Best Biotechnology Engineer El Monte Near Me

4worldlovers: Following thorough review by our genetic experts, our hereditary cancer panels have been updated to reflect the latest research and recommendations and now include up to 153 genes.

Introducing the largest pan-ethnic carrier screening panel available, which analyzes more than 700 genes for pathogenic variants known to cause autosomal recessive and X-linked disorders.

Increase the effectiveness of medications while reducing the risk of adverse drug reactions with PGx testing, available clinically through Fulgent, or at-home through Picture Genetics.

Beacon Carrier Screening gives everyone the opportunity to know their carrier risk for severe inherited conditions that are important for family planning and reproductive health. Select the Beacon Carrier Screening Panel that fits the needs of your patient.

Parkinson Disease Comprehensive NGS Panel Alzheimer and Dementia NGS Panel Parkinson-Alzheimer-Dementia NGS Panel

Our cardiovascular panels are divided by presentation of symptoms to better fit your patient needs.

Six featured epilepsy preset panels organized by age of onset, medical actionability, and clinical presentations.

Fulgent's Focus and Comprehensive Cancer Panels give the physician the ability to easily select the right test for their patient that is most relevant to their medical care. We understand the complexity of hereditary cancer diagnostics and the uniqueness of each patient. Explore the best option for your patient needs.

Fulgent offers free specimen collection kits for physicians and genetic counselors within the continental United States.

4worldlovers: Discover a healthier you with personalized health care driven by your genetics.


Already have data from a DNA test? Upload your data for free.

Our enhanced DNA reports provide clear, personalized guidance and actionable insights on a wide range of topics including health, wellness, and genealogy.

Our enhanced DNA reports provide dynamic, actionable insights on a wide range of topics.

Our health reports provide insight into what you can do right now to decrease the likelihood you’ll get a particular disease or to limit its impact on you.

Whether you have data from another DNA test or are sequencing for the first time, our technology uses the latest genetic research for the most comprehensive DNA analysis.

Sequence 100% of your genome with our at-home kit or upload your DNA data from any source, including 23andMe and Ancestry.

Our enhanced reports and apps offer personalized guidance on health, rare disease, medication reactions, nutrition, genealogy, and more.

Genetic science evolves and our technology keeps you learning and benefiting from new DNA discoveries throughout your life.

"The customer service is truly excellent and expedient. And the value for the cost is the best I've seen in a product of this sort. As soon as possible I am buying kits for family and friends because it has such far-reaching positive effects on health and preventitive care."

Start by ordering the world’s most comprehensive DNA test kit.

If you’ve taken a DNA test elsewhere, upload your raw DNA data for free to get started.

Obtains data on around 3 billion positions within your genome (100% of your genome). Also includes the ability to download your raw genome data files for no additional fee. This includes FASTQ, BAM and VCFs covering all genetic variations: Single Nucleotide Polymorphisms (SNPs), Insertions and Deletions (INDELs), Structural Variations (SVs), Copy Number Variations (CNVs) and Mitochondrial Heteroplasmy (MITO).

Next-generation DNA sequencing, comprehensive analysis, and your choice of enhanced health reports, all in one place.

We provide one-of-a-kind DNA storage technologies that keep your data secure and private throughout your life. Our ethic is simple:

Our genome sequencing technology is fundamentally different from other DNA tests. We obtain 100% of your DNA data while other DNA test providers obtain data on less than 0.1%.

Our proprietary technology makes it easy to store, access, and analyze the information in your DNA with clinical-grade comprehensiveness and robustness. We make DNA-based insights more accessible and understandable.