SLMSuite: a suite of algorithms for segmenting genomic profiles

BACKGROUND: The identification of copy number variants (CNVs) is essential to study human genetic variation and to understand the genetic basis of mendelian disorders and cancers. At present, genome-wide detection of CNVs can be achieved using microarray or second generation sequencing (SGS) data. A...

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Detalles Bibliográficos
Autores principales: Orlandini, Valerio, Provenzano, Aldesia, Giglio, Sabrina, Magi, Alberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5490196/
https://www.ncbi.nlm.nih.gov/pubmed/28659129
http://dx.doi.org/10.1186/s12859-017-1734-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5490196/
https://www.ncbi.nlm.nih.gov/pubmed/28659129
http://dx.doi.org/10.1186/s12859-017-1734-5

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