. 2020 Nov 2;49(D1):D884–D891. doi: 10.1093/nar/gkaa942

Ensembl 2021

Kevin L Howe ¹, Premanand Achuthan ², James Allen ³, Jamie Allen ⁴, Jorge Alvarez-Jarreta ⁵, M Ridwan Amode ⁶, Irina M Armean ⁷, Andrey G Azov ⁸, Ruth Bennett ⁹, Jyothish Bhai ¹⁰, Konstantinos Billis ¹¹, Sanjay Boddu ¹², Mehrnaz Charkhchi ¹³, Carla Cummins ¹⁴, Luca Da Rin Fioretto ¹⁵, Claire Davidson ¹⁶, Kamalkumar Dodiya ¹⁷, Bilal El Houdaigui ¹⁸, Reham Fatima ¹⁹, Astrid Gall ²⁰, Carlos Garcia Giron ²¹, Tiago Grego ²², Cristina Guijarro-Clarke ²³, Leanne Haggerty ²⁴, Anmol Hemrom ²⁵, Thibaut Hourlier ²⁶, Osagie G Izuogu ²⁷, Thomas Juettemann ²⁸, Vinay Kaikala ²⁹, Mike Kay ³⁰, Ilias Lavidas ³¹, Tuan Le ³², Diana Lemos ³³, Jose Gonzalez Martinez ³⁴, José Carlos Marugán ³⁵, Thomas Maurel ³⁶, Aoife C McMahon ³⁷, Shamika Mohanan ³⁸, Benjamin Moore ³⁹, Matthieu Muffato ⁴⁰, Denye N Oheh ⁴¹, Dimitrios Paraschas ⁴², Anne Parker ⁴³, Andrew Parton ⁴⁴, Irina Prosovetskaia ⁴⁵, Manoj P Sakthivel ⁴⁶, Ahamed I Abdul Salam ⁴⁷, Bianca M Schmitt ⁴⁸, Helen Schuilenburg ⁴⁹, Dan Sheppard ⁵⁰, Emily Steed ⁵¹, Michal Szpak ⁵², Marek Szuba ⁵³, Kieron Taylor ⁵⁴, Anja Thormann ⁵⁵, Glen Threadgold ⁵⁶, Brandon Walts ⁵⁷, Andrea Winterbottom ⁵⁸, Marc Chakiachvili ⁵⁹, Ameya Chaubal ⁶⁰, Nishadi De Silva ⁶¹, Bethany Flint ⁶², Adam Frankish ⁶³, Sarah E Hunt ⁶⁴, Garth R IIsley ⁶⁵, Nick Langridge ⁶⁶, Jane E Loveland ⁶⁷, Fergal J Martin ⁶⁸, Jonathan M Mudge ⁶⁹, Joanella Morales ⁷⁰, Emily Perry ⁷¹, Magali Ruffier ⁷², John Tate ⁷³, David Thybert ⁷⁴, Stephen J Trevanion ⁷⁵, Fiona Cunningham ⁷⁶, Andrew D Yates ⁷⁷, Daniel R Zerbino ⁷⁸, Paul Flicek ^79,^✉

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

² European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

³ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁴ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁵ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁶ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁷ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁸ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁹ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

¹⁰ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

¹¹ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

¹² European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

¹³ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

¹⁴ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

¹⁵ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

¹⁶ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

¹⁷ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

¹⁸ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

¹⁹ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

²⁰ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

²¹ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

²² European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

²³ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

²⁴ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

²⁵ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

²⁶ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

²⁷ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

²⁸ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

²⁹ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

³⁰ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

³¹ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

³² European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

³³ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

³⁴ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

³⁵ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

³⁶ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

³⁷ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

³⁸ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

³⁹ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁴⁰ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁴¹ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁴² European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁴³ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁴⁴ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁴⁵ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁴⁶ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁴⁷ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁴⁸ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁴⁹ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁵⁰ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁵¹ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁵² European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁵³ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁵⁴ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁵⁵ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁵⁶ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁵⁷ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁵⁸ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁵⁹ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁶⁰ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁶¹ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁶² European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁶³ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁶⁴ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁶⁵ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁶⁶ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁶⁷ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁶⁸ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁶⁹ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁷⁰ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁷¹ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁷² European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁷³ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁷⁴ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁷⁵ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁷⁶ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁷⁷ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁷⁸ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

⁷⁹ European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK

^✉

To whom correspondence should be addressed. Tel: +44 1223 492 581; Fax: +44 1223 494 468; Email: flicek@ebi.ac.uk

