Sequence More.
Spend Less.

Your libraries are ready. Your project shouldn’t have to wait. Move your study forward with our flexible partial lane sequencing, starting from just 1 Gb — for about the price of a cup of coffee.

New customer offer: Save up to 30% on full-lane sequencing.

Discover Our Supported Library Types

Have a project in mind or want to explore other library types and platform configurations? Let’s connect over coffee.

Standard & Bulk NGS Libraries

Sequencing for your prepared DNA and RNA libraries.

  • Whole Genome Sequencing (WGS) PCR-Free, Ultra-Low Input, Population Genomics
  • Whole Exome Sequencing (WES) High-depth capture for clinical & cancer genomics
  • RNA Sequencing (RNA-Seq) PolyA mRNA, Total RNA with Ribosomal Depletion
  • Metagenomics (Meta) 16S / 18S / ITS Amplicon & Shotgun Metagenomics
  • Epigenomics & Regulation ATAC-Seq, ChIP-Seq, Methyl-Seq
  • Targeted Amplicon Sequencing Custom gene panels & viral surveillance

Single-Cell & Single-Nucleus Libraries

Sequencing for your prepared single-cell and single-nucleus libraries.

  • 10x Genomics 3′ / 5′ Gene Expression, Single-Cell ATAC-Seq, Single-Cell V(D)J Profiling, Feature Barcode, CITE-seq, Flex
  • Parse Biosciences Evercode Whole Transcriptome Analysis (WTA)
  • BD Rhapsody™ System Whole Transcriptome Analysis (WTA), TCR & BCR Profiling, Sample Tag
  • Illumina Single Cell Solutions Compatible single-cell RNA/DNA assays
  • NanoString Single-cell and spatial reporter/barcode library profiling

Spatial Transcriptomics & Genomics Libraries

Sequencing for studies that place molecular insights within tissue context.

  • 10x Genomics Visium / Visium HD Single-cell scale spatial profiling (FFPE & Fresh-Frozen)
  • MGI Stereo-seq Ultra-high resolution spatial transcriptomics (FFPE & Fresh-Frozen)
  • Curio Bioscience (Curio Seeker) High-resolution Slide-seq spatial transcriptomics

Proteomics Libraries for Sequencing

Sequencing for DNA-based libraries generated by protein profiling assays.

  • Olink® Proteomics Explore HT & Reveal libraries
  • NULISAseq™ Libraries

Stay tuned to our Melbourne Logistics Centre!

Free sample pickup is coming soon to Melbourne.


Ready to Sequence Your Libraries?

Complete the form below and our team will contact you to discuss your project requirements and promotional eligibility.
By registering on this page, you are consenting and agreeing for Novogene to contact you, assist with your request, and store your information per our privacy policy. You can change your email preferences at any time.
Terms and Conditions

  • Complimentary local pickup service is available for samples within the Melbourne metropolitan area.
  • Free demultiplexing service is included for all qualifying sequencing runs under this promotion.
  • This promotion applies exclusively to pre-made library sequencing on NovaSeq X Plus and DNBseq platforms. Valid for new customers located in Australia and New Zealand.
  • All PO and samples must be received at Novogene facility by December 15, 2026.
  • This promotion cannot be combined with any other offer or discount. Novogene reserves the right to amend or discontinue this promotion.
 
 
 
About Novogene
Novogene is a pioneer in applying cutting-edge molecular biology technology and high-performance computing to research in the fields of life science and human health. Our vision is to continue as a global leader in the delivery of genomics services and solutions. With one of the largest sequencing capacities in the world, we utilise our deep scientific knowledge, first-class customer service and unsurpassed data quality to help clients realise their research goals in the rapidly evolving world of genomics. Novogene is committed to become your trusted genomics partner.
 
For more information, visit amea.novogene.com
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