Laundering CNV data for candidate process prioritization in brain disorders

BACKGROUND: Prioritization of genomic data has become a useful tool for uncovering the phenotypic effect of genetic variations (e.g. copy number variations or CNV) and disease mechanisms. Due to the complexity, brain disorders represent a major focus of genomic research aimed at revealing pathologic...

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Detalles Bibliográficos
Autores principales: Zelenova, Maria A., Yurov, Yuri B., Vorsanova, Svetlana G., Iourov, Ivan Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Methodology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933640/
https://www.ncbi.nlm.nih.gov/pubmed/31890034
http://dx.doi.org/10.1186/s13039-019-0468-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6933640/
https://www.ncbi.nlm.nih.gov/pubmed/31890034
http://dx.doi.org/10.1186/s13039-019-0468-7

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