PMCID: PMC7778975 PMID: 33137190

Abstract

The Ensembl project (https://www.ensembl.org) annotates genomes and disseminates genomic data for vertebrate species. We create detailed and comprehensive annotation of gene structures, regulatory elements and variants, and enable comparative genomics by inferring the evolutionary history of genes and genomes. Our integrated genomic data are made available in a variety of ways, including genome browsers, search interfaces, specialist tools such as the Ensembl Variant Effect Predictor, download files and programmatic interfaces. Here, we present recent Ensembl developments including two new website portals. Ensembl Rapid Release (http://rapid.ensembl.org) is designed to provide core tools and services for genomes as soon as possible and has been deployed to support large biodiversity sequencing projects. Our SARS-CoV-2 genome browser (https://covid-19.ensembl.org) integrates our own annotation with publicly available genomic data from numerous sources to facilitate the use of genomics in the international scientific response to the COVID-19 pandemic. We also report on other updates to our annotation resources, tools and services. All Ensembl data and software are freely available without restriction.

INTRODUCTION

Ensembl accelerates worldwide genomic research by integrating, harmonizing and annotating genome data and disseminating it via a coherent and consistent set of interfaces and tools. We import primary data from archive resources such as INSDC (1), dbSNP (2) and the European Variation Archive (EVA, https://www.ebi.ac.uk/eva), and add value via detailed and comprehensive annotation of transcript structures (3), genomic variants (4) and regulatory regions (5). We also enable the study of evolution by large-scale comparison of genomes and gene products across many species (6). These data can be accessed via our website, programmatically via a number of application programming interfaces (APIs) (7,8), and downloaded in numerous standard file formats. We develop and make available a variety of tools for genomic analysis, including the Ensembl Variant Effect Predictor (VEP) (9). Our software, database and tools infrastructure is freely available and is used to power the nonvertebrate genome resources provided by the clade-specific Ensembl Genomes websites (10), collaborating resources such as WormBase (11), and community-oriented databases focused on branches of the taxonomy, such as AvianBase (12) and LepBase (http://lepbase.org).

Genome research has evolved significantly since the publication of the human genome 20 years ago (13). Genome medicine is developing rapidly across the world as a diagnostic tool for rare diseases, for prioritization and selection of cancer treatments, and for many other applications. At the same time, we are in the midst of the sixth mass extinction (14), and loss of biodiversity is entwined with many of the key challenges faced by human society today including pandemic zoonotic diseases, climate change, food security, availability of drugs and vaccines, and renewable energy. Genomics will play an increasingly important role in biomedical and biodiversity science, and a key aim for Ensembl is to evolve accordingly by developing our reference annotation resources and genomics infrastructure platform to support these applications.

This year, we have enhanced our reference transcript, regulatory and variation annotation in human, vertebrate model organisms, and other species of high socioeconomic importance. For example, our human genome resources have seen three updates to the Ensembl/GENCODE reference transcript set, continued collaborative work within the Matched Annotation from NCBI and EMBL-EBI (MANE) project, enriched regulatory data for enhancer activity and microRNA-gene interactions, and variation annotation incorporating new structural variants and allele frequency data.

Large-scale biodiversity sequencing projects, such as the Vertebrate Genomes Project (https://vertebrategenomesproject.org/) and the Darwin Tree of Life Project (https://www.darwintreeoflife.org/), are generating high-quality genome assemblies at an accelerating pace. Supporting these projects and others under the umbrella of the Earth BioGenome Project (15) is a priority development area for us. We previously reported on our efforts to re-engineer our evidence-based automated transcript annotation pipeline to achieve an order-of-magnitude increase in efficiency (16). This year, we have consolidated this work to deliver our largest annual increase in supported genomes, while creating a new mechanism—Ensembl Rapid Release—for the dissemination and distribution of genomes as soon as they are annotated. We have also created a sub-portal of Ensembl for the Vertebrate Genomes Project, which acts as a template for further project or community-specific windows into Ensembl data.

As well as an annotation resource, Ensembl is also a comprehensive technology platform for the management, analysis and dissemination of genomic data. We have enriched our website and services with new ways of accessing data, and have developed a new interface for exploring multidimensional Track Hubs. At the same time, work on our redesigned website (17) and APIs continues apace, with recent innovations including a new prototype API.

