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TSEBRA: transcript selector for BRAKER.

Lars Gabriel1,2, Katharina J Hoff1,2, Tomáš Brůna3

  • 1Institute of Mathematics and Computer Science, University of Greifswald, Walther-Rathenau-Str. 47, 17489, Greifswald, Germany.

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|November 26, 2021
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Summary
This summary is machine-generated.

TSEBRA is a new software that combines gene predictions from BRAKER1 and BRAKER2, improving accuracy for eukaryotic genome annotation. This tool effectively utilizes both RNA-seq and protein evidence for more reliable gene prediction.

Keywords:
Evidence integrationGene predictionGenome annotationProtein homologyProtein-coding genesRNA-seq

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Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • BRAKER pipelines (BRAKER1, BRAKER2) automate eukaryotic gene annotation using statistical models and extrinsic evidence.
  • BRAKER1 utilizes RNA-seq data, while BRAKER2 uses cross-species protein databases.
  • Current BRAKER versions do not effectively integrate both RNA-seq and protein evidence simultaneously, leading to unexploited data.

Purpose of the Study:

  • To develop a software tool, TSEBRA, that integrates gene predictions from BRAKER1 and BRAKER2.
  • To enhance the accuracy of eukaryotic gene annotation by leveraging both RNA-seq and protein evidence.

Main Methods:

  • TSEBRA selects optimal gene predictions from BRAKER1 and BRAKER2 outputs.
  • It employs a rule-based system to compare overlapping transcript scores based on RNA-seq and protein evidence support.
  • Evaluated on 11 eukaryotic genomes.

Main Results:

  • TSEBRA achieves higher accuracy than BRAKER1 or BRAKER2 when used independently.
  • TSEBRA demonstrates competitive performance compared to the EVidenceModeler tool.
  • The software effectively combines complementary evidence for improved gene prediction.

Conclusions:

  • TSEBRA is a user-friendly and efficient software for eukaryotic gene annotation.
  • It enhances the BRAKER pipeline by integrating both RNA-seq and homologous protein evidence.
  • Facilitates more comprehensive and accurate gene prediction sets for novel genome projects.