Spring Promotion for Metagenomic Sequencing

US$69 for 5Gb clean data, US$99 for 10Gb clean data

For a Limited Time Only!

 

Request a Free Quote

Top Quality Metagenomic Data at Unbeatable Price!

BGI has been providing world-class metagenomic sequencing services for more than 10 years. We have processed over 96,000 samples from partners across the world on our own DNBSEQTM technology platforms and have published more than 70 papers in the world's leading journals.

For a limited time, we are offering a spring discount for our metagenomic sequencing services, including both library construction and sequencing:

US$69 for 5Gb clean data
US$99 for 10Gb clean data


Key Terms and Conditions:

- This promotion cannot be accumulated with any other offer.
- The promotion terms are only eligible for contracts signed before June 30th, 2022.
- This promotion includes library construction and sequencing.
- Sequencing performed on DNBSEQTM, PE150.
-This promotion is for metagenomic sequencing 5Gb and 10Gb packages only.
- Additional terms may apply, contact us for details.

 

Why Choose BGI’s Metagenomic Sequencing Service?

Experienced provider with more than 96,000 samples sequenced on DNBSEQ™ platforms

Guaranteed data quality at unbeatable pricing

Professional project support from our in-house experts

Metagenomic Sequencing Service Overview

P3

Sample
Requirements

  • Intact genomic DNA ≥1 μg

  • Concentration ≥12.5 ng/μL

  • Volume ≥15 μL

P4

Library
Construction

  • 300-400bp short insert library 

P5

Sequencing
Standards

  • PE150

  • Guaranteed ≥80% of bases with quality score of ≥Q30

P6

Data Delivery
Details

  • Typical 30 working days delivery from sample QC acceptance to filtered clean data availability

  • Data available in standard FASTQ file formats

  • Custom bioinformatics analysis options available

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 metagenomic 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.