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1.
Nature ; 496(7446): 498-503, 2013 Apr 25.
Artículo en Inglés | MEDLINE | ID: mdl-23594743

RESUMEN

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.


Asunto(s)
Secuencia Conservada/genética , Genoma/genética , Pez Cebra/genética , Animales , Cromosomas/genética , Evolución Molecular , Femenino , Genes/genética , Genoma Humano/genética , Genómica , Humanos , Masculino , Meiosis/genética , Anotación de Secuencia Molecular , Seudogenes/genética , Estándares de Referencia , Procesos de Determinación del Sexo/genética , Proteínas de Pez Cebra/genética
2.
Database (Oxford) ; 2011: bar030, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-21785142

RESUMEN

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/.


Asunto(s)
Clasificación/métodos , Bases de Datos Genéticas , Almacenamiento y Recuperación de la Información/métodos , Animales , Anopheles/genética , Biología Computacional , Genoma/genética , Humanos , Sistemas de Lectura Abierta/genética , Polimorfismo de Nucleótido Simple/genética , Motor de Búsqueda
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