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Related Concept Videos

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...
Ribosomal RNA Synthesis02:53

Ribosomal RNA Synthesis

Ribosome synthesis is a highly complex and coordinated process involving more than 200 assembly factors. The synthesis and processing of ribosomal components occurs not only in the nucleolus but also in the nucleoplasm and the cytoplasm of eukaryotic cells.
Ribosome biogenesis begins with the synthesis of 5S and 45S pre-rRNAs by distinct RNA polymerases. The primary transcripts are extensively processed and modified before they are bound and folded by ribosomal proteins and assembly factors,...
Ribosomal RNA Synthesis02:53

Ribosomal RNA Synthesis

Ribosome synthesis is a highly complex and coordinated process involving more than 200 assembly factors. The synthesis and processing of ribosomal components occurs not only in the nucleolus but also in the nucleoplasm and the cytoplasm of eukaryotic cells.
Ribosome biogenesis begins with the synthesis of 5S and 45S pre-rRNAs by distinct RNA polymerases. The primary transcripts are extensively processed and modified before they are bound and folded by ribosomal proteins and assembly factors,...
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...
Improving Translational Accuracy02:07

Improving Translational Accuracy

Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
Protein Folding Quality Check in the RER01:29

Protein Folding Quality Check in the RER

ER is the primary site for the maturation and folding of soluble and transmembrane secretory proteins. The calnexin cycle is a specific chaperone system that folds and assesses the confirmation of N-glycosylated proteins before they can exit the ER lumen. The primary players of this quality check pipeline are the lectins, ER-resident chaperones, and a glucosyl transferase enzyme. In case the calnexin system in the lumen fails to salvage a misfolded protein, it is transported to the cytoplasm...

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Updated: Jun 28, 2026

De novo Identification of Actively Translated Open Reading Frames with Ribosome Profiling Data
08:23

De novo Identification of Actively Translated Open Reading Frames with Ribosome Profiling Data

Published on: February 18, 2022

The Ribosomal Database Project: improved alignments and new tools for rRNA analysis.

J R Cole1, Q Wang, E Cardenas

  • 1Center for Microbial Ecology and Department of Microbiology and Molecular Genetics, Michigan State University, East Lansing, MI 48824, USA. colej@msu.edu

Nucleic Acids Research
|November 14, 2008
PubMed
Summary
This summary is machine-generated.

The Ribosomal Database Project (RDP) now offers enhanced bacterial and archaeal small subunit rRNA analysis tools. New features improve alignment quality, streamline ultra-high-throughput sequencing data processing, and aid taxonomic and instructional tasks.

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Global Identification of Co-Translational Interaction Networks by Selective Ribosome Profiling
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Global Identification of Co-Translational Interaction Networks by Selective Ribosome Profiling

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De novo Identification of Actively Translated Open Reading Frames with Ribosome Profiling Data
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Global Identification of Co-Translational Interaction Networks by Selective Ribosome Profiling
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Global Identification of Co-Translational Interaction Networks by Selective Ribosome Profiling

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Area of Science:

  • Microbiology
  • Bioinformatics
  • Computational Biology

Background:

  • The Ribosomal Database Project (RDP) is a crucial resource for bacterial and archaeal small subunit ribosomal RNA (rRNA) sequence data.
  • Accurate rRNA alignments and analysis tools are essential for microbial ecology and evolutionary studies.
  • Existing tools required improvements in alignment quality and processing of large datasets.

Purpose of the Study:

  • To enhance the Ribosomal Database Project (RDP) with improved alignment strategies and new analysis tools.
  • To facilitate the analysis of ultra-high-throughput rRNA sequencing data.
  • To provide better tools for taxonomic assignment and educational purposes.

Main Methods:

  • Implemented Infernal, a secondary structure-aware aligner, for improved rRNA sequence alignment.
  • Developed a new Pyrosequencing Pipeline to automate and simplify the analysis of large rRNA sequencing libraries.
  • Introduced Taxomatic for visualizing taxonomic inconsistencies and a class Assignment Generator for instructors.

Main Results:

  • Achieved higher quality and more consistent rRNA alignments with faster processing.
  • Enabled automated data processing for ultra-high-throughput sequencing, reducing computational intensity.
  • Provided tools for rapid taxonomic error detection and correction, alongside customizable educational materials.

Conclusions:

  • The enhanced RDP offers significantly improved capabilities for analyzing bacterial and archaeal rRNA data.
  • New tools streamline complex analyses, making high-throughput sequencing data more accessible.
  • The RDP continues to be a vital resource, now with expanded functionality for research and education.