Analysis of the Metatranscriptome of Microbial Communities by Comparison of Different Assembly Tools Reveals Improved Functional Annotation

C. Badapanda
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引用次数: 3

Abstract

Before the advent of Next Generation Sequencing (NGS) technology, data generation of uncultured species along with the analysis of microbial data was limited. Advancement in the sequencing technology has revolutionized the sequencing of individual genome as well as metagenome. NGS technology coupled with the development of algorithm for analysis of NGS data have increased our understanding of microbial community structure [1,2]. In met genomic study, the information of all genes are used to interpret microbial identities up to the species or strain level [3] whereas, metatranscriptomic study reveals the gene expression patterns of active genes and their functionality in different pathways [4,5]. In both the pipeline (met genomic and metatranscriptomic), it is important to assemble the reads into contigs which represents gene objects. However, there are various challenges associated with the assembly of metatranscriptome and metagenome data, which is addressed below:
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通过比较不同组装工具对微生物群落的超转录组进行分析,揭示了功能注释的改进
在下一代测序(NGS)技术出现之前,未培养物种的数据生成以及微生物数据分析受到限制。测序技术的进步使个体基因组和元基因组的测序发生了革命性的变化。NGS技术加上NGS数据分析算法的发展,增加了我们对微生物群落结构的了解[1,2]。在基因组学研究中,所有基因的信息被用来解释微生物的特性,直至物种或菌株水平b[3],而亚转录组学研究揭示了活性基因的基因表达模式及其在不同途径中的功能[4,5]。在这两个管道中(met基因组和亚转录组),将reads组装成代表基因对象的contigs是很重要的。然而,与元转录组和元基因组数据的组装相关的各种挑战,如下所述:
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