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XMRF: an R package to fit Markov Networks to high-throughput genetics data
BACKGROUND: Technological advances in medicine have led to a rapid proliferation of high-throughput “omics” data. Tools to mine this data and discover disrupted disease networks are needed as they hold the key to understanding complicated interactions between genes, mutations and aberrations, and ep...
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| Publicat a: | BMC Syst Biol |
|---|---|
| Autors principals: | , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2016
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5009817/ https://ncbi.nlm.nih.gov/pubmed/27586041 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12918-016-0313-0 |
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