GenomeCAT: a versatile tool for the analysis and integrative visualization of DNA copy number variants

BACKGROUND: The analysis of DNA copy number variants (CNV) has increasing impact in the field of genetic diagnostics and research. However, the interpretation of CNV data derived from high resolution array CGH or NGS platforms is complicated by the considerable variability of the human genome. There...

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Detalles Bibliográficos
Autores principales: Tebel, Katrin, Boldt, Vivien, Steininger, Anne, Port, Matthias, Ebert, Grit, Ullmann, Reinhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217618/
https://www.ncbi.nlm.nih.gov/pubmed/28061750
http://dx.doi.org/10.1186/s12859-016-1430-x

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5217618/
https://www.ncbi.nlm.nih.gov/pubmed/28061750
http://dx.doi.org/10.1186/s12859-016-1430-x

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