Leading Edge Genomic Services & Solutions

Start Your NGS Projects at Novogene Cambridge Genomics Centre

RNA Sequencing
Human Whole Genome Sequencing
Whole Exome Sequencing
Metagenomics Sequencing
Plant and Animal Resequencing
Lane Sequencing
Free Shipment in Q3

Novogene is a leading provider of genomic services and solutions with cutting edge NGS and bioinformatics expertise. It utilizes scientific excellence and unsurpassed data quality to help our clients realize their research goals. With over 2,000 employees, multiple locations around the world, 49 NGS related patents, and over 400 publications in top tier journal such as Nature and Science, the company has rapidly become a world-leader in NGS services. Novogene Cambridge Genomics Centre provide an important base for Novogene to serve its European customers and contribute to human health across Europe.

*For European Customers Only

  • NOVOGENE (UK) COMPANY LTD
  • 25 Cambridge Science Park
  • Milton Road
  • Cambridgeshire, CB4 0FW
  • United Kingdom
  • T:+44(0)1223 628750
  • E:europe@novogene.com
  • W:en.novogene.com

Fast Lane Sequencing in 7 Workig days

Better-Performance NovaSeq 6000
Quick & Exclusive Technical Support
Ultra-Fast Turnaround-Time
at Novogene Cambridge Genomics Centre



Please contact europe@novogene.com or your local representative for details.

*For European Customers Only

NovaSeq 6000 Sequencing Offer

NovaSeq RNA-Seq Promotion - $189/sample ≥ 24 samples per batch

Novogene Advantages:

• Two-week turnaround time, after library QC confirmation
• Complementary data QC
• High quality data delivered as FASTQ file, at a competitive price
• Extensive expertise in NGS services and solutions

Service Highlights:

• Applications range from Whole Genome to Epigenetic and Transcriptome sequencing projects
• Premade library samples only
• Platform: Novaseq 6000
• Flow cell and sequencing strategy: S4(PE150)

Promotion Terms:

• Promotion valid for samples and PO arriving before June 30, 2019
• Data analysis is available at additional cost

诺禾致源

NovaSeq RNA-Seq Promotion - $189/sample ≥ 24 samples per batch

phone 916-252-0068-383      email inquiry_us@novogene.com     web en.novogene.com

Only for North and South America

Thrilled: New Human Exome Promotion

Thrilled: New Human Exome Promotion

Sequencing on HUMAN EXOME is more cost effective than whole genome
sequencing. But have you ever thought Novogene is now forwarding human whole
exome sequencing (hWES) to lower edge in cost?

NovaSeq RNA-Seq Promotion - $189/sample ≥ 24 samples per batch

Novogene Advantages

•   Scalable capacity of sequencing
•   High quality data with ideal price
•   Comprehensive data analysis

Service Highlights

•   PE150 reads from Illumina platform
•   Validated Agilent SureSelect Human All Exon V6 Kit
•   Data quality guaranteed (Q30>80%)
•   Comprehensive standard analysis pipeline

Promotion Terms

•   Only applicable for non-FFPE human samples
•   Promotion 1&2 can be combined
•   Promotion valid for samples and PO arriving before September 30, 2019

novaseq 6000

*Substantial promotions are available for pre-made library sequencing service.

*Promotion service is for research use only.

phone +1-916-252-0068-383 (Novogene America)      email inquiry_us@novogene.com
phone +44-1223-804-151 (Novogene Europe)             email europe@novogene.com 
web en.novogene.com

New RNA-Seq Promotion

NovaSeq RNA-Seq Promotion - $189/sample ≥ 24 samples per batch
World’s Largest Capacity
NovaSeq 6000, HiSeq X, and PacBio Sequel
Sequencing labs in California, China, and Singapore

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

Comprehensive Data Analysis
Transcriptome analysis and RNA-Seq quantification

Alternative offer for ≥ 24 samples:
Free bioinformatics analysis with $199/sample

$199/sample for projects with < 24 samples

Substantial discount available for a full NovaSeq flowcell

contact us

novaseq 6000

Pricing applies to eukaryotic samples only.

