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Genomic & Bioinformatics Services

Comprehensive whole genome sequencing and genomic analysis for stem cell research, genome editing and cell therapy development.

WGS-Based Genomic Analysis from Discovery to Clinical Development

REPROCELL provides whole-genome sequencing (WGS)-based bioinformatics services to support stem cell research, genome editing, and cell therapy development. Our analyses help characterize cell lines, evaluate genome editing outcomes, assess genomic stability, and generate data packages for research, translational, and clinical-stage programs. 

For regulated projects, genomic analyses are performed through qualified laboratory partners operating under appropriate quality systems and certifications.

Available Reports & Analysis Packages

Choose from our portfolio of ready-to-order reports or request a custom analysis.

Report Typical Application
✓ OncoPanel Report (400+ genes) Cancer-associated variant screening
✓ Copy Number Variation (CNV) Chromosomal alterations
✓ Mitochondrial Genome Analysis mtDNA integrity
✓ Off-Target Analysis Gene-editing verification
✓ HLA Typing Cell therapy development
✓ Blood Group Genotyping Donor characterization
✓ STR Profiling Cell line authentication
✓ Genomic Stability Report Long-term culture monitoring
✓ Donor-to-Product Comparability Development tracking
✓ Disease/Indication Variant Report * Targeted variant analysis
✓ Custom Bioinformatics Report Tailored analyses

* For research use only; not intended for clinical diagnosis

Research Applications

  • Cell line characterization

  • Cell line authentication

  • Gene-editing assessment

  • Clone selection

  • Genomic profiling

  • Comparative cell line analysis

Cell Therapy Applications

  • Donor characterization

  • iPSC Seed Clone characterization

  • MCB/WCB characterization

  • Donor-to-product comparability

  • Gene-editing safety assessment

  • Product characterization

  • Disease variant analysis *
 * For research use only, not intended for clinical diagnosis

Featured Workflow

Donor-to-Product Comparability Analysis

Assess genomic integrity, identify genomic and emerging variants, and evaluate comparability across key stages of your cell therapy development program. 

Featured Workflow Bioinformatics page

 
INCLUDES
 
Genome Integrity Monitoring
Detect structural variants, CNVs and copy-neutral LOH.
Acquired Variant Detection
Identify SNVs, indels and variants acquired over time. 
Clone Selection Support
Compare genomic profiles to inform clone selection.
Comparative Genomic Analysis
Track genomic changes across clones and passages. 
Product Characterization

Characterize genomic features relevant to product quality.

Regulatory-Supporting Evidence
Generate traceable data for regulatory submissions. 


Why REPROCELL?

Where Genomics Meets Stem Cell Expertise

Sequencing tells you what changed. REPROCELL helps you understand why it matters.

Our unique combination of stem cell biology, genome engineering, and bioinformatics transforms genomic data into actionable insights for research, translational development, and cell therapy.

Explore Relevant Pages:

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All REPROCELL Services — Stem Cell, Drug Discovery, and Analytical