Package: cn.mops 1.51.0
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Gundula Povysil
cn.mops: cn.mops - Mixture of Poissons for CNV detection in NGS data
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++.
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cn.mops.pdf |cn.mops.html✨
cn.mops/json (API)
# Install 'cn.mops' in R: |
install.packages('cn.mops', repos = c('https://bioc.r-universe.dev', 'https://cloud.r-project.org')) |
- CNVRanges - Genomic locations and indices of the simulated CNVs.
- X - A simulated data set for CNV detection from NGS data.
- XRanges - A simulated data set for CNV detection from NGS data.
- exomeCounts - Read counts from exome sequencing for CNV detection
On BioConductor:cn.mops-1.51.0(bioc 3.20)cn.mops-1.50.0(bioc 3.19)
This package does not link to any Github/Gitlab/R-forge repository. No issue tracker or development information is available.
Last updated 2 months agofrom:ee78d2ead0
Exports:calcFractionalCopyNumberscalcIntegerCopyNumberscn.mopscnvrcnvsexomecn.mopsgetReadCountsFromBAMgetSegmentReadCountsFromBAMgrhaplocn.mopsindividualCalliniCallintegerCopyNumberlocalAssessmentsmakeRobustCNVRnormalizeChromosomesnormalizedDatanormalizeGenomeparamsposteriorProbsreferencecn.mopssampleNamessegmentsegmentationsegplotshowsinglecn.mops
Dependencies:askpassBHBiobaseBiocGenericsBiocParallelBiostringsbitopscodetoolscpp11crayoncurlformatRfutile.loggerfutile.optionsGenomeInfoDbGenomeInfoDbDataGenomicRangeshttrIRangesjsonlitelambda.rmimeopensslR6RhtslibRsamtoolsS4VectorssnowsysUCSC.utilsXVectorzlibbioc