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TEspeX: consensus-specific quantification of transposable element expression preventing biases from exonized
Federico Ansaloni1,2, Nicolò Gualandi1, Mauro Esposito1
1Area of Neuroscience, Scuola Internazionale Superiore di Studi Avanzati (SISSA), Trieste 34136, Italy.
Bioinformatics (Oxford, England)
|July 25, 2022
Summary
Transposable elements (TEs) expression quantification is improved by TEspeX. This new pipeline accurately measures TE transcription, distinguishing active TEs from fragments within other transcripts.
Area of Science:
- Genomics
- Molecular Biology
- Bioinformatics
Background:
- Transposable elements (TEs) are vital genetic components influencing biological processes.
- Accurate quantification of TE expression is crucial for understanding their roles.
- Existing tools struggle to differentiate active TE transcription from TE fragments in other transcripts.
Purpose of the Study:
- To develop a computational pipeline, TEspeX, for precise quantification of transposable element expression at the consensus level.
- To address the limitation of existing tools in distinguishing autonomous TE transcription from TE sequences within canonical transcripts.
Main Methods:
- TEspeX pipeline utilizes Illumina RNA-seq short reads.
- The method quantifies TE expression by specifically excluding reads from inactive TE fragments embedded in canonical transcripts.
- Implementation in Python 3.
Main Results:
- TEspeX enables accurate quantification of transposable element expression.
- The pipeline effectively distinguishes transcription from autonomous TEs versus TE fragments within other transcripts.
- Avoids misinterpretation of expression changes due to TE-containing non-TE transcripts.
Conclusions:
- TEspeX provides a robust solution for accurate transposable element expression analysis.
- This tool enhances the study of TE functions in biological pathways.
- Facilitates more reliable research on the impact of transposable elements in genomics and transcriptomics.
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