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相关概念视频

RNA-seq03:21

RNA-seq

9.8K
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...
9.8K
RACE - Rapid Amplification of cDNA Ends02:35

RACE - Rapid Amplification of cDNA Ends

6.3K
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...
6.3K
Ribosome Profiling02:24

Ribosome Profiling

3.5K
Ribosome profiling or ribo-sequencing is a deep sequencing technique that produces a snapshot of active translation in a cell. It selectively sequences the mRNAs protected by ribosomes to get an insight into a cell’s translation landscape at any given point in time.
Applications of ribosome profiling
Ribosome profiling has many applications, including in vivo monitoring of translation inside a particular organ or tissue type and quantifying new protein synthesis levels.
The technique...
3.5K
Leaky Scanning02:28

Leaky Scanning

5.1K
During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA.  Marilyn Kozak discovered that the sequence RCCAUGG (where R...
5.1K
Pre-mRNA Processing: Modification of pre-mRNA Ends01:35

Pre-mRNA Processing: Modification of pre-mRNA Ends

9.2K
In eukaryotic cells, transcripts made by RNA polymerase are modified and processed before exiting the nucleus. Unprocessed RNA is called precursor mRNA or pre-mRNA to distinguish it from mature mRNA.
Once about 20-40 ribonucleotides have been joined together by RNA polymerase, a group of enzymes adds a cap to the 5' end of the growing transcript. In this process, a 5' phosphate is replaced by modified guanosine that has a methyl group attached (7-methyl guanosine). This 5' cap helps...
9.2K
pre-mRNA Processing02:01

pre-mRNA Processing

52.6K
In eukaryotic cells, transcripts made by RNA polymerase are modified and processed before exiting the nucleus. Unprocessed RNA is called precursor mRNA or pre-mRNA to distinguish it from mature mRNA.
Once about 20-40 ribonucleotides have been joined together by RNA polymerase, a group of enzymes adds a “cap” to the 5’ end of the growing transcript. In this process, a 5’ phosphate is replaced by modified guanosine that has a methyl group attached to it (7-Methyl...
52.6K

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相关实验视频

Updated: Jun 7, 2025

Single Read and Paired End mRNA-Seq Illumina Libraries from 10 Nanograms Total RNA
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Single Read and Paired End mRNA-Seq Illumina Libraries from 10 Nanograms Total RNA

Published on: October 27, 2011

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识别mRNA转录的挑战从长读测序数据开始和结束.

Ezequiel Calvo-Roitberg1, Rachel F Daniels1, Athma A Pai2

  • 1RNA Therapeutics Institute, University of Massachusetts Chan Medical School, Worcester, Massachusetts 01605, USA.

Genome research
|November 20, 2024
PubMed
概括

长读测序 (LRS) 提供了全面的RNA分析,但难以准确地定义mRNA开始和结束地点. 本研究详细介绍了RNA生物学中精确终端表征的挑战和解决方案.

科学领域:

  • 分子生物学分子生物学
  • 基因组学就是基因组学.
  • 生物信息学是一种生物信息学.

背景情况:

  • 长读测序 (LRS) 承诺对全长mRNA异型进行全面分析.
  • 目前的LRS应用面临着覆盖率低,错误率高和计算管道限制等挑战.
  • 精确的mRNA终端特征 (转录起点和终点点) 是至关重要的,但在LRS中未得到充分研究.

研究的目的:

  • 用LRS技术识别和量化评估mRNA终端的挑战.
  • 评估这些挑战对LRS数据的生物学解释的影响.
  • 审查实验和计算方面的进展,以改进终端端的特性.

主要方法:

  • 对LRS数据的分析,重点是基因末端的读取不一致性.
  • 对现有和新兴的终端终端确定实验技术的审查.
  • 对计算策略的评估,以准确量化mRNA开始和结束地点.

主要成果:

  • 读取LRS通常无法准确地表示注释或经验衍生的mRNA开始和结束位置.
  • 在LRS读取坐标的不一致性给终端端分析带来了重大挑战.
  • 最近的进展显示,有望缓解这些问题,并确定了特定的用例.

更多相关视频

3' End Sequencing Library Preparation with A-seq2
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3' End Sequencing Library Preparation with A-seq2

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Author Spotlight: AQRNA-seq Role in Mapping Small RNAs and Unraveling Protein Translation Mechanisms
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Author Spotlight: AQRNA-seq Role in Mapping Small RNAs and Unraveling Protein Translation Mechanisms

Published on: February 2, 2024

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相关实验视频

Last Updated: Jun 7, 2025

Single Read and Paired End mRNA-Seq Illumina Libraries from 10 Nanograms Total RNA
14:49

Single Read and Paired End mRNA-Seq Illumina Libraries from 10 Nanograms Total RNA

Published on: October 27, 2011

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3' End Sequencing Library Preparation with A-seq2
12:01

3' End Sequencing Library Preparation with A-seq2

Published on: October 10, 2017

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Author Spotlight: AQRNA-seq Role in Mapping Small RNAs and Unraveling Protein Translation Mechanisms
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Author Spotlight: AQRNA-seq Role in Mapping Small RNAs and Unraveling Protein Translation Mechanisms

Published on: February 2, 2024

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结论:

  • 精确的mRNA终端与LRS结尾的表征对于完整的分子划分和理解调节作用至关重要.
  • 解决终端端分析中的LRS限制对于推进RNA生物学至关重要.
  • 未来的发展是必要的,以提高基于LRS的终端端确定精度和可靠性.