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Fulgent Genetics

48 Orders Completed
Temple City, California, US

About Fulgent Genetics

**Fulgent offers services and/or reagents specific to COVID-19 research. Submit a quote request containing the word ‘COVID-19’ to receive more details.**

Fulgent is a leader in genetic and genomic clinical testing, a publicly traded company located in Los Angeles, California. We are a technology-driven company with extensive academic/clinical experience and capabilities in Next Generation Sequencing and bioinformatics. This distinction has advanced us to the forefront of the rapidly advancing genetic and genomic testing industry. We offer the most expansive set of clinical genetic tests in the world, including 18,000+ single gene tests, 300+ preset panels, rearrangement testing, clinical exome/trios, whole exome/trios, whole genome and our All-in-One reflex test. We are a CLIA and CAP accredited laboratory focused on providing clinical as well as research services. *Mission* Develop flexible and affordable genetic testing to improve patient lives. Founded in 2011, Fulgent began with two simple ideas; flexibility and affordability. Today, we strive to create the most effective and wide ranging genetic tests and sequencing services on the market. All of this is done in the pursuit of advancing personalized medicine and bettering the everyday lives of patients. *Why Fulgent ?* 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 all services. Our approach has always been simple: provide testing based on the specific needs of clinicians and their patients. *Customer Support* Our support philosophy is simple: answer our client's questions quickly and accurately. Currently 95% of incoming calls are addressed by the first person that answers the phone. 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 your questions. For the other 5% of calls our team will quickly will find the resource you need, whether it is a genetic counselor, lab, or even our accounting team.

Certifications & Qualifications

CLIA/CAP

Diversity Certificates

Minority owned business Small business

Our Services (33)


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Tumor Mutation Burden Analysis

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Tumor Profiling

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Single Cell Gene Expression Analysis

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Single Cell RNA-Seq

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Illumina Sequencing

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Targeted Cancer Gene Panel

Price on request

A comprehensive view of 139 genes and regions of interest known to be associated with various types of inherited cancers. This approach utilizes deep sequencing (>99.9% of bases covered at 50X minimum) to allow for high sensitivity variant calling. Additional options including copy number variant analysis are available upon request.

Specifications
Minimum Order Quantity: 10 samples
Reads: Paired-end 2 x 150bp
Services Included: Library Preparation, Sequencing, Alignment, QC Check, Annotation
Delivery Format: FASTQ, BAM, VCF, Coverage summary
Turnaround Time: 2-3 weeks

Bladder cancer Oncology Breast cancer Colorectal cancer Gastric Cancer Liver cancer Ovarian Cancer Lung Cancer Pancreatic cancer Prostate Cancer Melanoma Illumina HiSeq Illumina HiSeq 2000 Illumina HiSeq 4000 Illumina HiSeq X Illumina Novaseq Illumina Illumina HiSeq Illumina HiSeq 2500 Illumina X Ten Blood DNA Buccal swab Biofluids Genomics Biology Drug Discovery Show 27 more tags Show less

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Mitochondrial DNA Sequencing

Price on request

Mitochondrial DNA sequencing enables analysis of the mitochondrial genome, of which there are hundreds of copies in every human cell. This service can be a powerful tool for researchers interested in mitochondrial disorders and mechanisms of aging.

Specifications
Minimum Order Quantity: 6 samples
Services Included: Library Preparation, Sequencing, Alignment, QC Check Output
Number of Reads: 2M Reads
Delivery Format: FASTQ, BAM, Coverage summary (VCF Option)
Turnaround Time: 3-5 weeks

Illumina Illumina HiSeq

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Sanger Sequencing

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Whole Genome Sequencing

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

Specifications
Coverage: >30X
Number of Reads: 400-450M Reads
Platform: Illumina HiSeq X Ten
Delivery Format: FASTQ/BAM
Turnaround Time: 2-3 weeks

Oncology Cardiovascular Dental Metabolism and Endocrinology Hearing loss Respiratory Immunology Hepatology Musculoskeletal/Orthopedic CNS/Neurology Nephrology and Urology Sexually transmitted diseases Dermatology Illumina HiSeq X Ten Illumina HiSeq X Illumina HiSeq 4000 Illumina MiSeqDx Illumina MiSeq Genetic Disease Illumina Illumina Novaseq Whole Genome Sequencing Whole Genome Illumina HiSeq Illumina HiSeq 2500 Illumina X Ten Kapa Hyper PCR-Free sample prep kit Blood gDNA DNA FFPE tissue Fresh Tissue Frozen Tissue Biofluids Buccal swab Show 35 more tags Show less

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Whole Exome Sequencing (WES)

Price on request

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

Specifications
Coverage: 100x
Number of Reads: 35-40M Reads
Platform: Illumina HiSeq 4000
Delivery Format: FASTQ/BAM
Turnaround Time: 2-4 weeks

100X coverage, 2x150 reads. Turnaround time is 2-3 weeks. ~24M reads; 14Gb. Delivered in FASTQ/BAM format. Additional $50 for vcf file.

