Rare variants analysis using penalization methods for whole genome sequence data

BACKGROUND: Availability of affordable and accessible whole genome sequencing for biomedical applications poses a number of statistical challenges and opportunities, particularly related to the analysis of rare variants and sparseness of the data. Although efforts have been devoted to address these...

Descripción completa

Detalles Bibliográficos
Autores principales: Yazdani, Akram, Yazdani, Azam, Boerwinkle, Eric
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670502/
https://www.ncbi.nlm.nih.gov/pubmed/26637205
http://dx.doi.org/10.1186/s12859-015-0825-4

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670502/
https://www.ncbi.nlm.nih.gov/pubmed/26637205
http://dx.doi.org/10.1186/s12859-015-0825-4

Ejemplares similares