4.3 Article

Comparison of library construction kits for mRNA sequencing in the Illumina platform

Journal

GENES & GENOMICS
Volume 41, Issue 10, Pages 1233-1240

Publisher

SPRINGER
DOI: 10.1007/s13258-019-00853-3

Keywords

Transcriptome sequencing; RNA-Seq; Library prep kit; Poly A selection

Funding

  1. Bio & Medical Technology Development Program of the National Research Foundation (NRF) - Ministry of Science ICT [2016M3A9B6026776]
  2. National Research Foundation of Korea [2016M3A9B6026776] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Background The emergence of next-generation sequencing (NGS) technologies has made a tremendous contribution to the deciphering and significance of transcriptome analysis in biological fields. Since the advent of NGS technology in 2007, Illumina, Inc. has provided one of the most widely used sequencing platforms for NGS analysis. Objective Although reagents and protocols provided by Illumina are adequately performed in transcriptome sequencing, recently, alternative reagents and protocols which are relatively cost effective are accessible. However, the kits derived from various manufacturers have advantages and disadvantages when researchers carry out the transcriptome library construction. Methods We compared them using a variety of protocols to produce Illumina-compatible libraries based on transcriptome. Three different mRNA sequencing kits were selected for this study: TruSeq (R) RNA Sample Preparation V2 (Illumina, Inc., USA), Universal Plus mRNA-Seq (NuGEN, Ltd., UK), and NEBNext (R) Ultra (TM) Directional RNA Library Prep Kit for Illumina (R) (New England BioLabs, Ltd., USA). We compared them focusing on cost, experimental time, and data output. Results The quality and quantity of sequencing data obtained through the NGS technique were strongly influenced by the type of the sequencing library kits. It suggests that for transcriptome studies, researchers should select a suitable library construction kit according to the goal and resources of experiments. Conclusion The present work will help researchers to choose the right sequencing library construction kit for transcriptome analyses.

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