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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Vydáno v:BMC Syst Biol
Hlavní autoři: Wan, Ying-Wooi, Allen, Genevera I., Baker, Yulia, Yang, Eunho, Ravikumar, Pradeep, Anderson, Matthew, Liu, Zhandong
Médium: Artigo
Jazyk:Inglês
Vydáno: BioMed Central 2016
Témata:
Research
On-line přístup: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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