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Accurate binning of metagenomic contigs via automated clustering sequences using information of genomic signatures and marker genes

机译:通过使用基因组特征和标记基因的信息,通过自动聚类序列精确分叉Metagenomic Contigs

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摘要

Metagenomics, the application of shotgun sequencing, facilitates the reconstruction of the genomes of individual species from natural environments. A major challenge in the genome recovery domain is to agglomerate or 'bin' sequences assembled from metagenomic reads into individual groups. Metagenomic binning without consideration of reference sequences enables the comprehensive discovery of new microbial organisms and aids in the microbial genome reconstruction process. Here we present MyCC, an automated binning tool that combines genomic signatures, marker genes and optional contig coverages within one or multiple samples, in order to visualize the metagenomes and to identify the reconstructed genomic fragments. We demonstrate the superior performance of MyCC compared to other binning tools including CONCOCT, GroopM, MaxBin and MetaBAT on both synthetic and real human gut communities with a small sample size (one to 11 samples), as well as on a large metagenome dataset (over 250 samples). Moreover, we demonstrate the visualization of metagenomes in MyCC to aid in the reconstruction of genomes from distinct bins. MyCC is freely available at http://sourceforge.net/projects/sb2nhri/files/MyCC/.
机译:Metagenomics,霰弹枪测序的应用,促进了从自然环境中重建个体种类的基因组。基因组恢复结构域中的主要挑战是从代理读入单个组的聚集或“垃圾箱”序列。在不考虑参考序列的情况下,Metagenomic Binning能够综合发现新的微生物生物和艾滋病在微生物基因组重建过程中。在这里,我们呈现MyCC,是一种自动分子工具,其将基因组签名,标记基因和可选的葡萄饼覆盖物结合在一个或多个样品中,以便可视化梅曲线和鉴定重建的基因组片段。我们展示了Mycc的卓越性能与其他融合工具相比,包括CONCOCT,GROPM,MAXBIN和METABAT在合成和真正的人体肠道社区上具有小样本大小(一到11个样本)以及大的METAGENOME数据集(过度) 250个样本)。此外,我们证明了Mycc中的Metagenomes的可视化,以帮助重建不同垃圾箱的基因组。 MyCC在http://sourceforge.net/projects/sb2nhri/files/mycc/上自由提供。

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