Empower your research with Novogene Long-reads Sequencing Solutions!
Long-read sequencing is a powerful technique used to sequence longer DNA or RNA fragments compared to traditional short-read sequencing methods. The extended read lengths offer several advantages, including improved de novo assembly, enhanced mapping certainty, accurate identification of transcript isoforms, and the ability to detect structural variants. This methodology enables the direct detection of base modifications, such as methylation, providing valuable information about epigenetic regulation and other biological processes.
Long-reads sequencing offers increased accuracy in the analysis of complex genomics regions. Further, aid researchers gain deeper insights across various research areas.
Discover our range of sequencing offers and featured articles below to learn more.
Which Long-reads sequencing offer
should I go for?
Embrace Long-Read Sequencing this season! Seize our current promotions to kickstart your projects.
Offer NOT included above? Explore more of our other long-reads sequencing services:
Discover our ongoing promotions
Limited promotion for the first 100 only. T&C apply.
Up to 40% off for long-reads genome sequencing
For the first 100 cells only.
40% off for sequencing on the latest PacBio RevioTM system. Offer includes 1 HiFi library preparation and 1 SMRT cell. Learn more.
Looking for other platforms? Here's 20% off for sequencing on the PacBio Sequel IIe/ Nanopore PromethION system. Learn more.
Up to 30% off Early Bird price for Isoform sequencing.
For the first 100 samples only.
110GB of HiFi reads per SMRT cell
for our validation data on Revio
The Revio offers 15× Boost in throughput, as compared to the previous Sequel II system, empowering Novogene to offer high-throughput HiFi long-read sequencing and direct methylation detection for a wide range of applications.
Featured articles in Long-Reads Sequencing
Exploring the Power of Whole Genome Sequencing: A Beginner’s Guide to Long-read sequencing
Learn about the comparison and specifications of short-read and long-read sequencing platforms for WGS, and explore the key benefits of employing long-read in your research:
- PacBio HiFi libraries with 99.9% accuracy rate
- Nanopore Q20+ system
- Read length(N50): ≥15K
- No GC and PCR bias
Using long-read sequencing technology to explore the complex structure of transcripts
The Iso-Seq has unparalleled advantages in the complex structural analysis. These advantages include the direct acquisition of full-length transcript sequences, the discovery of new genes and new transcripts, as well as the identification of fusion genes. Read more.
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 novogene.com/amea-en/.
For more information, visit novogene.com/amea-en/.
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