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Comparative analysis of grapevine whole-genome gene predictions, functional annotation, categorization and integration of the predicted gene sequences

机译:葡萄全基因组基因预测,功能注释,预测基因序列的分类和整合的比较分析

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Background The first draft assembly and gene prediction of the grapevine genome (8X base coverage) was made available to the scientific community in 2007, and functional annotation was developed on this gene prediction. Since then additional Sanger sequences were added to the 8X sequences pool and a new version of the genomic sequence with superior base coverage (12X) was produced. Results In order to more efficiently annotate the function of the genes predicted in the new assembly, it is important to build on as much of the previous work as possible, by transferring 8X annotation of the genome to the 12X version. The 8X and 12X assemblies and gene predictions of the grapevine genome were compared to answer the question, “Can we uniquely map 8X predicted genes to 12X predicted genes?” The results show that while the assemblies and gene structure predictions are too different to make a complete mapping between them, most genes (18,725) showed a one-to-one relationship between 8X predicted genes and the last version of 12X predicted genes. In addition, reshuffled genomic sequence structures appeared. These highlight regions of the genome where the gene predictions need to be taken with caution. Based on the new grapevine gene functional annotation and in-depth functional categorization, twenty eight new molecular networks have been created for VitisNet while the existing networks were updated. Conclusions The outcomes of this study provide a functional annotation of the 12X genes, an update of VitisNet, the system of the grapevine molecular networks, and a new functional categorization of genes. Data are available at the VitisNet website ( http://www.sdstate.edu/ps/research/vitis/pathways.cfm ).
机译:背景技术葡萄基因组的初步组装和基因预测(8X基本覆盖率)于2007年提供给科学界,并在该基因预测上开发了功能注释。从那时起,将其他Sanger序列添加到8X序列库中,并产生了具有更高碱基覆盖率(12X)的新版本的基因组序列。结果为了更有效地注释新装配中预测的基因的功能,重要的是通过将基因组的8X注释转移到12X版本来尽可能多地利用先前的工作。比较了葡萄基因组的8X和12X装配体以及基因预测,以回答以下问题:“我们能否将8X预测基因唯一映射到12X预测基因?”结果表明,尽管装配和基因结构预测相差太大,无法在它们之间进行完整的映射,但是大多数基因(18,725个)显示8X预测基因与最新版本的12X预测基因之间是一对一的关系。另外,改组的基因组序列结构出现了。这些突出显示了需要谨慎进行基因预测的基因组区域。基于新的葡萄基因功能注释和深入的功能分类,为VitisNet创建了28个新的分子网络,同时更新了现有的网络。结论这项研究的结果提供了12X基因的功能注释,VitisNet的更新,葡萄分子网络系统以及基因的新功能分类。数据可从VitisNet网站(http://www.sdstate.edu/ps/research/vitis/pathways.cfm)获得。

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