CLIA Services from the Name You Know and Trust


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Clinical Services

To support clinical applications, GENEWIZ has established next generation sequencing and Sanger-based CLIA-compliant workflows ensuring high-quality laboratory testing for accurate and consistent sequencing results.​

Our clinical lab is certified by The Centers for Medicare & Medicaid Services (CMS) through the Clinical Laboratory Improvement Amendments (CLIA) and accredited by the College of American Pathologists (CAP) for providing clinical sequencing.


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Features & Benefits

Superior data quality that exceeds manufacturer’s benchmarks​
Industry-leading turnaround time delivers results when you
need it​
Ph.D.-level support during the entire project, including free consultations
Complementary NGS and Sanger services provide variant discovery-to-validation workflows​

Clinical Next Generation Sequencing

GENEWIZ offers clinical NGS at two levels:

Research Use Only NGS in CLIA Environment

Sequencing performed in a CLIA-certified, CAP-accredited laboratory by CLIA-trained personnel on CLIA-qualified equipment. Recommended if data is used for research purposes only.

CLIA-Validated NGS

Our CLIA-validated assays provide the highest level of clinical regulatory compliance, including enhanced QA oversight and laboratory director signoff. Recommended if data is used for diagnostic purposes.

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    Whole Genome

    CLIA Environment | CLIA-Validated

    Uncover mutations in coding and non-coding regions, including structural and copy number variants.


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    Whole Exome

    CLIA Environment | CLIA-Validated

    Probe protein-coding regions of the genome at high depth with uniform coverage.


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    RNA-Seq

    CLIA Environment

    Profile the transcriptome to measure gene expression levels or discover novel transcripts.​


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    Whole Genome Metagenomics

    CLIA Environment

    Identify and compare the microbial species within clinical samples.​



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Clinical Sanger-Based Sequencing

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    Sanger Sequencing

    CLIA Sanger sequencing is best utilized to elucidate complex regions or to confirm variants uncovered by genome-wide techniques.

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    Variant Confirmation (PCR + Sanger)

    Reliable method for initial analysis or orthogonal confirmation of next generation sequencing, microarrays, or qPCR results.

CERTIFICATIONS

  • CMS CLIA Certificate

  • CAP Certificate

  • NJ Clinical Lab License