The SAMN03320098_v1.1 assembly was submitted by BGI, Shenzhen on January 2016. The assembly is on scaffold level, consisting of 314,963 contigs assembled into 164,173 scaffolds. The N50 size is the length such that 50% of the assembled genome lies in blocks of the N50 size or longer. The N50 length for the contigs is 18,758 while the scaffold N50 is 945,738.
The gene annotation process was carried out using a combination of protein-to-genome alignments, annotation mapping from a suitable reference species and RNA-seq alignments (where RNA-seq data with appropriate meta data were publicly available). For each candidate gene region, a selection process was applied to choose the most appropriate set of transcripts based on evolutionary distance, experimental evidence for the source data and quality of the alignments.Small ncRNAs were obtained using a combination of BLAST and Infernal/RNAfold. Pseudogenes were calculated by looking at genes with a large percentage of non-biological introns (introns of <10bp), where the gene was covered in repeats, or where the gene was single exon and evidence of a functional multi-exon paralog was found elsewhere in the genome. lincRNAs were generated via RNA-seq data where no evidence of protein homology or protein domains could be found in the transcript.
In accordance with the Fort Lauderdale Agreement, please check the publication status of the genome/assembly before publishing any genome-wide analyses using these data.
General information about this species can be found in Wikipedia.
|Assembly||SAMN03320098_v1.1, INSDC Assembly GCA_001515625.1, Dec 2015|
|Golden Path Length||1,655,786,410|
|Annotation method||Full genebuild|
|Genebuild started||Oct 2018|
|Genebuild released||Dec 2019|
|Genebuild last updated/patched||Mar 2020|
|Non coding genes||2,161|
|Small non coding genes||2,012|
|Long non coding genes||98|
|Misc non coding genes||51|
|Genscan gene predictions||85,786|