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RNA-seq data analysis for bacterial transcriptomics | 10900
Transcriptomics: Open Access

Transcriptomics: Open Access
Open Access

ISSN: 2329-8936

+44 1223 790975

RNA-seq data analysis for bacterial transcriptomics


3rd International Conference on Transcriptomics

October 30-31, 2017 Bangkok, Thailand

Yahaya Yabo, P Monsieurs and N Leys

Universiteit Brussel, Belgium

Posters & Accepted Abstracts: Transcriptomics

Abstract :

The advent of high-throughput sequencing technologies has played a significant role in the transition of biomedical research from in vivo to in silico approach. RNA-seq has emerged as one of the technologies used in the analysis of all RNA populations found in a cell or group of cells and effectively dominating the existing methods used such as the microarray technology. Several tools have been recommended for the analysis of mostly eukaryotic RNA-seq data to determine differentially expressed genes under varying conditions or treatment groups. However, up until now no consensus has been reached on the best analytical tool/tools to adopt in the analysis, especially for bacterial RNA-seq data analysis. This work systematically compared different combinations of alignment algorithms and differential gene expression analytical tools with the aim of selecting the best alignment and differential gene expression tools that will improve the process of analyzing bacterial RNA-seq data to determine most of the differentially expressed genes under different experimental conditions with high accuracy. As a proof of concept for benchmarking the selected tools, we used real-life, paired-end and RNA-seq reads of 150 nt length obtained from sequenced libraries of Cupriavidus metallidurans (NA4 strain) using Illumina HiSeq 2000 platform. The evaluated alignment algorithms showed comparable performance in aligning reads to the reference genome. Among the tested tools for differential gene expression analysis, edgeR detected more number of genes while DESeq2 was found to be more stringent and tends to prevent some low expressed genes with fold changes around the cut-off to be considered as differentially expressed genes, as such lowering the number of false positive detections. We propose base on our benchmarking results a pipeline for the analysis of RNA-seq data for bacterial transcriptomics.

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