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1.
Nucleic Acids Res ; 49(D1): D1058-D1064, 2021 01 08.
Article in English | MEDLINE | ID: mdl-33170210

ABSTRACT

The Zebrafish Information Network (ZFIN) (https://zfin.org/) is the database for the model organism, zebrafish (Danio rerio). ZFIN expertly curates, organizes, and provides a wide array of zebrafish genetic and genomic data, including genes, alleles, transgenic lines, gene expression, gene function, mutant phenotypes, orthology, human disease models, gene and mutant nomenclature, and reagents. New features at ZFIN include major updates to the home page and the gene page, the two most used pages at ZFIN. Data including disease models, phenotypes, expression, mutants and gene function continue to be contributed to The Alliance of Genome Resources for integration with similar data from other model organisms.


Subject(s)
Computational Biology/methods , Databases, Genetic , Genome/genetics , Genomics/methods , Zebrafish/genetics , Animals , Animals, Genetically Modified , Data Mining/methods , Gene Expression , Humans , Internet , Models, Animal , Mutation , Phenotype , Zebrafish Proteins/genetics
2.
Nucleic Acids Res ; 47(D1): D867-D873, 2019 01 08.
Article in English | MEDLINE | ID: mdl-30407545

ABSTRACT

The Zebrafish Information Network (ZFIN) (https://zfin.org/) is the database for the model organism, zebrafish (Danio rerio). ZFIN expertly curates, organizes and provides a wide array of zebrafish genetic and genomic data, including genes, alleles, transgenic lines, gene expression, gene function, mutant phenotypes, orthology, human disease models, nomenclature and reagents. New features at ZFIN include increased support for genomic regions and for non-coding genes, and support for more expressive Gene Ontology annotations. ZFIN has recently taken over maintenance of the zebrafish reference genome sequence as part of the Genome Reference Consortium. ZFIN is also a founding member of the Alliance of Genome Resources, a collaboration of six model organism databases (MODs) and the Gene Ontology Consortium (GO). The recently launched Alliance portal (https://alliancegenome.org) provides a unified, comparative view of MOD, GO, and human data, and facilitates foundational and translational biomedical research.


Subject(s)
Databases, Genetic , Genome/genetics , Genomics , Zebrafish/genetics , Animals , Gene Expression/genetics , Gene Ontology , Humans , Molecular Sequence Annotation , Mutation/genetics , Phenotype
3.
Nucleic Acids Res ; 45(D1): D758-D768, 2017 01 04.
Article in English | MEDLINE | ID: mdl-27899582

ABSTRACT

The Zebrafish Model Organism Database (ZFIN; http://zfin.org) is the central resource for zebrafish (Danio rerio) genetic, genomic, phenotypic and developmental data. ZFIN curators provide expert manual curation and integration of comprehensive data involving zebrafish genes, mutants, transgenic constructs and lines, phenotypes, genotypes, gene expressions, morpholinos, TALENs, CRISPRs, antibodies, anatomical structures, models of human disease and publications. We integrate curated, directly submitted, and collaboratively generated data, making these available to zebrafish research community. Among the vertebrate model organisms, zebrafish are superbly suited for rapid generation of sequence-targeted mutant lines, characterization of phenotypes including gene expression patterns, and generation of human disease models. The recent rapid adoption of zebrafish as human disease models is making management of these data particularly important to both the research and clinical communities. Here, we describe recent enhancements to ZFIN including use of the zebrafish experimental conditions ontology, 'Fish' records in the ZFIN database, support for gene expression phenotypes, models of human disease, mutation details at the DNA, RNA and protein levels, and updates to the ZFIN single box search.


Subject(s)
Databases, Genetic , Genetic Association Studies/methods , Genomics/methods , Search Engine , Zebrafish/genetics , Animals , Computational Biology/methods , Data Curation , Disease Models, Animal , Gene Expression , Genetic Predisposition to Disease , Genotype , Humans , Mutation , Phenotype
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