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    <title>New Packages: Bioconductor</title>
    <link>http://www.bioconductor.org/</link>
    <description>New Bioconductor Packages (devel branch)</description>
    <language>en-us</language>
    <copyright/>
    <generator>ruby</generator>
  <item><title>http://bioconductor.org/packages/2.13/bioc/html/flowFit.html flowFit Estimate proliferation in cell-tracking dye studies</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Davide Rambaldi</author><description disable-output-escaping='yes'>This package estimate the proliferation of a cell population in cell-tracking dye studies. The package uses an R implementation of the Levenberg-Marquardt algorithm (minpack.lm) to fit a set of peaks (corresponding to different generations of cells) over the proliferation-tracking dye distribution in a FACS experiment.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/flowFit.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/clonotypeR.html clonotypeR Identify and analyse B and T cell receptors at a high throughput.</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Charles Plessy &lt;plessy@riken.jp&gt;</author><description disable-output-escaping='yes'>Identify and analyse B and T cell receptors at a high throughput. The genes encoding T cell receptors and B cell receptors (the antibodies) are created by somatic recombination, generating an immense combination of V, (D) and J segments. Additional processes during the recombination create extra sequence diversity between the V an J segments.  Collectively, this hyper-variable region is called the CDR3 loop. . The purpose of this package is to process and quantitatively analyse millions of V-CDR3-J combination, called clonotypes, from multiple libraries.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/clonotypeR.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/XVector.html XVector Representation and manpulation of external sequences</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>H. Pages and P. Aboyoun</author><description disable-output-escaping='yes'>Memory efficient S4 classes for storing sequences &quot;externally&quot; 	(behind an R external pointer, or on disk).
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/XVector.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/sSeq.html sSeq Shrinkage estimation of dispersion in Negative Binomial models for RNA-seq experiments with small sample size</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Danni Yu &lt;dyu@purdue.edu&gt;,  Wolfgang Huber &lt;whuber@embl.de&gt; and  Olga Vitek &lt;ovitek@purdue.edu&gt;</author><description disable-output-escaping='yes'>The purpose of this package is to discover the genes that are  differentially expressed between two conditions in RNA-seq experiments. Gene  expression is measured in counts of transcripts and modeled with the Negative  Binomial (NB) distribution using a shrinkage approach for dispersion  estimation. The method of moment (MM) estimates for dispersion are shrunk  towards an estimated target, which minimizes the average squared difference  between the shrinkage estimates and the initial estimates. The exact per-gene  probability under the NB model is calculated, and used to test the hypothesis  that the expected expression of a gene in two conditions identically follow a  NB distribution.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/sSeq.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/SplicingGraphs.html SplicingGraphs Create, manipulate, visualize splicing graphs, and assign RNA-seq reads 	to them</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>D. Bindreither, M. Carlson, M. Morgan, H. Pages</author><description disable-output-escaping='yes'>This package allows the user to create, manipulate, and visualize 	splicing graphs and their bubbles based on a gene model for a given 	organism. Additionally it allows the user to assign RNA-seq reads to 	the edges of a set of splicing graphs, and to summarize them.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/SplicingGraphs.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/BiSeq.html BiSeq Processing and analyzing bisulfite sequencing data</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Katja Hebestreit, Hans-Ulrich Klein</author><description disable-output-escaping='yes'>The BiSeq package provides useful classes and functions to handle and analyze targeted bisulfite sequencing (BS) data such as reduced-representation bisulfite sequencing (RRBS) data. In particular, it implements an algorithm to detect differentially methylated regions (DMRs). The package takes already aligned BS data from one or multiple samples.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/BiSeq.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/triplex.html triplex Search and visualize intramolecular triplex-forming sequences in DNA</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Jiri Hon, Matej Lexa, Tomas Martinek and Kamil Rajdl with contributions from Daniel Kopecek</author><description disable-output-escaping='yes'>This package provides functions for identification and  visualization of potential intramolecular triplex patterns in DNA sequence. The main functionality is to detect the positions of subsequences capable of  folding into an intramolecular triplex (H-DNA) in a much larger sequence.  The potential H-DNA (triplexes) should be made of as many cannonical  nucleotide triplets as possible. The package includes visualization showing  the exact base-pairing in 1D, 2D or 3D.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/triplex.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/prebs.html prebs Probe region expression estimation for RNA-seq data for improved microarray comparability</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Karolis Uziela and Antti Honkela</author><description disable-output-escaping='yes'>The prebs package aims at making RNA-sequencing (RNA-seq) data more comparable to microarray data. The comparability is achieved by summarizing sequencing-based expressions of probe regions using a modified version of RMA algorithm. The pipeline takes mapped reads in BAM format as an input and produces either gene expressions or original microarray probe set expressions as an output.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/prebs.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/piano.html piano Platform for integrative analysis of omics data</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Leif Varemo &lt;piano.rpkg@gmail.com&gt; and Intawat Nookaew &lt;piano.rpkg@gmail.com&gt;</author><description disable-output-escaping='yes'>Piano performs gene set analysis using various statistical methods, from different gene level statistics and a wide range of gene-set collections. Furthermore, the Piano package contains functions for combining the results of multiple runs of gene set analyses.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/piano.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/MMDiff.html MMDiff Statistical Testing for ChIP-Seq data sets</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Gabriele Schweikert</author><description disable-output-escaping='yes'>This package detects statistically significant difference between read enrichment profiles in different ChIP-Seq samples. To take advantage of shape differences it uses Kernel methods (Maximum Mean Discrepancy, MMD).
