dSimer

dSimer computes disease-disease similarity using nine methods to quantify relationships among diseases for genomics and molecular biology research.


Key Features:

  • Nine similarity methods: Implements nine distinct methods for computing disease-disease similarity.
  • Standard cosine similarity: Includes a cosine similarity measure for vector-space comparison of disease feature vectors.
  • Function-based methods: Provides eight function-based methods to capture different biological dimensions of disease relationships.
  • Visualization: Produces heatmaps and network representations of disease similarity results.
  • Biological data integration: Integrates with extensive biological datasets commonly used in disease-disease association studies.

Scientific Applications:

  • Disease association studies: Quantifies and visualizes similarities to identify potential genetic or environmental links between diseases.
  • Interdisciplinary research: Facilitates analyses that combine genomic, molecular, and other biological data through statistical methods and visualizations.
  • Software development within Bioconductor: Supports interoperability and package-based development workflows in the Bioconductor ecosystem.

Methodology:

Implemented in the R programming language and distributed as a Bioconductor package; follows Bioconductor standards including package interoperability, formal initial review, and automated testing.

Topics

Collections

Details

License:
GPL-2.0
Tool Type:
command-line tool, library
Operating Systems:
Linux, Windows, Mac
Programming Languages:
R
Added:
1/17/2017
Last Updated:
11/25/2024

Operations

Publications

Huber W, Carey VJ, Gentleman R, Anders S, Carlson M, Carvalho BS, Bravo HC, Davis S, Gatto L, Girke T, Gottardo R, Hahne F, Hansen KD, Irizarry RA, Lawrence M, Love MI, MacDonald J, Obenchain V, Oleś AK, Pagès H, Reyes A, Shannon P, Smyth GK, Tenenbaum D, Waldron L, Morgan M. Orchestrating high-throughput genomic analysis with Bioconductor. Nature Methods. 2015;12(2):115-121. doi:10.1038/nmeth.3252. PMID:25633503. PMCID:PMC4509590.

Documentation

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