2013
DOI: 10.1371/journal.pone.0075448
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NeSSM: A Next-Generation Sequencing Simulator for Metagenomics

Abstract: BackgroundMetagenomics can reveal the vast majority of microbes that have been missed by traditional cultivation-based methods. Due to its extremely wide range of application areas, fast metagenome sequencing simulation systems with high fidelity are in great demand to facilitate the development and comparison of metagenomics analysis tools.ResultsWe present here a customizable metagenome simulation system: NeSSM (Next-generation Sequencing Simulator for Metagenomics). Combining complete genomes currently avai… Show more

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Cited by 67 publications
(67 citation statements)
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References 42 publications
(42 reference statements)
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“…While quality control methods were previously suggested, they only focussed on the genome (potentially missing alternatively spliced variants that would have been detected by studying the transcriptome) [80,81], or on the proteome (potentially missing mRNAs whose translation is downregulated by microRNAs [83,84] or covered aspects of the data such as GC content [40], noise [12,13] source material quality [62,63,67,70,86], different experimental methods [64][65][66][71][72][73][74][76][77][78][79] or read quality [87][88][89][90][91][92][93][94][95], with few investigations focusing on the tissuespecificity issues [75,96], even when two or more methods were used in the same study [97][98][99][100][101]. A common shortcoming of many previous attempts is that tissue specificity of the genes was reported [102][103][104][105][106][1...…”
Section: Existing Expression Data Quality Control Methods and Their Amentioning
confidence: 99%
“…While quality control methods were previously suggested, they only focussed on the genome (potentially missing alternatively spliced variants that would have been detected by studying the transcriptome) [80,81], or on the proteome (potentially missing mRNAs whose translation is downregulated by microRNAs [83,84] or covered aspects of the data such as GC content [40], noise [12,13] source material quality [62,63,67,70,86], different experimental methods [64][65][66][71][72][73][74][76][77][78][79] or read quality [87][88][89][90][91][92][93][94][95], with few investigations focusing on the tissuespecificity issues [75,96], even when two or more methods were used in the same study [97][98][99][100][101]. A common shortcoming of many previous attempts is that tissue specificity of the genes was reported [102][103][104][105][106][1...…”
Section: Existing Expression Data Quality Control Methods and Their Amentioning
confidence: 99%
“…A complementary metagenome was simulated using the same set of 73 bacterial genomes used for the aforementioned simulated MT [12]. Simulated reads were obtained using the NeSSM MG simulator (default settings) [79]. The simulated mock community is designated as SM within this article [79].…”
Section: Acknowledgementsmentioning
confidence: 99%
“…Simulated reads were obtained using the NeSSM MG simulator (default settings) [79]. The simulated mock community is designated as SM within this article [79]. The simulated data along with the corresponding reference genomes used to generate the MG data are made available via LCSB WebDav (https://webdav-r3lab.uni.lu/public/R3lab/IMP/datasets/) and is archived on Zenodo [80].…”
Section: Acknowledgementsmentioning
confidence: 99%
“…It offers the possibility to explore data characteristics as a near 16 continuum and subject software to a previously unavailable degree of testing 17 thoroughness.…”
mentioning
confidence: 99%
“…From read simulation in isolation, field advancements such as 22 metagenomics have been accompanied soon after by simulators reflecting their specific 23 data characteristics and evolving experimental methodology [2,16,34]. 24 We introduce Sim3C, a software package designed to simulate data generated by HiC 25 and other 3C-based proximity ligation (PL) sequencing protocols.…”
mentioning
confidence: 99%