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/MMDiff.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/GENE.E.html GENE.E Interact with GENE-E from R</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Joshua Gould</author><description disable-output-escaping='yes'>Interactive exploration of matrices in GENE-E.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/GENE.E.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/PAPi.html PAPi Predict metabolic pathway activity based on metabolomics data</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Raphael Aggio</author><description disable-output-escaping='yes'>The Pathway Activity Profiling - PAPi - is an R package for predicting the activity of metabolic pathways based solely on a metabolomics data set containing a list of metabolites identified and their respective abundances in different biological samples. PAPi generates hypothesis that improves the final biological interpretation. See Aggio, R.B.M; Ruggiero, K. and Villas-Boas, S.G. (2010) - Pathway Activity Profiling (PAPi): from metabolite profile to metabolic pathway activity. Bioinformatics.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/PAPi.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/antiProfiles.html antiProfiles Implementation of gene expression anti-profiles</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Hector Corrada Bravo, Rafael A. Irizarry and Jeffrey T. Leek</author><description disable-output-escaping='yes'>Implements gene expression anti-profiles as described in Corrada Bravo et al., BMC Bioinformatics 2012, 13:272 doi:10.1186/1471-2105-13-272.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/antiProfiles.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/copynumber.html copynumber Segmentation of single- and multi-track copy number data by penalized least squares regression.</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Gro Nilsen, Knut Liestoel and Ole Christian Lingjaerde.</author><description disable-output-escaping='yes'>Penalized least squares regression is applied to fit piecewise constant curves to copy number data to locate genomic regions of constant copy number. Procedures are available for individual segmentation of each sample, joint segmentation of several samples and joint segmentation of the two data tracks from SNP-arrays. Several plotting functions are available for visualization of the data and the segmentation results.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/copynumber.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/geNetClassifier.html geNetClassifier classify diseases and build associated gene networks using gene expression profiles</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Sara Aibar, Celia Fontanillo and Javier De Las Rivas. Bioinformatics and Functional Genomics Group. Cancer Research Center (CiC-IBMCC, CSIC/USAL). Salamanca. Spain.</author><description disable-output-escaping='yes'>Comprehensive package to automatically train a multi-class SVM classifier based on gene expression data. Provides transparent selection of gene markers, their coexpression networks, and an interface to query the classifier.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/geNetClassifier.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/SeqGSEA.html SeqGSEA Gene Set Enrichment Analysis (GSEA) of RNA-Seq Data: integrating differential expression and splicing</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Xi Wang &lt;Xi.Wang@newcastle.edu.au&gt;</author><description disable-output-escaping='yes'>The package generally provides methods for gene set enrichment analysis of high-throughput RNA-Seq data by integrating differential expression and splicing. It uses negative binomial distribution to model read count data, which accounts for sequencing biases and biological variation. Based on permutation tests, statistical significance can also be achieved regarding each gene&apos;s differential expression and splicing, respectively.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/SeqGSEA.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/DASiR.html DASiR Distributed Annotation System in R</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Oscar Flores, Anna Mantsoki</author><description disable-output-escaping='yes'>R package for programmatic retrieval of information from DAS servers
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/DASiR.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/metagenomeSeq.html metagenomeSeq Statistical analysis for sparse high-throughput sequencing</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Joseph Nathaniel Paulson, Mihai Pop,  Hector Corrada Bravo</author><description disable-output-escaping='yes'>metagenomeSeq is designed to determine features (be it Operational Taxanomic Unit (OTU), species, etc.) that are differentially abundant between two or more groups of multiple samples. metagenomeSeq is designed to address the effects of both normalization and under-sampling of microbial communities on disease association detection and the testing of feature correlations.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/metagenomeSeq.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/AnnotationHub.html AnnotationHub A client for retrieving Bioconductor objects from AnnotationHub</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Marc Carlson</author><description disable-output-escaping='yes'>A client for retrieving data from the Bioconductor AnnotationHub online services.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/AnnotationHub.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/ROntoTools.html ROntoTools R Onto-Tools suite</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Calin Voichita &lt;calin@wayne.edu&gt; and Sorin Draghici &lt;sorin@wayne.edu&gt;</author><description disable-output-escaping='yes'>Suite of tools for functional analysis
