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1.
Nucleic Acids Res ; 45(D1): D896-D901, 2017 01 04.
Artículo en Inglés | MEDLINE | ID: mdl-27899670

RESUMEN

The NHGRI-EBI GWAS Catalog has provided data from published genome-wide association studies since 2008. In 2015, the database was redesigned and relocated to EMBL-EBI. The new infrastructure includes a new graphical user interface (www.ebi.ac.uk/gwas/), ontology supported search functionality and an improved curation interface. These developments have improved the data release frequency by increasing automation of curation and providing scaling improvements. The range of available Catalog data has also been extended with structured ancestry and recruitment information added for all studies. The infrastructure improvements also support scaling for larger arrays, exome and sequencing studies, allowing the Catalog to adapt to the needs of evolving study design, genotyping technologies and user needs in the future.


Asunto(s)
Bases de Datos de Ácidos Nucleicos , Estudio de Asociación del Genoma Completo/métodos , Programas Informáticos , Minería de Datos , Genómica/métodos , Humanos , Anotación de Secuencia Molecular , National Human Genome Research Institute (U.S.) , Estados Unidos , Interfaz Usuario-Computador , Navegador Web
2.
Nucleic Acids Res ; 44(D1): D746-52, 2016 Jan 04.
Artículo en Inglés | MEDLINE | ID: mdl-26481351

RESUMEN

Expression Atlas (http://www.ebi.ac.uk/gxa) provides information about gene and protein expression in animal and plant samples of different cell types, organism parts, developmental stages, diseases and other conditions. It consists of selected microarray and RNA-sequencing studies from ArrayExpress, which have been manually curated, annotated with ontology terms, checked for high quality and processed using standardised analysis methods. Since the last update, Atlas has grown seven-fold (1572 studies as of August 2015), and incorporates baseline expression profiles of tissues from Human Protein Atlas, GTEx and FANTOM5, and of cancer cell lines from ENCODE, CCLE and Genentech projects. Plant studies constitute a quarter of Atlas data. For genes of interest, the user can view baseline expression in tissues, and differential expression for biologically meaningful pairwise comparisons-estimated using consistent methodology across all of Atlas. Our first proteomics study in human tissues is now displayed alongside transcriptomics data in the same tissues. Novel analyses and visualisations include: 'enrichment' in each differential comparison of GO terms, Reactome, Plant Reactome pathways and InterPro domains; hierarchical clustering (by baseline expression) of most variable genes and experimental conditions; and, for a given gene-condition, distribution of baseline expression across biological replicates.


Asunto(s)
Bases de Datos Genéticas , Perfilación de la Expresión Génica , Plantas/metabolismo , Proteínas/metabolismo , Proteómica , Animales , Línea Celular Tumoral , Humanos , Plantas/genética , Interfaz Usuario-Computador
3.
Nucleic Acids Res ; 43(Database issue): D1113-6, 2015 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-25361974

RESUMEN

The ArrayExpress Archive of Functional Genomics Data (http://www.ebi.ac.uk/arrayexpress) is an international functional genomics database at the European Bioinformatics Institute (EMBL-EBI) recommended by most journals as a repository for data supporting peer-reviewed publications. It contains data from over 7000 public sequencing and 42,000 array-based studies comprising over 1.5 million assays in total. The proportion of sequencing-based submissions has grown significantly over the last few years and has doubled in the last 18 months, whilst the rate of microarray submissions is growing slightly. All data in ArrayExpress are available in the MAGE-TAB format, which allows robust linking to data analysis and visualization tools and standardized analysis. The main development over the last two years has been the release of a new data submission tool Annotare, which has reduced the average submission time almost 3-fold. In the near future, Annotare will become the only submission route into ArrayExpress, alongside MAGE-TAB format-based pipelines. ArrayExpress is a stable and highly accessed resource. Our future tasks include automation of data flows and further integration with other EMBL-EBI resources for the representation of multi-omics data.


Asunto(s)
Bases de Datos Genéticas , Perfilación de la Expresión Génica , Análisis de Secuencia por Matrices de Oligonucleótidos , Genómica , Secuenciación de Nucleótidos de Alto Rendimiento , Internet , Programas Informáticos
4.
Nucleic Acids Res ; 42(Database issue): D926-32, 2014 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-24304889

RESUMEN

Expression Atlas (http://www.ebi.ac.uk/gxa) is a value-added database providing information about gene, protein and splice variant expression in different cell types, organism parts, developmental stages, diseases and other biological and experimental conditions. The database consists of selected high-quality microarray and RNA-sequencing experiments from ArrayExpress that have been manually curated, annotated with Experimental Factor Ontology terms and processed using standardized microarray and RNA-sequencing analysis methods. The new version of Expression Atlas introduces the concept of 'baseline' expression, i.e. gene and splice variant abundance levels in healthy or untreated conditions, such as tissues or cell types. Differential gene expression data benefit from an in-depth curation of experimental intent, resulting in biologically meaningful 'contrasts', i.e. instances of differential pairwise comparisons between two sets of biological replicates. Other novel aspects of Expression Atlas are its strict quality control of raw experimental data, up-to-date RNA-sequencing analysis methods, expression data at the level of gene sets, as well as genes and a more powerful search interface designed to maximize the biological value provided to the user.


