Comprehensive Selection of Services

Fulgent provides comprehensive NGS-based clinical and research sequencing services with competitive prices and fast turnaround times.

Our team consists of bioinformaticians and scientists who are pioneers in the field of NGS-based genetic testing, equipping Fulgent with the knowledge and experience to push us to the forefront of science and technology. Our state-of-the-art sequencing platforms give us tremendous sequencing capacity, ensuring that we can handle projects of all size and scale.

Clinical Quality

As a CLIA-certified and CAP-accredited clinical laboratory, we adhere to the strictest quality control standards in the industry. All samples that we receive undergo several QC checks throughout the laboratory process, starting from before extraction and continuing through the library, sequencing, and post-sequencing phases.

We utilize sophisticated barcoding and tag systems to track each sample and prevent sample mix-up, and we follow a unidirectional workflow that is highly integrated with our in-house developed laboratory information management system (LIMS) to ensure that every sample is tracked and handled proficiently. If you have any questions about quality standards, please contact us at SeqService@fulgentgenetics.com

Fast Turnaround Times

We have a very streamlined and highly automated laboratory workflow, which ensures that we can deliver clinical-grade quality at very competitive turnaround times.

All samples follow the same general flow, which begins with accessioning the sample, and then proceeding with extraction -> library prepartion -> sequencing -> analysis. Once results are ready, they will be delivered via secure FTP.

Cutting Edge Technology

As a laboratory built around NGS-technology we offer an impressive array of state-of-the-art sequencing platforms – each designed for different sequencing needs and applications. Our broad suite of sequencers ensures that we can provide affordable, fast, and high-quality sequencing services for diverse projects of virtually any scale.

  • NovaSeq
  • HiSeq X Ten
  • HiSeq 4000
  • NextSeq
  • MiSeq
WGS & WES

Whole Genome Sequencing

The most comprehensive approach to genomic testing - WGS analyzes the entire genome so you can be confident that you covered all your bases.

Whole Exome Sequencing

A more targeted approach than WGS, WES looks across the relatively small protein-coding region of the genome.

Methylation Sequencing

Whole Genome Bisulfite Sequencing

A powerful approach to epigenetic studies, whole genome bisulfite sequencing looks at methylation patterns across the entire genome to reveal valuable information on chromatin remodeling and gene expression.

Cancer Sequencing

Inherited Cancer Research Sequencing

Deep sequencing of 139 genes and regions of interest known to be associated with various types of inherited cancers.

RNA Sequencing

We provide flexible RNA sequencing services - from small RNA and miRNA sequencing to sequencing of the coding transcriptome and the whole transcriptome.

Mitochondrial DNA Sequencing

Sequencing of the small mitochondrial genome (16,569 bp) - can be a powerful tool for researchers interested in mitchondrial disorders and mechanisms of aging.

Rent-a-Lane Services

Didn't find exactly what you were looking for? We offer the option to rent a variety of state-of-the-art sequencing platforms, allowing you to customize sequencing projects depending on your specific needs. You can select from Illumina NovaSeq, HiSeq4000, and MiSeq – each of which is designed for different sequencing applications.