Our Agrigenomics Services and Solutions

Our Agrigenomics Solutions | Promotions | Featured Publications

Empowering Agrigenomics Studies - Plant and Animal Sequencing

Genetics plays a crucial role in global food security and biodiversity. With a growing population at pace, advances in genomics sequencing help identify desirable traits selection in animal breeding and crop genetic engineering.

Researchers acquire high-quality reference genomes for newly discovered species by de novo genome assembly and annotation using the PacBio/Nanopore sequencing and find key variants by population studies using resequencing, genotyping and array data. In addition, further mechanisms underlying wanted traits could be enlightened by epigenetics studies.

At Novogene, we offer a comprehensive range of solutions with dedicated technical support to help you overcome the complexities of genomics sequencing. Leveraging on our efficient workflow and strict quality control protocols, you can be sure of cost-effective and reliable genomics data to empower your agrigenomics projects.

Helping to achieve your research goal is what truly matters to us, so that's why we placed the utmost importance on providing reliable services that you can rely upon:

Competitive Turn-Around Time (TAT) with real-time experiment tracking from sample QC to data delivery
Our highly competent Technical Specialists and Sales Representatives are located in-country* to provide better support for your projects

*Direct sales countries. Otherwise, we work with our network of global partners.

Are you ready to get started on your Agrigenomics studies?

Request for a non-obligatory scientific consultation on your experimental design with us now.

Our Agrigenomics Solutions

Novogene Agrigenomics Services and Solutions

Click to learn more about each of our Agrigenomics services:

Long Reads Sequencing

Long read solutions offer answers that can only be derived from intact long sequences. Addressable areas apply to all applications- De novo Sequencing, Whole Genome Sequencing, Isoform Sequencing, Full-length 16S Amplicon, etc.

De novo Sequencing

In de novo genome sequencing, researchers utilize long-read sequencing, Hi-C and Bionano optical maps to assembly a highly contiguous, complete, and correct genome ever. High quality genomes could be of great significance for downstream data mining.

Whole Genome Sequencing

Variations including SNP, InDel, CNV and SV are found by whole-genome sequencing. For population studies, BSA/GWAS/genetic map analyses could be applied to find significant variations that matter to specific traits.

Genotyping

Genotyping-by-Sequencing is a genetic screening method for discovering novel plant and animal SNPs and performing genotyping studies. For some applications like genotype screening and genetic mapping, sequence-based genotyping provides a lower-cost alternative to arrays for studying genetic variation.

Epigenetics

In Epigenetics, researchers examine how cells control gene activity without altering the DNA sequences. Popular approaches include Whole Genome Bisulfite Sequencing, ChIP-seq, RIP-seq, etc.

2022 PacBio-Novogene APAC Human Genetics HiFi-SeqXP

Submit your 300-word proposal for a chance to win up to seven (7) SMRT Cells 8M worth of free sequencing, and see the HiFi sequencing difference for yourself.

Novogene is proud to be the co-sponsor for the 2022 PacBio APAC Human Genetics HiFi-SeqXP. Submit your proposal now.

PacBio-Novogene SMRT Grant for Plant and Animal Sciences

The PacBio-Novogene SMRT Grant for Plant and Animal Sciences has ended. We are currently evaluating the proposals and will contact all participants in May 2022. Not a recipient of the grant? All successful applicants will receive USD200 HiFi sequencing vouchers for your project.

[Featured Publication]
Horizontal gene transfer of Fhb7 from fungus underlies Fusarium head blight resistance in wheat

We introduce you to the work of Prof. Hongwei WANG and Prof. Lingran KONG at the Shangdong Agricultural University. Together with their global collaborators, and the help of Novogene de novo sequencing services and bioinformatics expertise, the group elegantly demonstrated evidence that T.elongatum has gained Fhb7 through horizontal gene transfer (HGT) from an endophytic Epichloe species, shaping the plant genome evolution. Learn more about the publication here.

[Featured Publication]
Chromosome-scale de novo assembly of a yellow-seeded B.juncrea

Nuclear and organelle phylogenies of 490 accessions worldwide supported that B.juncea is most likely a single origin in West Asia, 8,000 - 14,000 years ago, via natural interspecific hybridization. Take a closer look at the study whereby the group mapped the species expansion and, via NGS analysis by Novogene, demonstrated the domestication history and provided a comprehensive insight into the evolution of B.juncrea. Learn more about the publication here.

Publications

View some of the recent publications that were supported by Novogene solutions below and more at our website.

Genome of Tripterygium wilfordii and identification of cytochrome P450 involved in triptolide biosynthesis

Nature Communications. 2020 Feb 20;11(1):971

Tu L., Su P. & et. al

DOI: 10.1038/s41467-020-14776-1 PMID: 32080175

The chromosome-level wintersweet (Chimonanthus praecox) genome provides insights into floral scent biosynthesis and flowering in winter

Genome Biology 21, 200 (2020)

Shang, J., Tian, J., Cheng, H. et al.

DOI: 10.1186/s13059-020-02088-y

A chromosome-level genome assembly of garlic (Allium sativum) provides insights into genome evolution and Allicin Biosynthesis

Molecular Plant. 2020 Sep 7;13(9):1328-1339.