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/ROntoTools.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/eiR.html eiR Accelerated similarity searching of small molecules</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Kevin Horan</author><description disable-output-escaping='yes'>The eiR package provides utilities for accelerated structure similarity 	searching of very large small molecule data sets using an embedding and 	indexing approach.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/eiR.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/CNORfeeder.html CNORfeeder Integration of CellNOptR to add missing links</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>F.Eduati</author><description disable-output-escaping='yes'>This package integrates literature-constrained and data-driven methods to infer signalling networks from perturbation experiments. It permits to extends a given network with links derived from the data via various inference methods, and uses information on physical interactions of proteins to guide and validate the integration of links.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/CNORfeeder.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/BaseSpaceR.html BaseSpaceR R SDK for BaseSpace RESTful API</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Adrian Alexa</author><description disable-output-escaping='yes'>A rich R interface to Illumina&apos;s BaseSpace cloud computing 	     environment, enabling the fast development of data analysis and 	     visualisation tools.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/BaseSpaceR.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/SPEM.html SPEM S-system parameter estimation method</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Xinyi YANG Developer, Jennifer E. DENT Developer and Christine NARDINI Supervisor</author><description disable-output-escaping='yes'>This package can optimize the parameter in S-system models given time series data
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/SPEM.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/SeqArray.html SeqArray Big Data Management of Genome-wide Sequencing Variants</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Xiuwen Zheng</author><description disable-output-escaping='yes'>Big data management of genome-wide variants using the CoreArray library, where genotypic data and annotations are stored in an array-oriented manner, offering efficient access of genetic variants using the R language.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/SeqArray.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/RNASeqPower.html RNASeqPower Sample size for RNAseq studies</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author/><description disable-output-escaping='yes'>RNA-seq, sample size
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/RNASeqPower.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/pathview.html pathview a tool set for pathway based data integration and visualization</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Weijun Luo</author><description disable-output-escaping='yes'>Pathview is a tool set for pathway based data integration and visualization. It maps and renders a wide variety of biological data on relevant pathway graphs. All users need is to supply their data and specify the target pathway. Pathview automatically downloads the pathway graph data, parses the data file, maps user data to the pathway, and render pathway graph with the mapped data. In addition, Pathview also seamlessly integrates with pathway and gene set analysis tools for large-scale and fully automated analysis.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/pathview.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/jmosaics.html jmosaics Joint analysis of multiple ChIP-Seq data sets</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Xin Zeng</author><description disable-output-escaping='yes'>jmosaics detects enriched regions of ChIP-seq data sets jointly.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/jmosaics.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/HCsnip.html HCsnip Semi-supervised adaptive-height snipping of the Hierarchical Clustering tree</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Askar Obulkasim</author><description disable-output-escaping='yes'>Decompose given hierarchical clustering tree into non-overlapping clusters in a semi-supervised way by using available patients follow-up information as guidance. Contains functions for snipping HC tree, various cluster quality evaluation criteria, assigning new patients to one of the two given HC trees, testing the significance of clusters with permutation argument and clusters visualization using sample&apos;s molecular entropy.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/HCsnip.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/epigenomix.html epigenomix Epigenetic and gene expression data normalization and integration with mixture models</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Hans-Ulrich Klein, Martin Schaefer</author><description disable-output-escaping='yes'>A package for the integrative analysis of microarray based gene expression and histone modification data obtained by ChIP-seq. The package provides methods for data preprocessing and matching as well as methods for fitting bayesian mixture models in order to detect genes with differences in both data types.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/epigenomix.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/dexus.html dexus DEXUS - Identifying Differential Expression in RNA-Seq Studies with Unknown Conditions or without Replicates</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Guenter Klambauer</author><description disable-output-escaping='yes'>DEXUS identifies differentially expressed genes in RNA-Seq data under all possible study designs such as studies without replicates, without sample groups, and with unknown conditions. DEXUS works also for known conditions, for example for RNA-Seq data with two or multiple conditions. RNA-Seq read count data can be provided both by the S4 class Count Data Set and by read count matrices. Differentially expressed transcripts can be visualized by heatmaps, in which unknown conditions, replicates, and samples groups are also indicated. This software is fast since the core algorithm is written in C. For very large data sets, a parallel version of DEXUS is provided in this package. DEXUS is a statistical model that is selected in a Bayesian framework by an EM algorithm. DEXUS does not need replicates to detect differentially expressed transcripts, since the replicates (or conditions) are estimated by the EM method for each transcript. The method provides an informative/non-informative value to extract differentially expressed transcripts at a desired significance level or power.