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Next Generation Sequencing (NGS)

  The Next-Generation Sequencing (NGS) Analysis Laboratory at Diagnomics is a hub of advanced genomic research and applications. Equipped with cutting-edge Illumina sequencing technology, our lab delivers accurate, high-throughput sequencing solutions tailored to a variety of clinical and research needs.


Key Features of Our NGS Laboratory

  • Advanced Illumina Sequencers:
    • Our facility is powered by Illumina platforms, including systems capable of performing:
      • Whole-genome sequencing (WGS)
      • Whole-exome sequencing (WES)
      • Transcriptome analysis (RNA-Seq)
      • Targeted panel sequencing for specific genes or regions.
  • Comprehensive NGS Services:
    • Clinical Applications: Including oncology, rare disease diagnostics, pharmacogenomics, and personalized medicine.
    • Research Applications: Covering areas like population genomics, evolutionary biology, and microbiome studies.
    • Epigenomic Sequencing: Such as methylation sequencing and chromatin profiling.
  • Applications of Our NGS Services:
    • Identification of genetic variants associated with diseases.
    • Cancer mutation profiling and liquid biopsy solutions.
    • Transcriptomic insights for understanding gene expression patterns.
    • Microbial and metagenomic analysis for health and environmental studies.
  • Expert Workflow and Quality Standards:
    • Sample Preparation: Precise extraction and library preparation techniques optimized for various sample types (blood, tissue, cfDNA, etc.).
    • Data Generation: Utilizing Illumina’s proprietary sequencing-by-synthesis (SBS) technology for unparalleled accuracy.
    • Bioinformatics Pipeline: From raw data processing to advanced interpretation, we provide actionable insights using industry-leading tools.
  • Collaborative Expertise:
    • Our team of genomics experts works closely with clients to design and execute projects, ensuring alignment with their research goals and clinical objectives.
    • We prioritize communication, customization, and delivering insights that matter.


Why Choose Diagnomics for NGS?

  • Precision: Illumina sequencing technology ensures exceptional accuracy and depth.
  • Flexibility: Customizable sequencing strategies for diverse applications.
  • Innovation: Stay at the forefront of genomic research with cutting-edge solutions.
  • Experience: A decade of expertise in delivering NGS services to global partners.


At Diagnomics, our NGS Laboratory bridges the power of Illumina sequencing with innovative bioinformatics to uncover genomic insights that drive meaningful advances in healthcare, research, and beyond. Let us partner with you to unlock the potential of your next NGS project.

Microarray

 At Diagnomics, our Microarray Analysis Laboratory is at the forefront of precision genomics, delivering high-quality genetic and epigenetic insights using advanced microarray technologies. We specialize in providing tailored solutions to meet the diverse needs of researchers, clinicians, and industry partners.


Key Features of Our Laboratory

  • State-of-the-Art Technology:
    • Our laboratory primarily utilizes Illumina microarray platforms, renowned for their accuracy, reliability, and high-throughput capabilities. This technology ensures robust data quality and comprehensive genomic coverage.
  • Comprehensive Services:
    • Genotyping for disease risk assessment, ancestry analysis, and pharmacogenomics.
    • Methylation profiling for epigenetic studies, focusing on health, wellness, and disease biomarkers.
    • Custom array services, designed to suit specific project requirements.
  • Applications of Our Microarray Services:
    • Precision medicine and personalized healthcare.
    • Wellness and preventive health programs.
    • Population genomics and cohort studies.
    • Research in oncology, cardiovascular diseases, and metabolic disorders.
  • Expertise and Quality Assurance:
    • Our team includes highly trained specialists with extensive experience in array data processing and analysis.
    • We adhere to stringent quality control measures at every stage of the workflow to ensure reproducibility and accuracy.
  • Data Analysis and Interpretation:
    • We provide end-to-end support, from raw data generation to advanced bioinformatics analysis.
    • Our interpretative insights empower actionable decisions in clinical and research settings.


Why Choose Diagnomics?

  • Reliability: Over a decade of expertise in genomics, serving clients globally.
  • Customization: Flexibility to adapt protocols and analyses to your unique needs.
  • Efficiency: High-throughput systems for rapid turnaround times without compromising quality.
  • Collaboration: Dedicated support for project planning, execution, and result interpretation.


At Diagnomics, we bridge the gap between cutting-edge genomics technology and meaningful applications, enabling breakthroughs in health, wellness, and disease management. Contact us to explore how our Illumina microarray services can power your next project.

Genotyping

  The Genotyping Service Laboratory at Diagnomics specializes in delivering high-quality, accurate, and cost-effective genotyping solutions. Using the QuantStudio™ 12K Flex Real-Time PCR System, our laboratory provides flexible and scalable services tailored to research, clinical, and industrial needs.


Key Features of Our Genotyping Laboratory

  • State-of-the-Art Technology:
    • The QuantStudio™ 12K Flex Real-Time PCR System is a versatile platform that supports a wide range of genotyping assays, offering high-throughput capabilities and precise data for single-nucleotide polymorphisms (SNPs) and other genetic markers.
  • Comprehensive Genotyping Services:
    • SNP Genotyping: Identification of genetic variations for population studies, disease association, and pharmacogenomics.
    • Copy Number Variation (CNV) Analysis: High-resolution detection of CNVs associated with diseases.
    • Allelic Discrimination Assays: Precise genotyping for clinical and research applications.
    • Custom Assay Development: Tailored genotyping solutions for specific research needs.
  • Applications of Our Genotyping Services:
    • Precision Medicine: Identification of genetic predispositions to diseases and drug responses.
    • Agrigenomics: Genotyping for crop improvement and livestock breeding.
    • Population Genetics: Genetic diversity studies and ancestry research.
    • Pharmacogenomics: Optimizing drug therapies based on genetic markers.
  • Expert Workflow and Quality Standards:
    • Sample Handling: Rigorous protocols to ensure sample integrity and reproducibility.
    • Assay Flexibility: Capable of running up to 12,000 data points per run for large-scale projects.
    • Data Accuracy: Robust algorithms for precise genotyping and efficient discrimination of alleles.
    • Quality Control: Comprehensive checks at every stage to ensure reliable results.
  • Customized Support and Bioinformatics:
    • Our team provides personalized consultation to design and execute genotyping projects.
    • Post-analysis support includes data interpretation and integration with broader research objectives.


Why Choose Diagnomics for Genotyping?

  • Precision and Speed: Fast turnaround times with uncompromising accuracy using the QuantStudio 12K Flex system.
  • Scalability: Accommodates projects of all sizes, from small research studies to large population surveys.
  • Customization: Flexibility to develop and adapt assays for specific needs.
  • Experience: Proven track record of delivering reliable genotyping data for diverse applications.


At Diagnomics, our Genotyping Service Laboratory bridges cutting-edge technology with scientific expertise to unlock genetic insights that matter. Partner with us to power your research, clinical, or industrial projects with unparalleled accuracy and efficiency.

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