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相关概念视频

Chromatin Immunoprecipitation- ChIP02:36

Chromatin Immunoprecipitation- ChIP

12.1K
Chromatin immunoprecipitation, or ChIP, is an antibody-based technique used to identify sites on DNA that bind to transcription factors of interest or histone proteins. It also helps determine the type of histone modifications such as acetylation, phosphorylation, or methylation.
Types of ChIP
ChIP can be divided into two types - X-ChIP and N-ChIP. X-ChIP involves in vivo cross-linking of histones and regulatory proteins to DNA, fragmenting the DNA by sonication, and isolating the protein-DNA...
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Heterochromatin02:38

Heterochromatin

17.7K
The extent of chromatin compaction can be studied by staining chromatin using specific DNA binding dyes. Under the microscope, the dense-compacted regions that take up more dye are called heterochromatin. Heterochromatin is further classified into two forms – constitutive heterochromatin and facultative heterochromatin.
Constitutive heterochromatin: It is a highly compact region of chromatin that is mostly concentrated in the centromere and telomere. Unlike euchromatin, the amino acid at...
17.7K
Cooperative Binding of Transcription Regulators02:13

Cooperative Binding of Transcription Regulators

7.1K
Transcriptional regulators bind to specific cis-regulatory sequences in the DNA to regulate gene transcription. These cis-regulatory sequences are very short, usually less than ten nucleotide pairs in length. The short length means that there is a high probability of the exact same sequence randomly occurring throughout the genome.  Since regulators can also bind to groups of similar sequences, this further increases the chances of random binding. Transcriptional regulators form...
7.1K
Chromatin Modification in iPS Cells01:32

Chromatin Modification in iPS Cells

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Chromatin modification alters gene expression; therefore, scientists can add histone-modifying enzymes, histone variants, and chromatin remodeling complexes to somatic cells to aid reprogramming into pluripotent stem (iPS) cells.
Compact chromatin makes reprogramming difficult. Enzymes, such as histone demethylases and acetyltransferases, are often added during reprogramming to loosen the chromatin, making the DNA more accessible to transcription factors. Molecules that inhibit histone...
2.1K
Cis-regulatory Sequences02:02

Cis-regulatory Sequences

11.5K
Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
11.5K
Euchromatin01:01

Euchromatin

8.7K
The extent of chromatin compaction can be studied by staining chromatin using specific DNA binding dyes. Under the microscope, the dense-compacted regions take up more dye, appearing darker, while the less-compact areas take up less dye and appear lighter. Based on the compaction level, chromatins are classified into two primary forms – euchromatin and heterochromatin.
Euchromatin is the less dense region of the chromatin and stains lighter. Euchromatin contains histone H3 extensively...
8.7K

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相关实验视频

Updated: Jan 8, 2026

Author Spotlight: An Integrated Workflow to Study the Promoter-Centric Spatio-Temporal Genome Architecture in Scarce Cell Populations
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Author Spotlight: An Integrated Workflow to Study the Promoter-Centric Spatio-Temporal Genome Architecture in Scarce Cell Populations

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调控元件模块作为单细胞染色体分析的通用特性.

Chrysania Lim1, Javen Tan Yih Ruay1,2, Tim Stuart1

  • 1Genome Institute of Singapore (GIS), Agency for Science Technology and Research (A*STAR), 60 Biopolis Street, Genome, Singapore 138672, Republic of Singapore.

bioRxiv : the preprint server for biology
|December 19, 2025
PubMed
概括
此摘要是机器生成的。

我们开发了DNA调节元件模块 (REMO) 以标准化单细胞染色质可访问性数据分析. 雷莫改进了细胞状态分离,可扩展性和自动化的细胞类型注释,克服了数据集特定峰值区域的局限性.

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Formaldehyde-assisted Isolation of Regulatory Elements to Measure Chromatin Accessibility in Mammalian Cells
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Formaldehyde-assisted Isolation of Regulatory Elements to Measure Chromatin Accessibility in Mammalian Cells

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Single-Cell Factor Localization on Chromatin using Ultra-Low Input Cleavage Under Targets and Release using Nuclease
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Single-Cell Factor Localization on Chromatin using Ultra-Low Input Cleavage Under Targets and Release using Nuclease

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相关实验视频

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Author Spotlight: An Integrated Workflow to Study the Promoter-Centric Spatio-Temporal Genome Architecture in Scarce Cell Populations
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Formaldehyde-assisted Isolation of Regulatory Elements to Measure Chromatin Accessibility in Mammalian Cells
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Single-Cell Factor Localization on Chromatin using Ultra-Low Input Cleavage Under Targets and Release using Nuclease
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科学领域:

  • 基因组学就是基因组学.
  • 计算生物学 计算生物学
  • 表观遗传学 在表观遗传学中,表观遗传学是指表观遗传学.

背景情况:

  • 单细胞染色质可访问性数据提供了对各种生物状态中的DNA调节元素活性的见解.
  • 目前的分析方法由于缺乏标准化的特征而面临挑战,导致数据集特定的峰值区域阻碍了跨研究比较.

研究的目的:

  • 为人类基因组开发一套全面的DNA调控元件模块 (REMO).
  • 解决不同研究中分析和比较单细胞染色质可访问性数据的局限性.

主要方法:

  • 为人类基因组开发一套标准化的DNA调控元件模块 (REMO).
  • 应用REMO对单细胞染色质数据进行分析.
  • 为量化单细胞染色体可访问性数据创建存储效率高且可扩展的软件.

主要成果:

  • 与传统的峰值矩阵量化相比,REMO应用可以在低维空间中更好地分离细胞状态.
  • 在数据分析中,REMO方法显著提高了尺寸缩小步骤的可扩展性.
  • 通过使用REMO.启用了细胞类型的自动注释.

结论:

  • 雷莫为分析单细胞染色质可访问性数据提供了一个标准化的框架.
  • 开发的REMO方法提高了数据的可比性,可扩展性和细胞类型注释的准确性.
  • 新的软件有助于有效和可扩展量化单细胞染色体可访问性数据.