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Global sequence features based translation initiation site prediction in human genomic sequences.

Neelam Goel1, Shailendra Singh2, Trilok Chand Aseri2

  • 1Department of Information Technology, University Institute of Engineering and Technology, Sector-25, Panjab University, Chandigarh 160014, India.

Heliyon
|September 23, 2020
PubMed
Summary

This study introduces a novel computational method for predicting translation initiation sites (TIS) in human genomic sequences, achieving over 90% accuracy. The method enhances gene prediction by incorporating global sequence features for TIS identification.

Keywords:
Computer scienceGene predictionGenomic sequenceSupport vector machineTranslation initiation sitecDNAmRNA

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Area of Science:

  • Bioinformatics
  • Computational Biology
  • Genomics

Background:

  • Advancements in sequencing technology have increased the importance of gene prediction and genome annotation.
  • Accurate prediction of translation initiation sites (TIS) is crucial for identifying gene structures and functions.
  • Existing computational methods for TIS prediction have not specifically focused on human genomic sequences.

Purpose of the Study:

  • To develop and evaluate a novel computational method for predicting TIS in human genomic sequences.
  • To incorporate global sequence-based features to improve TIS prediction accuracy.
  • To assess the method's performance on both genomic and cDNA sequences.

Main Methods:

  • A new TIS prediction method was developed incorporating global sequence-based features.
  • Support Vector Machine (SVM) was employed to evaluate the predictive power of the selected features.
  • The method was tested on human genomic and cDNA sequences.

Main Results:

  • The proposed TIS prediction method achieved an accuracy exceeding 90%.
  • The method demonstrated effectiveness for both genomic and cDNA sequence types.
  • Experimental results confirmed the method's robust performance.

Conclusions:

  • The developed TIS prediction method is accurate and effective for human genomic sequences.
  • The method shows promise for integration into broader gene prediction systems.
  • This approach contributes to more precise genome annotation and gene function determination.