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相关概念视频

RNA-seq03:21

RNA-seq

10.1K
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...
10.1K
RACE - Rapid Amplification of cDNA Ends02:35

RACE - Rapid Amplification of cDNA Ends

6.4K
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...
6.4K
Ribosome Profiling02:24

Ribosome Profiling

3.6K
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...
3.6K
Pre-mRNA Processing: Modification of pre-mRNA Ends01:35

Pre-mRNA Processing: Modification of pre-mRNA Ends

9.5K
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...
9.5K
pre-mRNA Processing02:01

pre-mRNA Processing

53.0K
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...
53.0K
Leaky Scanning02:28

Leaky Scanning

5.2K
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...
5.2K

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相关实验视频

Updated: Jul 19, 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 Pai1

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

bioRxiv : the preprint server for biology
|August 7, 2023
PubMed
概括

长读数测序 (LRS) 具有很高的错误率,不准确地识别mRNA开始和结束位置. 一种新方法提高了终端精度,但可能会降低基因量化和异构体发现能力.

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) 提供了在RNA生物学中进行全长mRNA异形分析的潜力.
  • 在LRS数据中的高错误率为准确的转录基因分析带来了挑战.
  • 在表示转录开始和结束位置方面,LRS的准确性仍然不明确.

结论:

  • 在选择LRS方法和解释长时间读取的RNA测序数据时,建议谨慎.
  • 准确识别转录端末对于强大的转录组分析至关重要.
  • 需要进一步开发以平衡基于LRS的转录组学研究的准确性和灵敏性.

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Last Updated: Jul 19, 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

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