Mobile genomics: tools and techniques for tackling transposons. (30th March 2020)

• Record Type: Journal Article
• Authors: O'Neill, Kathryn; Brocks, David; Hammell, Molly Gale
• Is Part Of: Philosophical transactions. Volume 375:Number 1795(2020)
• Publication Date: 2020-03-30
• Subjects: transposable elements -- computational genomics -- retrotransposons -- single-cell analysis; Biology -- Periodicals; Science -- Periodicals; 570
• DOI: 10.1098/rstb.2019.0345
• Languages: English
• ISSNs: 0962-8436

Abstract

Abstract : Next-generation sequencing approaches have fundamentally changed the types of questions that can be asked about gene function and regulation. With the goal of approaching truly genome-wide quantifications of all the interaction partners and downstream effects of particular genes, these quantitative assays have allowed for an unprecedented level of detail in exploring biological interactions. However, many challenges remain in our ability to accurately describe and quantify the interactions that take place in those hard to reach and extremely repetitive regions of our genome comprised mostly of transposable elements (TEs). Tools dedicated to TE-derived sequences have lagged behind, making the inclusion of these sequences in genome-wide analyses difficult. Recent improvements, both computational and experimental, allow for the better inclusion of TE sequences in genomic assays and a renewed appreciation for the importance of TE biology. This review will discuss the recent improvements that have been made in the computational analysis of TE-derived sequences as well as the areas where such analysis still proves difficult. This article is part of a discussion meeting issue 'Crossroads between transposons and gene regulation'.