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Fulgent Genetics

Temple City CA

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.

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
Cardiovascular
metabolic
eye
neurological
Lung
Endocrine
Blood
Liver
Skin
Muscular
Skeletal
Sex Determination
Renal
Cardio
Dental
Hearing
Immune
Sex
Illumina
Genome
Whole Genome
Whole Exome Sequencing
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
Cardiovascular
Muscular Dystrophy
metabolic
eye
Lung
Endocrine
Blood
Liver
Skin
Muscular
Skeletal
Sex Determination
Renal
Cardio
Dental
Hearing
Immune
Nuerological
Nuerology
Sex
Illumina
Exome
Whole Exome
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
RNA Seq
Transcriptome
mRNA
Total RNA
RNA Sequencing
Whole Transcriptome
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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