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Related Concept Videos

RNA-seq03:21

RNA-seq

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RNA sequencing, or RNA-Seq, is a high-throughput sequencing technology used to study the transcriptome of a cell. Transcriptomics helps to interpret the functional elements of a genome and identify the molecular constituents of an organism. Additionally, it also helps in understanding the development of an organism and the occurrence of diseases. 
Before the discovery of RNA-seq, microarray-based methods and Sanger sequencing were used for transcriptome analysis. However, while...
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RNA Interference01:23

RNA Interference

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RNA interference (RNAi) is a process in which a small non-coding RNA molecule blocks the post-transcriptional expression of a gene by binding to its messenger RNA (mRNA) and preventing the protein from being translated.
This process occurs naturally in cells, often through the activity of genomically-encoded microRNAs. Researchers can take advantage of this mechanism by introducing synthetic RNAs to deactivate specific genes for research or therapeutic purposes. For example, RNAi could be used...
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RNA Structure01:23

RNA Structure

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Overview
The basic structure of RNA consists of a five-carbon sugar and one of four nitrogenous bases. Although most RNA is single-stranded, it can form complex secondary and tertiary structures. Such structures play essential roles in the regulation of transcription and translation.
Different Types of RNA Have the Same Basic Structure
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RNA Stability01:53

RNA Stability

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Intact DNA strands can be found in fossils, while scientists sometimes struggle to keep RNA intact under laboratory conditions. The structural variations between RNA and DNA underlie the differences in their stability and longevity. Because DNA is double-stranded, it is inherently more stable. The single-stranded structure of RNA is less stable but also more flexible and can form weak internal bonds. Additionally, most RNAs in the cell are relatively short, while DNA can be up to 250 million...
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RNA Splicing01:32

RNA Splicing

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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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RNA Editing02:23

RNA Editing

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RNA editing is a post-transcriptional modification where a precursor mRNA (pre-mRNA) nucleotide sequence is changed by base insertion, deletion, or modification. The extent of RNA editing varies from a few hundred bases, in mitochondrial DNA of trypanosomes, to a just single base, in nuclear genes of mammals. Even a single base change in the pre-mRNA can convert a codon for one amino acid into the codon for another amino acid or a stop codon. This type of re-coding can significantly affect the...
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Identification of Footprints of RNA:Protein Complexes via RNA Immunoprecipitation in Tandem Followed by Sequencing RIPiT-Seq
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An Efficient Algorithm for Sensitively Detecting Circular RNA from RNA-seq Data.

Xuanping Zhang1,2, Yidan Wang3,4, Zhongmeng Zhao5,6

  • 1School of Electronic and Information Engineering, Xi'an Jiaotong University, Xi'an 710049, China. zxp@mail.xjtu.edu.cn.

International Journal of Molecular Sciences
|September 26, 2018
PubMed
Summary
This summary is machine-generated.

A new algorithm, CIRCPlus, enhances circular RNA (circRNA) detection from RNA-seq data. It improves sensitivity while maintaining precision, especially for low-expression circRNAs.

Keywords:
RNA-seqde novo detectionhigh sensitivitylocal similar sequence

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Area of Science:

  • Bioinformatics
  • Genomics
  • Molecular Biology

Background:

  • Circular RNAs (circRNAs) are a significant class of non-coding RNAs.
  • Existing computational methods for circRNA detection from RNA-sequencing (RNA-seq) data exhibit variability in sensitivity and precision.
  • There is a need for improved algorithms to accurately identify circRNAs, particularly those with low expression levels.

Purpose of the Study:

  • To introduce CIRCPlus, a novel and efficient *de novo* algorithm for circRNA detection.
  • To enhance the sensitivity of circRNA detection while preserving acceptable precision.
  • To address limitations in existing circRNA detection methods.

Main Methods:

  • CIRCPlus identifies circRNA candidates by analyzing back-spliced junction reads.
  • It compares local similar sequences of spanning junction read pairs.
  • The algorithm leverages information from unbalanced spanning reads for improved detection.

Main Results:

  • CIRCPlus achieved up to 90% sensitivity in common simulation settings.
  • The algorithm demonstrated balanced sensitivity and reliability on real RNA-seq datasets.
  • Performance was validated against existing *de novo* methods using simulation and real data.

Conclusions:

  • CIRCPlus offers an improved approach for *de novo* circRNA detection from RNA-seq data.
  • The algorithm is particularly effective for detecting circRNAs with low expression levels.
  • CIRCPlus provides a sensitive and reliable tool for circRNA identification in bioinformatics research.