Ensembl 2020

Author:

Yates Andrew D1ORCID,Achuthan Premanand1,Akanni Wasiu1,Allen James1,Allen Jamie1,Alvarez-Jarreta Jorge1,Amode M Ridwan1,Armean Irina M1,Azov Andrey G1,Bennett Ruth1,Bhai Jyothish1,Billis Konstantinos1,Boddu Sanjay1,Marugán José Carlos1,Cummins Carla1,Davidson Claire1,Dodiya Kamalkumar1,Fatima Reham1,Gall Astrid1,Giron Carlos Garcia1,Gil Laurent1,Grego Tiago1,Haggerty Leanne1,Haskell Erin1,Hourlier Thibaut1,Izuogu Osagie G1,Janacek Sophie H1,Juettemann Thomas1,Kay Mike1,Lavidas Ilias1,Le Tuan1,Lemos Diana1,Martinez Jose Gonzalez1,Maurel Thomas1,McDowall Mark1,McMahon Aoife1,Mohanan Shamika1,Moore Benjamin1,Nuhn Michael1,Oheh Denye N1,Parker Anne1,Parton Andrew1,Patricio Mateus1,Sakthivel Manoj Pandian1,Abdul Salam Ahamed Imran1,Schmitt Bianca M1,Schuilenburg Helen1,Sheppard Dan1,Sycheva Mira1,Szuba Marek1,Taylor Kieron1,Thormann Anja1,Threadgold Glen1,Vullo Alessandro1,Walts Brandon1,Winterbottom Andrea1,Zadissa Amonida1,Chakiachvili Marc1,Flint Bethany1,Frankish Adam1,Hunt Sarah E1,IIsley Garth1,Kostadima Myrto1,Langridge Nick1,Loveland Jane E1ORCID,Martin Fergal J1,Morales Joannella1,Mudge Jonathan M1,Muffato Matthieu1,Perry Emily1,Ruffier Magali1,Trevanion Stephen J1,Cunningham Fiona1,Howe Kevin L1ORCID,Zerbino Daniel R1,Flicek Paul1ORCID

Affiliation:

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

Abstract

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.

Funder

Wellcome Trust

National Human Genome Research Institute

National Institutes of Health

Biotechnology and Biological Sciences Research Council

Horizon 2020

European Molecular Biology Laboratory

Publisher

Oxford University Press (OUP)

Subject

Genetics

Reference47 articles.

1. The International Nucleotide Sequence Database Collaboration;Nakamura;Nucleic Acids Res.,2013

2. dbSNP: the NCBI database of genetic variation;Sherry;Nucleic Acids Res.,2001

3. The NIH Roadmap Epigenomics Mapping Consortium;Bernstein;Nat. Biotechnol.,2010

4. The Genotype-Tissue Expression (GTEx) pilot analysis: multitissue gene regulation in humans;Consortium;Science,2015

5. The Ensembl gene annotation system;Aken;Database J. Biol. Databases Curation,2016

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3