The following pages link to CNV-seq (Q29821):
Displaying 9 items.
- MGP-HMM: detecting genome-wide CNVs using an HMM for modeling mate pair insertion sizes and read counts (Q312518) (← links)
- Change-point model on nonhomogeneous Poisson processes with application in copy number profiling by next-generation DNA sequencing (Q439133) (← links)
- Modeling read counts for CNV detection in exome sequencing data (Q458185) (← links)
- Modeling the next generation sequencing read count data for DNA copy number variant study (Q906234) (← links)
- Modeling the evolution space of breakage fusion bridge cycles with a stochastic folding process (Q907112) (← links)
- A penalized regression approach for DNA copy number study using the sequencing data (Q2325029) (← links)
- A Statistical Change-Point Analysis Approach for Modeling the Ratio of Next Generation Sequencing Reads (Q2833043) (← links)
- An online copy number variant detection method for short sequencing reads (Q5130271) (← links)
- Beta approximation of ratio distribution and its application to next generation sequencing read counts (Q5138517) (← links)
