Fulgent Genetics

Fulgent Genetics Fulgent Genetics is a CAP and CLIA certified clinical laboratory in Los Angeles that's dedicated to improving patient care. Why Fulgent ?

Mission
Developing flexible and affordable genetic testing that improves the everyday lives of those around us. Founded in 2011, Fulgent began with two simple ideas; flexibility and affordability. Today, we strive to create the most effective and wide ranging tests on the market. All of this is done in the pursuit of bettering the everyday lives of our customers. We shine brightest when meaningful

relationships, passion, and purpose come together. We are committed to working side-by-side with every one of our clients. This is essential to a strong and successful relationship and is our core way of doing business. We have collaborated with some of the top clinicians in our field who have assisted us in creating our panels, report formatting, and improvements to our website. Our approach has always been simple: provide testing based on the specific needs of clinicians and their patients. Customer Support
Our support philosophy has always been simple: answer our client's questions quickly and accurately. We do not have a receptionist or an automated system, we have a dedicated team of customer support staff that can answer a wide variety of questions, so you can spend more time with what is really important, patients.

18,000+ single gene tests. 900+ panel tests. One lab. Reproductive health, oncology, rare disease, pharmacogenomics, ana...
08/25/2026

18,000+ single gene tests. 900+ panel tests. One lab.

Reproductive health, oncology, rare disease, pharmacogenomics, anatomic pathology — our menu spans a lot of ground. Providers and institutions shouldn't have to juggle multiple labs to get a full picture of a patient's care.

If you could ask for one new panel or test to be added to a lab's menu, what would it be?

Our team's contributions to the field of genomics take a lot of forms — peer-reviewed publications, conference posters, ...
08/20/2026

Our team's contributions to the field of genomics take a lot of forms — peer-reviewed publications, conference posters, presentations, even podcast appearances.

Case in point: Jay Shaw, MS, CGC, spoke with Progyny last year on their "This is Infertility" podcast. In her episode ("Fertility 101: The Basics of Genetics and Genetic Testing"), she explores how genetic testing informs fertility care, IVF, and pregnancy planning.

You can find this episode link, along with the rest of our team's published and presented work, on our Publications page: https://web.fulgentgenetics.com/resources/publications

What kind of content — papers, talks, podcasts — do you find most useful for staying current in the field?

Ever wondered how we approach a variant reclassification, or when segregation testing might be recommended? Our testing ...
08/18/2026

Ever wondered how we approach a variant reclassification, or when segregation testing might be recommended?

Our testing policies — including our variant reclassification policy, segregation testing policy, and exome/genome reanalysis policy — are all available for clinicians and genetic counselors to reference directly.

Visit our testing policies page: https://web.fulgentgenetics.com/resources/testing-policies

What's a policy or process that you wish were easier to find or understand?

Fulgent is care.Behind every report is a team that takes the relationship seriously — with clinicians who call us with q...
08/13/2026

Fulgent is care.

Behind every report is a team that takes the relationship seriously — with clinicians who call us with questions, and patients navigating results that matter to their lives. We're proud of the relationships we've built.

What's made a lab feel like a true partner to you, rather than just a vendor?

Fulgent is quality.Our genomic panels and proprietary pipelines are built by leaders in the field. As a CLIA-certified, ...
08/12/2026

Fulgent is quality.

Our genomic panels and proprietary pipelines are built by leaders in the field. As a CLIA-certified, CAP-accredited lab, quality is built into our procedures at every step, with multiple lab directors overseeing clinical analysis.

What does quality look like to you when you're evaluating a lab partner?

Fulgent is flexible.No two patients (or providers) have exactly the same needs. That's why our tests are built to be tai...
08/11/2026

Fulgent is flexible.

No two patients (or providers) have exactly the same needs. That's why our tests are built to be tailored: from focused panels to comprehensive ones, you can design around the clinical question in front of you rather than adhering to a one-size-fits-all menu.

Where has flexibility in testing made the biggest difference in your practice?

