clinical and research decisions.
Reach us at
genomics(AT)semanticweb(DOT)tech
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Explore technology, channel, strategic, and investment partnership with Semantic Web Tech.
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partnership(AT)semanticweb(DOT)tech
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