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Related Concept Videos

lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

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 (lncRNA)...
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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 (lncRNA)...
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The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.
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Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
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Related Experiment Video

Updated: May 10, 2026

RNA Next-Generation Sequencing and a Bioinformatics Pipeline to Identify Expressed LINE-1s at the Locus-Specific Level
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Linc2GO: a human LincRNA function annotation resource based on ceRNA hypothesis.

Ke Liu1, Zhangming Yan, Yuchao Li

  • 1MOE Key Laboratory of Bioinformatics, State Key Laboratory of Biomembrane and Membrane Biotechnology, School of Life Sciences, Tsinghua University, Beijing, China.

Bioinformatics (Oxford, England)
|June 25, 2013
PubMed
Summary
This summary is machine-generated.

Linc2GO is a new database providing functional annotations for human long intergenic non-coding RNAs (lincRNAs). It utilizes the competing endogenous RNA hypothesis to predict lincRNA functions, aiding research in this understudied area.

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Area of Science:

  • Genomics
  • Molecular Biology
  • Bioinformatics

Background:

  • High-throughput sequencing has identified numerous long intergenic non-coding RNAs (lincRNAs).
  • The functions of most lincRNAs remain largely unknown.
  • A dedicated database for lincRNA function annotation is crucial for advancing research.

Purpose of the Study:

  • To introduce Linc2GO, a novel web resource for comprehensive functional annotations of human lincRNAs.
  • To facilitate the study of lincRNA functions by providing accessible annotation data.

Main Methods:

  • Integration of microRNA-mRNA and microRNA-lincRNA interaction data.
  • Application of the competing endogenous RNA (ceRNA) hypothesis for functional prediction.
  • Development of a user-friendly web resource.

Main Results:

  • Linc2GO provides functional annotations for human lincRNAs.
  • The database is the first to employ the ceRNA hypothesis for predicting lincRNA functions.
  • Comprehensive data integration enables robust functional predictions.

Conclusions:

  • Linc2GO addresses the need for lincRNA functional annotation.
  • The use of the ceRNA hypothesis offers a novel approach to understanding lincRNA roles.
  • This resource will support further investigations into lincRNA biology.