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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...

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Related Experiment Video

Updated: Jun 16, 2026

Cost-Efficient Transcriptomic-Based Drug Screening
06:40

Cost-Efficient Transcriptomic-Based Drug Screening

Published on: February 23, 2024

SeqTrim: a high-throughput pipeline for pre-processing any type of sequence read.

Juan Falgueras1, Antonio J Lara, Noé Fernández-Pozo

  • 1Departamento de Lenguajes y Ciencias de la Computación, Universidad de Málaga, Málaga, Spain.

BMC Bioinformatics
|January 22, 2010
PubMed
Summary

SeqTrim is an efficient pipeline for pre-processing DNA sequences, including next-generation sequencing data. It removes artefacts and improves sequence quality, outperforming other pre-processing tools.

Related Experiment Videos

Last Updated: Jun 16, 2026

Cost-Efficient Transcriptomic-Based Drug Screening
06:40

Cost-Efficient Transcriptomic-Based Drug Screening

Published on: February 23, 2024

Area of Science:

  • Bioinformatics
  • Genomics
  • Computational Biology

Background:

  • High-throughput sequencing generates vast amounts of data, necessitating high-quality and reliable sequences.
  • Database contamination from artefactual sequences is a growing concern, exacerbated by technologies like pyrosequencing.
  • Customizable pre-processing algorithms are essential for managing and ensuring the accuracy of sequencing data.

Purpose of the Study:

  • To develop and implement SeqTrim, an efficient pipeline for pre-processing diverse sequence reads.
  • To provide a configurable tool that identifies and removes various sequence artefacts.
  • To enhance sequence quality and reliability for downstream genomic analyses.

Main Methods:

  • SeqTrim integrates existing and novel algorithms for sequence pre-processing.
  • It identifies and removes low-quality, vector, adaptor, low complexity, and contaminant sequences.
  • The pipeline detects chimeric reads and sequence inserts, offering multiple input/output formats for workflow integration.

Main Results:

  • SeqTrim is available as a web and standalone command-line application.
  • It effectively removes artefacts without over-trimming, performing well across various library types (EST, SSH, genomic DNA) and pyrosequencing reads.
  • SeqTrim demonstrates superior performance compared to other pre-processing tools.

Conclusions:

  • SeqTrim is an efficient and configurable pipeline for pre-processing all types of sequence reads, including next-generation sequencing.
  • Its user-friendly interface allows detailed monitoring of pre-processing stages and individual sequence verification.
  • SeqTrim provides more comprehensive information and better artefact removal than existing pre-processors.