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Genome Variation Map: a data repository of genome variations in BIG Data Center.

Identifieur interne : 000E73 ( Main/Exploration ); précédent : 000E72; suivant : 000E74

Genome Variation Map: a data repository of genome variations in BIG Data Center.

Auteurs : Shuhui Song [République populaire de Chine] ; Dongmei Tian [République populaire de Chine] ; Cuiping Li [République populaire de Chine] ; Bixia Tang [République populaire de Chine] ; Lili Dong [République populaire de Chine] ; Jingfa Xiao [République populaire de Chine] ; Yiming Bao [République populaire de Chine] ; Wenming Zhao [République populaire de Chine] ; Hang He [République populaire de Chine] ; Zhang Zhang [République populaire de Chine]

Source :

RBID : pubmed:29069473

Descripteurs français

English descriptors

Abstract

The Genome Variation Map (GVM; http://bigd.big.ac.cn/gvm/) is a public data repository of genome variations. As a core resource in the BIG Data Center, Beijing Institute of Genomics, Chinese Academy of Sciences, GVM dedicates to collect, integrate and visualize genome variations for a wide range of species, accepts submissions of different types of genome variations from all over the world and provides free open access to all publicly available data in support of worldwide research activities. Unlike existing related databases, GVM features integration of a large number of genome variations for a broad diversity of species including human, cultivated plants and domesticated animals. Specifically, the current implementation of GVM not only houses a total of ∼4.9 billion variants for 19 species including chicken, dog, goat, human, poplar, rice and tomato, but also incorporates 8669 individual genotypes and 13 262 manually curated high-quality genotype-to-phenotype associations for non-human species. In addition, GVM provides friendly intuitive web interfaces for data submission, browse, search and visualization. Collectively, GVM serves as an important resource for archiving genomic variation data, helpful for better understanding population genetic diversity and deciphering complex mechanisms associated with different phenotypes.

DOI: 10.1093/nar/gkx986
PubMed: 29069473
PubMed Central: PMC5753358


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<term>Access to Information (MeSH)</term>
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<term>Animals, Domestic (genetics)</term>
<term>Base Sequence (MeSH)</term>
<term>Big Data (MeSH)</term>
<term>Data Curation (MeSH)</term>
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<term>Genome (MeSH)</term>
<term>Genome, Human (MeSH)</term>
<term>Genotype (MeSH)</term>
<term>High-Throughput Nucleotide Sequencing (MeSH)</term>
<term>Humans (MeSH)</term>
<term>Plants (genetics)</term>
<term>Species Specificity (MeSH)</term>
<term>User-Computer Interface (MeSH)</term>
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<term>Animaux domestiques (génétique)</term>
<term>Bases de données génétiques (MeSH)</term>
<term>Curation de données (MeSH)</term>
<term>Génome (MeSH)</term>
<term>Génome humain (MeSH)</term>
<term>Génotype (MeSH)</term>
<term>Génétique des populations (MeSH)</term>
<term>Humains (MeSH)</term>
<term>Interface utilisateur (MeSH)</term>
<term>Mégadonnées (MeSH)</term>
<term>Plantes (génétique)</term>
<term>Prévision (MeSH)</term>
<term>Spécificité d'espèce (MeSH)</term>
<term>Systèmes de gestion de bases de données (MeSH)</term>
<term>Séquence nucléotidique (MeSH)</term>
<term>Séquençage nucléotidique à haut débit (MeSH)</term>
<term>Variation génétique (MeSH)</term>
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<term>Big Data</term>
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<term>Databases, Genetic</term>
<term>Forecasting</term>
<term>Genetic Variation</term>
<term>Genetics, Population</term>
<term>Genome</term>
<term>Genome, Human</term>
<term>Genotype</term>
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<term>Species Specificity</term>
<term>User-Computer Interface</term>
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<term>Bases de données génétiques</term>
<term>Curation de données</term>
<term>Génome</term>
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<div type="abstract" xml:lang="en">The Genome Variation Map (GVM; http://bigd.big.ac.cn/gvm/) is a public data repository of genome variations. As a core resource in the BIG Data Center, Beijing Institute of Genomics, Chinese Academy of Sciences, GVM dedicates to collect, integrate and visualize genome variations for a wide range of species, accepts submissions of different types of genome variations from all over the world and provides free open access to all publicly available data in support of worldwide research activities. Unlike existing related databases, GVM features integration of a large number of genome variations for a broad diversity of species including human, cultivated plants and domesticated animals. Specifically, the current implementation of GVM not only houses a total of ∼4.9 billion variants for 19 species including chicken, dog, goat, human, poplar, rice and tomato, but also incorporates 8669 individual genotypes and 13 262 manually curated high-quality genotype-to-phenotype associations for non-human species. In addition, GVM provides friendly intuitive web interfaces for data submission, browse, search and visualization. Collectively, GVM serves as an important resource for archiving genomic variation data, helpful for better understanding population genetic diversity and deciphering complex mechanisms associated with different phenotypes.</div>
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<AbstractText>The Genome Variation Map (GVM; http://bigd.big.ac.cn/gvm/) is a public data repository of genome variations. As a core resource in the BIG Data Center, Beijing Institute of Genomics, Chinese Academy of Sciences, GVM dedicates to collect, integrate and visualize genome variations for a wide range of species, accepts submissions of different types of genome variations from all over the world and provides free open access to all publicly available data in support of worldwide research activities. Unlike existing related databases, GVM features integration of a large number of genome variations for a broad diversity of species including human, cultivated plants and domesticated animals. Specifically, the current implementation of GVM not only houses a total of ∼4.9 billion variants for 19 species including chicken, dog, goat, human, poplar, rice and tomato, but also incorporates 8669 individual genotypes and 13 262 manually curated high-quality genotype-to-phenotype associations for non-human species. In addition, GVM provides friendly intuitive web interfaces for data submission, browse, search and visualization. Collectively, GVM serves as an important resource for archiving genomic variation data, helpful for better understanding population genetic diversity and deciphering complex mechanisms associated with different phenotypes.</AbstractText>
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<ForeName>Shuhui</ForeName>
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