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Results 1 - 10 of 12 found.
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segmentSeq : Methods for identifying small RNA loci from high-throughput sequencing data

Package: segmentSeq
Type: Package
Title: Methods for identifying small RNA loci from high-throughput
sequencing data
Version: 2.6.0
Date: 2010-01-20
Author: Thomas J. Hardcastle
Maintainer: Thomas J. Hardcastle <tjh48@cam.ac.uk>
Description: High-throughput sequencing technologies allow the production of large volumes of short sequences, which can be aligned to the genome to create a set of matches to the genome. By looking for regions of the genome which to which there are high densities of matches, we can infer a segmentation of the genome into regions of biological significance. The methods in this package allow the simultaneous segmentation of data from multiple samples, taking into account replicate data, in order to create a consensus segmentation. This has obvious applications in a number of classes of sequencing experiments, particularly in the discovery of small RNA loci and novel mRNA transcriptome discovery.
License: GPL-3
LazyLoad: yes
Depends: R (>= 2.3.0), methods, baySeq (>= 1.99.0), ShortRead,
GenomicRanges, IRanges, S4Vectors
Suggests: BiocStyle, BiocGenerics
Imports: graphics, grDevices, utils
biocViews: MultipleComparison, Sequencing, Alignment,
DifferentialExpression, QualityControl, DataImport
Packaged: 2016-05-04 04:02:57 UTC; biocbuild
NeedsCompilation: no

● Data Source: BioConductor
● BiocViews: Alignment, DataImport, DifferentialExpression, MultipleComparison, QualityControl, Sequencing
1 images, 25 functions, 1 datasets
● Reverse Depends: 0

systemPipeR : systemPipeR: NGS workflow and report generation environment

Package: systemPipeR
Type: Package
Title: systemPipeR: NGS workflow and report generation environment
Version: 1.6.2
Date: 2016-02-26
Author: Thomas Girke
Maintainer: Thomas Girke <thomas.girke@ucr.edu>
biocViews: Genetics, Infrastructure, DataImport, Sequencing, RNASeq,
RiboSeq, ChIPSeq, MethylSeq, SNP, GeneExpression, Coverage,
GeneSetEnrichment, Alignment, QualityControl
Description: R package for building and running automated end-to-end analysis workflows for a wide range of next generation sequence (NGS) applications such as RNA-Seq, ChIP-Seq, VAR-Seq and Ribo-Seq. Important features include a uniform workflow interface across different NGS applications, automated report generation, and support for running both R and command-line software, such as NGS aligners or peak/variant callers, on local computers or compute clusters. Efficient handling of complex sample sets and experimental designs is facilitated by a consistently implemented sample annotation infrastructure. Instructions for using systemPipeR are given in the Overview Vignette (HTML). The remaining Vignettes, linked below, are workflow templates for common NGS use cases.
Depends: Rsamtools, Biostrings, ShortRead, methods
Imports: BiocGenerics, GenomicRanges, GenomicFeatures,
SummarizedExperiment, VariantAnnotation, rjson, ggplot2, grid,
limma, edgeR, DESeq2, GOstats, GO.db, annotate, pheatmap,
BatchJobs
Suggests: ape, RUnit, BiocStyle, knitr, rmarkdown, biomaRt,
BiocParallel
VignetteBuilder: knitr
SystemRequirements: systemPipeR can be used to run external
command-line software (e.g. short read aligners), but the
corresponding tool needs to be installed on a system.
License: Artistic-2.0
URL: https://github.com/tgirke/systemPipeR
NeedsCompilation: no
Packaged: 2016-05-16 04:51:50 UTC; biocbuild

● Data Source: BioConductor
● BiocViews: Alignment, ChIPSeq, Coverage, DataImport, GeneExpression, GeneSetEnrichment, Genetics, Infrastructure, MethylSeq, QualityControl, RNASeq, RiboSeq, SNP, Sequencing
33 images, 39 functions, 0 datasets
● Reverse Depends: 0

rSFFreader : rSFFreader reads in sff files generated by Roche 454 and Life Sciences Ion Torrent sequencers

Package: rSFFreader
Type: Package
Title: rSFFreader reads in sff files generated by Roche 454 and Life
Sciences Ion Torrent sequencers
Version: 0.20.0
Date: 2011-10-02
Author: Matt Settles <mattsettles@gmail.com>, Sam Hunter, Brice Sarver,
Ilia Zhbannikov, Kyu-Chul Cho
Maintainer: Matt Settles <mattsettles@gmail.com>
Description: rSFFreader reads sequence, qualities and clip point values
from sff files generated by Roche 454 and Life Sciences Ion
Torrent sequencers into similar classes as are present for fastq files.
License: Artistic-2.0
Depends: ShortRead (>= 1.23.17)
Imports: methods, Biostrings, IRanges
Suggests: xtable
LinkingTo: S4Vectors, IRanges, XVector, Biostrings
Collate: allClasses.R allGenerics.R methods-Misc.R methods-SffHeader.R
methods-SffReads.R methods-SffReadsQ.R readSFF.R
biocViews: DataImport, Sequencing
NeedsCompilation: yes
Packaged: 2016-05-04 04:46:02 UTC; biocbuild

● Data Source: BioConductor
● BiocViews: DataImport, Sequencing
8 images, 11 functions, 0 datasets
● Reverse Depends: 0

HTSeqGenie : A NGS analysis pipeline.

