Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Alternative RNA Splicing02:18

Alternative RNA Splicing

24.6K
Alternative RNA splicing is the regulated splicing of exons and introns to produce different mature mRNAs from a single pre-mRNA. Unlike in constitutive splicing where a single gene produces a single type of mRNA, alternative splicing allows an organism to produce multiple proteins from a single gene and plays an important role in protein diversity.
There are five types of alternative RNA splicing that vary in the ways the pre-mRNA segments are removed or retained in the mature mRNA. The first...
24.6K
Alternative RNA Splicing02:18

Alternative RNA Splicing

4.8K
4.8K
RNA Splicing01:32

RNA Splicing

60.3K
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...
60.3K
Chromatin Structure and RNA Splicing02:41

Chromatin Structure and RNA Splicing

3.2K
3.2K
Pre-mRNA Processing: RNA Splicing01:36

Pre-mRNA Processing: RNA Splicing

6.5K
6.5K
Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

18.5K
Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
18.5K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Plasma GDF15 affects long-term dementia risk and alters neuroimmune signaling.

Science advances·2026
Same author

Characterization of the m<sup>6</sup>A Epitranscriptome in Fibroblast Senescence.

Molecular and cellular biology·2026
Same author

SIRT6 overexpression counteracts chromatin aging in the male murine liver.

Nature communications·2026
Same author

Glucose-6-Phosphate Dehydrogenase Modifies the Impact of Glucose on Arterial Aging in A Sex-Specific Manner.

Journal of the American Heart Association·2026
Same author

Senolytic Treatment With Fisetin Reverses Age-Related Endothelial Dysfunction Partially Mediated by SASP Factor CXCL12.

Aging cell·2026
Same author

Intercompartmental communication in senescence.

FEBS open bio·2026
Same journal

Molecular Interplay of PARN and Telomerase: Tail Modifiers and Disease Implications.

Wiley interdisciplinary reviews. RNA·2026
Same journal

Exploring New Frontiers in Bone Metabolism: Role and Potential of lncRNA DANCR.

Wiley interdisciplinary reviews. RNA·2026
Same journal

Functional Inclusion of RNA Biology in the Tethered Extracellular Matrix.

Wiley interdisciplinary reviews. RNA·2026
Same journal

Structural and Functional Diversity of RNA-Containing Toxin-Antitoxin Systems.

Wiley interdisciplinary reviews. RNA·2026
Same journal

Promoter-Targeting RNA Technologies: An Epigenetic Strategy for Gene Activation and Gene Silencing.

Wiley interdisciplinary reviews. RNA·2026
Same journal

LncRNA PCAT18: Roles and Mechanisms in Human Cancers.

Wiley interdisciplinary reviews. RNA·2026
查看所有相关文章

相关实验视频

Updated: Jan 9, 2026

Identification of Alternative Splicing and Polyadenylation in RNA-seq Data
08:35

Identification of Alternative Splicing and Polyadenylation in RNA-seq Data

Published on: June 24, 2021

6.3K

针对替代分离分析的计算工具的全面概述

Hieu Tran1, Nirad Banskota1, Myriam Gorospe2

  • 1Computational Biology and Genomics Core, Laboratory of Genetics and Genomics, National Institute on Aging, National Institutes of Health, Baltimore, Maryland, USA.

Wiley interdisciplinary reviews. RNA
|December 1, 2025
PubMed
概括
此摘要是机器生成的。

替代拼接 (AS) 产生了对细胞功能至关重要的蛋白质多样性. 本综述比较了用于分析分子生物学研究中AS事件的关键RNA测序工具.

关键词:
拼接的计算分析.短读和长读测序的测序.转录组分析 转录组分析

更多相关视频

Using RNA-sequencing to Detect Novel Splice Variants Related to Drug Resistance in In Vitro Cancer Models
09:58

Using RNA-sequencing to Detect Novel Splice Variants Related to Drug Resistance in In Vitro Cancer Models

Published on: December 9, 2016

14.3K
Using the E1A Minigene Tool to Study mRNA Splicing Changes
10:25

Using the E1A Minigene Tool to Study mRNA Splicing Changes

Published on: April 22, 2021

5.4K

相关实验视频

Last Updated: Jan 9, 2026

Identification of Alternative Splicing and Polyadenylation in RNA-seq Data
08:35

Identification of Alternative Splicing and Polyadenylation in RNA-seq Data

Published on: June 24, 2021

6.3K
Using RNA-sequencing to Detect Novel Splice Variants Related to Drug Resistance in In Vitro Cancer Models
09:58

Using RNA-sequencing to Detect Novel Splice Variants Related to Drug Resistance in In Vitro Cancer Models

Published on: December 9, 2016

14.3K
Using the E1A Minigene Tool to Study mRNA Splicing Changes
10:25

Using the E1A Minigene Tool to Study mRNA Splicing Changes

Published on: April 22, 2021

5.4K

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:

  • 替代拼接 (AS) 是产生转录组和蛋白组多样性的关键机制.
  • AS影响细胞分化,组织特异性和适应环境刺激.
  • 了解AS对于理解生物复杂性和疾病机制至关重要.

研究的目的:

  • 审查和比较用于替代拼接分析的突出的计算工具.
  • 讨论各种AS检测工具的优点,局限性和实际可用性.
  • 根据生物背景和研究需求,为选择合适的AS分析工具提供指导.

主要方法:

  • 对替代拼接分析工具的文献综述.
  • 对rMATS,SUPPA2,LeafCutter,MISO,DEXSeq,MAJIQ,StringTie和袖珍链条进行了比较分析.
  • 评估工具功能,计算要求和易用性.

主要成果:

  • 每个工具都有独特的优势和局限性,用于检测特定的替代拼接事件.
  • 工具的选择取决于数据类型,研究问题和可用的计算资源等因素.
  • 对这些工具的全面理解有助于研究人员进行有效的AS分析.

结论:

  • 选择AS分析工具会对研究结果产生重大影响.
  • 对工具的知情选择对于准确解释替代拼接数据至关重要.
  • 这一审查促进了AS分析工具在分子生物学和疾病研究中的最佳应用.