This week, Fulgent is headed to Asheville for !Our team is excited to discuss the latest developments in our genomic te...
07/13/2026

This week, Fulgent is headed to Asheville for !

Our team is excited to discuss the latest developments in our genomic testing services, including:

🔸 FulGenome – Our whole genome sequencing solution, now covering 64 repeat expansions in a single assay.
🔸 RISE – RNA-Integrated Sequencing Evaluation, a combination of WES or WGS analysis with simultaneous transcriptomic analysis by RNA sequencing.
🔸 TruPath Genome — Short-read repeat expansion analysis on the Illumina NovaSeq X platform that captures long-range genomic insights with a single assay.

Stop by our booth in Salon A-B for more information on these and other sequencing services at Fulgent.

This Thursday: single-cell resolution meets spatial context. Join Fulgent and 10x Genomics at 10 AM EST / 1 PM PST for a...
07/13/2026

This Thursday: single-cell resolution meets spatial context.

Join Fulgent and 10x Genomics at 10 AM EST / 1 PM PST for a live webinar exploring how Chromium and Visium work together to answer translational research questions that bulk transcriptomics and single-modality approaches leave open.

We’ll have two presentations that cover the entire workflow:
🔸 Lauren Neves, PhD (10x Genomics) — Resolving tissue heterogeneity, immune context, and mechanism of action.
🔸 Budha Banerjee, PhD (Fulgent BioPharma Services) — 10x Genomics as a cost-effective discovery platform complementing bulk transcriptomics and pathology.

Fulgent is also rewarding your curiosity — webinar attendees get access to a special discount on a pilot 10x project with Fulgent.

There's still time to register: 508cccfc-e322-4cc7-8bc7-07e7ad79bf21@ad54e8f7-b08a-4284-a291-badc52a99092" rel="ugc" target="_blank">https://events.teams.microsoft.com/event/508cccfc-e322-4cc7-8bc7-07e7ad79bf21@ad54e8f7-b08a-4284-a291-badc52a99092

July 16 | 10:30–11:30 a.m. PT

Discover how pairing Chromium and Visium can resolve tissue heterogeneity, immune context, and mechanism of action with ...
07/06/2026

Discover how pairing Chromium and Visium can resolve tissue heterogeneity, immune context, and mechanism of action with Dr. Lauren Neves in a double-feature webinar.

Dr. Neves is the Science and Technology Advisor at 10x Genomics, supporting biopharma researchers across Northern California and Los Angeles with spatial transcriptomics and single-cell RNAseq. She joined 10x in 2022 as a field application scientist, bringing a decade of molecular biology knowledge across academia and life science tool providers to our conversation.

Register today | July 16, 10:00 – 11:00 am PT
https://ow.ly/ZpKb50Zky3e

We'll be at in ExCeL London, July 5–8.If your work touches reproductive genetics, preconception screening, or prenatal...
07/01/2026

We'll be at in ExCeL London, July 5–8.
If your work touches reproductive genetics, preconception screening, or prenatal diagnosis, we'd love to connect and discuss our reproductive services:

🔸 Beacon Carrier Screening — NGS–based, comprehensive screening for up to 1,000+ genes. Assess reproductive risk in individuals or couples with customizable panels tailored to your clinical needs.
🔸 Beacon Exome – our latest option for couples, which expands testing scope while reducing counseling burden.
🔸 Infertility Gene Panels — identify underlying genetic causes of infertility to help inform and optimize IVF planning.
🔸 KNOVA NIPT — screens for severe autosomal dominant conditions that, collectively, are more common than Down syndrome.
🔸 CE-IVDR approved testing for 6,717 genes.

Come visit us at booth C16!

Address

4399 Santa Anita Avenue
El Monte, CA
91731

Opening Hours

Monday 7am - 6pm
Tuesday 7am - 6pm
Wednesday 7am - 6pm
Thursday 7am - 6pm
Friday 7am - 6pm

Telephone

+16263500537

Website

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