snr

snr provides visual analytics for exploration and interpretation of large-scale RNA-Seq data generated by Next-Generation Sequencing (NGS).


Key Features:

  • Visual analytics: Analytical visualization for exploration and pattern identification in complex RNA-Seq datasets.
  • Integration with public repositories: Contextualization of experimental RNA-Seq data by comparing with profiles from ArrayExpress and other public sources.
  • Data querying and extraction: Retrieval and extraction of datasets that share similar gene expression signatures for comparative analysis.
  • Scalability for differential expression profiles: Capability to operate on large collections of RNA-Seq differential expression profiles.

Scientific Applications:

  • Exploration of differential expression profiles: Analysis of large RNA-Seq differential expression collections, demonstrated on 1,543 mouse profiles from ArrayExpress.
  • Hypothesis generation: Comparative analyses with public RNA-Seq profiles to support formulation of novel molecular hypotheses.

Methodology:

snr applies visual analytics combined with integration of external RNA-Seq repositories to transform, query, and compare large-scale RNA-Seq differential expression data.

Topics

Details

License:
MIT
Maturity:
Mature
Cost:
Free of charge
Tool Type:
command-line tool
Operating Systems:
Linux, Windows, Mac
Programming Languages:
R, JavaScript
Added:
5/22/2019
Last Updated:
6/16/2020

Operations

Publications

Klemm P, Frommolt P, Kornfeld J. s·nr: a visual analytics framework for contextual analyses of private and public RNA-seq data. BMC Genomics. 2019;20(1). doi:10.1186/s12864-018-5396-0. PMID:30678634. PMCID:PMC6346532.

PMID: 30678634
PMCID: PMC6346532
Funding: - Deutsche Forschungsgemeinschaft: KO4728/1.1 - European Research Council: 675014