The Ensembl Browser: Difference between revisions
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I am trying to learn how Ensembl is structured. As Ensembl itself does not have a wiki, nor a forum | I am trying to learn how Ensembl is structured. As Ensembl itself does not have a wiki, nor a forum, I'll document it here. | ||
Some ideas: | Some ideas: |
Revision as of 08:35, 7 June 2010
I am trying to learn how Ensembl is structured. As Ensembl itself does not have a wiki, nor a forum, I'll document it here.
Some ideas:
- Everything is in mysql databases. No flat text files. Database schema documentation
- Can be accessed via Perl API (slow) or via biomart.org (~table browser, fast and convenient) or via direct sql queries (very complex schema)
- 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 (oct 09) is 56
- 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 Often they have been replaced by others.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 usually the only way to get more information.
The databases:
All versions of the genomes are on the same server. Some ideas to help you find your way:
- species_name_version_obscureNumber is the format of the individual species database (see below)
- 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 ??
The 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.
The pipeline:
- Their pipeline systems inserts jobs into a mysql database as well
- 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)
Documentation:
- Most documentation is not accessible from the Ensembl homepage. You have to dig into the CVS repositories to find "pipeline_docs": [1] The file overview.txt gives a very good introduction.