Design and validation of an oligonucleotide microarray for the detection of genomic rearrangements associated with common hereditary cancer syndromes

BACKGROUND: Conventional Sanger sequencing reliably detects the majority of genetic mutations associated with hereditary cancers, such as single-base changes and small insertions or deletions. However, detection of genomic rearrangements, such as large deletions and duplications, requires special te...

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Detalles Bibliográficos
Autores principales: Mancini-DiNardo, Debora, Judkins, Thaddeus, Woolstenhulme, Nick, Burton, Collin, Schoenberger, Jeremy, Ryder, Matthew, Murray, Adam, Gutin, Natalia, Theisen, Aaron, Holladay, Jayson, Craft, Jonathan, Arnell, Christopher, Moyes, Kelsey, Roa, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4174268/
https://www.ncbi.nlm.nih.gov/pubmed/25204323
http://dx.doi.org/10.1186/s13046-014-0074-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4174268/
https://www.ncbi.nlm.nih.gov/pubmed/25204323
http://dx.doi.org/10.1186/s13046-014-0074-9

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