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Related Concept Videos

RNA-seq03:21

RNA-seq

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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...
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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
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Related Experiment Video

Updated: Jun 8, 2025

Obtaining High-Quality Transcriptome Data from Cereal Seeds by a Modified Method for Gene Expression Profiling
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Lasy-Seq: A High-Throughput 3' RNA-Seq Method for Large-Scale Transcriptome Profiling in Rice.

Natsumi Mori-Moriyama1, Atsushi J Nagano2,3

  • 1Faculty of Agriculture, Ryukoku University, Shiga, Japan.

Methods in Molecular Biology (Clifton, N.J.)
|November 5, 2024
PubMed
Summary

Lasy-Seq offers a low-cost, easy method for preparing 3' RNA-sequencing libraries. This high-throughput technique simplifies sample indexing and pooling, reducing processing time for hundreds of samples.

Keywords:
3′ RNA-seqHigh-throughput RNA-seqLarge-scale RNA-seqScalable RNA-seqTranscriptome

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Area of Science:

  • Molecular Biology
  • Genomics
  • Biotechnology

Background:

  • RNA sequencing (RNA-seq) is crucial for gene expression analysis.
  • Traditional library preparation methods can be time-consuming and costly.
  • 3' RNA-seq focuses on the 3' end of transcripts, offering a cost-effective approach.

Purpose of the Study:

  • To introduce Lasy-Seq, a novel, streamlined library preparation method for 3' RNA-seq.
  • To demonstrate the efficiency and scalability of Lasy-Seq for high-throughput applications.
  • To reduce the cost and hands-on time associated with RNA-seq library preparation.

Main Methods:

  • Lasy-Seq utilizes oligo(dT) primers with unique index sequences.
  • Simultaneous reverse transcription (RT) and sample indexing are performed in a single step.
  • Post-RT steps are consolidated for pooled samples, eliminating individual processing.

Main Results:

  • Lasy-Seq enables high-throughput library preparation for 3' RNA-seq.
  • The method allows for simultaneous RT and sample indexing.
  • Complex library pools from hundreds of samples can be prepared in days.

Conclusions:

  • Lasy-Seq significantly simplifies and accelerates the RNA-seq library preparation workflow.
  • This method is suitable for processing a large number of samples efficiently.
  • Lasy-Seq presents a cost-effective and easy-to-use alternative for 3' RNA-seq.