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lncRNA - Long Non-coding RNAs02:39

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In humans, more than 80% of the genome gets transcribed. However, only around 2% of the genome codes for proteins. The remaining part produces non-coding RNAs which includes ribosomal RNAs, transfer RNAs, telomerase RNAs, and regulatory RNAs, among other types. A large number of regulatory non-coding RNAs have been classified into two groups depending upon their length – small non-coding RNAs, such as microRNA, which are less than 200 nucleotides in length, and long non-coding RNA...
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Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
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Data resources and computational methods for lncRNA-disease association prediction.

Nan Sheng1, Lan Huang1, Yuting Lu2

  • 1Key Laboratory of Symbol Computation and Knowledge Engineering of Ministry of Education, College of Computer Science and Technology, Jilin University, Changchun, China.

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|January 7, 2023
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Summary

This review explores long non-coding RNA-disease association (LDA) prediction, highlighting computational methods crucial for understanding disease pathogenesis. It categorizes 64 methods and discusses future trends in this vital area of genomic research.

Keywords:
Computational methodsData resourcesLncRNA-disease association predictionLong non-coding RNAs

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Area of Science:

  • Genomics
  • Computational Biology
  • Bioinformatics

Background:

  • Long non-coding RNAs (lncRNAs) play diverse roles in genome regulation, influencing disease pathogenesis.
  • Understanding lncRNA-disease associations (LDAs) is crucial for deciphering disease mechanisms.
  • Computational models significantly aid systematic biology and experimental research in this field.

Purpose of the Study:

  • To review representative diseases linked to lncRNAs, including cancers, cardiovascular, and neurological diseases.
  • To introduce publicly available resources for lncRNA and disease data.
  • To systematically categorize and discuss computational methods for LDA prediction.

Main Methods:

  • Categorization of 64 computational LDA prediction methods into five groups: machine learning, network propagation, matrix factorization/completion, deep learning, and graph neural networks.
  • Discussion of common evaluation methods and metrics used in LDA prediction.
  • Identification of current challenges and future trends in the field.

Main Results:

  • A comprehensive overview of 64 computational methods for LDA prediction, classified into distinct categories.
  • Introduction to relevant public resources for lncRNA-disease research.
  • Analysis of evaluation strategies and metrics for assessing prediction accuracy.

Conclusions:

  • LDA prediction is a rapidly advancing field with significant implications for understanding disease pathogenesis.
  • The review provides a structured overview of existing computational approaches and resources.
  • Future research should focus on addressing current challenges and leveraging emerging trends in LDA prediction.