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Fulgent Genetics

Temple City, California, US

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... Show more »

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.

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Fulgent Genetics has not listed any services.

Targeted Cancer Gene Panel
Starting at $400.00 per sample

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... Show more »

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

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Illumina HiSeq 4000
Illumina HiSeq 2000
Illumina HiSeq X
Cancer
Melanoma
Buccal swab
Biology
Drug Discovery
Colorectal cancer
Illumina
saliva
Illumina HiSeq
Illumina HiSeq 2500
DNA
Genomics
illumina hiseq 4000
Prostate Cancer
Illumina X Ten
Breast cancer
Illumina HiSeq
EDTA Whole Blood
Lung Cancer
Ovarian Cancer
Gastric Cancer
Illumina Novaseq
Illumina
Pancreatic cancer
Liver cancer
Novaseq
Bladder cancer
Mitochondrial DNA Sequencing
Starting at $400.00 per sample

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... Show more »

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

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Illumina HiSeq
Illumina
Sanger Sequencing
Price on request
Request a quote for more information about this service.
Whole Genome Sequencing
Starting at $1,200.00 per sample

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

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

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Illumina MiSeq sequencing system
Illumina HiSeq X Ten
Illumina HiSeq 4000
Illumina MiSeqDx
Illumina HiSeq X
Cancer
Immunology
Muscular diseases
Sex Determination
Buccal swab
CNS/Neurology
Illumina
saliva
isolated DNA
Illumina HiSeq
Illumina HiSeq 2500
Frozen Tissue
Cardiovascular
illumina hiseq 4000
Illumina X Ten
gDNA
Whole Genome Sequencing
Whole Genome
Dermatology
Dental
Respiratory
EDTA Whole Blood
Nephrology and Urology
Kapa Hyper PCR-Free sample prep kit
Illumina Novaseq
Fresh Tissue
Genetic disease
FFPE
Sexually transmitted diseases
Metabolism and Endocrinology
Musculoskeletal/Orthopedic
Hepatology
Hearing loss
Whole Exome Sequencing (WES)
Starting at $500.00 per sample

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... Show more »

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.

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Illumina MiSeq sequencing system
Illumina HiSeq X Ten
Illumina HiSeq 4000
Illumina MiSeqDx
Illumina HiSeq X
Immunology
Muscular Dystrophy
Muscular diseases
Sex Determination
Buccal swab
CNS/Neurology
Illumina
saliva
Genomics
Cardiovascular
gDNA
Dermatology
Dental
Respiratory
EDTA Whole Blood
Nephrology and Urology
Illumina Novaseq
Fresh Tissue
Fresh Frozen
FFPE
Sexually transmitted diseases
Metabolism and Endocrinology
Musculoskeletal/Orthopedic
Hepatology
Hearing loss
DNA Methylation Analysis
Starting at $1,500.00 per sample

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: 30X
* TAT: 2-3 weeks
* Read Length: 2 x 150bp and 2 x 75
*... Show more »

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: 30X
* TAT: 2-3 weeks
* Read Length: 2 x 150bp and 2 x 75
* Platform: Illumina HiSeq X Ten
* Sample types accepted: Extracted DNA, Blood ($50 extra for extraction from blood)

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Illumina HiSeq X Ten
Genomics
Illumina X Ten
whole genome bisulfite sequencing
WGBS
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... Show more »

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

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Illumina MiSeq sequencing system
Illumina HiSeq X Ten
Illumina HiSeq 4000
Single Gene Sequencing
Price on request

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

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

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
Starting at $430.00 per sample

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... Show more »

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
Starting at $400.00 per sample

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... Show more »

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

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Illumina MiSeq sequencing system
Illumina NextSeq 500 sequencing system
Illumina HiSeq X Ten
Illumina HiSeq 4000
RNA-Seq
RNA CaptureSeq
Starting at $550.00 per sample

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... Show more »

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

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Illumina MiSeq sequencing system
Illumina HiSeq X Ten
Illumina HiSeq 4000
Illumina MiSeqDx
Illumina HiSeq X
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... Show more »

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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Clinical Research
Price on request
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Clinical Molecular Diagnostics
Price on request
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Biology
Price on request
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Biochemistry & Molecular Biology
Price on request
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Nucleic Acid Services
Price on request
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DNA Services
Price on request
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DNA Sequencing
Price on request
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Next Generation Sequencing (NGS)
Price on request
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Targeted Gene Sequencing
Price on request
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Epigenetic Studies
Price on request
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RNA Services
Price on request
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RNA Sequencing
Price on request
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Whole Exome Sequence Capture
Price on request
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RNA Extraction and Purification
Price on request
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DNA Extraction and Purification
Price on request
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2018-09-24 09:45:39 -0400

Net Promoter Score of 10 received for Ultra-High-Throughput Sequencing.

Additional Ratings: satisfaction with deliverable: 10, satisfaction with timeliness: 10.
2018-09-18 17:36:29 -0400

Net Promoter Score of 10 received for Ultra-High-Throughput Sequencing.

Additional Ratings: satisfaction with deliverable: 10, satisfaction with timeliness: 10.
2018-08-20 17:03:16 -0400

Net Promoter Score of 10 received for Ultra-High-Throughput Sequencing.

Additional Ratings: satisfaction with deliverable: 10, satisfaction with timeliness: 10.
2018-08-20 17:02:28 -0400

Net Promoter Score of 10 received for Ultra-High-Throughput Sequencing.

Additional Ratings: satisfaction with deliverable: 10, satisfaction with timeliness: 10.
2018-08-03 09:34:00 -0400

Net Promoter Score of 9 received for Ultra-High-Throughput Sequencing.

Additional Ratings: satisfaction with deliverable: 10, satisfaction with timeliness: 10.
2018-07-28 22:18:02 -0400

Net Promoter Score of 10 received for Ultra-High-Throughput Sequencing.

Additional Ratings: satisfaction with deliverable: 10, satisfaction with timeliness: 10.
2018-07-23 17:27:22 -0400

Net Promoter Score of 10 received for Ultra-High-Throughput Sequencing.

Additional Ratings: satisfaction with deliverable: 10, satisfaction with timeliness: 10.
2018-07-23 17:26:56 -0400

Net Promoter Score of 10 received for Ultra-High-Throughput Sequencing.

Additional Ratings: satisfaction with deliverable: 10, satisfaction with timeliness: 10.
2018-07-23 17:26:33 -0400

Net Promoter Score of 10 received for Ultra-High-Throughput Sequencing.

Additional Ratings: satisfaction with deliverable: 10, satisfaction with timeliness: 10.
2018-07-23 17:25:52 -0400

Net Promoter Score of 10 received for Ultra-High-Throughput Sequencing.

Additional Ratings: satisfaction with deliverable: 10, satisfaction with timeliness: 10.
2018-06-08 08:45:34 -0400

Net Promoter Score of 10 received for Ultra-High-Throughput Sequencing.

Additional Ratings: satisfaction with deliverable: 10, satisfaction with timeliness: 10.

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