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  • Deep Learning

Multi-View Hypergraph Neural Network for Disease-Gene Association Prediction

An explainable bioinformatics framework that predicts disease-gene associations from biological networks.

Overview

Multi-view hypergraphs are constructed from protein-protein interaction and pathway data, and hypergraph neural encoders learn gene embeddings through structured message propagation. Contrastive alignment improves consistency between the two biological views, and predictions are backed by evidence from gene ontology, pathway co-membership and PPI connectivity — reaching 0.9434 validation AUC.

Problem Statement

Ordinary graphs model only pairwise gene relationships, but biological interactions are frequently many-to-many. Predictions that cannot cite biological evidence are not actionable for a researcher.

Proposed Solution

Represent the biology as hypergraphs so group-level interactions survive the encoding, align multiple biological views contrastively, and attach explicit ontology and pathway evidence to each predicted association.

Key Features

  • Multi-View Hypergraph Construction

    Builds views from protein-protein interaction and pathway data.

  • Hypergraph Neural Encoders

    Learns gene embeddings via structured message propagation.

  • Contrastive Alignment

    Improves consistency between the two biological views.

  • Explainable Predictions

    Evidence from gene ontology, pathway co-membership, and PPI connectivity; 0.9434 validation AUC.

Technologies Used

Deep Learning

  • Hypergraph neural networks
  • PyTorch Geometric
  • Contrastive learning

Bioinformatics

  • PPI networks
  • Gene Ontology
  • Pathway databases
  • NetworkX

Evaluation

  • AUC
  • Cross-validation
  • Scikit-Learn

Project Workflow

  1. 1

    Network construction

    Hypergraph views are built from PPI and pathway data.

  2. 2

    Embedding

    Hypergraph encoders learn gene representations.

  3. 3

    View alignment

    Contrastive loss aligns the two biological views.

  4. 4

    Prediction

    Disease-gene associations are scored.

  5. 5

    Evidence

    Ontology and pathway evidence is attached to each call.

What You'll Receive

  • Complete, runnable source code with folder structure
  • Project report and technical documentation
  • Ready-to-present PPT content
  • Setup and installation walkthrough
  • Line-by-line project explanation session
  • Viva question bank with answers
  • Bug fixing and troubleshooting help
  • Post-delivery support after submission

Frequently Asked Questions

How much does this project cost?

Every project is quoted individually, because the price depends on the modules you need, your technology stack, your college's format and your deadline. Send us the project name on WhatsApp and we'll share a quote the same day.

Can the project be customised to my college requirements?

Yes. Share your guide's requirements, preferred technology stack and abstract format, and we adapt the modules, dataset or UI accordingly.

Will I be able to explain this project during my viva?

That is the point of the explanation session. We walk you through the architecture, every module, the flow of data and the results, and hand over a viva question bank with answers.

What if the project does not run on my laptop?

We help you with setup end to end — dependencies, environment, database and configuration — over chat or a call until it runs on your machine.

Do I get support after submission?

Yes. Post-delivery support is included, so you can come back for fixes, doubts or demo help even after the project is delivered.

Want This Project?

Get complete source code, documentation, PPT, explanation, and support.

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