WIDDE: a Web-Interfaced next generation database for genetic diversity exploration, with a first application in
Guilhem Sempéré1, Katayoun Moazami-Goudarzi2, André Eggen3
1CIRAD, UMR INTERTRYP, F34398, Montpellier, France. guilhem.sempere@cirad.fr.
BMC Genomics
|November 18, 2015
Summary
WIDDE is a new database for exploring cattle genetic diversity using SNP data. It helps manage and analyze large datasets, aiding researchers in understanding bovine biodiversity.
Area of Science:
- Genomics
- Bioinformatics
- Population Genetics
Background:
- Next-generation sequencing generates vast genetic data, posing storage and analysis challenges.
- Efficient management of dense genotyping datasets, especially for cattle, is crucial but difficult.
Purpose of the Study:
- To develop a user-friendly database for managing and exploring cattle genetic diversity.
- To provide a platform for analyzing single nucleotide polymorphism (SNP) data across various cattle populations.
Main Methods:
- Developed WIDDE (Web-Interfaced Next Generation Database), a versatile tool for various species and marker types.
- Created a cattle-specific version with over 750,000 SNPs across 129 populations and 7 outgroup species.
- Implemented data filtering, export options, principal component analysis, and user data integration.
Main Results:
- WIDDE offers a comprehensive dataset for global cattle genetic diversity.
- Users can analyze their own data alongside WIDDE's extensive cattle genetic information.
- The database facilitates population assignment and ancestry estimation for user samples.
Conclusions:
- The cattle WIDDE database is the first of its kind for SNP genotyping data, valuable for bovine biodiversity research.
- WIDDE's generic design allows for future expansion to other species and marker types.
- The database structure supports easy integration of new tools and data formats for enhanced genetic diversity exploration.
More Related Videos
Related Concept Videos
Next-generation Sequencing
101.0K
The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
101.0K
Genetic Variation
1.6K
Genetic variation is the diversity in DNA sequences found among individuals of the same species. This diversity is crucial for a species' survival because it helps organisms adapt to environmental changes. Genetic variation begins with fertilization, where an egg and sperm cell merge. Each of these cells carries 23 chromosomes, up to 46 in the fertilized egg. Chromosomes are long DNA strands that contain genes, the basic units of heredity.
Genes exist in different versions called alleles,...
Genes exist in different versions called alleles,...
1.6K
Applications of Molecular Taxonomy
653
Molecular taxonomy has revolutionized the understanding and classification of bacteria, providing precise insights into their diversity, evolutionary relationships, and ecological roles. By utilizing molecular techniques such as DNA sequencing and fingerprinting, researchers have made significant strides in various fields related to bacterial studies.Resolving Taxonomic AmbiguitiesMolecular taxonomy has been instrumental in distinguishing closely related bacterial species initially thought to...
653
Genome-wide Association Studies-GWAS
16.6K
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...
16.6K
Genomics
41.7K
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...
41.7K
Evolutionary Relationships through Genome Comparisons
7.2K
Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
7.2K


