Leading Edge Genomic Services & Solutions

New RNA-Seq Promotion

World’s Largest Capacity
25 NovaSeq 6000, 30 HiSeq X, and 20 PacBio Sequel
Sequencing labs in California, China, and Singapore

High Quality Data & Affordable Prices
Q30 80%, exceeding Illumina’s official guarantee
Fast turnaround
100,000+ samples sequenced

Comprehensive Data Analysis
Transcriptome analysis and RNA-Seq quantification
to discover novel transcripts, differential
expressions, and function annotations

Substantial discount available for a full NovaSeq flowcell (>1000 GB)

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novaseq 6000
Promotion valid through April 30, 2018, for Americas customers only!
Pipeline for Transcriptome Analysis

Pipeline for RNA Sequencing Service Transcriptome
Pipeline for RNA-Seq Quantification
Pipeline for RNA Sequencing Service Quantification

Whole Genome Sequencing Services

 

Whole Genome Sequencing Services

World’s Largest Sequencing Capacity

30 HiSeq X and 25 NovaSeq 6000 sequencers deliver rapid turnaround time

Extensive Whole Genome Sequencing Experience

Successfully sequenced hundreds of thousands of genomes

Informatics Expertise Providing Publication-Ready Results

Cutting-edge bioinformatics pipeline for SNP/InDel/CNV/SV detection

High Quality Guaranteed – Q30 Score Exceeds Illumina’s Official Standards

Sample Type Raw Data (Gb) Q20 (%) Q30 (%) GC Content (%)
Human 100.32 97.61 94.30 42.67
Human 101.08 97.28 93.56 41.47
Human 102.60 96.85 93.85 41.39
Human 100.37 97.00 92.97 41.54
Human 113.12 96.89 92.73 41.40

 

Promotion valid through April 30, 2018, for Americas customers only
Your Partner in the “X” Era of Whole Genome Sequencing

Novogene is a leading provider of genomic services and solutions with cutting edge NGS and bioinformatics expertise that enables our customers to achieve their research goals. We possess the largest NGS capacities in the world, delivering publication ready data rapidly at highly competitive pricing.

Novogene offers a track record of performance and reliability. We have completed nearly 20,000 projects for more than 10,000 global customers, and have had over 950 customer research papers published, often in top-ranked journals such as Nature and Science.

Novogene - HiSeq X Ten

Bioinformatics Specialist (Beijing, China)

Location: Beijing, China

The Bioinformatics Specialist will consult with researchers to analyze problems, recommend technology-based solutions, or determine computational strategies. He/she will oversee the collection and analysis of high throughput sequencing data generated by Novogene or other research groups. He/she will provide customized solutions in data analysis directly to our customers and also assist in any after sales problems.

Benefits:
Competitive salary and benefits, excellent training opportunities

Click here to download a pdf copy of the job description/requirements.

If you’re interested in applying for this position, please send your resume or CV to: hr-recruiting@novogene.com

PacBio Promotion

Novogene Advantages
  • The world’s largest SMRT sequencing capacity – 20 PacBio Sequel systems
  • Deep experience – In 2017, we sequenced 500 Iso-Seq samples, as well as 1200 PacBio libraries for 400 projects, generating 45 Tb of data
  • Expert bioinformatics analysis
  • Diverse sequencing strategies combining PacBio Sequel with additional platforms
Featured PacBio Services
Learn more about Novogene’s
PacBio sequencing services by 
downloading our informational brochure

Novogene Customer Publications
Zhang, G. Q. et al. 2017. The Apostasia genome and the evolution of orchids.
Nature 549, 379–383 (2017)

Li, Y. et al. 2017. Scallop genome reveals molecular adaptations to semi-sessile life and neurotoxins.
Nature Communications 8(1): 1721.

Zhao, G. et al. 2017. The Aegilops tauschii genome reveals multiple impacts of transposons.
Nature Plants 3(12): 946.

*For plants, mammals, birds, and insects
Promotion valid through April 30, 2018, for Americas customers only

PAG 2018

Ready for sunny San Diego? We are excited to see you at PAG 2018!
As a leading provider of genomic services and solutions, we are dedicated to providing fast turnaround time for projects of any size with the world’s largest NGS capacity at our state-of-the-art US sequencing lab at highly competitive prices!
See below for some highlighted services for animal and plant research!

Highlighted Services for PAG Attendees

RNA Sequencing

Learn More

Plant & Animal Whole Genome Sequencing

Learn More

PacBio Sequel Based de novo Sequencing

Learn More

Novogene Advantages

  • Rich experience: successfully sequenced >370,000 samples for >10,000 global customers
  • Quick turnaround time: finish projects in as fast as 2 weeks
  • Diverse sequencing platforms: access to 30 HiSeq X, 25 NovaSeq and 20 PacBio Sequel, the largest sequencing capacity in the world
  • Advanced data analysis for projects of all sizes
  • State-of-the-art California lab in the US, and branches worldwide

Celebrating the Arrival of NovaSeq at Novogene’s California Lab

 

RNA-Seq at $199/Sample
World’s Largest Capacity
25 NovaSeq 6000, 30 HiSeq X, and 20 PacBio Sequel

High Quality Data & Affordable Prices
Our latest NovaSeq systems enable highly affordable RNA-Seq and exome sequencing services with fast turnaround. See our Exome Sequencing Promotion!

Substantial discount available for a full NovaSeq flow cell (>1000 GB)

Also check out our Whole Genome Sequencing service on HiSeq X Ten

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novaseq 6000

Human Whole Exome Sequencing Promotion

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• High quality data

Illumina PE150, Q30 ≥ 80%, 6G or 12G raw data guaranteed

• Latest capture kit

Agilent SureSelect Human
All Exon V6 Kit (58M)

• Extraordinary expertise

>2,000 exome projects completed
World’s largest capacity

Turnaround time: 22 working days after samples pass QC (for samples ≤ 30)

 

 

Comprehensive Analysis Available at an Additional $49/Sample

STANDARD ANALYSIS SOFTWARE
Employing widely-accepted open software
Data quality control Rigorous in-house pipeline
Alignment with reference, statistics of
sequencing depth and coverage
BWA, Samtools, Picard
SNP and InDel calling,
annotation and statistics
GATK, ANNOVAR
Somatic SNP/InDel/CNV calling,
annotation and statistics

(for paired tumor samples)
SNP: MuTect
InDel: Strelka
CNV: Control-freec
Annotation: ANNOVAR
STANDARD ANALYSIS
Data quality control
Alignment with reference, statistics of
sequencing depth and coverage
SNP and InDel calling,
annotation and statistics
Somatic SNP/InDel/CNV calling,
annotation and statistics

(for paired tumor samples)
SOFTWARE
Employing widely-accepted open software
Rigorous in-house pipeline
BWA, Samtools, Picard
GATK, ANNOVAR
SNP: MuTect
InDel: Strelka
CNV: Control-freec
Annotation: ANNOVAR