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Co-clustering phenome–genome for phenotype classification and disease gene discovery

Understanding the categorization of human diseases is critical for reliably identifying disease causal genes. Recently, genome-wide studies of abnormal chromosomal locations related to diseases have mapped >2000 phenotype–gene relations, which provide valuable information for classifying diseases...

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Bibliografiska uppgifter
Huvudupphovsmän: Hwang, TaeHyun, Atluri, Gowtham, Xie, MaoQiang, Dey, Sanjoy, Hong, Changjin, Kumar, Vipin, Kuang, Rui
Materialtyp: Artigo
Språk:Inglês
Publicerad: Oxford University Press 2012
Ämnen:
Länkar:https://ncbi.nlm.nih.gov/pmc/articles/PMC3479160/
https://ncbi.nlm.nih.gov/pubmed/22735708
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gks615
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