Pages that link to "Item:Q458185"

The following pages link to Modeling read counts for CNV detection in exome sequencing data (Q458185):

Displaying 3 items.

• MGP-HMM: detecting genome-wide CNVs using an HMM for modeling mate pair insertion sizes and read counts (Q312518) (← links)
• The number of candidate variants in exome sequencing for Mendelian disease under no genetic heterogeneity (Q382543) (← links)
• Modeling the next generation sequencing read count data for DNA copy number variant study (Q906234) (← links)