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

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

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

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

Each new dataset requires writing custom analysis code from scratch

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

Democratizes genomics: No coding required to explore complex datasets

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

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

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

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)