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Disease gene identification by random walk on multigraphs merging heterogeneous genomic and phenotype data
BACKGROUND: High throughput experiments resulted in many genomic datasets and hundreds of candidate disease genes. To discover the real disease genes from a set of candidate genes, computational methods have been proposed and worked on various types of genomic data sources. As a single source of gen...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3521411/ https://www.ncbi.nlm.nih.gov/pubmed/23282070 http://dx.doi.org/10.1186/1471-2164-13-S7-S27 |