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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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Shranjeno v:
Bibliografske podrobnosti
izdano v:Mol Cytogenet
Main Authors: Zelenova, Maria A., Yurov, Yuri B., Vorsanova, Svetlana G., Iourov, Ivan Y.
Format: Artigo
Jezik:Inglês
Izdano: BioMed Central 2019
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6933640/
https://ncbi.nlm.nih.gov/pubmed/31890034
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13039-019-0468-7
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