The COVID-19 pandemic is unprecedented in its mobilization of the global scientific community, with many researchers refocusing their work to help understand the disease, treat its symptoms and slow its transmission. We have contributed to the effort by creating a browser and tools for the genome of the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus that causes COVID-19. The reference sequence acts as a foundation for exploring data pertaining to the molecular genetics of virus transmission and pathogenicity, and our established tools such as the Ensembl VEP are a useful platform for exploring the variation between viral isolates.

REFERENCE ANNOTATION FOR KEY SPECIES

We have enriched our reference human transcript annotation, which is created as part of the GENCODE consortium (18). One area of focus this year has been re-examining and extending the annotation for genes implicated with COVID-19 infection and response, which has resulted thus far in the addition or amendment of over 4000 transcripts. These data are currently available as a Track Hub (19), and will be made available as part of the full Ensembl/GENCODE transcript set in an imminent Ensembl release. We previously reported (17) on a new collaboration with the NCBI—MANE Select—that aims to produce a single reference transcript for every human protein gene with identical structure between Ensembl/GENCODE and RefSeq (20). In our recent v0.91 of MANE Select (July 2020), 84% of human protein-coding genes are covered (up from 67% last year). We have been working closely with clinical partners to prioritize loci for inclusion in MANE Select, and we expect close to full coverage of all clinical genes with confirmed association with human disease to be available imminently. This includes the 59 genes considered to be clinically actionable by the American College of Medical Genetics and Genomics (ACMG) (21).

We have broadened and deepened our reference human regulatory annotation. This year, we incorporated updated enhancer activity data from VISTA (22) and miRNA/gene interactions from Tarbase v8 (23). We also refreshed our regulatory annotation for GRCh37, in recognition of the widespread use of this previous human assembly. Our GRCh37 regulatory annotation now represents over 100 human epigenomes, cataloguing over half a million elements covering 16% of the genome from over 9TB of experimental data from the Roadmap Epigenomics (24), ENCODE (25) and BLUEPRINT (26) projects.

Our high-quality reference human gene and regulatory annotation underpin the interpretation of genetic variation in human populations. We have enhanced our variant collections by updating to the latest versions of multiple resources including dbSNP and the Genome Aggregation Database (gnomAD, (27)), and added new human allele frequency data from the Gambian Genome Variation project (28). We have also integrated new structural variant data from sources including gnomAD, ClinVar (29) and the NCBI Curated Common Structural Variants set (https://www.ncbi.nlm.nih.gov/dbvar/studies/nstd186).

Beyond human, provision of annotation resources for model organisms and species of socioeconomic importance continues to be a key activity area. For example, we are part of the AQUA-FAANG consortium (https://www.aqua-faang.eu), which is focused the functional genomics of the six most economically important fish species in European aquaculture: European Seabass, Gilthead Seabream, Atlantic Salmon, Rainbow Trout, Common Carp and Turbot. We have produced detailed gene annotations for all six species, with work underway to add regulatory annotation. We have also integrated variant data for Atlantic Salmon from the EVA.

We support multiple strain/breed genomes for model organisms and farmed/companion animals, and we previously reported on the incorporation of 17 laboratory mouse strains (30) and 12 pig breeds (17). This year we have added additional breed genomes for sheep (Rambouillet), goat (Black bengal) and dog (Great Dane, Banshi and German Shepherd) as well as three strains of common carp.

SUPPORTING BIODIVERSITY GENOMICS

In the past year, we have annotated and integrated 83 new vertebrate genomes across diverse clades (see Figure 1). Notable among the additions are kakapo, golden eagle, small tree finch, wild duck, Indian cobra, mainland tiger snake and tuatara (31).

Our plans to rapidly increase the number of genomes that we annotate, compare and disseminate require us to make continual improvements to our gene annotation and comparative genomics workflows. We are focused both on increasing throughput and most effectively using the available experimental evidence to increase annotation accuracy. This year, we have enhanced our gene annotation pipeline with a new module for incorporating long-read transcriptomic data produced by the Oxford Nanopore Technologies platform. This was first used for annotating the kakapo genome and allows us to more confidently capture full-length transcript structures including a better representation of untranslated regions.

The traditional Ensembl data distribution model is one of periodic integrated and versioned releases in which every genome is comprehensively annotated, compared to other genomes and made available via our complete set of tools and services. Integrated releases involve the complex orchestration of a number of large-scale analyses and processes across the whole Ensembl project. This means that there can sometimes be a delay of multiple months between our production of the primary gene and transcript annotation and when a genome is available via an Ensembl release.

