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Related Concept Videos

RNA-seq03:21

RNA-seq

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 microarray-based...
Next-generation Sequencing03:00

Next-generation Sequencing

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.
Sanger Sequencing01:57

Sanger Sequencing

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...
Ribosome Profiling02:24

Ribosome Profiling

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 helps...

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Related Experiment Video

Updated: May 10, 2026

Amplicon Sequencing using the Long-Read Sequencing Technologies
08:57

Amplicon Sequencing using the Long-Read Sequencing Technologies

Published on: August 29, 2025

The advantages of SMRT sequencing.

Richard J Roberts, Mauricio O Carneiro, Michael C Schatz

    Genome Biology
    |July 5, 2013
    PubMed
    Summary

    Single-molecule, real-time (SMRT) sequencing offers long reads, modified base detection, and high accuracy. This makes SMRT sequencing an ideal approach for the complete sequencing of small genomes.

    Area of Science:

    • Genomics
    • Molecular Biology
    • Next-Generation Sequencing

    Background:

    • Next-generation sequencing (NGS) technologies are rapidly advancing.
    • Single-molecule, real-time (SMRT) sequencing is a notable NGS technology.
    • SMRT sequencing is often overlooked despite its capabilities.

    Discussion:

    • SMRT sequencing provides long reads, enabling comprehensive genome assembly.
    • It offers direct detection of modified bases, crucial for epigenomic studies.
    • High accuracy of SMRT sequencing ensures reliable variant calling.

    Key Insights:

    • SMRT sequencing is a powerful tool for small genome sequencing.
    • Its long reads facilitate the complete assembly of complex genomes.
    • Modified base detection adds another layer of biological insight.

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    Published on: August 4, 2016

    Outlook:

    • Further adoption of SMRT sequencing for small genome projects is anticipated.
    • Integration of SMRT data with other NGS platforms may enhance genomic analyses.
    • Continued technological advancements will likely expand SMRT sequencing applications.