Genomic Testing from Fulgent Genetics

DNA sequencing automation in a clinical laboratory.

FEATURED

FulGenome Delivers the Full Genomic Picture

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.

The optional addition of RNA analysis (RISE) enables deeper characterization of functional impact, providing a powerful tool for clinicians.

Explore Our Full Genomic Testing Suite

Whole genome sequencing with optional RNA analysis for unparalleled variant detection

Rapid Whole Genome Sequencing

Full genomic sequencing with fast turnaround for time-sensitive diagnoses

Analysis of over 6,500 genes for diagnosis of inherited conditions

Whole Exome Sequencing

Analysis of over 20,000 genes for diagnosis of unresolved conditions

Chromosomal Sequencing Analysis

Genetic testing for early diagnosis of pediatric syndromes

Mitochondrial Genome

Full mitochondrial genome sequencing to detect mtDNA variants and heteroplasmy

RNA-Integrated Sequence Evaluation (RISE)

Integrated DNA and RNA sequencing for complex or undiagnosed cases

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