Simpute: An Efficient Solution for Dense Genotypic Data

Single nucleotide polymorphism (SNP) data derived from array-based technology or massive parallel sequencing are often flawed with missing data. Missing SNPs can bias the results of association analyses. To maximize information usage, imputation is often adopted to compensate for the missing data by...

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Detalles Bibliográficos
Autores principales: Lin, Yen-Jen, Chang, Chun-Tien, Tang, Chuan Yi, Hsieh, Wen-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3581137/
https://www.ncbi.nlm.nih.gov/pubmed/23509783
http://dx.doi.org/10.1155/2013/813912

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3581137/
https://www.ncbi.nlm.nih.gov/pubmed/23509783
http://dx.doi.org/10.1155/2013/813912

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