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)
Cited by
1207 articles.
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