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lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

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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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Transcription01:10

Transcription

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Transcription is the process of synthesizing RNA from a DNA sequence by RNA polymerase. It is the first step in producing a protein from a gene sequence. Additionally, many other proteins and regulatory sequences are involved in the proper synthesis of messenger RNA (mRNA). Regulation of transcription is responsible for the differentiation of all the different types of cells and often for the proper cellular response to environmental signals.
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Isolation of High-density Lipoproteins for Non-coding Small RNA Quantification
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Computational Methods for Mapping, Assembly and Quantification for Coding and Non-coding Transcripts.

Isaac A Babarinde1, Yuhao Li1, Andrew P Hutchins1

  • 1Department of Biology, Southern University of Science and Technology, 1088 Xueyuan Lu, Shenzhen, China.

Computational and Structural Biotechnology Journal
|June 14, 2019
PubMed
Summary
This summary is machine-generated.

High-throughput RNA sequencing (RNA-Seq) offers deep biological insights but increases computational demands. This review details RNA-Seq analysis pipelines, their challenges, and their utility for studying coding and non-coding RNAs.

Keywords:
GenomeLong non-coding RNARNA-SeqTranscriptTransposable element

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Area of Science:

  • Genomics
  • Bioinformatics
  • Molecular Biology

Background:

  • Gene expression measurement is crucial for understanding biological functions.
  • High-throughput sequencing technologies like RNA-Seq have revolutionized the scale of transcriptional analysis.
  • Increased data complexity necessitates advanced computational approaches.

Purpose of the Study:

  • To review common computational pipelines for RNA-Seq data analysis.
  • To discuss the strengths and weaknesses of these pipelines for RNA analysis.
  • To address challenges in analyzing repetitive elements like transposable elements.

Main Methods:

  • Review of existing literature on RNA-Seq computational pipelines.
  • Analysis of strengths and weaknesses of assembly, quantification, and analysis methods.
  • Discussion of strategies for handling transposable elements in transcript assembly.

Main Results:

  • RNA-Seq analysis pipelines vary in their suitability for different biological questions.
  • Assembly and quantification of coding and non-coding RNAs present distinct challenges.
  • Repetitive elements, such as transposable elements, complicate transcript assembly.

Conclusions:

  • RNA-Seq is a powerful and versatile technology for biological research.
  • Understanding computational pipeline limitations is essential for accurate RNA-Seq data interpretation.
  • Continued development in bioinformatics is needed to fully leverage RNA-Seq data.