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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.
Package details |
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Author | Anna Eames Seffernick [aut, cre, cph] (<https://orcid.org/0000-0003-0848-4604>), Stanley Pounds [aut], Xueyuan Cao [aut] |
Maintainer | Anna Eames Seffernick <anna.seffernick@stjude.org> |
License | GPL (>= 3) |
Version | 1.1.0 |
URL | https://annaseffernick.github.io/BEAMR/ https://github.com/annaSeffernick/BEAMR |
Package repository | View on CRAN |
Installation |
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