Myoluc2.0 (GCA_000147115.1) is the latest assembly of the microbat or little brown bat (Myotis lucifugus), sequenced to 7X coverage. The genome sequencing and assembly are provided by the Broad Institute as part of the Mammalian Genome Project.
The N50 size is the length such that 50% of the assembled genome lies in blocks of the N50 size or longer. The N50 size of scaffolds is 4.3Mb. The total of all scaffolds is 1.96Gb.
The genome assembly represented here corresponds to GenBank Assembly ID GCA_000147115.1
The gene set for microbat was built using the Ensembl pipeline. Gene models are based on genewise alignments of microbat proteins, mammal proteins as well as genetically distance proteins from other species, including most vertebrate proteins from Uniprot. Additionally, dog and cow proteins were aligned using exonerate. The protein based gene models were then extended using microbat and cow cDNA. In addition to the coding transcript models, non-coding RNAs and pseudogenes were annotated
Mammalian Genome Project
Myotis lucifugus is one of 24 mammals that will be sequenced as part of the Mammalian Genome Project, funded by the National Institutes of Health (NIH). A group of species were chosen to maximise the branch length of the evolutionary tree while representing the diversity of mammalian species. The aim is to increase our understanding of functional elements, especially in the human genome.
General information about this species can be found in Wikipedia.
|Assembly||Myoluc2.0, INSDC Assembly GCA_000147115.1, Sep 2010|
|Golden Path Length||2,034,575,300|
|Genebuild method||Full genebuild|
|Genebuild started||Dec 2010|
|Genebuild released||Jun 2011|
|Genebuild last updated/patched||Jun 2011|
Genes and/or transcript that contains an open reading frame (ORF).
|Small non coding genes||4,408|
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.||26,840|
|Genscan gene predictions||68,558|