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Using hierarchical similarity to examine the genetics of Behçet’s disease

OBJECTIVE: Behçet’s disease (BD) is a multisystem inflammatory disease that affects patients along the historic silk road. Thus far, the pathogenesis of the disease has proved elusive due to the complex genetic interactions of the disease. In this paper, we seek to clarify the genetic factors of the...

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Detalles Bibliográficos
Autores principales: Shenoi, Samuel J., Baker, Erich J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8434716/
https://www.ncbi.nlm.nih.gov/pubmed/34507623
http://dx.doi.org/10.1186/s13104-021-05767-6
Descripción
Sumario:OBJECTIVE: Behçet’s disease (BD) is a multisystem inflammatory disease that affects patients along the historic silk road. Thus far, the pathogenesis of the disease has proved elusive due to the complex genetic interactions of the disease. In this paper, we seek to clarify the genetic factors of the disease while also uncovering other diseases of interest that present with a similar genotype as BD. RESULTS: To do this, we employ a convergent functional genomics approach by leveraging the hierarchical similarity tool available in Geneweaver. Through our analysis, we were able to ascertain 7 BD consensus genes and 16 autoimmune diseases with genetic overlap with BD. The results of our study will inform further research into the pathogenesis of Behçet’s disease. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13104-021-05767-6.