TEspeX: consensus-specific quantification of transposable element expression preventing biases from exonized fragments.
basic_science · Level V
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- Record sourced from PubMed, PMID 35876845.
- Also identified by DOI 10.1093/bioinformatics/btac526 and PMC identifier 9477521.
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Abstract
Transposable elements (TEs) play key roles in crucial biological pathways. Therefore, several tools enabling the quantification of their expression were recently developed. However, many of the existing tools lack the capability to distinguish between the transcription of autonomously expressed TEs and TE fragments embedded in canonical coding/non-coding non-TE transcripts. Consequently, an apparent change in the expression of a given TE may simply reflect the variation in the expression of the transcripts containing TE-derived sequences. To overcome this issue, we have developed TEspeX, a pipeline for the quantification of TE expression at the consensus level. TEspeX uses Illumina RNA-seq short reads to quantify TE expression avoiding counting reads deriving from inactive TE fragments embedded in canonical transcripts. The tool is implemented in python3, distributed under the GNU General Public License (GPL) and available on Github at https://github.com/fansalon/TEspeX (Zenodo URL: https://doi.org/10.5281/zenodo.6800331). Supplementary data are available at Bioinformatics online.
Medical subject headings
- DNA Transposable Elements
- High-Throughput Nucleotide Sequencing