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NGS LIMS

Simplifying Molecular Testing, Sequencing Workflows, and Clinical Reporting

Modern molecular diagnostics and genomics laboratories manage increasingly complex workflows involving molecular assays, DNA/RNA sample processing, sequencing, quality control, variant interpretation, and clinical reporting. As testing volumes continue to grow, laboratories need a platform that ensures complete traceability, operational efficiency, and secure data management.

Molecular Diagnostics & NGS LIMS is an enterprise Laboratory Information Management System designed for molecular diagnostics and Next-Generation Sequencing laboratories. It brings every stage of the laboratory workflow together into one centralized platform—helping laboratories streamline operations, reduce manual processes, improve turnaround times, and deliver reliable diagnostic results.

  • Molecular Diagnostics Laboratories
  • Clinical Genomics Laboratories
  • Genetic Testing Laboratories
  • Oncology & Precision Medicine Centres
  • Infectious Disease Laboratories
  • Public Health Laboratories
  • Hospital Molecular Laboratories
  • Research & Academic Institutions
  • Pharmaceutical & Biotechnology Companies

Core Capabilities

  • Molecular Test Workflow Management
  • DNA & RNA Sample Management
  • End-to-End Sample Traceability
  • Sequencing Workflow Management
  • Quality Control Management
  • Variant Review & Interpretation
  • Clinical Report Generation
  • Patient Portal & Report Access
  • Laboratory Analytics & Dashboards
  • Multi-site Laboratory Management

Why Choose Labsols?

  • End-to-End Laboratory Workflow Management
  • Complete Sample Traceability
  • Workflow Automation
  • Centralized Laboratory Operations
  • Improved Turnaround Time
  • Secure Data Management
  • Real-Time Laboratory Visibility
  • Enterprise Scalability
  • Multi-site Laboratory Support
  • Cloud or On-Premise Deployment

Complete Laboratory Workflow

Labsols Molecular Diagnostics & NGS LIMS

Patient Registration

Register patient demographics and test request.

Sample Collection

Collect blood, tissue or other specimen.

Sample Accessioning

Barcode generation and laboratory accession.

DNA / RNA Extraction

Automated or manual nucleic acid extraction.

Molecular Testing

PCR, qPCR and molecular diagnostic testing.

Library Preparation

NGS library preparation workflow.

NGS Sequencing

Sequence samples using supported sequencers.

Quality Control

Validate sequencing quality and coverage.

Variant Interpretation

Analyze variants using clinical databases.

Clinical Review

Pathologist and clinician validation.

Report Generation

Create finalized clinical reports.

Patient Portal

Secure online access to laboratory reports.