2015
DOI: 10.1016/j.gpb.2015.10.003
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Web Resources for Metagenomics Studies

Abstract: The development of next-generation sequencing (NGS) platforms spawned an enormous volume of data. This explosion in data has unearthed new scalability challenges for existing bioinformatics tools. The analysis of metagenomic sequences using bioinformatics pipelines is complicated by the substantial complexity of these data. In this article, we review several commonly-used online tools for metagenomics data analysis with respect to their quality and detail of analysis using simulated metagenomics data. There ar… Show more

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Cited by 33 publications
(17 citation statements)
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“…The advent of Next-Generation Sequencing (NGS) technologies has made it possible to perform sequencing based metagenomic analysis. NGS aids in complete decoding of the entire community [5]. Healthy population of microbes in CWS is essential for the optimized removal of pollutants in the system.…”
Section: Introductionmentioning
confidence: 99%
“…The advent of Next-Generation Sequencing (NGS) technologies has made it possible to perform sequencing based metagenomic analysis. NGS aids in complete decoding of the entire community [5]. Healthy population of microbes in CWS is essential for the optimized removal of pollutants in the system.…”
Section: Introductionmentioning
confidence: 99%
“…The most important contribution of these two alignment-free methods (OPD and BLSOM) is to predict the functions of the increasingly large number of functionunknown proteins derived from poorly characterized organisms, such as those studied using metagenomic approaches (Dudhagara et al, 2015;Noecker et al, 2017), and thus to serve a new and powerful tool in the postgenome era.…”
Section: Discussionmentioning
confidence: 99%
“…The GS De Novo Assembler (Roche) was used to trim and group the data (i.e., adapter, linker and primer sequences) based on MID as well as generate consensus sequences of the DNA libraries. The assembled contigs were used in a metagenomic analysis with the CAMERA database [27] [28].…”
Section: Next-generation Sequencingmentioning
confidence: 99%