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FulGenome - Whole Genome Sequencing Analysis NGS Panel

Message
FulGenome is a next-generation whole genome sequencing (WGS) solution designed to provide comprehensive genomic insights through a single, streamlined report. Leveraging advanced sequencing technology and our proprietary bioinformatics pipeline, FulGenome delivers enhanced variant detection, including single nucleotide variants (SNVs), copy number variants (CNVs), genome-wide del/dups, mitochondrial genome alterations, and repeat expansions. 


Test Code
FULGENOME (WHOLE GENOME SEQUENCING)


Includes
Genes: 20,000+


Preferred Specimen
Blood (two 4ml EDTA tubes, lavender top) or saliva/buccal swabs. 


Methodology
Whole genome sequencing by PCR-free NGS; confirmatory ancillary assays may include Sanger sequencing, qPCR, RP-PCR, and/or MLPA.

Performing Laboratory
Fulgent Genetics.
4399 Santa Anita Ave
El Monte, CA 91731

Additional Information
Click here

Last Updated: February 19, 2026


The CPT Codes provided in this document are based on AMA guidelines and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payor being billed. Any Profile/panel component may be ordered separately. Reflex tests are performed at an additional charge.