Package: HTSeqGenie
Imports: BiocGenerics (>= 0.2.0), S4Vectors (>= 0.9.25), IRanges (>=
1.21.39), GenomicRanges (>= 1.23.21), Rsamtools (>= 1.8.5),
Biostrings (>= 2.24.1), chipseq (>= 1.6.1), hwriter (>= 1.3.0),
Cairo (>= 1.5.5), GenomicFeatures (>= 1.9.31), BiocParallel,
parallel, tools, rtracklayer (>= 1.17.19), GenomicAlignments,
VariantTools (>= 1.7.7), GenomeInfoDb, SummarizedExperiment,
methods
Maintainer: Jens Reeder <reeder.jens@gene.com>
License: Artistic-2.0
Title: A NGS analysis pipeline.
Type: Package
LazyLoad: yes
Author: Gregoire Pau, Jens Reeder
Description: Libraries to perform NGS analysis.
Version: 4.2.0
Depends: R (>= 3.0.0), gmapR (>= 1.8.0), ShortRead (>= 1.19.13),
VariantAnnotation (>= 1.8.3)
Suggests: TxDb.Hsapiens.UCSC.hg19.knownGene, LungCancerLines,
org.Hs.eg.db
RoxygenNote: 5.0.1
NeedsCompilation: no
Packaged: 2016-05-04 04:46:04 UTC; biocbuild

● Data Source: BioConductor
● 0 images, 129 functions, 0 datasets
● Reverse Depends: 0

Rolexa : Statistical analysis of Solexa sequencing data

Package: Rolexa
Type: Package
Title: Statistical analysis of Solexa sequencing data
Version: 1.27.0
Date: 2009-10-06
Author: Jacques Rougemont, Arnaud Amzallag, Christian Iseli, Laurent Farinelli, Ioannis Xenarios, Felix Naef
Maintainer: Jacques Rougemont <jacques.rougemont@epfl.ch>
Depends: R (>= 2.9.0), graphics, grDevices, methods, ShortRead
Imports: mclust, Biostrings, graphics, grDevices, IRanges, methods,
ShortRead, stats
Enhances: fork
Description: Provides probabilistic base calling, quality checks and diagnostic plots for Solexa sequencing data
License: GPL-2
biocViews: Sequencing, DataImport, Preprocessing, QualityControl
NeedsCompilation: no
Packaged: 2015-10-14 02:09:02 UTC; biocbuild

● Data Source: BioConductor
● BiocViews: DataImport, Preprocessing, QualityControl, Sequencing
● 0 images, 9 functions, 0 datasets
● Reverse Depends: 0

Rqc : Quality Control Tool for High-Throughput Sequencing Data

Package: Rqc
Type: Package
Title: Quality Control Tool for High-Throughput Sequencing Data
Version: 1.6.2
Author: Welliton Souza, Benilton Carvalho <beniltoncarvalho@gmail.com>
Maintainer: Welliton Souza <well309@gmail.com>
Description: Rqc is an optimised tool designed for quality control and
assessment of high-throughput sequencing data. It performs parallel
processing of entire files and produces a report which contains a set
of high-resolution graphics.
License: GPL (>= 2)
Depends: BiocParallel, ShortRead, ggplot2
Imports: BiocGenerics, Biostrings, IRanges, methods, S4Vectors, knitr
(>= 1.7), BiocStyle, plyr, markdown, grid, reshape2, digest,
Rcpp (>= 0.11.6), biovizBase, shiny, Rsamtools,
GenomicAlignments, GenomicFiles
LinkingTo: Rcpp
Suggests: testthat
VignetteBuilder: knitr
biocViews: Sequencing, QualityControl, DataImport
URL: https://github.com/labbcb/Rqc
RoxygenNote: 5.0.1
NeedsCompilation: yes
Packaged: 2016-05-16 05:02:37 UTC; biocbuild

● Data Source: BioConductor
● BiocViews: DataImport, QualityControl, Sequencing
13 images, 26 functions, 0 datasets
● Reverse Depends: 0

