2015
DOI: 10.4172/jpb.1000381
|View full text |Cite
|
Sign up to set email alerts
|

A Comparison of Three Bioinformatics Pipelines for the Analysis of Preterm Gut Microbiota using 16S rRNA Gene Sequencing Data

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

2
87
0
4

Year Published

2016
2016
2023
2023

Publication Types

Select...
4
3
2

Relationship

0
9

Authors

Journals

citations
Cited by 100 publications
(93 citation statements)
references
References 28 publications
2
87
0
4
Order By: Relevance
“…-Presence of PCR inhibitors (Juen & Traugott, 2006) digestion (Arai, Welch, Dunsmuir, Jacobs, & Ladouceur, 2003) (Pompanon et al, 2012) Gómez, Swift, & Dawson, 2017) -& Thomas, 2010) (Gonzalez, Portillo, Belda-Ferre, & Mira, 2012) estimates (Plummer & Twin, 2015) Sample Collection DNA extraction PCR Sequencing Bio-informatics 1.…”
Section: Potential Biases Stage Of Protocolmentioning
confidence: 99%
“…-Presence of PCR inhibitors (Juen & Traugott, 2006) digestion (Arai, Welch, Dunsmuir, Jacobs, & Ladouceur, 2003) (Pompanon et al, 2012) Gómez, Swift, & Dawson, 2017) -& Thomas, 2010) (Gonzalez, Portillo, Belda-Ferre, & Mira, 2012) estimates (Plummer & Twin, 2015) Sample Collection DNA extraction PCR Sequencing Bio-informatics 1.…”
Section: Potential Biases Stage Of Protocolmentioning
confidence: 99%
“…A comparison of these three bioinformatic pipelines has been conducted by Plummer et al [41] using 16S rRNA gut microbial data. The study concluded that all of the three pipelines were able to generate similar and reliable results with common limitation the ability to classify at the species level due to the type of data.…”
Section: Mg-rastmentioning
confidence: 99%
“…It is important to recognise that due to some possible pitfalls in sample processing, the abundance of specific bacterial species and overall community composition can be distorted, thus hampering the analysis and threatening the validity of the research findings [14]. In addition, a key limitation of using 16S rRNA gene analysis for genus and species level classification is that related bacterial species may be indistinguishable due to near identical 16S rRNA gene sequences [15]. The potential for different data analysis approaches to impact on outcomes has also been recognised.…”
Section: Introductionmentioning
confidence: 99%
“…The potential for different data analysis approaches to impact on outcomes has also been recognised. Plummer et al [15] compared three pipelines commonly used for 16S rRNA gene analysis: QIIME, MG-RAST and mothur. Favourably, their results showed that the three pipelines assessed produce comparable results for analysis of faecal samples, in terms of alpha diversity analysis and usability.…”
Section: Introductionmentioning
confidence: 99%