Asunto(s)
Bases de Datos Genéticas , Perfilación de la Expresión Génica , Genómica , Humanos , Internet , Análisis de Secuencia por Matrices de Oligonucleótidos , Proteínas/genética , Proteínas/metabolismo , Isoformas de ARN/metabolismo , Análisis de Secuencia de ARN
5.
Nucleic Acids Res ; 41(Database issue): D987-90, 2013 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-23193272

RESUMEN

The ArrayExpress Archive of Functional Genomics Data (http://www.ebi.ac.uk/arrayexpress) is one of three international functional genomics public data repositories, alongside the Gene Expression Omnibus at NCBI and the DDBJ Omics Archive, supporting peer-reviewed publications. It accepts data generated by sequencing or array-based technologies and currently contains data from almost a million assays, from over 30 000 experiments. The proportion of sequencing-based submissions has grown significantly over the last 2 years and has reached, in 2012, 15% of all new data. All data are available from ArrayExpress in MAGE-TAB format, which allows robust linking to data analysis and visualization tools, including Bioconductor and GenomeSpace. Additionally, R objects, for microarray data, and binary alignment format files, for sequencing data, have been generated for a significant proportion of ArrayExpress data.


Asunto(s)
Bases de Datos Genéticas , Genómica , Análisis por Micromatrices , Bases de Datos Genéticas/estadística & datos numéricos , Bases de Datos Genéticas/tendencias , Secuenciación de Nucleótidos de Alto Rendimiento , Internet , Programas Informáticos , Interfaz Usuario-Computador
6.
Nucleic Acids Res ; 39(Database issue): D1002-4, 2011 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-21071405

RESUMEN

The ArrayExpress Archive (http://www.ebi.ac.uk/arrayexpress) is one of the three international public repositories of functional genomics data supporting publications. It includes data generated by sequencing or array-based technologies. Data are submitted by users and imported directly from the NCBI Gene Expression Omnibus. The ArrayExpress Archive is closely integrated with the Gene Expression Atlas and the sequence databases at the European Bioinformatics Institute. Advanced queries provided via ontology enabled interfaces include queries based on technology and sample attributes such as disease, cell types and anatomy.


Asunto(s)
Bases de Datos Genéticas , Perfilación de la Expresión Génica , Genómica , Secuenciación de Nucleótidos de Alto Rendimiento , Análisis de Secuencia por Matrices de Oligonucleótidos , Expresión Génica
7.
Bioinformatics ; 26(19): 2470-1, 2010 Oct 01.
Artículo en Inglés | MEDLINE | ID: mdl-20733062

RESUMEN

UNLABELLED: Computational methods in molecular biology will increasingly depend on standards-based annotations that describe biological experiments in an unambiguous manner. Annotare is a software tool that enables biologists to easily annotate their high-throughput experiments, biomaterials and data in a standards-compliant way that facilitates meaningful search and analysis. AVAILABILITY AND IMPLEMENTATION: Annotare is available from http://code.google.com/p/annotare/ under the terms of the open-source MIT License (http://www.opensource.org/licenses/mit-license.php). It has been tested on both Mac and Windows.


Asunto(s)
Perfilación de la Expresión Génica , Análisis de Secuencia por Matrices de Oligonucleótidos , Programas Informáticos , Biología Computacional/métodos , Bases de Datos Factuales , Anotación de Secuencia Molecular , Interfaz Usuario-Computador
8.
Genome Biol ; 19(1): 21, 2018 02 15.
Artículo en Inglés | MEDLINE | ID: mdl-29448949

RESUMEN

The accurate description of ancestry is essential to interpret, access, and integrate human genomics data, and to ensure that these benefit individuals from all ancestral backgrounds. However, there are no established guidelines for the representation of ancestry information. Here we describe a framework for the accurate and standardized description of sample ancestry, and validate it by application to the NHGRI-EBI GWAS Catalog. We confirm known biases and gaps in diversity, and find that African and Hispanic or Latin American ancestry populations contribute a disproportionately high number of associations. It is our hope that widespread adoption of this framework will lead to improved analysis, interpretation, and integration of human genomics data.


Asunto(s)
Estudio de Asociación del Genoma Completo/normas , Genómica/normas , Variación Genética , Humanos , Grupos Raciales
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