Simultaneous discovery of rare and common segment variants

DOI10.1093/BIOMET/ASS059zbMath1284.62658OpenAlexW2130974386WikidataQ41481404 ScholiaQ41481404MaRDI QIDQ5411020

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Publication date: 22 April 2014

Published in: Biometrika (Search for Journal in Brave)

Full work available at URL: http://europepmc.org/articles/pmc3696347

zbMATH Keywords

information poolingDNA copy number variantspopulation structural variants

Mathematics Subject Classification ID

Applications of statistics to biology and medical sciences; meta analysis (62P10) Medical applications (general) (92C50)

Related Items (12)

Scalable change-point and anomaly detection in cross-correlated data with an application to condition monitoring ⋮ A combined SR-CUSUM procedure for detecting common changes in panel data ⋮ Subset Multivariate Collective and Point Anomaly Detection ⋮ Univariate mean change point detection: penalization, CUSUM and optimality ⋮ Optimal detection of multi-sample aligned sparse signals ⋮ Collective Anomaly Detection in High-Dimensional Var Models ⋮ Maximum pairwise Bayes factors for covariance structure testing ⋮ Localising change points in piecewise polynomials of general degrees ⋮ Real Time Anomaly Detection And Categorisation ⋮ Sequential model selection-based segmentation to detect DNA copy number variation ⋮ Higher criticism: \(p\)-values and criticism ⋮ Higher criticism for large-scale inference, especially for rare and weak effects

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