The Helomnix Platform

A structured disease modeling framework that integrates multi-omics data into reusable Digital Twin Maps and interpretable biological states.

Helomnix applies this disease intelligence framework through collaborative analytical engagements with translational research teams.

From multi-omics inputs to structured biological outputs —
supporting biomarker discovery, target prioritization, and program-level biological insight in hematologic diseases.

How the Platform Works

Helomnix structures heterogeneous molecular data into reproducible disease-state models through a biology-grounded analytical framework.

1

Multi-Omics Integration

Bulk RNA-seq, single-cell data, proteomics, exome sequencing, digital pathology, and clinical annotations are harmonized and integrated at the cohort level.

2

Digital Twin Map Construction

Latent biological programs are identified and organized into a structured reference map of interpretable disease states — built once and reused across studies and programs.

3

Cohort Projection & State Assignment

New patient cohorts are mapped onto the reference framework without retraining. Each sample is assigned to its closest biological state for structured comparison across programs.

4

Structured Biological Outputs

The framework produces state definitions, molecular signatures, pathway context, and evidence-linked reports — supporting biomarker discovery, target prioritization, and translational research decisions.

Delivery model: collaborative programs with clear milestones and reusable disease state maps as the primary deliverable.

Request the Platform Architecture Brief

A technical overview of the Helomnix Digital Twin modeling architecture — covering reference map design, projection logic, and program-level translational integration.

Outcome-agnostic reference map construction grounded in intrinsic disease biology
Deterministic cohort projection and stable state assignment
Fixed coordinate topology enabling cross-cohort comparability
Structured reporting framework for translational program integration
Get the Solution Brief

Available upon request for scientific and translational program discussions.

Operational Integration & Governance

Helomnix operates as structured translational infrastructure — with version-locked reference maps, deterministic outputs, and reproducible analytical logic built into every engagement.

Governance Controls

  • Version-locked reference maps with stable, documented topology
  • Deterministic projection of new cohorts without model retraining
  • Separation of state construction and outcome evaluation to prevent analytical leakage
  • Transparent state definitions with recorded projection logic and parameters
  • Reproducible cohort outputs generated from fixed inputs and versioned artifacts

Program Integration

  • Retrospective projection of historical cohorts and trial datasets
  • Mechanism-aware stratification workflows for cohort segmentation
  • Target and biomarker context analysis across functional states
  • Support for prospective enrichment strategy discussions and study design inputs

Helomnix outputs are structured for cross-functional review across translational biology, biomarker strategy, and clinical development teams.

Data InputsReference Map (Version-Locked)Deterministic ProjectionStructured Translational Report

Stable reference structure — consistent cross-cohort comparability.

Core Analytical Engines

Foundational components of the Helomnix disease intelligence framework — built to convert multi-omics data into reusable biological states and reference maps.

Multi-Modal Integration Engine

Unified Molecular Representations

Integrates bulk RNA-seq, scRNA-seq, proteomics, and exome data into sample-level molecular representations with latent feature extraction

  • Multi-modal companion diagnostic development
  • Regulatory-ready biomarker discovery with cross-validation
  • Latent dimension extraction for advanced patient modeling
Digital Twin Map™

Reusable State Map & Cohort Contextualization

Visual 2D topological map of patient molecular profiles. Projects new patients onto the map to identify the most similar digital twins for biological context matching

  • Cohort alignment to reference state maps
  • Compound-biology relationship characterization across subgroups
  • Molecular subtype classification for translational workflows
Preclinical Response Profiling

AI-Powered Compound Profiling

Deep learning framework characterizing preclinical response patterns and compound–state alignment across a broad compound library using multi-omics digital twin representations

  • Preclinical response profiling and compound–state alignment across a broad compound library
  • Mechanistic alignment characterization to support study design
  • Compound–state association mapping for drug-biology alignment

Translational Workflows Enabled by the Platform

Reusable workflows built on Digital Twin Maps — supporting cohort definition, biomarker exploration, and target prioritization across hematology programs.

Multi-Omics Integration

Data fusion engine integrating bulk RNA-seq, scRNA-seq, proteomics, and exome sequencing into unified patient representations across multiple molecular layers.