Cardiovascular Dental Metabolism and Endocrinology Hearing loss Immunology Hepatology Respiratory Muscular Dystrophy Musculoskeletal/Orthopedic CNS/Neurology Nephrology and Urology Sexually transmitted diseases Dermatology Illumina HiSeq X Ten Illumina HiSeq X Illumina HiSeq 4000 Illumina MiSeq Illumina MiSeqDx Illumina Illumina Novaseq Genomics gDNA Blood FFPE tissue Frozen Tissue Fresh Tissue Biofluids Buccal swab Show 28 more tags Show less

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DNA Methylation Analysis

Price on request

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 differential gene expression. Specifications: * Coverage: 20X * TAT: 2-3 weeks * Read Length: 2 x 150bp * Platform: Illumina HiSeq X Ten and NovaSeq * Sample types accepted: Extracted DNA, Blood ($50 extra for extraction from blood)

Illumina HiSeq X Ten Genomics whole genome bisulfite sequencing WGBS Illumina X Ten

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Small RNA Sequencing

Starting at $250.00 per sample

Small interfering RNA (Si-RNA) are small double-stranded RNA molecules, typically 21-25 base-pairs in length. Like miRNA, Si-RNA play a central role in RNA interference. We Provide the tools to discover known and novel Si-RNAs at unmatched resolution.

Specifications:
Sample Type Accepted: Whole Blood, Extracted Total RNA
Turnaround Time: 4-5 weeks
Platform: Illumina MiSeq
Number of Reads: 15M reads
Read Length: 1 x 40bp

Illumina HiSeq 4000 Illumina HiSeq X Ten Illumina MiSeq

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Single Gene Sequencing

Price on request

Fulgent offers sequencing of over 18,000 single genes. Please contact for pricing details.


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Gene Panel Testing

Price on request

Clinical Sequencing

We offer a wide variety of disease panels that cover numerous clinical areas including: cancer, epilepsy, cardiology, neurology and many more.

Please contact for further pricing details


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Transcriptome Sequencing and Profiling

Price on request

rRNA Depleted Total RNA Sequencing

Selective removal of ribosomal RNA (rRNA) allows for a more efficient transcriptome analysis in degraded/low quality samples. This option is recommended for transcriptome analysis of FFPE samples. The minimum order quantity for Total RNA sequencing is 8 samples and we can ensure a turnaround time of 3-5 weeks.

total RNASeq Specifications & Prices:
2X 50 bp PE, 20M Reads $430
2X 75 bp PE, 20M Reads $450
2X 100bp PE, 20M Reads $470
2X 150bp PE, 20M Reads $500
2X 50 bp PE, 40M Reads $700
2X 75 bp PE, 40M Reads $715
2X 100bp PE, 40M Reads $730
2X 150bp PE, 40M Reads $770
2X 50 bp PE, 80M Reads $1150
2X 75 bp PE, 80M Reads $1170
2X 100bp PE, 80M Reads $1190
2X 150bp PE, 80M Reads $1230
2X 50 bp PE, 100M Reads $1360
2X 75 bp PE, 100M Reads $1400
2X 100bp PE, 100M Reads $1440
2X 150bp PE, 100M Reads $1500


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mRNA Sequencing

Price on request

By selectively targeting mRNAs using poly(T) oligomers, we can look across the entire transcriptome to measure gene expression levels, and to detect changes arising from different environmental conditions and disease states. We accept a minimum of 8 samples for mRNA sequencing and ensure a turnaround time of 3-4 weeks .

mRNASeq Specifications & Price List:
2X 50 bp PE, 20M Reads $400
2X 75 bp PE, 20M Reads $420
2X 100bp PE, 20M Reads $440
2X 150bp PE, 20M Reads $475
2X 50 bp PE, 40M Reads $665
2X 75 bp PE, 40M Reads $685
2X 100bp PE, 40M Reads $700
2X 150bp PE, 40M Reads $740
2X 50 bp PE, 80M Reads $1120
2X 75 bp PE, 80M Reads $1140
2X 100bp PE, 80M Reads $1160
2X 150bp PE, 80M Reads $1200
2X 50 bp PE, 100M Reads $1325
2X 75 bp PE, 100M Reads $1365
2X 100bp PE, 100M Reads $1385
2X 150bp PE, 100M Reads $1425

Illumina HiSeq 4000 Illumina HiSeq X Ten Illumina MiSeq Illumina NextSeq 500 sequencing system RNA-Seq

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RNA CaptureSeq

Price on request

The coding transcriptome represents all coding regions of mRNA molecules within a cell at any given moment. Coding regions are selectively targeted, allowing the capture of specific transcripts. This method is good for both high quality and degraded RNA.

Specifications:
Sample Type Accepted: Whole Blood, Extracted Total RNA
Turnaround Time: 3-5 weeks
Number of Reads: >~60M reads (ask for price on 200m reads)
Read Length: 2 x 1500bp

Illumina HiSeq 4000 Illumina HiSeq X Illumina HiSeq X Ten Illumina MiSeq Illumina MiSeqDx

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Ultra-High-Throughput Sequencing

Price on request

Rent a full lane on Illumina NovaSeq, HiSeq 4000 and MiSeq. The NovaSeq and HiSeq4000 are ideal for large-scale and very high-throughput sequencing projects – full lane sequencing on our Illumina machines generates more than 400 million reads, equivalent to roughly 16 exomes sequenced at a coverage of 100X.

Platform: Illumina NovaSeq / HiSeq 4000
Read Length: 2x150 bp
Number of Reads: ≥400 million
Turnaround Time: 3-5 weeks (varies)


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Biology

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DNA Sequencing

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DNA Services

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Nucleic Acid Services

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Next Generation Sequencing (NGS)

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RNA Sequencing

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Targeted Gene Sequencing

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Whole Exome Sequence Capture

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RNA Extraction and Purification

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DNA Extraction and Purification

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Clinical Research

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RNA Services

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Epigenetic Studies

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Biochemistry & Molecular Biology

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Clinical Molecular Diagnostics

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