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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
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
lncRNA - Long Non-coding RNAs02:39

lncRNA - Long Non-coding RNAs

8.5K
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...
8.5K
Next-generation Sequencing03:00

Next-generation Sequencing

87.5K
The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
Although all next-generation methods use different technologies, they all share a set of standard features....
87.5K
Translation01:31

Translation

14.6K
Translation is the process of synthesizing proteins from the genetic information carried by messenger RNA (mRNA). Following transcription, it constitutes the final step in the expression of genes. This process is carried out by ribosomes, complexes of protein and specialized RNA molecules. Ribosomes, transfer RNA (tRNA), and other proteins produce a chain of amino acids—the polypeptide—as the end product of translation.
Translation Produces the Building Blocks of Life
Proteins are...
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相关实验视频

Updated: Jun 7, 2025

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

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长读RNA测序:一种用于探索人类疾病中转录组复杂性的变革性技术.

Isabelle Heifetz Ament1, Nicole DeBruyne2, Feng Wang3

  • 1Department of Biology, University of Pennsylvania, Philadelphia, PA 19104, USA.

Molecular therapy : the journal of the American Society of Gene Therapy
|November 20, 2024
PubMed
概括
此摘要是机器生成的。

长读RNA测序 (RNA-seq) 提供了对人类转录组的全面视图,超过了短读方法. 这项技术对于了解人类疾病中的RNA变异至关重要.

关键词:
基因组RNA的修饰是RNA的修饰.在RNA-seqqq.这种异形异形是什么?长时间阅读翻译学 翻译学 翻译学 翻译学

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Targeted RNA Sequencing Assay to Characterize Gene Expression and Genomic Alterations
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Targeted RNA Sequencing Assay to Characterize Gene Expression and Genomic Alterations

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Identification of Key Factors Regulating Self-renewal and Differentiation in EML Hematopoietic Precursor Cells by RNA-sequencing Analysis

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相关实验视频

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Targeted RNA Sequencing Assay to Characterize Gene Expression and Genomic Alterations
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科学领域:

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

背景情况:

  • 短读RNA测序 (RNA-seq) 在捕获全长转录时存在局限性.
  • 了解完整的转录组对于生物研究和疾病研究至关重要.

研究的目的:

  • 提供长期阅读RNA测序技术的概述.
  • 为了突出其优势比短读RNA-seq.
  • 总结最近在人类转录组学方面的进展和应用.

主要方法:

  • 对长时间读取的RNA测序现有文献的审查.
  • 对实验和计算方法的分析.
  • 人类疾病研究中的各种应用的汇编.

主要成果:

  • 长读RNA-seq使全长转录的端到端测序成为可能.
  • 它揭示了RNA物种和短读方法遗漏的特征.
  • 最近的进步增强了它对转录学学的力量.

结论:

  • 长读RNA测序是全面的人类转录组研究的强大工具.
  • 它对于探索人类疾病中的转录组变异越来越重要.
  • 这项技术是未来转录原子研究的基础.