This is the preliminary display of the Coelacanth (Latimeria chalumnae) genome produced by the Broad Institute. Illumina techology was used to produced this high quality draft. The whole genome shotgun data was assembled with Allpaths. The genome is 2.9gb in length;,composed of 291,828 contigs with an N50 value of 12.6kb and 22,818 scaffolds with an N50 value of 765kb.
The genome assembly represented here corresponds to GenBank Assembly ID GCA_000225785.1
The Ensembl genome annotation pipeline was used to identify genes. Models built from Coelacanth proteins and cDNAs have been given priority over predictions from other vertebrate species. 6,671 transcript models made from paired end Illumina RNA-Seq were added into the gene set where they added a novel model or splice variant. RNA-Seq data was also used to add UTR to non species specific models. The total gene set contains 19,697 protein coding genes with a further 2,894 ncRNAs and 141 pseudogenes.
General information about this species can be found in Wikipedia.
|Assembly||LatCha1, INSDC Assembly GCA_000225785.1, Sep 2011|
|Golden Path Length||2,860,591,921|
|Genebuild method||Full genebuild|
|Genebuild started||Sep 2011|
|Genebuild released||Oct 2011|
|Genebuild last updated/patched||Nov 2012|
Genes and/or transcript that contains an open reading frame (ORF).
|Short non coding genes|
Short non coding genes are usually fewer than 200 bases long. They may be transcribed but are not translated. In Ensembl, genes with the following biotypes are classed as short non coding genes: miRNA, miscRNA, rRNA, tRNA, ncRNA, scRNA, snlRNA, snoRNA, snRNA, tRNA, and also the pseudogenic form of these biotypes. The majority of the short non coding genes in Ensembl are annotated automatically by our ncRNA pipeline.
A pseudogene shares an evolutionary history with a functional protein-coding gene but it has been mutated through evolution to contain frameshift and/or stop codon(s) that disrupt the open reading frame.
|Gene transcriptsNucleotide sequence resulting from the transcription of the genomic DNA to mRNA. One gene can have different transcripts or splice variants resulting from the alternative splicing of different exons in genes.||26,660|
|Genscan gene predictions||103,879|