The redesigned Ensembl genome browser (see below) will support the release of genomes quickly after annotation and allow for their exploration via a core set of functionality and tools before their incorporation into an integrated release. In advance of the release of our new website and in support of the Darwin Tree of Life and other emerging nodes of the Earth BioGenome Project, we have created a new sub-portal of our current website for early access to annotated genomes. Ensembl Rapid Release (https://rapid.ensembl.org) is updated every 2 weeks with new genomes being added quickly after primary annotation. Core functionality on the site includes (i) a genome browser for every genome with tracks for primary gene annotation and repeats; (ii) functional annotation of annotated gene products using InterProScan (32); (iii) BLAST search of user-supplied sequences against the genome and its gene sequences; and (iv) download files of the genome and annotations in a variety of standard formats. Ensembl Rapid Release hosts both vertebrate and nonvertebrate genomes with the latter to be integrated into the appropriate Ensembl Genomes website (10). In the next year, we plan to add additional functionality to Ensembl Rapid Release, including homologies, gene symbols, additional genome browser tracks and programmatic access.

As we add more genomes to Ensembl, finding relevant data collections becomes increasingly important. To this end, we are creating community-oriented gateways for specific collections of genomes based initially on nodes of the Earth BioGenome Project. These act as landing pages for the annotated genomes arising from these projects with easy one-click access to key resources such as annotation files and the genome browser. Our first such gateway is for the Vertebrate Genomes Project (https://projects.ensembl.org/vgp) and one for the Darwin Tree of Life is planned for the next year. In future, we will extend the concept to create genome collections and sub-portals aimed at specific scientific communities such as agricultural genomics or parasitology and pathology.

TOOLS AND SERVICES

The capabilities of the Ensembl VEP have been expanded in several ways over the past year. For example, the Ensembl VEP can now standardize the representation of ambiguous insertion/deletion variants prior to consequence prediction, which addresses anomalous differences in predicted molecular consequences when variants in repetitive genomic regions are described in multiple equivalent ways. Another major enhancement is the reporting of variant synonyms, which enables improved navigation to additional information in resources such as ClinVar, UniProt and PharmGKB (33). Other improvements include enriched annotation of potential splicing impact (using scores from SpliceAI (34)), incorporation of phenotype association and variant citation data from DisGeNET (35), and protein annotations from neXtProt (36).

We previously introduced the Ensembl Transcript Archive (Tark) (17), which tracks changes to transcript structures across different annotation sources, releases and genome builds (http://dev-tark.ensembl.org). Ensembl Tark now includes all versioned human transcript sets from RefSeq and Ensembl/GENCODE, and contains an up-to-date list of MANE Select transcripts. In the next year, we will add support for Locus Reference Genomic (37) reference sequences.

We have made numerous improvements to our main website portal (https://www.ensembl.org). An example is our redesigned interface for configuring multi-dimensional Track Hubs. For 2D Hubs, we present a simple matrix as before, but where the Track Hub provider uses more than two dimensions the new interface allows for easier discovery and selection of these tracks (see Figure 2).

Figure 2. — The Blueprint Signal Track Hub. The primary dimensions of the Hub, Sample description and Experiment, are used to create the track selection matrix. Other dimensions within the data are shown in a panel on the right (e.g. Analysis group and Analysis Type), and tracks can be filtered by clicking on any of the types within those. Even greater granularity of track selection can be achieved by selecting tracks from a pop-up menu associated with each individual cell of the matrix.

Our new genome browser is currently in beta at http://2020.ensembl.org. We have recently focused on the development of key workflows such as viewing summary information about a gene, selecting transcripts and downloading sequence information. In tandem, we are developing a new API designed for the needs of modern, responsive web applications based on the GraphQL standard (graphql.org). The Ensembl GraphQL API enables the fine-grained request and delivery of specific slices of data. It is initially being developed primarily for our new website, and we aim for a public prototype in the next year.

SUPPORTING COVID-19 GENOMICS

COVID-19 is caused by SARS-CoV-2, which has spread across the globe since emerging in late 2019. Our SARS-CoV-2 genome browser and related resources (https://covid-19.ensembl.org) support genomics-based approaches to the study of the virus.

