SubPatCNV: approximate subspace pattern mining for mapping copy-number variations

BACKGROUND: Many DNA copy-number variations (CNVs) are known to lead to phenotypic variations and pathogenesis. While CNVs are often only common in a small number of samples in the studied population or patient cohort, previous work has not focused on customized identification of CNV regions that on...

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Detalles Bibliográficos
Autores principales: Johnson, Nicholas, Zhang, Huanan, Fang, Gang, Kumar, Vipin, Kuang, Rui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Software
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4305219/
https://www.ncbi.nlm.nih.gov/pubmed/25591662
http://dx.doi.org/10.1186/s12859-014-0426-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4305219/
https://www.ncbi.nlm.nih.gov/pubmed/25591662
http://dx.doi.org/10.1186/s12859-014-0426-7

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