CLIA Whole Genome Sequencing

GENEWIZ offers CLIA-compliant whole genome sequencing as a comprehensive analysis of the entire genome to uncover mutations in coding and non-coding regions, including structural and copy number variants.

Our CLIA-compliant next generation sequencing services provide sensitive and unbiased detection of genetic variants. These assays enable clinical researchers to answer focused biological questions using genome-scale information, fueling the advancement of precision medicine and biomarker discovery.

CLIA whole exome sequencing is available for more targeted genomic analysis.

We also offer RUO whole genome sequencing for your non-clinical needs.


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Features & Benefits

Flexible data analysis and regulatory oversight to meet study requirements
PCR-free protocols provide unbiased sequence information
Ph.D.-level support during the entire project, including free consultations
Variant confirmation via Sanger sequencing available for a streamlined CLIA-compliant workflow

FROM SEQUENCING TO DISCOVERY

1. SUBMIT SAMPLES

Submit DNA or blood sample

2. SEQUENCE

Sequencing on the Illumina® NovaSeq™ 6000

3. ANALYZE DATA

Receive raw data files and variant report

Service Levels

Service Level* Data & Report
(FASTQ, BAM & VCF)
QA Oversight Lab Director Signature
CLIA Environment

CLIA-Validated Service

Included | Not Available

*All service levels are performed by CLIA-trained personnel in a CLIA-certified lab with CLIA-qualified equipment.

Request Your CLIA Whole Genome Sequencing Quote

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Email | Phone (1-877-GENEWIZ (436-3949), Ext. 1)