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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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| Huvudupphovsmän: | , , , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Oxford University Press
2012
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| 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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