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LIS System for genomics and molecular biology laboratories

Complete platform for precision medicine and next-generation sequencing (NGS).

Specialized genomics system that ensures total control of the analytical cycle, from sample reception to the release of molecular reports. Developed for laboratories operating with next-generation sequencing (NGS), molecular testing, and high-complexity genomic analysis.

Complete management of samples and aliquots in genomics

Individualized control of biological material.

Comprehensive management from reception to final processing, with specific traceability for each type of genetic material:

  • Intelligent fractionation: Individualized control of each generated aliquot
  • Configurable flows: Specific workflows for DNA, RNA, cfDNA, and other biological materials
  • Optimized internal logistics: Organization by department and grouping of exams by routine
  • Tracked movement: Every material transfer recorded with date, time, and responsible party

Control laboratory processes

Full traceability and regulatory compliance

Complete audit trail for genomics.

Unalterable historical record of all interventions in the analytical cycle:

  • Data integrity: The system prevents deletion or overwriting of original information
  • Complete logging: Date, time, and person responsible for every action
  • Version history: Tracking of all changes to reports and results
  • Guaranteed compliance: Architecture prepared for audits and accreditations

Complete management of samples and aliquots in genomics

Benchtop control.

Unified management of manual and automated stages:

  • Process monitors: Real-time visualization of the status of each sample
  • Service Orders (SO): Automatic generation for sample grouping
  • Individual traceability: Even in batch processing, each sample maintains its identity
  • Quality checkpoints: Mandatory validations at critical stages

Library preparation and NGS sequencing

Specialized modules for critical processes

Strict control over the most sensitive stages of the genomic workflow:

Management of indexes and barcodes

  • Controlled registration of indexes used
  • Prevention of combination duplication
  • Automatic sample-index-barcode association
  • Complete logging for troubleshooting

Pool creation and management

  • Intelligent sample grouping for sequencing
  • Automatic generation of sample sheets for sequencers
  • Calculation of concentrations and dilutions
  • Direct interface with Illumina, Thermo Fisher, and other manufacturers' equipment

NGS flow monitoring

  • Centralized visualization: extraction → library preparation → pooling → sequencing
  • Real-time bottleneck identification
  • Tracking of kits and reagents per run
  • Cost control per sample/panel

Integration with bioinformatics and data analysis

90% reduction in report preparation time.

Automated communication with genomic analysis tools:

Integration with analysis pipelines
  • Automatic reception of results from bioinformatics software
  • Import of VCF, BAM, and other genomic formats
  • Automatic variant classification (pathogenic, benign, VUS)
  • Annotation with clinical databases (ClinVar, OMIM, HGMD)
Configurable reports by exam type
  • Specific templates: oncology panels, exome, carrier screening, pharmacogenomics
  • Automatic inclusion of identified variants
  • Structured clinical interpretation
  • Standardized HGVS nomenclature
  • Adaptable layouts by health insurance provider or requesting physician
Comprehensive
interfacing
  • Direct connection with automated extractors (QIASymphony, Maxwell, MagNA Pure)
  • Integration with real-time PCR equipment
  • Interfacing with sequencers from multiple manufacturers
  • Bidirectional communication with hospital systems (HL7/FHIR)

Management dashboard for molecular genomics

Business intelligence for genomic laboratories.

Complete analytical view of the operational scenario for strategic decision-making:

Operational indicators
  • TAT by exam type (panels, exome, genome)
  • Productivity by department and by analyst
  • NGS run success rate
  • Identification of flow bottlenecks
Financial indicators
  • Cost per exam/per run
  • Reagent and kit utilization
  • Revenue projection per panel
  • Equipment ROI
Quality indicators
  • Reprocessing rate
  • QC metrics (coverage, read quality)
  • Contamination control
  • Compliance with validated protocols

Compliance with national and international standards

The foundation for genomics accreditations.

Architecture developed to meet the rigorous quality standards required in clinical genomics.

Supported Accreditations:

  • PALC (Clinical Laboratory Accreditation Program - SBPC/ML)
  • CAP (College of American Pathologists) - Molecular Pathology
  • ISO 15189 (Medical Laboratories)
  • CLIA (Clinical Laboratory Improvement Amendments)
  • ANVISA (compliance with RDC 302 and specific regulations)

Compliance features:

  • Non-conformity management
  • Control of corrective and preventive actions
  • Method and process validation
  • Management of proficiency testing and interlaboratory comparison trials
  • Audit-ready evidence

Why choose MotionLIS Genomics?

Proven Benefits.

90% reduction in report preparation time

Direct integration with bioinformatics.

Zero index errors

Rigorous control of barcodes and sample sheets.

Full traceability

From the blood tube to the molecular report.From the blood tube to the molecular report.

Guaranteed compliance

Approved by national and international accreditations.

Scalability

From PCR to whole-genome sequencing.

Measurable ROI

Optimization of NGS runs and reduction in reprocessing.

Request a demo

Discover how MotionLIS Genomics can transform your genomic laboratory’s operations.

Contact our team to schedule a personalized demo.

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