Multiple samples aCGH analysis for rare CNVs detection

BACKGROUND: DNA copy number variations (CNV) constitute an important source of genetic variability. The standard method used for CNV detection is array comparative genomic hybridization (aCGH). RESULTS: We propose a novel multiple sample aCGH analysis methodology aiming in rare CNVs detection. In co...

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Detalles Bibliográficos
Autores principales: Sykulski, Maciej, Gambin, Tomasz, Bartnik, Magdalena, Derwińska, Katarzyna, Wiśniowiecka-Kowalnik, Barbara, Stankiewicz, Paweł, Gambin, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3691624/
https://www.ncbi.nlm.nih.gov/pubmed/23758813
http://dx.doi.org/10.1186/2043-9113-3-12

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3691624/
https://www.ncbi.nlm.nih.gov/pubmed/23758813
http://dx.doi.org/10.1186/2043-9113-3-12

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