The reference sequence represented in Ensembl (INSDC accession GCA_009858895.3) is the RNA genome isolated from one of the first cases in Wuhan (38) and is widely used as a standard reference for variant calling and to root phylogenetic analyses. We have annotated the reference genome with genic features using a slightly adapted version of our annotation pipeline. Annotation of the ORF1ab/ORF1a locus in particular is complicated by a programmed-1 ribosome slippage in the translation of one of its two polyprotein products (39). The Ensembl data-model and database schema allows us to represent this situation elegantly as a sequence edit, allowing our annotation pipeline to store the transcript structure correctly and our API to produce the correct peptide products.

To enrich our gene structure annotation, we have added structural RNAs from Rfam (40), full cross-references to annotated entries at Uniprot (41) and RefSeq, functional annotation from the Gene Ontology Consortium (42), and annotation of protein domains from InterProScan. For the latter, we created a genome browser track projecting the protein-domain annotations onto the genome, facilitating a genome-oriented view of the gene projects (including the nonstructural cleavage products of ORF1a/ORF1ab). We also display a collection of other tracks on the genome browser, including the annotation that was submitted to INSDC as part of the publication of the reference genome (38), and community annotation of sites and regions resulting from an effort coordinated by the UCSC genome browser (43).

We are integrating and annotating identified variants in the genome of SARS-Cov-2 using Ensembl VEP. This has been an active area of research during the pandemic, with many countries undergoing concerted programs of isolate sequencing. For example, the COVID-19 data portal (https://www.covid19dataportal.org) has developed a pipeline employing LoFreq (44) to identify variants in publicly available SARS-CoV-2 genomes sequenced and deposited in the European Nucleotide Archive. We currently display variants from 5106 SARS-CoV2 samples, with significant growth expected in future releases. To complement our own analysis of the public data, we also display annotated variants from real-time pathogen surveillance resource Nextstrain (45), using sequence data acquired from the virus data sharing platform GISAID (46). As reported by De Maio et al. (https://virological.org/t/issues-with-sars-cov-2-sequencing-data/473), some sites in the SARS-CoV-2 are associated with unreliable variant calls, due to artifacts in sample preparation, sequencing technology and consensus calling. We have created a genome browser track for these sites to display which variants identified in the various datasets should be treated with caution.

Future releases of the portal will include new data as it emerges, additional tools (including sequence search) and comparative genomics views to enable the comparison of SARS-CoV-2 genome and gene products with those of related coronaviruses found in other species.

USER SUPPORT AND TRAINING

We maintain a close relationship with our global user community via our helpdesk (https://www.ensembl.org/Help/Contact or helpdesk@ensembl.org), and through our developer mailing list (https://lists.ensembl.org/mailman/listinfo/dev) we facilitate a network of bioinformaticians using the Ensembl platform.

We also directly train researchers throughout the world in the use of the Ensembl (http://training.ensembl.org). Traditionally, we have designed in-person courses aimed at wet-lab researchers and clinicians, developers and educators, with all courses tailored to suit the needs of a host institute or to fit in as part of a series. The COVID-19 pandemic has seen nearly all of our training in 2020 delivered on-line. This included an Ensembl component in a virtual training course for the Pan African Bioinformatics Network for the Human Heredity and Health in Africa consortium, H3ABioNet, reaching >1300 participants across 16 countries. We remain committed to in-person training but acknowledge that virtual training will occupy a larger proportion of our portfolio in the post-COVID-19 world.

CONCLUSION

While Ensembl resources are used in many different ways by thousands of researches across the world, our mission can be viewed from three broad perspectives. The first is enabling the fine-grained interpretation of genomic variation via the provision of comprehensive reference annotation for human, model organisms and other species of socioeconomic importance exemplified by our updates of the MANE Select transcript set and our enhanced reference regulatory and variation annotation resources. The second perspective is enabling genomic approaches to the study of biodiversity, this year seeing improvements to the breadth and depth of genomes we annotate and serve and the development of the Ensembl Rapid Release platform. The third perspective is enabling genome bioinformatics via the development of an extensive and reusable genomics infrastructure platform, with improved Ensembl Tark, enhanced website configuration options and accelerated work on our new genome browser. Finally, cutting across these three perspectives, we have integrated Ensembl's first viral genome to create our SARS-CoV-2 genome browser.

