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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...
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Genome Annotation and Assembly

The genome refers to all of the genetic material in an organism. It can range from a few million base pairs in microbial cells to several billion base pairs in many eukaryotic organisms. Genome assembly refers to the process of taking the DNA sequencing data and putting it all back together in a correct order to create a close representation of the original genome. This is followed by the identification of functional elements on the newly assembled genome, a process called genome annotation.
RACE - Rapid Amplification of cDNA Ends02:35

RACE - Rapid Amplification of cDNA Ends

Rapid Amplification of cDNA Ends, or RACE, is one of the most effective methods to obtain a full-length cDNA from an mRNA sequence between a known internal region to the unknown sequence at the 5’ or 3’ end. The unknown region is cloned in the cDNA by a gene-specific primer that binds the known end, and a hybrid primer that attaches a predefined anchor sequence to the unknown end of the cDNA. The sequence in between is amplified by PCR with an anchor primer and a gene-specific primer.
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Related Experiment Video

Updated: Jun 24, 2026

Informatic Analysis of Sequence Data from Batch Yeast 2-Hybrid Screens
09:14

Informatic Analysis of Sequence Data from Batch Yeast 2-Hybrid Screens

Published on: June 28, 2018

dCAS: a desktop application for cDNA sequence annotation.

Yongjian Guo1, Jose M C Ribeiro, Jennifer M Anderson

  • 1Bioinformatics and Computational Biosciences Branch, Office of Cyber Infrastructure and Computational Biology and Laboratory of Malaria and Vector Research, National Institute of Allergy and Infectious Diseases, Bethesda, MD 20892, USA. guoyo@mail.nih.gov

Bioinformatics (Oxford, England)
|March 26, 2009
PubMed
Summary

Desktop cDNA Annotation System (dCAS) is a new application for automated analysis of expressed sequence tags (ESTs). This tool simplifies gene expression studies by providing user-friendly sequence cleaning, clustering, assembly, and annotation on a personal computer.

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Introductory Analysis and Validation of CUT&RUN Sequencing Data
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Introductory Analysis and Validation of CUT&RUN Sequencing Data

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Informatic Analysis of Sequence Data from Batch Yeast 2-Hybrid Screens
09:14

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Published on: June 28, 2018

Introductory Analysis and Validation of CUT&RUN Sequencing Data
04:58

Introductory Analysis and Validation of CUT&RUN Sequencing Data

Published on: December 13, 2024

Area of Science:

  • Bioinformatics
  • Molecular Biology
  • Genomics

Background:

  • Gene regulation and expression are fundamental to biological advancement.
  • Expressed sequence tag (EST) sequence assembly and analysis offer valuable insights.
  • Existing tools may lack user-friendliness or comprehensive functionality.

Purpose of the Study:

  • To develop a user-friendly desktop application for automated EST analysis.
  • To provide biologists with a convenient tool for extracting biological meaning from sequence data.
  • To streamline the process of EST cleaning, clustering, assembly, and annotation.

Main Methods:

  • Development of a standalone desktop application named dCAS (Desktop cDNA Annotation System).
  • Implementation of automated workflows for EST data processing.
  • Provision of a cross-platform installer and associated sequence databases.

Main Results:

  • dCAS offers automated cleaning, clustering, assembly, and annotation of EST sequences.
  • The application is designed for operation on a desktop computer.
  • dCAS provides a more convenient and user-friendly solution compared to existing tools.

Conclusions:

  • dCAS facilitates the extraction of biological meaning from EST sequence data.
  • The application enhances the efficiency and accessibility of gene expression analysis for biologists.
  • dCAS represents a significant improvement in user-friendly bioinformatics tools for sequence analysis.