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Related Concept Videos

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Alternative RNA splicing is the regulated splicing of exons and introns to produce different mature mRNAs from a single pre-mRNA. Unlike in constitutive splicing where a single gene produces a single type of mRNA, alternative splicing allows an organism to produce multiple proteins from a single gene and plays an important role in protein diversity.
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Splicing is the process by which eukaryotic RNA is edited before its translation into protein. The RNA strand transcribed from eukaryotic DNA is called the primary transcript. The primary transcripts that become mRNAs are called precursor messenger RNAs (pre-mRNAs). Eukaryotic pre-mRNA contains alternating sequences of exons and introns. Exons are nucleotide sequences that code for proteins, whereas introns are the non-coding regions. In RNA splicing, introns are removed and exons are bonded...
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Many proteins’ biological role depends on their interactions with their ligands, small molecules that bind to specific locations on the protein known as ligand-binding sites. Ligand-binding sites are often conserved among homologous proteins as these sites are critical for protein function.
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Novel Object Recognition Test for the Investigation of Learning and Memory in Mice
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DeepDSSR: Deep Learning Structure for Human Donor Splice Sites Recognition.

Tanvir Alam1, Mohammad Tariqul Islam2, Mowafa Househ1

  • 1Information and Computing Technology Division, College of Science and Engineering, Hamad Bin Khalifa University (HBKU), Doha, Qatar.

Studies in Health Technology and Informatics
|July 27, 2019
PubMed
Summary
This summary is machine-generated.

DeepDSSR, a novel deep learning model, accurately predicts human donor splice sites. This advancement improves understanding of gene structure and mRNA variants, outperforming existing methods.

Keywords:
bidirectional long short-term memoryconvolution neural networkdeep learningdonor splice sites

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Area of Science:

  • Genomics
  • Computational Biology
  • Bioinformatics

Background:

  • Alternative splicing in humans generates diverse mRNA and protein isoforms.
  • Accurate splice site identification is essential for understanding gene structure and functional variants.
  • Existing computational methods for splice site detection require further improvement.

Purpose of the Study:

  • To develop a novel deep learning-based computational method for predicting human donor splice sites.
  • To enhance the accuracy of splice site recognition in human pre-messenger RNA.
  • To provide a robust tool for analyzing gene structure and alternative splicing.

Main Methods:

  • Development of DeepDSSR (deep donor splice site recognizer), a deep learning architecture.
  • Training and evaluation using a publicly available, imbalanced benchmark dataset.
  • Comparative analysis against leading deep learning-based methods for donor splice site detection.

Main Results:

  • DeepDSSR demonstrates comparable performance to existing leading deep learning methods.
  • Performance evaluation metrics indicate that DeepDSSR outperforms current deep learning-based approaches.
  • The model effectively addresses the challenge of predicting human donor splice sites.

Conclusions:

  • DeepDSSR represents a significant advancement in the computational prediction of human donor splice sites.
  • The developed method offers improved accuracy over existing deep learning techniques.
  • Future work will focus on enhancing predictive capabilities and developing acceptor splice site prediction.