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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.
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Identification of Alternative Splicing and Polyadenylation in RNA-seq Data
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TSSi--an R package for transcription start site identification from 5' mRNA tag data.

C Kreutz1, J S Gehring, D Lang

  • 1Institute for Physics, University of Freiburg, Germany. ckreutz@fdm.uni-freiburg.de

Bioinformatics (Oxford, England)
|April 20, 2012
PubMed
Summary

This study introduces TSSi, an R package for identifying transcription start sites (TSSs) using 5' mRNA tag sequencing data. It offers a robust framework to accurately pinpoint TSSs by modeling data distributions and errors.

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Transcription Start Site Mapping Using Super-low Input Carrier-CAGE
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Transcription Start Site Mapping Using Super-low Input Carrier-CAGE

Published on: June 26, 2019

Area of Science:

  • Genomics
  • Molecular Biology
  • Bioinformatics

Background:

  • High-throughput sequencing is crucial for studying transcriptional mechanisms.
  • Existing peak prediction methods are unsuitable for identifying transcription start sites (TSSs) due to distinct noise patterns in TSS data.
  • Accurate TSS identification is vital for understanding gene regulation.

Purpose of the Study:

  • To present the R package TSSi for heuristic identification of transcription start sites (TSSs).
  • To provide a framework adaptable to user-defined probabilistic assumptions for data distribution and systematic errors.
  • To offer a regularization procedure for noise reduction and improved TSS prediction accuracy.

Main Methods:

  • Development of the R package TSSi.
  • Utilizing 5' mRNA tag sequencing data for TSS identification.
  • Implementing a heuristic framework with probabilistic assumptions for data and error modeling.
  • Incorporating a regularization procedure for noise reduction.

Main Results:

  • The TSSi package provides a novel heuristic framework for TSS identification.
  • The framework allows user adaptation of probabilistic assumptions for data and error modeling.
  • A regularization procedure effectively reduces noise and minimizes false TSS predictions.
  • The package is available via Bioconductor.

Conclusions:

  • TSSi offers a specialized and adaptable solution for accurate transcription start site identification from 5' mRNA tag data.
  • The package enhances the analysis of transcriptional mechanisms by improving TSS prediction accuracy.
  • The heuristic framework and noise reduction capabilities make TSSi a valuable tool for researchers.