Genomic copy number variation analysis in multiple system atrophy

Genomic copy number variation analysis in multiple system atrophy

Abstract Genomic variation includes single-nucleotide variants, small insertions or deletions (indels), and copy number variants (CNVs). CNVs affect gene expression by altering the genome structure and transposable elements within a region. CNVs are greater than 1 kb in size; hence, CNVs can produce...

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Bibliographic Details
Main Authors: Yuka Hama, Masataka Katsu, Ichigaku Takigawa, Ichiro Yabe, Masaaki Matsushima, Ikuko Takahashi, Takayuki Katayama, Jun Utsumi, Hidenao Sasaki
Format: Article
Language:English
Published: BMC 2017-11-01
Series:Molecular Brain
Subjects:
Genomic DNA
Copy number variation
Multiple system atrophy
Array-comparative genome hybridization
Online Access:http://link.springer.com/article/10.1186/s13041-017-0335-6

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http://link.springer.com/article/10.1186/s13041-017-0335-6

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