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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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Next-generation Sequencing03:00

Next-generation Sequencing

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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.
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Sanger Sequencing01:57

Sanger Sequencing

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DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
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Ribosome Profiling02:24

Ribosome Profiling

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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.
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Updated: Apr 23, 2026

Author Spotlight: AQRNA-seq Role in Mapping Small RNAs and Unraveling Protein Translation Mechanisms
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Alternative applications for distinct RNA sequencing strategies.

Leng Han, Kasey C Vickers, David C Samuels

    Briefings in Bioinformatics
    |September 24, 2014
    PubMed
    Summary

    High-throughput RNA sequencing (RNAseq) now surpasses microarrays for transcriptome analysis. RNAseq offers deep insights into gene expression, epigenetic regulation, and DNA variations, advancing genomic research.

    Keywords:
    RNAseqSNPdata miningexogenous RNAmutation

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    Area of Science:

    • Genomics
    • Molecular Biology
    • Bioinformatics

    Background:

    • High-throughput RNA sequencing (RNAseq) has become the preferred method for mRNA profiling and transcriptome analysis.
    • Advances in library preparation, platform accessibility, and cost-efficiency have driven RNAseq adoption over microarrays.

    Purpose of the Study:

    • To review the current state of transcriptome sequencing using RNAseq.
    • To discuss the diverse applications and capabilities of RNAseq in genomic analysis.

    Main Methods:

    • Review of current RNA sequencing methodologies and technologies.
    • Analysis of RNAseq data for various applications including expression profiling, epigenetic analysis, and mutation detection.

    Main Results:

    • RNAseq provides comprehensive transcriptome profiling for both long and short RNA species.
    • RNAseq enables assessment of transcriptional elongation, DNA variance, allele-specific expression, and somatic mutations.
    • Combining RNAseq and DNA sequencing offers powerful genomic analysis capabilities.

    Conclusions:

    • RNAseq offers deeper insights into transcriptional regulation and output compared to traditional miRNA and mRNA profiling.
    • RNAseq is a versatile tool for identifying genetic variations and understanding complex biological processes.