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Special Promotion: DNBSEQTM RNA sequencing from $129 per sample* 

(A limited time offer)

 

DNBSEQTM RNA Sequencing

Here at BGI, customer service, and satisfaction are at the heart of what we do. With more than two decades of experience delivering RNA sequencing projects to customers across the world, we believe the formula for success is simple:

- Quality data

- Delivered on time

- At a price point that doesn't max out the project budget

In every project, we strive to meet these criteria. Read on for more details about our RNA sequencing services. You may also request a consultation or no-obligation quotes today. We're sure you won't be disappointed! 

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RNA Sequencing Service Overview

P3

Sample
Requirements

  • Human tissue/ Rat: Total RNA ≥200ng, Concentration ≥10ng  / μl. RIN≥7.0 28S/18S≥1.0
  • Human whole blood: Total RNA ≥500ng, Concentration ≥40ng/μl. RIN≥7.0 28S/18S≥1.0
  • Animal: Total RNA ≥1μg, Concentration ≥40ng/μl. RIN≥7.0 28S/18S≥1.0
  • Fungi: Total RNA ≥1μg, Concentration ≥40ng/μ. RIN≥6.5 28S/18S≥1.0
  • Plant: Total RNA ≥1μg, Concentration ≥40ng/μl. RIN≥6.5 28S/18S≥1.0
  • Insects: Total RNA ≥1μg, Concentration ≥40ng/μl.
  • Prokaryotes: Total RNA ≥1μg, Concentration ≥40ng/μl. RIN≥7.0 23S/16S≥1.0
P4

Library
Construction

  • Multiple choices for mRNA enrichment and rRNA removal kits

P5

Sequencing
Standards

  • ≥30 Million reads per sample recommended
  • Guaranteed ≥80% of bases with quality score of ≥Q30
  • Stranded and non-stranded sequencing is available

P6

Data Delivery
Details

  • Typical 30 working days from sample QC acceptance to filtered raw data availability
  • Expedited services are available, contact your local BGI specialist for details
  • Raw data and bioinformatics analysis are available in standard file formats

 

Contact Us

Please tell us about your project, ask us a question, or request a free no-obligation quote. We are always happy to help.

Our DNBSEQ™ Sequencing Technology

 

BGI RNA sequencing services are typically executed with our proprietary DNBSEQ™ NGS technology platform, for great sequencing data at the lowest cost in the industry.

DNBSEQ is a proprietary sequencing technology, first developed by BGI's Complete Genomics subsidiary in Silicon Valley, and can offer advantages in terms of lower amplification error rates and much lower duplication rates for some sequencing applications. In addition, studies have shown the index hopping rate in DNBSEQ platforms can be much lower when compared to that of other platforms.

Download our RNA Sequencing Service Overview

* Terms and conditions:

  1. For sequencing services, this promotion is valid for contracts signed before February 28th, 2023, and samples submitted before March 31st, 2023.
  2. Each of these promotions is independent and cannot be combined with each other.
  3. This is a limited and conditional offer subject to the actual execution of the contract and BGI reserves the right to void the promotions and revert to its standard list price if the Partner does not comply with the conditions listed above.
  4. For customers in US and Canada only.

CopyrightⒸ Innomics 2024. All trademarks are the property of Innomics or their respective owners. This website contains information on products targeted to a wide range of audiences and could contain product details or information otherwise not accessible or valid in your country. Please be aware that we do not take any responsibility for accessing such information, which may not comply with any legal process, regulation, registration, or usage in the country of your origin. For Research Use Only. Not for use in diagnostic procedures (except as specifically noted). Unless otherwise informed, certain sequencers and sequencing reagents are not available in selected countries or regions. Please get in touch with a representative for regional availability. The company reserves the right of final interpretation.