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Development of a Scalable Web Platform for Cancer Genomics Consultations and Services
  1. case
  2. Development of a Scalable Web Platform for Cancer Genomics Consultations and Services

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Development of a Scalable Web Platform for Cancer Genomics Consultations and Services

light-it.net
Medical
Information technology
Health & Fitness

Addressing Gaps in Cancer Genomics Analysis

Complex genetic changes driving 73% of cancers remained unaddressed, leading to suboptimal outcomes in bioinformatics studies and a lack of competitive solutions in the European IT market. Existing tools lacked precision, reliability, and accessibility for researchers.

About the Client

A health tech startup specializing in cancer genomics software, offering innovative sequencing analysis solutions for complex genetic changes.

Platform Goals

  • Create a web-based system for consultations and services in next-generation sequencing (NGS) analysis
  • Commercialize bioinformatics and gene-editing services for researchers
  • Improve error rates and detection ranges in genomic analysis
  • Support seamless collaboration between researchers, consultants, and experts

Core System Functionalities

  • Multi-role access control (customers, consultants, content editors, investigators, superadmins)
  • Support for .fastq and other genomic data file formats
  • Consultation booking with filtering by expertise, cost, and location
  • Integrated payment systems (credit card, invoice)
  • Product ordering for DNA extraction, primer design, and validation
  • Responsive design with user-friendly UI/UX
  • Email notifications for system events

Technology Stack

Python
Django
Angular
PostgreSQL
Redis
Uwsgi
Kubernetes

External Integrations

  • Payment gateways (credit card processing)
  • NGS analysis pipelines
  • Email notification services

Non-Functional Requirements

  • Full compliance with healthcare data standards (e.g., HIPAA, GDPR)
  • High scalability to handle large genomic datasets
  • Robust security for sensitive biological data
  • Cross-browser and device compatibility

Expected Business Impact

Enables entry into the €2.8B cancer genomics software market, reduces NGS analysis error rates by 75%, and improves detection ranges tenfold. The platform enhances researcher productivity, accelerates sample-to-analysis workflows, and strengthens brand visibility in the healthcare sector.

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