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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.

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Related Experiment Video

Updated: Jun 12, 2026

DNA Sequence Recognition by DNA Primase Using High-Throughput Primase Profiling
08:04

DNA Sequence Recognition by DNA Primase Using High-Throughput Primase Profiling

Published on: October 8, 2019

WebPrInSeS: automated full-length clone sequence identification and verification using high-throughput sequencing

Andreas Massouras1, Frederik Decouttere, Korneel Hens

  • 1Laboratory of Systems Biology and Genetics, Institute of Bioengineering, School of Life Sciences, Ecole Polytechnique Fédérale de Lausanne, CH-1015 Lausanne, Switzerland.

Nucleic Acids Research
|May 27, 2010
PubMed
Summary
This summary is machine-generated.

WebPrInSeS is a new web server tool that uses high-throughput sequencing (HTS) data for automated clone sequence identification and verification. This cost-effective solution aids researchers in analyzing experimental libraries and screening results efficiently.

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Novel Sequence Discovery by Subtractive Genomics
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Last Updated: Jun 12, 2026

DNA Sequence Recognition by DNA Primase Using High-Throughput Primase Profiling
08:04

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Published on: October 8, 2019

G2-seq: A High Throughput Sequencing-based Technique for Identifying Late Replicating Regions of the Genome
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Published on: March 22, 2018

Novel Sequence Discovery by Subtractive Genomics
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Novel Sequence Discovery by Subtractive Genomics

Published on: January 25, 2019

Area of Science:

  • Genomics
  • Bioinformatics
  • Molecular Biology

Background:

  • High-throughput sequencing (HTS) offers rapid and cost-effective DNA sequencing.
  • Integrating HTS into experimental pipelines requires specialized software tools.
  • Automated analysis of sequencing data is crucial for large-scale biological studies.

Purpose of the Study:

  • To develop a web server tool, WebPrInSeS, for automated sequence identification and verification using HTS data.
  • To provide efficient solutions for analyzing open-reading frame (ORF) clone libraries and screening experiments.
  • To facilitate the incorporation of HTS data into diverse experimental workflows.

Main Methods:

  • WebPrInSeS consists of two applications: WebPrInSeS-C for clone library verification and WebPrInSeS-E for library screening analysis.
  • Both tools utilize de novo assembly algorithms to process HTS data.
  • The system supports HTS data from all three major sequencing platforms.

Main Results:

  • WebPrInSeS enables automated, full-length clone sequence identification and verification.
  • The tool efficiently processes user-defined ORF clone libraries.
  • WebPrInSeS successfully identifies positive hits in cDNA or ORF-based library screening experiments, such as yeast one- or two-hybrid assays.

Conclusions:

  • WebPrInSeS offers an integrated, cost-effective, and efficient solution for sequence verification and clone identification.
  • The web server tool simplifies the analysis of HTS data for researchers.
  • WebPrInSeS supports a wide range of applications in molecular biology and genomics research.