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 also available for more targeted genomic analysis.


Request Quote   
Building

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

add text here

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