A bootstrap-based approach to integrate multiple forms of high dimensional genomic data with multiple clinical endpoints. This method is used to find clinically meaningful groups of genomic features, such as genes or pathways. A manuscript describing this method is in preparation.
Version: 1.1.0 Depends: R (≥ 2.10) Imports: dplyr, ggmosaic, ggplot2, ggpubr, logistf, magrittr, MASS, purrr, rlist, stats, stringr, survival, survminer Suggests: rmarkdown Published: 2024-07-27 DOI: 10.32614/CRAN.package.BEAMR Author: Anna Eames Seffernick [aut, cre, cph], Stanley Pounds [aut], Xueyuan Cao [aut] Maintainer: Anna Eames Seffernick <anna.seffernick at stjude.org> BugReports: https://github.com/annaSeffernick/BEAMR/issues License: GPL (≥ 3) URL: https://annaseffernick.github.io/BEAMR/, https://github.com/annaSeffernick/BEAMR NeedsCompilation: no Materials: README NEWS CRAN checks: BEAMR results Documentation: Downloads: Linking:Please use the canonical form https://CRAN.R-project.org/package=BEAMR to link to this page.
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