Pages that link to "Item:Q3011149"
From MaRDI portal
The following pages link to False discovery rates and copy number variation (Q3011149):
Displaying 10 items.
- Multiple Testing of Local Extrema for Detection of Change Points (Q143270) (← links)
- FDR-control in multiscale change-point segmentation (Q153065) (← links)
- Finding causative genes from high-dimensional data: an appraisal of statistical and machine learning approaches (Q309421) (← links)
- Optimal detection of multi-sample aligned sparse signals (Q888496) (← links)
- A scoring criterion for rejection of clustered \(p\)-values (Q1662188) (← links)
- A double application of the Benjamini-Hochberg procedure for testing batched hypotheses (Q2397957) (← links)
- Sequential model selection-based segmentation to detect DNA copy number variation (Q2827192) (← links)
- Detecting Genomic Aberrations Using Products in a Multiscale Analysis (Q3064252) (← links)
- A multilevel model to address batch effects in copy number estimation using SNP arrays (Q3303648) (← links)
- Simultaneous discovery of rare and common segment variants (Q5411020) (← links)
