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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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Two structural features of the DNA molecule provide a basis for the mechanisms of heredity: the four nucleotide bases and its double-stranded nature. The Watson-Crick model of double-helical DNA structure, proposed in 1952, drew heavily upon the X-ray crystallography work of researchers Rosalind Franklin and Maurice Wilkins. Watson, Crick, and Wilkins jointly received the Nobel Prize in Physiology or Medicine for their work in 1962. Franklin was, controversially, excluded from the prize for...
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Corrigendum: NCNet: Deep Learning Network Models for Predicting Function of Non-Coding DNA.

Hanyu Zhang1,2, Che-Lun Hung3,4,5,6, Meiyuan Liu7

  • 1College of Computing and Informatics, Providence University, Taichung City, Taiwan.

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|September 24, 2019
PubMed
Summary
This summary is machine-generated.

This study corrects a previous article DOI. It ensures accurate citation and retrieval of genetic research findings for the scientific community.

Keywords:
LSTMNon-coding DNAdeep learningresidual learningsequence to sequence learning

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Area of Science:

  • Genetics
  • Bioinformatics

Context:

  • Correction of a previously published article DOI.
  • Ensuring accurate citation and data retrieval.

Purpose:

  • To provide the correct Digital Object Identifier (DOI) for a specific article.
  • To facilitate proper referencing and access to the research.

Summary:

  • The article DOI 10.3389/fgene.2019.00432 has been corrected.
  • This ensures the scientific record is accurate.

Impact:

  • Improved accessibility to genetic research.
  • Enhanced integrity of scientific literature.
  • Facilitation of future research citing this work.