Pages that link to "Item:Q906234"
From MaRDI portal
The following pages link to Modeling the next generation sequencing read count data for DNA copy number variant study (Q906234):
Displaying 11 items.
- MGP-HMM: detecting genome-wide CNVs using an HMM for modeling mate pair insertion sizes and read counts (Q312518) (← links)
- Modeling read counts for CNV detection in exome sequencing data (Q458185) (← links)
- Single-sample SNP detection by empirical Bayes method using next-generation sequencing data (Q1747473) (← links)
- A penalized regression approach for DNA copy number study using the sequencing data (Q2325029) (← links)
- Car sequencing versus mixed-model sequencing: a computational study (Q2514809) (← links)
- A Statistical Change-Point Analysis Approach for Modeling the Ratio of Next Generation Sequencing Reads (Q2833043) (← links)
- Dynamic linear model for the identification of miRNAs in next-generation sequencing data (Q2893375) (← links)
- BM-map: Bayesian mapping of multireads for next-generation sequencing data (Q2893378) (← links)
- A modified information criterion for tuning parameter selection in 1d fused LASSO for inference on multiple change points (Q5107787) (← links)
- An online copy number variant detection method for short sequencing reads (Q5130271) (← links)
- Statistical method for modeling sequencing data from different technologies in longitudinal studies with application to Huntington disease (Q6071002) (← links)
