Cargando…
Accuracy of CNV Detection from GWAS Data
Several computer programs are available for detecting copy number variants (CNVs) using genome-wide SNP arrays. We evaluated the performance of four CNV detection software suites—Birdsuite, Partek, HelixTree, and PennCNV-Affy—in the identification of both rare and common CNVs. Each program's pe...
Autores principales: | Zhang, Dandan, Qian, Yudong, Akula, Nirmala, Alliey-Rodriguez, Ney, Tang, Jinsong, Gershon, Elliot S., Liu, Chunyu |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3020939/ https://www.ncbi.nlm.nih.gov/pubmed/21249187 http://dx.doi.org/10.1371/journal.pone.0014511 |
Ejemplares similares
-
GWAS Significance Thresholds for Deep Phenotyping Studies Can Depend Upon Minor Allele Frequencies and Sample Size
por: Asif, Huma, et al.
Publicado: (2020) -
Ethical and public policy challenges for pharmacogenomics
por: Gershon, Elliot S., et al.
Publicado: (2014) -
Finding Predictors of Leg Defects in Pigs Using CNV-GWAS
por: Getmantseva, Lyubov, et al.
Publicado: (2023) -
A rare mutation of CACNA1C in a patient with Bipolar disorder, and decreased gene expression associated with a Bipolar-associated common SNP of CACNA1C in brain
por: Gershon, Elliot S., et al.
Publicado: (2013) -
Ximmer: a system for improving accuracy and consistency of CNV calling from exome data
por: Sadedin, Simon P, et al.
Publicado: (2018)