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/dexus.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/deltaGseg.html deltaGseg deltaGseg</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Diana Low, Efthymios Motakis</author><description disable-output-escaping='yes'>Identifying distinct subpopulations through multiscale time series analysis
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/deltaGseg.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/ARRmNormalization.html ARRmNormalization Adaptive Robust Regression normalization for Illumina methylation data</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Jean-Philippe Fortin, Celia M.T. Greenwood, Aurelie Labbe.</author><description disable-output-escaping='yes'>Perform the Adaptive Robust Regression method (ARRm) for the normalization of methylation data from the Illumina Infinium HumanMethylation 450k assay.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/ARRmNormalization.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/gCMAPWeb.html gCMAPWeb A web interface for gene-set enrichment analyses</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Thomas Sandmann</author><description disable-output-escaping='yes'>The gCMAPWeb R package provides a graphical user interface for the gCMAP package. gCMAPWeb uses the Rook package and can be used either on a local machine, leveraging R&apos;s internal web server, or run on a dedicated rApache web server installation. gCMAPWeb allows users to search their own data sources and instructions to generate reference datasets from public repositories are included with the package. The package supports three common types of analyses, specifically queries with 1. one or two sets of query gene identifiers, whose members are expected to show changes in gene expression in a consistent direction. For example, an up-regulated gene set might contain genes activated by a transcription factor, a down-regulated geneset targets repressed by the same factor. 2. a single set of query gene identifiers, whose members are expected to show divergent differential expression (non-directional query). For example, members of a particular signaling pathway, some of which may be up- some down-regulated in response to a stimulus. 3. a query with the complete results of a differential expression profiling experiment. For example, gene identifiers and z-scores from a previous perturbation experiment. gCMAPWeb accepts three types of identifiers: EntreIds, gene Symbols and microarray probe ids and can be configured to work with any species supported by Bioconductor. For each query submission, significantly similar reference datasets will be identified and reported in graphical and tabular form.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/gCMAPWeb.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/SANTA.html SANTA Spatial Analysis of Network Associations</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Alex Cornish and Florian Markowetz</author><description disable-output-escaping='yes'>This package provides methods for measuring the strength of association between a network and a phenotype. It does this by measuring clustering of the phenotype across the network. Vertices can also be individually ranked by their strength of association with high-weight vertices.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/SANTA.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/proteinProfiles.html proteinProfiles Protein Profiling</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Julian Gehring</author><description disable-output-escaping='yes'>Significance assessment for distance measures of time-course 	     protein profiles
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/proteinProfiles.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/DESeq2.html DESeq2 Differential gene expression analysis based on the negative binomial distribution</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Michael Love (MPIMG Berlin), Simon Anders, Wolfgang Huber (EMBL Heidelberg)</author><description disable-output-escaping='yes'>Estimate variance-mean dependence in count data from high-throughput sequencing assays and test for differential expression based on a model using the negative binomial distribution
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/DESeq2.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/chimera.html chimera A package for detection and secondary analysis of fusion products</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Raffaele A Calogero, Matteo Carrara, Marco Beccuti, Francesca Cordero</author><description disable-output-escaping='yes'>This package facilitates the characterisation of fusion products events. It allows to import fusion data results from the following fusion finders:  bellerophontes, deFuse, FusionFinder, FusionHunter, mapSplice, tophat-fusion, FusionMap, STAR.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/chimera.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/CAGEr.html CAGEr Analysis of CAGE (Cap Analysis of Gene Expression) sequencing data for precise mapping of transcription start sites and promoterome mining</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Vanja Haberle, Department of Biology, University of Bergen, Norway &lt;vanja.haberle@bio.uib.no&gt;</author><description disable-output-escaping='yes'>Preprocessing of CAGE sequencing data, identification and normalization of transcription start sites and downstream analysis of transcription start sites clusters (promoters).
