A Simple Guideline to Assess the Characteristics of RNA-Seq Data.

Next-generation sequencing (NGS) techniques have been used to generate various molecular maps including genomes, epigenomes, and transcriptomes. Transcriptomes from a given cell population can be profiled via RNA-seq. However, there is no simple way to assess the characteristics of RNA-seq data syst...

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Publicado en:BioMed Research International pp. 1 - 10
Autores principales: Son, Keunhong, Yu, Sungryul, Shin, Wonseok, Han, Kyudong, Kang, Keunsoo
Formato: pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell 11/04/2018
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 11/04/2018
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1155/2018/2906292
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        atl: A Simple Guideline to Assess the Characteristics of RNA-Seq Data.
      aug:
        au:
          Son, Keunhong
          Yu, Sungryul
          Shin, Wonseok
          Han, Kyudong
          Kang, Keunsoo
        affil: Department of Microbiology, College of Natural Sciences, Dankook University, Cheonan 31116, Republic of Korea
      sug:
        subj:
          RNA
          Sequence Analysis Methods
          Human
          Factor Analysis
          Gene Expression
          Carcinoma, Ductal
      ab: Next-generation sequencing (NGS) techniques have been used to generate various molecular maps including genomes, epigenomes, and transcriptomes. Transcriptomes from a given cell population can be profiled via RNA-seq. However, there is no simple way to assess the characteristics of RNA-seq data systematically. In this study, we provide a simple method that can intuitively evaluate RNA-seq data using two different principal component analysis (PCA) plots. The gene expression PCA plot provides insights into the association between samples, while the transcript integrity number (TIN) score plot provides a quality map of given RNA-seq data. With this approach, we found that RNA-seq datasets deposited in public repositories often contain a few low-quality RNA-seq data that can lead to misinterpretations. The effect of sampling errors for differentially expressed gene (DEG) analysis was evaluated with ten RNA-seq data from invasive ductal carcinoma tissues and three RNA-seq data from adjacent normal tissues taken from a Korean breast cancer patient. The evaluation demonstrated that sampling errors, which select samples that do not represent a given population, can lead to different interpretations when conducting the DEG analysis. Therefore, the proposed approach can be used to avoid sampling errors prior to RNA-seq data analysis.
      pubtype: Academic Journal
      doctype:
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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