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GeneNetwork
Developer(s)GeneNetwork Development Team, University of Tennessee
Stable release
0.9 / 13 September 2010
Operating systemCross-platform web-based
LicenseAffero General Public License
Websitehttp://www.genenetwork.org/

GeneNetwork is a database and open source bioinformatics software resource for systems genetics.[2] This resource is used to study gene regulatory networks that link DNA sequence variants to corresponding differences in gene and protein expression and to differences in traits such as health and disease risk. Data sets in GeneNetwork are typically are made up of large collections of genotypes (e.g., SNPs) and phenotypes that are obtained from groups of related individuals, including human families, experimental crosses of strains of mice and rats, and organisms as diverse as Drosophila melanogaster, Arabidopsis thaliana, and barley.[3] The inclusion of genotypes for all individuals makes it practical to carry out web-based gene mapping to discover those regions of the genome that contribute to differences in gene expression, cell function, anatomy, physiology, and behavior among individuals.

History

GeneNetwork was originally created at the University of Tennessee in Memphis in 2000-2001. It was developed as a web-adapted version of Kenneth F. Manly's Map Manager program and was initially called WebQTL.[4] Gene mapping data were incorporated for several mouse recombinant inbred strains. By early 2003, the first large Affymetrix gene expression data sets (whole mouse brain mRNA and hematopoietic stem cells) were incorporated and the system was renamed.[5] [6] GeneNetwork is now developed by an international group of open source developers and has mirror and development sites in Europe, Asia, and Australia.

Organization and Use

GeneNetwork consists of two major components:

  • Massive collections of genetic, genomic, and phenotype data for large families
  • Sophisticated statistical analysis and gene mapping software that enable analysis of regulatory networks and genotype-to-phenotype relations

Four levels of data are usually obtained for each family or population:

  1. DNA sequences and genotypes
  2. Gene expression values using microarray, RNA-seq, or proteomic methods (molecular phenotypes)
  3. Standard phenotypes of the type that are part of a typical medical record (e.g., blood chemistry, body weight)
  4. Annotation files and metadata.

The combined data types are housed together in a single relational database, but are conceptually organized and divided by species and family. The system is implemented as a LAMP (software bundle) stack.

GeneNetwork is primarily used by researchers but has also been adopted successfully for undergraduate courses in genetics (see YouTube example), bioinformatics, physiology, and psychology.[7] Researchers and students typically retrieve sets of genotypes and phenotypes from one or more families and use built-in statistical and mapping functions to explore relations among variables and to assemble networks of associations. Key steps include the analysis of these factors:

  1. The range of variation of traits
  2. Covariation among traits (scatterplots and correlations)
  3. Architecture of larger networks of traits
  4. Quantitative trait locus mapping and causal models of the linkage between sequence differences and phenotype differences

Data Sources

Massive expression data sets are submitted by researchers directly or are extracted from repositories such as National Center for Biotechnology Information Gene Expression Omnibus. A wide variety of cells and tissues are included--from single cell populations of the immune system, specific tissues (retina, prefrontal cortex), to entire systems (whole brain, lung, muscle, heart, fat, kidney, flower, even whole plant embryos). A typical data set is often based on hundreds of fully genotyped individuals and may also include biological replicates. Genotypes and phenotypes are taken from peer-reviewed papers. GeneNetwork includes annotation files for several RNA profiling platforms (Affymetrix, Illumina, and Agilent). RNA-seq data are also available for BXD recombinant inbred mice. Content and nomenclature are reviewed and edited by curators. Updates on coverage of species, families, tissues and measurement types are available at this site: [1].

Topics of annotation include the following:

Tools and Features

There are tools on the site for a wide range of functions that range from simple graphical displays of variation in gene expression or other phenotypes, scatter plots of pairs of traits (Pearson or rank order), construction of both simple and complex network graphs, analysis of principal components and synthetic traits, QTL mapping using marker regression, interval mapping, and pair scans for epistatic interactions. Most functions work with up to 100 traits and several functions work with an entire transcriptome.

The database can be browsed and searched at the main search page. An on-line tutorial is available. Users can also download the primary data sets as text files, Excel, or in the case of network graphs, as SBML.

Code

GeneNetwork is an open source project released under the Affero General Public License (AGPLv3). The majority of code is written in Python, but includes modules and other code written in C and JavaScript. GeneNetwork also calls statistical procedures written in R.[citation needed]


See also

References

  1. ^ A Brief History R : Past and Future History, Ross Ihaka, Statistics Department, The University of Auckland, Auckland, New Zealand, available from the CRAN website
  2. ^ Morahan, G; Williams, RW (2007). "Systems genetics: the next generation in genetics research?". Novartis Foundation symposium. 281: 181–8, discussion 188–91, 208–9. PMID 17534074.
  3. ^ Druka, A; Druka, I; Centeno, AG; Li, H; Sun, Z; Thomas, WT; Bonar, N; Steffenson, BJ; Ullrich, SE (2008). "Towards systems genetic analyses in barley: Integration of phenotypic, expression and genotype data into GeneNetwork". BMC genetics. 9: 73. doi:10.1186/1471-2156-9-73. PMC 2630324. PMID 19017390.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  4. ^ Chesler, EJ; Lu, L; Wang, J; Williams, RW; Manly, KF (2004). "WebQTL: rapid exploratory analysis of gene expression and genetic networks for brain and behavior". Nature neuroscience. 7 (5): 485–6. doi:10.1038/nn0504-485. PMID 15114364.
  5. ^ Chesler, EJ; Lu, L; Shou, S; Qu, Y; Gu, J; Wang, J; Hsu, HC; Mountz, JD; Baldwin, NE (2005). "Complex trait analysis of gene expression uncovers polygenic and pleiotropic networks that modulate nervous system function". Nature genetics. 37 (3): 233–42. doi:10.1038/ng1518. PMID 15711545.
  6. ^ Bystrykh, L; Weersing, E; Dontje, B; Sutton, S; Pletcher, MT; Wiltshire, T; Su, AI; Vellenga, E; Wang, J (2005). "Uncovering regulatory pathways that affect hematopoietic stem cell function using 'genetical genomics'". Nature genetics. 37 (3): 225–32. doi:10.1038/ng1497. PMID 15711547.
  7. ^ Grisham, W; Schottler, NA; Valli-Marill, J; Beck, L; Beatty, J (2010). "Teaching bioinformatics and neuroinformatics by using free web-based tools". CBE life sciences education. 9 (2): 98–107. doi:10.1187/cbe.09-11-0079. PMC 2879386. PMID 20516355.
Related resources

Other systems genetics and network databases

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