Pipeline for Transcriptome Analysis

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

NovoPM Cancer Panel

The Novogene Precision Medicine 2.0 (NovoPM 2.0) comprehensive genomic profiling test for solid tumors is a next generation sequencing (NGS)-based assay that analyzes 484 genes for clinically important alterations at the DNA level. These genes are known to be relevant for the diagnosis and/or treatment of various solid tumors according to National Comprehensive Cancer Network (NCCN) guidelines and the medical literature.

Comprehensive Result

  • Complete coding regions of 468 genes and the introns of 43 genes
  • 4 types of genomic abnormality: SNV, InDel, CNV and Fusion
  • TMB, bTMB and MSI helping guide cancer immunotherapies

Reliable Performance

  • Comprehensive analytical validation
  • Rigorous quality control
  • State-of-the-art bioinformatics pipeline

Flexible Requirement

  • Applicable to various sample types: extracted DNA, FFPE tissue, extracted ctDNA and blood samples;
  • Acceptable for paired tumor-normal samples or tumor sample alone.

For research use only. The content provided herein may relate to products that have not been officially approved by healthcare authorities in China and is thus for research use only. The content of this document is subject to change without notice. 2018 Novogene Co., LTD. All rights reserved. All trademarks are the property of Novogene Co., LTD and its subsidiaries unless otherwise specified.

Click “Learn More” to visit our website and download our brochure for detailed information and validation report.

Meta-omics Promotion

Meta-Omics Promotion

Explore microbial diversity with Novogene’s NGS expertise

Meta-omics Promotion

Bioinformatics Analysis for all Meta-Omics Projects

Promotional pricing available for 12 GB Data too!

CONTACT US TO LEARN MORE

The Novogene Advantage
Experience

Successfully completed thousands of metagenomic sequencing projects

Wide range of samples accepted: water, soil, human

End-to-end Service

High-quality sequencing, efficient workflow, and bioinformatics analysis at a cost-effective price

Comprehensive Analysis

Comprehensive analysis of community composition and function

Intra-group and inter-group comparative analysis

Deep functional annotation (KEGG, eGGNOG, and CAZy)

Integrative DNA & RNA analysis

novaseq 6000

Promotion valid for Americas customers only.

PacBio Summer Promotion

Novogene has the largest fleet of both PacBio and Illumina platforms. We are excited about Illumina’s acquisition of Pacific Biosciences and committed to utilizing the latest sequencing technology to provide high-quality data to our customers.
Novogene Advantages
  • The world’s largest SMRT sequencing capacity
  • 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
Bioinformatics Analysis for Iso-Seq Projects
Novogene Customer Publications
Zhang, G. Q. et al. 2017. The Apostasia genome and the evolution of orchids.
Nature 549(7672): 379.

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.

Promotion valid for Americas customers only.
877-230-9060 | support@novogene.com | en.novogene.com

Whole Genome Sequencing Services

 

Whole Genome Sequencing Services

World’s Largest Sequencing Capacity

HiSeq X and 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 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 1850 customer research papers published, often in top-ranked journals such as Nature and Science.

Novogene - HiSeq X Ten

NovaSeq Fleet

Novogene Celebrating the Launch of the NovaSeq Fleet
'HiSeq X

Novogene Advantages

  • World’s largest capacity
  • Unbeatable pricing
  • Industry leading data quality guarantee
  • Fast turnaround: deliver data within 2 WEEKS after samples pass library QC

Promotion Platforms

  • Full lane sequencing on HiSeq X
  • Full flow cell sequencing on NovaSeq

Services Included

  • Illumina platform sequencing (PE150)
  • Sequencing data quality control
  • Sequencing data delivered in FASTQ files
contact us

Notes

  • Data output and number of reads may vary depending on client library quality
  • Applies to whole genome sequencing, RNA sequencing, and exome sequencing

 

  • Library preparation and data analysis services available at additional cost