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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...
| Autores principales: | , , , , , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Oxford University Press
2019
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| Materias: | |
| 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 |