CoNVaQ: a web tool for copy number variation-based association studies

CoNVaQ: a web tool for copy number variation-based association studies

Abstract Background Copy number variations (CNVs) are large segments of the genome that are duplicated or deleted. Structural variations in the genome have been linked to many complex diseases. Similar to how genome-wide association studies (GWAS) have helped discover single-nucleotide polymorphisms...

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Bibliographic Details
Main Authors: Simon Jonas Larsen, Luisa Matos do Canto, Silvia Regina Rogatto, Jan Baumbach
Format: Article
Language:English
Published: BioMed Central 2018-05-01
Series:BMC Genomics
Subjects:
Copy number variation
Association studies
Online Access:http://link.springer.com/article/10.1186/s12864-018-4732-8

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http://link.springer.com/article/10.1186/s12864-018-4732-8

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