Project Vision: Automated Genomics Analysis Platform

From raw data to interactive exploration in minutes, not weeks

status
Data Extraction status
goal
Analysis Pipeline goal
impact
Discovery platform impact
proven
Tested on 3 datasets proven

❌ The Current State of Genomics Analysis

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Researchers spend weeks running standard analyses (DESeq2, GSEA) that only confirm known biology

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Unknown genes get ignored because there's no literature to reference

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Results come as static PDFs with tables that can't be explored interactively

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Each new dataset requires writing custom analysis code from scratch

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No easy way to navigate gene relationships or discover novel patterns

✅ Our Vision: End-to-End Analysis Platform

Upload your genomic data → Get an interactive web report with AI-powered exploration tools

1

Upload Data

RNA-seq counts, sample metadata, experimental design..

2

Configure Analysis

Choose analyses: clustering, networks, ML classification, dose-response. ML suggests optimal parameters.

3

Automated Processing

Backend runs full statistical pipeline: normalization, clustering, network analysis, enrichment..

4

Interactive Report

Deployed web app with force graphs, UMAP visualization, AI chatbots, gene prioritization..

🎯 Proof of Concept: Senescence Reversal Analysis

This site demonstrates the platform analyzing NANOG-mediated reversal of cellular aging in human muscle cells.

Dataset

Shahini et al. (2021) Science Advances

6,613 genes 15 samples
Conditions: Young myoblastsSenescent myoblastsNANOG treatment (5d, 10d, 15d)

Platform Features

• 8 gene clusters identified via UMAP and k-means
• Interactive force graphs - click any gene to explore its network
• ML classification - Type A (reversing markers), Type B (off-target responders), Type C (resistant markers)
• Dose-response analysis - temporal kinetics across 3 timepoints
• Multi-evidence scoring - combines network topology, expression patterns, statistics, ML predictions
• AI chatbots available - context-aware assistants trained on your data
• External integrations - MyGene, UniProt, STRING, PubMed for comprehensive gene info

Scientific Insights

• Type B genes (13.3%) respond strongly to NANOG but aren't senescence markers - revealing off-target effects
• 67.7% of genes are late responders requiring >10 days sustained treatment
• Force graph navigation reveals functional relationships between known and unknown genes

🔧 Reusable Components

Backend (Python)

  • ✓ Modular Python pipeline: clustering, network analysis, ML, enrichment
  • ✓ Works across mouse/human, aging/reprogramming contexts
  • ✓ Produces structured JSON outputs for frontend

Frontend (SvelteKit)

  • ✓ Force-directed network graphs (D3.js)
  • ✓ UMAP cluster visualization
  • ✓ Dose-response trajectory charts
  • ✓ Gene prioritization tables with sorting/filtering
  • ✓ Context-aware AI chatbots
  • ✓ External data integrations (MyGene, UniProt, STRING, PubMed)

🚧 Path to Full Automation

Backend Automation

  • ○ ML-assisted parameter selection (cluster count, thresholds)
  • ○ Automated analysis selection based on data type
  • ○ Smart preprocessing for different sequencing platforms
  • ○ Advanced network construction methods
  • ○ Batch processing for multiple datasets

Generic Frontend

  • ○ Configuration-driven UI (zero hardcoding per dataset)
  • ○ Dynamic component loading based on available analyses
  • ○ User-customizable dashboards
  • ○ Export reports (PDF, interactive HTML)

Platform Launch

  • ○ Upload interface for raw data
  • ○ Analysis wizard with ML suggestions
  • ○ Cloud processing backend
  • ○ Hosted reports with shareable links
  • ○ Collaboration features

👥 Who Benefits

Academic Researchers

Skip weeks of coding, get interactive results immediately, share live reports with collaborators

Biotech Companies

Rapid target discovery from internal datasets, standardized analysis pipelines, publication-ready figures

Core Facilities

Offer value-added services beyond raw data delivery, differentiate from competitors

Funding Agencies

Interactive reports make grant applications more compelling, demonstrate data-driven decision making

⭐ The Impact

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Democratizes genomics: No coding required to explore complex datasets

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Accelerates discovery: Find patterns in hours that would take weeks manually

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Reveals unknowns: Force graphs help researchers see relationships with uncharacterized genes

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Reproducible science: Every analysis documented with parameters, thresholds, software versions

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Share insights: Live web reports are more impactful than static PDFs

🚀 Try It Yourself

Explore this proof-of-concept analyzing 6,613 genes across young, senescent, and NANOG-treated myoblasts. Click through clusters, genes, and force graphs. Chat with AI assistants on every page. See what automated genomics analysis could look like.

Try these features:

  • → Navigate via force graphs - click any gene to explore its network
  • → Ask AI chatbots about mechanisms, pathways, or specific genes
  • → View dose-response trajectories with individual sample data

🛠️ Technical Stack

Backend: Python (pandas, scikit-learn, umap-learn, networkx, scipy, statsmodels)
Frontend: SvelteKit with Svelte 5, D3.js, Chart.js, Tailwind CSS
AI: Claude API with extended thinking, multiple agents, streaming responses
Deployment: Vercel (Pro plan with 800s timeouts)