Built by a Genome Analyst,
for Everyone

LYFE Sciences began as a personal project in 2023 to simplify genetic variant interpretation in day-to-day work. As a genome analyst, I frequently encountered the challenge of quickly accessing comprehensive and reliable genetic variant information.

To address this need, I built LYFE Sciences. an accessible, user-friendly tool that consolidates crucial genetic data in one place.

My main goal is to streamline variant analysis by reducing the need to navigate between multiple resources or pay for third-party applications.

I continually update LYFE Sciences with the latest AI architectures and enhancements to keep it practical, relevant, and useful for everyday clinical and research work.

LYFE Sciences is designed around the real workflows of genomic professionals. Rather than requiring users to juggle ClinVar, OncoKB, JAX-CKB, COSMIC, and other databases independently, Project HERA aggregates, normalises, and presents that data in a unified interface.

Every query runs against up-to-date sources so that interpretations reflect the latest evidence and not a static snapshot from months ago.

Project HERA is my third iteration of the LYFE SCIENCES project and is a modular AI pipeline for variant interpretation that integrates retrieval, normalization, framework selection, criterion assessment, and structured result generation into a single workflow.

It is designed around the idea that reliable AI needs controlled inputs, explicit evidence mapping, framework-aware decision logic, and outputs that are easy to audit and operationalize.

The pipeline combines automated evidence gathering with agentic-based decision making, prioritizes ClinGen and gene-specific specifications, and produces structured review artifacts for downstream systems.

Project HERA is an example of how AI-native pipelines can bridge language models, domain-specific logic, and production software architecture, without sacrificing the traceability that clinical use demands.

By sharing LYFE Sciences, I hope to make genetic analysis less overwhelming; helping others like myself improve their work.

Faster variant interpretation means analysts spend less time hunting for information!