DATA AVAILABILITY

All Ensembl integrated data are available without restriction from our website (https://www.ensembl.org), in bulk from our FTP site (ftp://ftp.ensembl.org) and programmatically via our REST API (https://rest.ensembl.org). Ensembl code is available from GitHub (https://github.com/Ensembl) under an open source Apache 2.0 license. News about our releases and services can be found our blog (https://www.ensembl.info), our announce mailing list (https://lists.ensembl.org/mailman/listinfo/announce), Twitter (@ensembl) and Facebook (https://facebook.com/Ensembl.org).

ACKNOWLEDGEMENTS

We wish to thank all of our user community and data providers for making their data available for reuse within Ensembl; Rob Finn and Bruno Contreras-Moreira for discussions and support for the COVID-19 browser; and the following members of EMBL-EBI’s technical services cluster for their continued support: Simone Badoer, Jonathan Barker, Andy Bryant, Sarah Butcher, Andy Cafferkey, Andrea Cristofori, Ray Coetzee, Salvatore Di Nardo, Pete Jokinen, Rodrigo Lopez, Zander Mears, Manuela Menchi, Sundeep Nanawa, Steven Newhouse and Jordi Valls.

Contributor Information

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

FUNDING

Wellcome Trust [WT108749/Z/15/Z]; National Human Genome Research Institue [U41HG007823, 2U41HG007234, U41HG010972, 2U24HG007497–05]. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health; Biotechnology and Biological Sciences Research Council [BB/N019563/1, BB/M011615/1, BB/S020152/1, BB/P016855/1, BB/S02011X/1, BB/P024602/1]; Wellcome Trust [WT104947/Z/14/Z, WT200990/Z/16/Z, WT201535/Z/16/Z, WT212925/Z/18/Z, WT218328/B/19/Z] British Council [414710385]; Save the Tasmanian Devil Program; ELIXIR: the research infrastructure for life-science data; European Molecular Biology Laboratory. This project has received funding from the European Union's Horizon 2020 research and innovation programme under grant agreement No 733161 (MultipleMS), No 825575 (EJP RD), No 817923 (AQUA-FAANG), No 817998 (GENE-SWitCH), No 815668 (BovReg). Funding for open access charge: Wellcome [WT108749/Z/15/Z].

Conflict of interest statement. Paul Flicek is a member of the Scientific Advisory Boards of Fabric Genomics, Inc. and Eagle Genomics, Ltd.

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Associated Data

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PERMALINK

Ensembl 2021

Kevin L Howe

Premanand Achuthan

James Allen

Jamie Allen

Jorge Alvarez-Jarreta

M Ridwan Amode

Irina M Armean

Andrey G Azov

Ruth Bennett

Jyothish Bhai

Konstantinos Billis

Sanjay Boddu

Mehrnaz Charkhchi

Carla Cummins

Luca Da Rin Fioretto

Claire Davidson

Kamalkumar Dodiya

Bilal El Houdaigui

Reham Fatima

Astrid Gall

Carlos Garcia Giron

Tiago Grego

Cristina Guijarro-Clarke

Leanne Haggerty

Anmol Hemrom

Thibaut Hourlier

Osagie G Izuogu

Thomas Juettemann

Vinay Kaikala

Mike Kay

Ilias Lavidas

Tuan Le

Diana Lemos

Jose Gonzalez Martinez

José Carlos Marugán

Thomas Maurel

Aoife C McMahon

Shamika Mohanan

Benjamin Moore

Matthieu Muffato

Denye N Oheh

Dimitrios Paraschas

Anne Parker

Andrew Parton

Irina Prosovetskaia

Manoj P Sakthivel

Ahamed I Abdul Salam

Bianca M Schmitt

Helen Schuilenburg

Dan Sheppard

Emily Steed

Michal Szpak

Marek Szuba

Kieron Taylor

Anja Thormann

Glen Threadgold

Brandon Walts

Andrea Winterbottom

Marc Chakiachvili

Ameya Chaubal

Nishadi De Silva

Bethany Flint

Adam Frankish

Sarah E Hunt

Garth R IIsley

Nick Langridge

Jane E Loveland

Fergal J Martin

Jonathan M Mudge

Joanella Morales

Emily Perry

Magali Ruffier

John Tate

David Thybert

Stephen J Trevanion

Fiona Cunningham

Andrew D Yates

Daniel R Zerbino