fcgr3bMXL

allGroups

bamFiles

copynumberGroups

objectCNVrd2

readCountMatrix

resultSegment

.Random.seed


This data set includes: segmentation results &#147;resultSegment&#148;,
information copy number &#147;copynumberGroups&#148; of <em>FCGR3B</em> gene.


datasets

CNVrd2 uses next-generation sequencing data to measure human gene copy number for multiple samples,
indentify SNPs tagging copy number variants and detect copy
number polymorphic genomic regions.

Hoang Tan Nguyen

CNVrd2

CNVrd2: a read depth-based method to detect and genotype complex common copy number variants from next generation sequencing data.

fcgr3bMXL function

All results analysed by the CNVrd2 package.

Format

This data set includes: segmentation results <dQuote>resultSegment</dQuote>,
information copy number <dQuote>copynumberGroups</dQuote> of <em>FCGR3B</em> gene.

fcgr3bMXL: MXL population data (The 1000 Genomes Project)

Description

Usage

Arguments

Format

References