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2.
Nature ; 496(7446): 498-503, 2013 Apr 25.
Artigo em Inglês | MEDLINE | ID: mdl-23594743

RESUMO

Zebrafish have become a popular organism for the study of vertebrate gene function. The virtually transparent embryos of this species, and the ability to accelerate genetic studies by gene knockdown or overexpression, have led to the widespread use of zebrafish in the detailed investigation of vertebrate gene function and increasingly, the study of human genetic disease. However, for effective modelling of human genetic disease it is important to understand the extent to which zebrafish genes and gene structures are related to orthologous human genes. To examine this, we generated a high-quality sequence assembly of the zebrafish genome, made up of an overlapping set of completely sequenced large-insert clones that were ordered and oriented using a high-resolution high-density meiotic map. Detailed automatic and manual annotation provides evidence of more than 26,000 protein-coding genes, the largest gene set of any vertebrate so far sequenced. Comparison to the human reference genome shows that approximately 70% of human genes have at least one obvious zebrafish orthologue. In addition, the high quality of this genome assembly provides a clearer understanding of key genomic features such as a unique repeat content, a scarcity of pseudogenes, an enrichment of zebrafish-specific genes on chromosome 4 and chromosomal regions that influence sex determination.


Assuntos
Sequência Conservada/genética , Genoma/genética , Peixe-Zebra/genética , Animais , Cromossomos/genética , Evolução Molecular , Feminino , Genes/genética , Genoma Humano/genética , Genômica , Humanos , Masculino , Meiose/genética , Anotação de Sequência Molecular , Pseudogenes/genética , Padrões de Referência , Processos de Determinação Sexual/genética , Proteínas de Peixe-Zebra/genética
3.
Database (Oxford) ; 2011: bar030, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-21785142

RESUMO

For a number of years the BioMart data warehousing system has proven to be a valuable resource for scientists seeking a fast and versatile means of accessing the growing volume of genomic data provided by the Ensembl project. The launch of the Ensembl Genomes project in 2009 complemented the Ensembl project by utilizing the same visualization, interactive and programming tools to provide users with a means for accessing genome data from a further five domains: protists, bacteria, metazoa, plants and fungi. The Ensembl and Ensembl Genomes BioMarts provide a point of access to the high-quality gene annotation, variation data, functional and regulatory annotation and evolutionary relationships from genomes spanning the taxonomic space. This article aims to give a comprehensive overview of the Ensembl and Ensembl Genomes BioMarts as well as some useful examples and a description of current data content and future objectives. Database URLs: http://www.ensembl.org/biomart/martview/; http://metazoa.ensembl.org/biomart/martview/; http://plants.ensembl.org/biomart/martview/; http://protists.ensembl.org/biomart/martview/; http://fungi.ensembl.org/biomart/martview/; http://bacteria.ensembl.org/biomart/martview/.


Assuntos
Classificação/métodos , Bases de Dados Genéticas , Armazenamento e Recuperação da Informação/métodos , Animais , Anopheles/genética , Biologia Computacional , Genoma/genética , Humanos , Fases de Leitura Aberta/genética , Polimorfismo de Nucleotídeo Único/genética , Ferramenta de Busca
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