Multiple modalities integrated per patient

Patient Molecular Subtyping

Unsupervised clustering identifies molecular subtypes in multiple myeloma (MM) and diffuse large B-cell lymphoma (DLBCL), revealing clinically relevant patient groups based on biological state rather than single markers.

Biology-driven patient stratification

Preclinical Response Profiling

Compound–state association mapping framework that characterizes preclinical response patterns across compound libraries, supporting translational hypothesis generation.

Compound library screening

XAI Biomarker Discovery

Explainable AI identifies robust gene signatures with mechanistic interpretability — designed for regulatory-aware biomarker development and companion diagnostic support.

Interpretable by construction

Digital Pathology AI

Deep learning models with attention mechanisms characterize molecular features from H&E slides — enabling virtual molecular profiling of archival cohorts without re-sequencing, and supporting cost-effective companion diagnostic development.

Image-omics integration

Knowledge Graph Explorer

Integrates gene essentiality evidence, preclinical response profiles, and pathway knowledge for systematic target contextualization and drug repurposing support.

Multi-source integration

Data Foundation

Curated multi-omics cohorts and proprietary in-vitro disease models designed for reproducible state modeling and cross-program reuse.

Multiple Myeloma Biobank

Longitudinal multi-omics cohort supporting state definition and biomarker contextualization in multiple myeloma.

Data modalities: Bulk RNA-seq, scRNA-seq, Proteomics, Exome sequencing
Sample types: Bone marrow aspirates (tumor), Peripheral blood (paired normal)
Clinical data: Survival outcomes, clinical outcome annotations, disease progression
Available for partnership

DLBCL Image-Omics Cohort

Integrated digital pathology and multi-omics for virtual molecular profiling and companion diagnostic development support

Data modalities: H&E digital pathology, Bulk RNA-seq, Mutation profiling, Clinical outcomes
AI capabilities: Molecular feature characterization from H&E, COO classification, multimodal analysis
Translational value: Virtual cohort screening, H&E-based companion diagnostic support, retrospective analysis
Available for partnership

AML Multi-Omics Biobank

Longitudinal multi-omics cohort supporting state definition and biomarker contextualization in acute myeloid leukemia.

Data modalities: Bulk RNA-seq, scRNA-seq, Proteomics, Exome sequencing
Sample types: Bone marrow aspirates, Peripheral blood (paired normal)
Clinical data: Clinical outcome annotations, survival outcomes, molecular evolution tracking
Available for partnership
UNIQUE

In-Vitro Plasma Cell Differentiation Model

Proprietary in-vitro model of normal plasma cell differentiation (Memory B-cell to Plasma cell). A functional state interrogation platform for mechanistic validation and perturbation studies — supporting research in myeloma, Waldenström macroglobulinemia, and autoimmunity without animal models.

Model capabilities: 4-stage differentiation trajectory with scRNAseq profiling at each stage
Applications: Functional state interrogation, CRISPR-based perturbation, mechanism discovery, companion diagnostic support
Access: Custom perturbation experiments (CRISPR, drug screening) + scRNAseq analysis via CHU partnership
Available for partnership

Data Modalities

Integrated data layers used to build and validate disease state maps.

Single-Cell Transcriptomics

Tumor heterogeneity profiling, microenvironment analysis, rare cell populations

10x Genomics, high-throughput scRNA-seq

Multi-Omics Integration

Bulk RNA + scRNA + Proteomics + Exome + Imaging for comprehensive molecular portraits

Multiple data layers integrated per patient

Gene Essentiality Data

Target validation using gene essentiality evidence from internal screens and curated reference data

Identify druggable dependencies

Clinical Annotations

Survival outcomes, clinical outcome annotations, disease progression with long-term follow-up

Biomarker contextualization

Engage the Helomnix Platform

Helomnix supports translational development programs through structured, reusable Digital Twin modeling. If you are advancing a clinical asset, refining stratification strategy, or exploring a target hypothesis, we can define a scoped analytical engagement.

Initiate a Scientific Discussion