文献检索文档翻译深度研究
Suppr Zotero 插件Zotero 插件
邀请有礼套餐&价格历史记录

新学期,新优惠

限时优惠:9月1日-9月22日

30天高级会员仅需29元

1天体验卡首发特惠仅需5.99元

了解详情
不再提醒
插件&应用
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
高级版
套餐订阅购买积分包
AI 工具
文献检索文档翻译深度研究
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2025

Ensembl 2020.

Ensembl 2020.

机构信息

European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK.

出版信息

Nucleic Acids Res. 2020 Jan 8;48(D1):D682-D688. doi: 10.1093/nar/gkz966.


DOI:10.1093/nar/gkz966
PMID:31691826
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7145704/
Abstract

The Ensembl (https://www.ensembl.org) is a system for generating and distributing genome annotation such as genes, variation, regulation and comparative genomics across the vertebrate subphylum and key model organisms. The Ensembl annotation pipeline is capable of integrating experimental and reference data from multiple providers into a single integrated resource. Here, we present 94 newly annotated and re-annotated genomes, bringing the total number of genomes offered by Ensembl to 227. This represents the single largest expansion of the resource since its inception. We also detail our continued efforts to improve human annotation, developments in our epigenome analysis and display, a new tool for imputing causal genes from genome-wide association studies and visualisation of variation within a 3D protein model. Finally, we present information on our new website. Both software and data are made available without restriction via our website, online tools platform and programmatic interfaces (available under an Apache 2.0 license) and data updates made available four times a year.

摘要

Ensembl(https://www.ensembl.org)是一个用于生成和分发基因组注释的系统,例如基因、变异、调控和比较基因组学,涵盖了脊椎动物亚门和关键模式生物。Ensembl 注释管道能够将来自多个提供者的实验和参考数据集成到一个单一的集成资源中。在这里,我们展示了 94 个新注释和重新注释的基因组,使 Ensembl 提供的基因组总数达到 227 个。这是自成立以来该资源的最大规模扩展。我们还详细介绍了我们在人类注释方面的持续努力、表观基因组分析和显示方面的发展、一种从全基因组关联研究中推断因果基因的新工具以及在 3D 蛋白质模型中显示变异的工具。最后,我们介绍了我们新网站的信息。我们的软件和数据可通过我们的网站、在线工具平台和编程接口(根据 Apache 2.0 许可证提供)无限制使用,并且每年更新四次数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba44/7145704/7d08f85d16c0/gkz966fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba44/7145704/18407908eec1/gkz966fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba44/7145704/7d08f85d16c0/gkz966fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba44/7145704/18407908eec1/gkz966fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ba44/7145704/7d08f85d16c0/gkz966fig2.jpg

相似文献

[1]
Ensembl 2020.

Nucleic Acids Res. 2020-1-8

[2]
Ensembl Genomes 2020-enabling non-vertebrate genomic research.

Nucleic Acids Res. 2020-1-8

[3]
Ensembl Genomes 2022: an expanding genome resource for non-vertebrates.

Nucleic Acids Res. 2022-1-7

[4]
Ensembl 2017.

Nucleic Acids Res. 2017-1-4

[5]
Ensembl 2021.

Nucleic Acids Res. 2021-1-8

[6]
Ensembl Plants: Integrating Tools for Visualizing, Mining, and Analyzing Plant Genomic Data.

Methods Mol Biol. 2017

[7]
The Ensembl Genome Browser: Strategies for Accessing Eukaryotic Genome Data.

Methods Mol Biol. 2018

[8]
Ensembl 2016.

Nucleic Acids Res. 2016-1-4

[9]
Ensembl 2022.

Nucleic Acids Res. 2022-1-7

[10]
Ensembl 2008.

Nucleic Acids Res. 2008-1

引用本文的文献

[1]
Comparative genomic insights into adaptation, selection signatures, and population dynamics in indigenous Indian sheep and foreign breeds.

Front Genet. 2025-8-21

[2]
Evolutionary diversification of ancestral genes across vertebrates and insects.

Genome Biol. 2025-9-4

[3]
Exon 11 Mutations in Breast Cancer: A Study From Pakistan.

Genet Res (Camb). 2025-8-26

[4]
LncRNA HSCHARME is altered in human cardiomyopathies and promotes stem cell-derived cardiomyogenesis via splicing regulation.

Nat Commun. 2025-8-23

[5]
Quantitative modeling of mRNA degradation reveals tempo-dependent mRNA clearance in early embryos.

Nucleic Acids Res. 2025-7-19

[6]
Paucity of optineurin gene variants in Indian juvenile open-angle glaucoma patients.

Indian J Ophthalmol. 2025-8-1

[7]
Analysis of metagenomic data.

Nat Rev Methods Primers. 2025

[8]
Cardiac Troponin C E135A Variant Impairs Myofilament Response to PKA Phosphorylation and Is Associated With Autosomal Dominant Dilated Cardiomyopathy With Diastolic Dysfunction.

Circ Genom Precis Med. 2025-7-17

[9]
TFBSFootprinter: a multiomics tool for prediction of transcription factor binding sites in vertebrate species.

Transcription. 2025

[10]
Host albumin redirects Candida albicans metabolism to engage an alternative pathogenicity pathway.

Nat Commun. 2025-7-12

本文引用的文献

[1]
An improved pig reference genome sequence to enable pig genetics and genomics research.

Gigascience. 2020-6-1

[2]
Haplotype-resolved genomes provide insights into structural variation and gene content in Angus and Brahman cattle.

Nat Commun. 2020-4-29

[3]
SPDI: data model for variants and applications at NCBI.

Bioinformatics. 2020-3-1

[4]
Flexible and scalable diagnostic filtering of genomic variants using G2P with Ensembl VEP.

Nat Commun. 2019-5-30

[5]
Ensembl variation resources.

Database (Oxford). 2018-1-1

[6]
SIFTS: updated Structure Integration with Function, Taxonomy and Sequences resource allows 40-fold increase in coverage of structure-based annotations for proteins.

Nucleic Acids Res. 2019-1-8

[7]
Ensembl 2019.

Nucleic Acids Res. 2019-1-8

[8]
Database resources of the National Center for Biotechnology Information.

Nucleic Acids Res. 2019-1-8

[9]
UniProt: a worldwide hub of protein knowledge.

Nucleic Acids Res. 2019-1-8

[10]
CADD: predicting the deleteriousness of variants throughout the human genome.

Nucleic Acids Res. 2019-1-8

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

推荐工具

医学文档翻译智能文献检索