Inferring human miRNA–disease associations via multiple kernel fusion on GCNII

Increasing evidence shows that the occurrence of human complex diseases is closely related to the mutation and abnormal expression of microRNAs(miRNAs). MiRNAs have complex and fine regulatory mechanisms, which makes it a promising target for drug discovery and disease diagnosis. Therefore, predicti...

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Detalles Bibliográficos
Autores principales: Lu, Shanghui, Liang, Yong, Li, Le, Liao, Shuilin, Ouyang, Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483142/
https://www.ncbi.nlm.nih.gov/pubmed/36134032
http://dx.doi.org/10.3389/fgene.2022.980497

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9483142/
https://www.ncbi.nlm.nih.gov/pubmed/36134032
http://dx.doi.org/10.3389/fgene.2022.980497

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