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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)...
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)...
RNA-seq03:21

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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. 
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Ribosome Profiling02:24

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RACE - Rapid Amplification of cDNA Ends02:35

RACE - Rapid Amplification of cDNA Ends

Rapid Amplification of cDNA Ends, or RACE, is one of the most effective methods to obtain a full-length cDNA from an mRNA sequence between a known internal region to the unknown sequence at the 5’ or 3’ end. The unknown region is cloned in the cDNA by a gene-specific primer that binds the known end, and a hybrid primer that attaches a predefined anchor sequence to the unknown end of the cDNA. The sequence in between is amplified by PCR with an anchor primer and a gene-specific primer.
Since the...
Organization of Genes02:07

Organization of Genes

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Updated: Jun 8, 2026

RNA Pull-down Procedure to Identify RNA Targets of a Long Non-coding RNA
09:36

RNA Pull-down Procedure to Identify RNA Targets of a Long Non-coding RNA

Published on: April 10, 2018

[Support vector data description for finding non-coding RNA gene].

Yingjie Zhao1, Zhengzhi Wang

  • 1College of Mechatronics Engineering and Automation, National University of Defense Technology, Changsha 410073, China. zhaoyingjie@nudt.edu.cn

Sheng Wu Yi Xue Gong Cheng Xue Za Zhi = Journal of Biomedical Engineering = Shengwu Yixue Gongchengxue Zazhi
|September 17, 2010
PubMed
Summary
This summary is machine-generated.

This study introduces a novel computational method for detecting non-coding RNA genes using Support Vector Data Description (SVDD) and k-means clustering. The approach effectively identifies these crucial genes in unlabeled sequences, improving accuracy in computational biology.

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Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay (EMSA) and DNA-affinity Precipitation Assay (DAPA)
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Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay (EMSA) and DNA-affinity Precipitation Assay (DAPA)

Published on: August 21, 2016

Area of Science:

  • Computational molecular biology
  • Bioinformatics
  • Genomics

Background:

  • Detecting non-coding RNA genes in unlabeled sequences is a significant challenge in computational biology.
  • Existing machine learning methods struggle with limited positive samples and the difficulty of defining appropriate negative samples.
  • Current approaches often introduce uncertainty by using random sequences as negative samples, leading to suboptimal performance.

Purpose of the Study:

  • To develop an improved method for non-coding RNA gene detection using Support Vector Data Description (SVDD).
  • To address the limitations of existing methods, particularly the challenge of negative sample definition and high false positive rates.
  • To enhance the accuracy and reliability of non-coding RNA gene identification in large unlabeled sequence datasets.

Main Methods:

  • Utilized Support Vector Data Description (SVDD) for learning and classification of non-coding RNA genes.
  • Employed k-means clustering prior to SVDD training to mitigate high false positive rates.
  • Constructed relevant features using Principal Component Analysis (PCA) and trained on experimentally validated non-coding RNA genes.

Main Results:

  • The combined k-means clustering and SVDD approach demonstrated effectiveness in detecting non-coding RNA genes.
  • The method showed improved performance compared to existing techniques, particularly in handling unlabeled sequences.
  • Validation on datasets from NONCODE databases and the E. coli genome confirmed the method's efficacy.

Conclusions:

  • The proposed method, integrating k-means clustering with SVDD and PCA, offers a robust solution for non-coding RNA gene detection.
  • This approach effectively overcomes the limitations associated with negative sample generation and improves classification accuracy.
  • The findings contribute a valuable tool for computational biologists and researchers in genomics and molecular biology.