Pages that link to "Item:Q5130271"

The following pages link to An online copy number variant detection method for short sequencing reads (Q5130271):

Displaying 7 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)
• Modeling the next generation sequencing read count data for DNA copy number variant study (Q906234) (← 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)
• Indels detection algorithm based on optimal split-read matching (Q3175576) (← links)
• Robust Detection and Identification of Sparse Segments in Ultrahigh Dimensional Data Analysis (Q5743146) (← links)