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

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 linked...

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Detalles Bibliográficos
Autores principales: Larsen, Simon Jonas, do Canto, Luisa Matos, Rogatto, Silvia Regina, Baumbach, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960125/
https://www.ncbi.nlm.nih.gov/pubmed/29776329
http://dx.doi.org/10.1186/s12864-018-4732-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960125/
https://www.ncbi.nlm.nih.gov/pubmed/29776329
http://dx.doi.org/10.1186/s12864-018-4732-8

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