Related Experiment Video
Updated: Mar 9, 2026

08:09
Annotation of Plant Gene Function via Combined Genomics, Metabolomics and Informatics
Published on: June 17, 2012
20.6K
Developing integrated crop knowledge networks to advance candidate gene discovery.
Keywan Hassani-Pak1, Martin Castellote2, Maria Esch1
1Rothamsted Research, Department of Computational and Systems Biology, UK.
Applied & Translational Genomics
|December 27, 2016
Summary
Understanding crop gene function is key to improving food security. This study presents a new method for integrating diverse biological data into knowledge networks, aiding gene discovery for crop enhancement.
Area of Science:
- Genomics and Bioinformatics
- Plant Science
- Computational Biology
Background:
- Enhancing crop productivity is crucial for global food security.
- Understanding biological mechanisms underlying crop traits (yield, disease resistance, nutrient/water use efficiency) is essential.
- Vast amounts of genomic data are available, but integrating them for functional insights is challenging due to data heterogeneity.
Purpose of the Study:
- To present a general approach for building genome-scale knowledge networks.
- To unify heterogeneous, interconnected datasets for effective knowledge mining and gene discovery.
- To facilitate crop improvement through systematic, evidence-based gene discovery.
Main Methods:
- Developed methods, workflows, and tools for creating and visualizing genome-scale knowledge networks.
- Integrated diverse datasets from multiple databases, addressing variable quality and coverage.
- Focused on major crop species, wheat and barley.
Main Results:
- Successfully built and visualized genome-scale knowledge networks for wheat and barley.
- Characterized the global properties of these knowledge networks.
- Demonstrated the value of integrated data for biological discovery using an example linking seed size to a barley WRKY transcription factor.
Conclusions:
- The developed approach provides a unified representation of complex biological data.
- Open-source software (Ondex) and knowledge resources (knetminer) are available for broader use.
- This work represents a significant step towards systematic gene discovery for crop improvement.
Related Concept Videos
Genetic Screens
5.8K
Genetic screens are tools used to identify genes and mutations responsible for phenotypes of interest. Genetic screens help identify individuals or a group of people at risk of developing genetic diseases and help them with early intervention, targeted therapy, and reproductive options.
Forward genetic screens
Forward or “classical” genetic screens involve creating random mutations in an organism’s DNA using radiation, mutagens, or insertion of additional bases, which...
Forward genetic screens
Forward or “classical” genetic screens involve creating random mutations in an organism’s DNA using radiation, mutagens, or insertion of additional bases, which...
5.8K
Genome-wide Association Studies-GWAS
16.3K
Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
GWAS does not require the identification of the target gene involved in...
GWAS does not require the identification of the target gene involved in...
16.3K
Pharmacogenomics: Identification of New Drug Targets
57
Advances in genomics have profoundly influenced drug discovery by increasing both the speed and accuracy of pharmaceutical development. Pharmacogenomics, which examines how genetic variation influences drug response, facilitates the identification of novel therapeutic targets and enables patient stratification for personalized treatment. These strategies contribute to improved drug efficacy, minimized adverse effects, and more efficient clinical trial design.Mapping genetic differences...
57
Genomics
41.2K
Genomics is the science of genomes: it is the study of all the genetic material of an organism. In humans, the genome consists of information carried in 23 pairs of chromosomes in the nucleus, as well as mitochondrial DNA. In genomics, both coding and non-coding DNA is sequenced and analyzed. Genomics allows a better understanding of all living things, their evolution, and their diversity. It has a myriad of uses: for example, to build phylogenetic trees, to improve productivity and...
41.2K
Single Nucleotide Polymorphisms-SNPs
19.2K
A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
19.2K

