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metaSHARK: software for automated metabolic network prediction from DNA sequence and its application to the genomes of Plasmodium falciparum and Eimeria tenella ud

机译:metasHaRK:DNa序列自动代谢网络预测软件及其在恶性疟原虫和柔嫩艾美耳球虫基因组中的应用

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摘要

The metabolic SearcH And Reconstruction Kitud(metaSHARK) is a new fully automated software packageudfor the detection of enzyme-encoding genesudwithin unannotated genome data and their visualizationudin the context of the surrounding metabolic network.udThe gene detection package (SHARKhunt) runsudon a Linux systemand requires only a set of raw DNAudsequences (genomic, expressed sequence tag and/udor genome survey sequence) as input. Its outputudmay be uploaded to our web-based visualizationudtool (SHARKview) for exploring and comparing dataudfrom different organisms. We first demonstrate theudutility of the software by comparing its results forudthe raw Plasmodium falciparum genome with theudmanual annotations available at the PlasmoDB andudPlasmoCyc websites. We then apply SHARKhunt toudthe unannotated genome sequences of the coccidianudparasite Eimeria tenella and observe that, at anudE-value cut-off of 10(-20), our software makes 142udadditional assertions of enzymatic function comparedudwith a recent annotation package workingudwith translated open reading frame sequences. Theudability of the software to cope with low levels ofudsequence coverage is investigated by analyzingudassemblies of the E.tenella genome at estimatedudcoverages from 0.5x to 7.5x. Lastly, as an exampleudof how metaSHARK can be used to evaluate theudgenomic evidence for specific metabolic pathways,udwe present a study of coenzyme A biosynthesis inudP.falciparum and E.tenella.
机译:代谢SearcH和重建工具包 ud(metaSHARK)是一个新型的全自动软件包 ud,用于检测酶编码基因 ud在未注释的基因组数据中并在周围代谢网络的背景下可视化 ud。 (SHARKhunt)在Linux系统上运行,并且仅需要一组原始DNA udsequences(基因组,表达的序列标签和/ 或udor基因组调查序列)作为输入。它的输出 ud可以上传到我们基于网络的可视化 udtool(SHARKview),以探索和比较来自不同生物的数据 ud。我们首先通过比较原始恶性疟原虫基因组的结果与PlasmoDB和 udPlasmoCyc网站上提供的 udmanual注释来证明该软件的 udutil。然后,我们将SHARKhunt应用于球虫 udparasite艾美球虫的未注释的基因组序列,并观察到,在 udE值截止值为10(-20)时,我们的软件对142个酶功能的常规断言进行了比较 ud一个最近的注释包,它已翻译了开放阅读框序列。通过分析大肠埃希氏菌(E.tenella)基因组的组装/估计覆盖率(从0.5x到7.5x),研究了该软件应对低水平 udsequence覆盖范围的能力。最后,作为一个例子,如何使用metaSHARK评估特定代谢途径的预算证据,我们对恶性疟原虫和大肠埃希菌中辅酶A的生物合成进行了研究。

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