Systems genetics of complex diseases using RNA-sequencing methods

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    Abstract

    Next generation sequencing technologies have enabled the generation of huge quantities of
    biological data, and nowadays extensive datasets at different ‘omics levels have been generated. Systems
    genetics is a powerful approach that allows to integrate different ‘omics level and understand the biological
    mechanisms behind complex diseases or traits. In the recent past, transcriptomic studies with microarrays
    have been replaced with the new powerful RNA-seq technologies. This has led to detection of novel gene
    transcripts, novel regulatory mechanisms, allele specific gene expression and numerous non-coding RNAs
    (ncRNAs). The integration of transcriptomics data with genomic data in a systems genetics context
    represents a valuable possibility to go deep into the causal and regulatory mechanisms that generate
    complex traits and diseases. However RNA-Seq data have to be treated carefully and the choice of the right
    methodology could have a great impact on the final results. Furthermore the integration of different level is
    not trivial. Here we give a comprehensive systems genetics overview of the methods and tools for analysis
    and the integration of RNA-Seq data including ncRNAs. We focused principally on merits and demerits of
    tools for post mapping quality control, normalization, differential expression analysis, gene network
    analysis, and integration of different omics data in order to generate a comprehensive guideline to systems
    genetics analysis using RNA-Seq data.
    Original languageEnglish
    JournalInternational Journal of Bioscience, Biochemistry and Bioinformatics
    Volume5
    Issue number4
    Pages (from-to)264-279
    Number of pages16
    ISSN2010-3638
    DOIs
    Publication statusPublished - 2015

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