The Ensembl Browser

I am trying to learn how Ensembl is structured. These notes are partially based on a workshop in 2010 at the EBI.

Basic Information

• Everything is in mysql databases. No flat text files.
• Everything is programmed in PERL (except the UCSC programs?)
• Main documentation start page
• Bert Overduin's homepage has a list of all slides and exercises - very handy!
• Parts of source code:
  • "core": genome database and related tools
  • "pipeline": the job scheduling system + config files
  • "analysis": all genome annotation tools and wrappers
• Subdirectories of source parts:
  • "scripts": command-line tools (mostly PERL)
  • "modules": perl modules for command-line tools
  • "sql": database schemas for scripts (remember that everything reads/writes to mysql

Pipeline / scheduling system

• Job description, input data description and commands are written to MySQL, the cluster writes the results back to mysql
• Each node will only extract part of the
• the paper has a rough general outline
• Basic schema is in ensembl-pipeline/sql/table.sql with some documentation
• The most useful documentation is in in CVS pipeline-docs
• The genebuild step is predicting genes
• The xref step is connecting predicted genes to external identifiers
• The compara step is aligning all genomes and predicted genes and then building phylogenetic trees for all proteins
• The biomart step is de-normalizing all databases for faster access (All older biomart versions are accessible via the archived old ensembl versions)

Genome data storage

• Basic schema is in ensembl/sql/table.sql, with quite a bit of documentation of the tables
• Can be accessed via Perl API (slow) or via biomart.org (~table browser, fast and convenient) or via direct sql queries
• Database schema documentation
• The database schema is very complex, due to self-referencing tables, whole-genome queries are not possible without biomart at reasonable speed
• An update of everything is done every 6 months. The old code, the old API and all databases are archived. Different mysql servers running on different ports are used to separated older archived from current versions.
  • Genes are not re-predicted each time but only when new data is added to the gene build. The starting month of the last update of a gene build is stored in genome_db.genebuild (not the month when the genebuild ended, so I don't see how you know if genes changed)
  • the current version can be found out with:

    select * from meta meta where meta_key in ("schema_version", "patch")

• Usually, each species has its own database, like in the UCSC browser. The current human one is 'homo_sapiens_core_56_37a'
• The Web interface is called "webcode", written in Perl and makes extensive use of inheritance (uh-oh), tool-support for reading the code might be helpful
• The database structure is very normalized. Whereas this is nice from a software engineering perspective, you cannot do large-scale requests. E.g. downloading all homologs between two genomes involves queries on self-referencing tables which take ages to resolve and will time out if run on their server. Use biomart for these types of requests.
• There are still a lot of older functions lingering in the source code. If a function returns null although it shouldn't have a look into the source code. Often they have been replaced by others. The ensembl-dev mailing list is a good way to get more information.
• Ensembl minimum install

Databases

All versions of the genomes are on the same server. Some ideas to help you find your way:

• Database names follow the schema <species>_<databaseType>_<releaseNumber>_<assemblyNumber>_<ChangesSinceLastAnnotation>
  • assembly number is the assembly version number from NCBI in the case of human
  • release is updated every 2 months
  • e.g. Homo_sapiens_core_59_37d
  • e.g. Homo_sapiens_core_58_37d
  • e.g. Homo_sapiens_core_57_37d
  • As you can see, the last letter is the most important one - you can see that there are no changes at all to the human annotations, as the final "d" has not changed!
• ensembl_compara includes homologies between proteins and genomes
• ensembl_go_version: Not used anymore? Was used to store gene ontology links.
• ensembl_website_version: Ensembl includes some sort of content management system. This databases includes help articles, bugs, news, the list of species on the frontpage etc. (This database looks somewhat similar to hgcentral)
• ensembl_ancestral_version ??

Species database

• Sequences can be accessed using different "coordinate systems", e.g. you can type in a chromsome location or alternatively a contig location. Both will be mapped to chromsome sequences. They are set up in the table 'coord_system'
• The sequences themselved are stored in the table 'dna' and information about them in 'seq_region'. There is a table dnac for compressed sequences but its empty.
• genes are linked to synonyms/names via xref-tables.

Documentation

• Most documentation is not accessible from the Ensembl homepage. Most useful documentation is available via "ensembl-doc" / "pipeline_docs": [1] The file overview.txt gives a very good introduction.