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

RNA-seq03:21

RNA-seq

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 microarray-based...

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

Transcriptional Profiling Shows Dampening of Interferon Gene Signatures by NAD<sup>+</sup> Augmentation in Ataxia-Telangiectasia.

International journal of molecular sciences·2026
Same author

Corrigendum to 'ZhuYang TongBi decoction ameliorates pulmonary fibrosis by degrading TGFBR via CAV1' [Fitoterapia 192 (2026) 107300].

Fitoterapia·2026
Same author

Protocol for identifying functional regulatory mutation blocks by integrating genome sequencing and transcriptome data.

STAR protocols·2026
Same author

BAGE: a Bayesian framework for age prediction based on PBMC gene expression data.

BMC bioinformatics·2026
Same author

Corrigendum to "ZhuYang TongBi decoction ameliorates pulmonary fibrosis by degrading TGFBR via CAV1" [Fitoterapia 192 (2026) 107300].

Fitoterapia·2026
Same author

Optimization of Permeable Cryoprotectants for <i>Neisseria meningitidis</i> Based on Assessment of Ice Inhibition and Cytotoxicity.

Biopreservation and biobanking·2026

相关实验视频

Updated: Jul 7, 2026

High-throughput Identification of Gene Regulatory Sequences Using Next-generation Sequencing of Circular Chromosome Conformation Capture 4C-seq
09:06

High-throughput Identification of Gene Regulatory Sequences Using Next-generation Sequencing of Circular Chromosome Conformation Capture 4C-seq

Published on: October 5, 2018

10.2K

EpiMapper:一种用于分析来自CUT&Tag的高吞吐量测序的新工具.

Jenny Sofie Dragland1, Gege Liu1, Hilde Loge Nilsen2

  • 1Department of Pathology, Oslo University Hospital - Norwegian Radium Hospital, Oslo, Norway.

Computers in biology and medicine
|January 20, 2025
PubMed
概括

EpiMapper是一个新的Python包,简化了表观基因组数据分析,用于诸如CUT&Tag测序等技术. 它有助于科学家解释基因表达和表观遗传标记研究的结果.

更多相关视频

High-Throughput Transcriptome Analysis for Investigating Host-Pathogen Interactions
14:58

High-Throughput Transcriptome Analysis for Investigating Host-Pathogen Interactions

Published on: March 5, 2022

4.1K
Author Spotlight: Investigating the Role of Repetitive DNA Misregulation in Cancer Initiation and Immunotherapy Resistance
04:58

Author Spotlight: Investigating the Role of Repetitive DNA Misregulation in Cancer Initiation and Immunotherapy Resistance

Published on: December 13, 2024

2.1K

相关实验视频

Last Updated: Jul 7, 2026

High-throughput Identification of Gene Regulatory Sequences Using Next-generation Sequencing of Circular Chromosome Conformation Capture 4C-seq
09:06

High-throughput Identification of Gene Regulatory Sequences Using Next-generation Sequencing of Circular Chromosome Conformation Capture 4C-seq

Published on: October 5, 2018

10.2K
High-Throughput Transcriptome Analysis for Investigating Host-Pathogen Interactions
14:58

High-Throughput Transcriptome Analysis for Investigating Host-Pathogen Interactions

Published on: March 5, 2022

4.1K
Author Spotlight: Investigating the Role of Repetitive DNA Misregulation in Cancer Initiation and Immunotherapy Resistance
04:58

Author Spotlight: Investigating the Role of Repetitive DNA Misregulation in Cancer Initiation and Immunotherapy Resistance

Published on: December 13, 2024

2.1K

科学领域:

  • 基因组学和表观遗传学
  • 生物信息学和计算生物学

背景情况:

  • 下一代测序使得通过表观遗传标记来理解基因表达调节的进步成为可能.
  • CUT&Tag (Cleavage Under Targets and Tagmentation) 是一种高效的表观基因组分析技术,其输入需求低,灵敏度高,背景低.
  • 对缺乏先进计算专业知识的研究人员来说,分析CUT&Tag,ATAC-seq和ChIP-seq数据带来了挑战.

研究的目的:

  • 开发EpiMapper,一个用户友好的Python包,用于简化CUT&Tag序列数据分析.
  • 为生物医学科学家提供一种可访问的工具来解释表观基因组分析结果.
  • 增强现有的分析协议,以提高功能和表观基因组数据的新功能.

主要方法:

  • 开发一个Python包,EpiMapper,集成质量控制,基因组注释和差异峰值分析.
  • 实施改进的功能,如可复制性评估和增强的可视化图表.
  • 使用涉及CUT&Tag和ATAC-seq数据集的三个案例研究验证EpiMapper.

主要成果:

  • EpiMapper成功地简化了CUT&Tag和类似的表观基因组测序技术的复杂数据分析管道.
  • 该包提供了从初始数据质量控制到高级注释和差异分析的全面功能.
  • 案例研究表明,EpiMapper可以准确地复制以前的发现,证实其可靠性和有效性.

结论:

  • EpiMapper为分析CUT&Tag,ATAC-seq和ChIP-seq数据提供了一个有价值的,易于使用的解决方案,赋予研究人员没有专门的计算技能的能力.
  • 该包提高了表观基因组分析结果的解释性,促进了基因表达调节方面的发现.
  • 经过验证的EpiMapper性能和全面的功能使其成为表观遗传学研究社区的重要工具.