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De Novo Assembly of Uca minax Transcriptome from Next Generation Sequencing

机译:从下一代测序的UCA Minax转录组的De Novo组装

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High-throughput cDNA sequencing (RNA-seq) is a very powerful technique to quantify gene expression in an unbiased way. The Crustacean family is among the groups of organisms sparsely represented in current genomic databases. Here we present transcriptome data from Uca minax (red-jointed fiddler crab) as an opportunity to extend our knowledge. Next generation sequencing was performed on six tissue samples from Uca minax using the Illumina HiSeq system. Six Transcriptome libraries were created using Trinity; a free, open-source software tool for de novo transcriptome assembly of high-throughput mRNA sequencing (RNA-seq) data with the absence of a reference genome. In addition, several tools that aid in management of data were used, such as RSEM, Bowtie, Blast, and IGV; a tool for visualizing RNA-seq analysis results. Fast quality control (FastQC) analysis of the raw sequenced files revealed that both adapter and PCR primer sequences were prevalently present, which may require a preprocessing step.
机译:高通量cDNA测序(RNA-SEQ)是一种非常强大的技术,以以无偏的方式定量基因表达。甲壳动物家族是在当前基因组数据库中稀疏地表示的生物体中。在这里,我们将来自UCA Minax(Red-Conned Fiddler Crab)的转录组数据作为扩展我们知识的机会。使用Illumina HiSeq系统,对来自UCA Minax的六个组织样本进行下一代测序。使用Trinity创建六种转录组文库;具有没有参考基因组的高通量mRNA测序(RNA-SEQ)数据的De Novo转录组合组装的自由的开源软件工具。此外,使用了有助于管理数据的几种工具,例如RSEM,Bowtie,Blast和IGV;一种可视化RNA-SEQ分析结果的工具。对原始测序文件的快度质量控制(FASTQC)分析显示,普遍存在的衔接子和PCR引物序列都可能需要预处理步骤。

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