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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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Detalles Bibliográficos
Publicado en:BMC Syst Biol
Autores principales: Wan, Ying-Wooi, Allen, Genevera I., Baker, Yulia, Yang, Eunho, Ravikumar, Pradeep, Anderson, Matthew, Liu, Zhandong
Formato: Artigo
Lenguaje:Inglês
Publicado: BioMed Central 2016
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Acceso en línea: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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