OTUbase : Provides structure and functions for the analysis of OTU data

Package: OTUbase
Type: Package
Title: Provides structure and functions for the analysis of OTU data
Description: Provides a platform for Operational Taxonomic Unit based
analysis
Version: 1.22.0
Date: 2010-09-10
Author: Daniel Beck, Matt Settles, and James A. Foster
Maintainer: Daniel Beck <danlbek@gmail.com>
Depends: R (>= 2.9.0), methods, S4Vectors, IRanges, ShortRead (>=
1.23.15), Biobase, vegan
Imports: Biostrings
License: Artistic-2.0
LazyLoad: yes
biocViews: Sequencing, DataImport
NeedsCompilation: no
Packaged: 2016-05-04 03:44:52 UTC; biocbuild

● Data Source: BioConductor
● BiocViews: DataImport, Sequencing
1 images, 14 functions, 0 datasets
Reverse Depends: 1

EDASeq : Exploratory Data Analysis and Normalization for RNA-Seq

Package: EDASeq
Version: 2.6.2
Title: Exploratory Data Analysis and Normalization for RNA-Seq
Description: Numerical and graphical summaries of RNA-Seq read data.
Within-lane normalization procedures to adjust for GC-content
effect (or other gene-level effects) on read counts: loess
robust local regression, global-scaling, and full-quantile
normalization (Risso et al., 2011). Between-lane normalization
procedures to adjust for distributional differences between
lanes (e.g., sequencing depth): global-scaling and
full-quantile normalization (Bullard et al., 2010).
Authors@R: c(person("Davide", "Risso", email = "risso.davide@gmail.com",
role = c("aut", "cre", "cph")),
person("Sandrine", "Dudoit", role = "aut"),
person("Ludwig", "Geistlinger", role = "ctb"))
Author: Davide Risso [aut, cre, cph], Sandrine Dudoit [aut], Ludwig Geistlinger [ctb]
Maintainer: Davide Risso <risso.davide@gmail.com>
Date: 08-30-2011
Depends: Biobase (>= 2.15.1), ShortRead (>= 1.11.42)
Imports: methods, graphics, BiocGenerics, IRanges (>= 1.13.9), DESeq,
aroma.light, Rsamtools (>= 1.5.75), biomaRt, Biostrings,
AnnotationDbi, GenomicFeatures, GenomicRanges
Suggests: BiocStyle, knitr, yeastRNASeq, leeBamViews, edgeR, KernSmooth
VignetteBuilder: knitr
License: Artistic-2.0
LazyLoad: yes
biocViews: Sequencing, RNASeq, Preprocessing, QualityControl,
DifferentialExpression
URL: https://github.com/drisso/EDASeq
BugReports: https://github.com/drisso/EDASeq/issues
NeedsCompilation: no
Packaged: 2016-05-16 03:02:34 UTC; biocbuild

● Data Source: BioConductor
● BiocViews: DifferentialExpression, Preprocessing, QualityControl, RNASeq, Sequencing
6 images, 17 functions, 2 datasets
Reverse Depends: 2

EatonEtAlChIPseq : ChIP-seq data of ORC-binding sites in Yeast excerpted from Eaton et al. 2010

Package: EatonEtAlChIPseq
Title: ChIP-seq data of ORC-binding sites in Yeast excerpted from Eaton
et al. 2010
Description: ChIP-seq analysis subset from "Conserved nucleosome positioning
defines replication origins" (PMID 20351051)
Version: 0.10.0
Author: Patrick Aboyoun <paboyoun@fhcrc.org>
Maintainer: Patrick Aboyoun <paboyoun@fhcrc.org>
Depends: GenomicRanges (>= 1.5.42), ShortRead, rtracklayer
License: Artistic 2.0
biocViews: ExperimentData, Saccharomyces_cerevisiae_Data,
SequencingData, ChIPSeqData, GEO
NeedsCompilation: no
Packaged: 2016-05-07 20:17:53 UTC; biocbuild

● Data Source: BioConductor
● BiocViews: ChIPSeqData, ExperimentData, GEO, Saccharomyces_cerevisiae_Data, SequencingData
● 0 images, 0 functions, 2 datasets
● Reverse Depends: 0

nucleR : Nucleosome positioning package for R

Package: nucleR
Type: Package
Title: Nucleosome positioning package for R
Version: 2.4.0
Date: 2016-02-24
Author: Oscar Flores, Ricard Illa
Maintainer: Ricard Illa <ricard.illa@irbbarcelona.org>
Description: Nucleosome positioning for Tiling Arrays and NGS experiments.
License: LGPL (>= 3)
Depends: ShortRead
Imports: methods, BiocGenerics, S4Vectors (>= 0.9.39), IRanges (>=
2.5.27), Biobase, GenomicRanges (>= 1.23.16), Rsamtools, stats,
graphics, parallel
Suggests: Starr
LazyLoad: yes
biocViews: ChIPSeq, Microarray, Sequencing, Genetics
NeedsCompilation: no
Packaged: 2016-05-04 04:09:14 UTC; biocbuild

● Data Source: BioConductor
● BiocViews: ChIPSeq, Genetics, Microarray, Sequencing
19 images, 16 functions, 2 datasets
● Reverse Depends: 0