MLSeq

MLSeq applies Support Vector Machines (SVM), bagged SVMs, Random Forest, and Classification And Regression Trees (CART) to analyze RNA-Seq data for classification, regression, and discovery of genomic features.


Key Features:

  • Machine Learning Integration: Integrates Support Vector Machines (SVM), bagged SVMs, Random Forest, and Classification And Regression Trees (CART) for classification and regression of RNA-Seq datasets.
  • Interoperability with Bioconductor: Integrates with the Bioconductor ecosystem in R to enable interaction with other Bioconductor packages.
  • Community-Driven Development: Part of the community-driven Bioconductor project comprising 934 interoperable packages and subject to formal review and automated testing.

Scientific Applications:

  • Genomic Data Analysis: Performs classification and pattern discovery on high-throughput RNA-Seq genomic datasets.
  • Interdisciplinary Research: Applies machine learning methods to genomics to support basic biological questions and applied biomedical research.

Methodology:

Applies Support Vector Machines (SVM), bagged SVMs, Random Forest, and Classification And Regression Trees (CART) to RNA-Seq data for classification and regression analyses.

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

Downloads