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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Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:BMC Syst Biol
Egile Nagusiak: Wan, Ying-Wooi, Allen, Genevera I., Baker, Yulia, Yang, Eunho, Ravikumar, Pradeep, Anderson, Matthew, Liu, Zhandong
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: BioMed Central 2016
Gaiak:
Research
Sarrera elektronikoa: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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