CLIA Whole Exome Sequencing

GENEWIZ offers CLIA-compliant whole exome sequencing as a powerful, cost-effective method to probe protein-coding regions of the genome at high depth and with uniform coverage.

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 genome sequencing is available for more comprehensive genomic analysis.

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


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Features & Benefits

Flexible data analysis and regulatory oversight to meet study requirements
Latest enrichment capture technology for uniform exome coverage
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 EXOME SEQUENCING QUOTE

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