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Our Genomic Solutions: Advanced NGS Services
Whole Exome Sequencing (WES)
Our WES services focus on decoding the protein-coding regions of the genome, offering unparalleled insights into genetic disorders and disease mechanisms.
Features:
- High coverage and accuracy for detecting rare variants.
- Comprehensive analysis of all exons for disease-related genes.
- Integration with bioinformatics pipelines for easy interpretation.
- Suitable for research, diagnostics, and personalized medicine applications.
Benefits:
- Accelerates the discovery of novel mutations.
- Enables the study of inhe
Tumor Profiling
Our tumor profiling services provide in-depth analysis of cancer-related genetic and molecular alterations to support precision oncology.
Features:
- DNA and RNA sequencing for comprehensive mutation detection.
- Identification of actionable biomarkers for targeted treatments.
- Analysis of copy number variations, structural variants, and gene fusions.
- Tumor mutational burden (TMB) and microsatellite instability (MSI) analysis.
Benefits:
- Facilitates personalized cancer treatment plans.
- Helps identify resistan
HLA Typing
Our high-resolution HLA typing solutions are designed for applications in immunogenetics, transplantation, and immune response research.
Features:
- High-throughput and high-accuracy sequencing for allele-level typing.
- Broad coverage of HLA class I and class II loci.
- Advanced bioinformatics tools for allele prediction and analysis.
- Suitable for solid organ and hematopoietic stem cell transplantation studies.
Benefits:
- Ensures transplant compatibility and reduces rejection risks.
- Supports autoimmune and in
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