CNVRanges


      This data set gives the starts, ends, and the integer copy number of the
      simulated CNVs in the data set <code><a rd-options="" href="/link/XRanges?package=cn.mops&version=1.18.0" data-mini-rdoc="cn.mops::XRanges">XRanges</a></code> object.

datasets

cn.mops (Copy Number estimation by a Mixture Of PoissonS)
is a data processing pipeline for copy number variations and
aberrations (CNVs and CNAs) from next generation sequencing
(NGS) data. The package supplies functions to convert BAM files
into read count matrices or genomic ranges objects, which are
the input objects for cn.mops. cn.mops models the depths of
coverage across samples at each genomic position. Therefore, it
does not suffer from read count biases along chromosomes. Using
a Bayesian approach, cn.mops decomposes read variations across
samples into integer copy numbers and noise by its mixture
components and Poisson distributions, respectively. cn.mops
guarantees a low FDR because wrong detections are indicated by
high noise and filtered out. cn.mops is very fast and written
in C++.

Guenter Klambauer

cn.mops

cn.mops - Mixture of Poissons for CNV detection in NGS data

CNVRanges function

A GRanges object with 20 rows and 40 value columns across 1 space.

Format

http://www.bioinf.jku.at/cnmops/cnmops.html.

Source


      This data set gives the starts, ends, and the integer copy number of the
      simulated CNVs in the data set <code><a rd-options='' href='XRanges'>XRanges</a></code> object.

CNVRanges: Genomic locations and indices of the simulated CNVs.

Description

Usage

Arguments

Format

Source

References