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Heat*seq: an interactive web tool for high-throughput sequencing experiment comparison with public data.

Guillaume Devailly1, Anna Mantsoki1, Anagha Joshi1

  • 1Department of Developmental Biology, The Roslin Institute, University of Edinburgh, Easter Bush Campus, Midlothian EH25 9RG, UK.

Bioinformatics (Oxford, England)
|July 6, 2016
PubMed
Summary
This summary is machine-generated.

Heat*seq is a new web tool enabling genome-wide comparison of high-throughput sequencing data, such as ChIP-seq and RNA-seq, against public domain experiments. This tool aids researchers lacking bioinformatics expertise in contextualizing their findings.

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Area of Science:

  • Genomics
  • Bioinformatics
  • Computational Biology

Background:

  • High-throughput sequencing experiments (e.g., ChIP-seq, RNA-seq) are increasingly accessible to smaller labs.
  • Comparing individual lab experiments to vast public domain data is challenging due to bioinformatics expertise limitations.
  • Existing tools offer gene-level comparisons but lack a genome-wide perspective.

Purpose of the Study:

  • To develop a web-based tool, Heat*seq, for genome-scale comparison of user-submitted high-throughput sequencing data against public domain repositories.
  • To provide researchers with a tool for contextualizing their experimental results within a broader genomic landscape.

Main Methods:

  • Development of Heat*seq, a web-tool facilitating genome-wide comparisons.
  • Integration of diverse high-throughput sequencing data types: chromatin immunoprecipitation followed by sequencing (ChIP-seq), RNA-sequencing (RNA-seq), and Cap Analysis of Gene Expression (CAGE).
  • Inclusion of over 12,000 public domain experiments across human, mouse, and Drosophila species.
  • Implementation of interactive correlation heatmaps with dynamic data subsetting capabilities.

Main Results:

  • Heat*seq enables genome-wide comparison of user experiments with public data.
  • The tool provides interactive correlation heatmaps for visualizing relationships between datasets.
  • Users can dynamically subset datasets to contextualize their experiments effectively.
  • High-quality figures and tables are generated and downloadable in multiple formats.

Conclusions:

  • Heat*seq addresses the need for accessible, genome-wide comparison of high-throughput sequencing data.
  • The tool empowers researchers, particularly those with limited bioinformatics expertise, to leverage public domain data.
  • Heat*seq facilitates deeper insights by enabling contextualization of experimental results within a large-scale genomic framework.