CNVRanger: association analysis of CNVs with gene expression and quantitative phenotypes

SUMMARY: Copy number variation (CNV) is a major type of structural genomic variation that is increasingly studied across different species for association with diseases and production traits. Established protocols for experimental detection and computational inference of CNVs from SNP array and next...

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Detalles Bibliográficos
Autores principales: da Silva, Vinicius, Ramos, Marcel, Groenen, Martien, Crooijmans, Richard, Johansson, Anna, Regitano, Luciana, Coutinho, Luiz, Zimmer, Ralf, Waldron, Levi, Geistlinger, Ludwig
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Applications Note
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887538/
https://www.ncbi.nlm.nih.gov/pubmed/31392308
http://dx.doi.org/10.1093/bioinformatics/btz632

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9887538/
https://www.ncbi.nlm.nih.gov/pubmed/31392308
http://dx.doi.org/10.1093/bioinformatics/btz632

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