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/CAGEr.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/biomvRCNS.html biomvRCNS Copy Number study and Segmentation for multivariate biological data</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Yang Du</author><description disable-output-escaping='yes'>In this package, a Hidden Semi Markov Model (HSMM) and one homogeneous  	segmentation model are designed and implemented for segmentation genomic data,  	with the aim of assisting in transcripts detection using high throughput technology  	like RNA-seq or tiling array, and copy number analysis using aCGH or sequencing.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/biomvRCNS.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/cisPath.html cisPath Visualization of the Shortest Functional Paths between Proteins.</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Likun Wang &lt;wanglk@hsc.pku.edu.cn&gt;</author><description disable-output-escaping='yes'>cisPath is an R package for identification and visualization of the shortest functional paths between proteins in the protein-protein interaction network.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/cisPath.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/MineICA.html MineICA Analysis of an ICA decomposition obtained on genomics data</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Anne Biton</author><description disable-output-escaping='yes'>The goal of MineICA is to make easier the interpretation of the interpretation of a decomposition obtained by Independent Component Analysis on transcriptomic data. It helps the biological interpretation of the components by studying their association with variables (e.g sample annotations) and gene sets, and enables the comparison of components from different datasets using correlation-based graph.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/MineICA.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/lpNet.html lpNet Linear Programming Model for Network Inference</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Bettina Knapp, Johanna Mazur, Lars Kaderali</author><description disable-output-escaping='yes'>lpNet takes perturbation data as input and generates an LP model which allows the inference of signaling networks. For parameter identification either leave-one-out cross-validation or stratified n-fold cross-validation can be used.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/lpNet.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/SomatiCA.html SomatiCA SomatiCA: identifying, characterizing, and quantifying somatic copy number aberrations from cancer genome sequencing</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Mengjie Chen &lt;mengjie.chen@yale.edu&gt;, Hongyu Zhao &lt;hongyu.zhao@yale.edu&gt;</author><description disable-output-escaping='yes'>SomatiCA is a software suite that is capable of identifying, characterizing, and quantifying somatic CNAs from cancer genome sequencing. First, it uses read depths and lesser allele frequencies (LAF) from mapped short sequence reads to segment the genome and identify candidate CNAs. Second, SomatiCA estimates the admixture rate from the relative copy-number profile of tumor-normal pair by a Bayesian finite mixture model. Third, SomatiCA quantifies absolute somatic copy-number and subclonality for each genomic segment to guide its characterization. Results from SomatiCA can be further integrated with single nucleotide variations (SNVs) to get a better understanding of the tumor evolution.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/SomatiCA.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/rBiopaxParser.html rBiopaxParser Parses BioPax files and represents them in R</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Frank Kramer</author><description disable-output-escaping='yes'>Parses BioPAX files and represents them in R, at the moment BioPAX level 2 and level 3 are supported.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/rBiopaxParser.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/HTSFilter.html HTSFilter Filter replicated high-throughput transcriptome sequencing data</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Andrea Rau, Melina Gallopin, Gilles Celeux, and Florence Jaffrezic</author><description disable-output-escaping='yes'>This package implements a filtering procedure for replicated transcriptome sequencing data based on a global Jaccard similarity index in order to identify genes with low, constant levels of expression across one or more experimental conditions.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/HTSFilter.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/MethylSeekR.html MethylSeekR Segmentation of Bis-seq data</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Lukas Burger, Dimos Gaidatzis, Dirk Schubeler and Michael Stadler</author><description disable-output-escaping='yes'>This is a package for the discovery of regulatory regions from Bis-seq data
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/MethylSeekR.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/DrugVsDisease.html DrugVsDisease Comparison of disease and drug profiles using Gene set Enrichment Analysis</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>C. Pacini</author><description disable-output-escaping='yes'>This package generates ranked lists of differential gene expression for either disease or drug profiles. Input data can be downloaded from Array Express or GEO, or from local CEL files. Ranked lists of differential expression and associated p-values are calculated using Limma. Enrichment scores (Subramanian et al. PNAS 2005) are calculated to a reference set of default drug or disease profiles, or a set of custom data supplied by the user. Network visualisation of significant scores are output in Cytoscape format.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/DrugVsDisease.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/PathNet.html PathNet An R package for pathway analysis using topological information</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Bhaskar Dutta &lt;bhaskar.dutta@gmail.com&gt;, Anders Wallqvist &lt;awallqvist@bhsai.org&gt;, and Jaques Reifman &lt;jreifman@bhsai.org&gt;</author><description disable-output-escaping='yes'>PathNet uses topological information present in pathways and  differential expression levels of genes (obtained from microarray experiment)  to identify pathways that are 1) significantly enriched and 2) associated  with each other in the context of differential expression. The algorithm is  described in: PathNet: A tool for pathway analysis using topological  information. Dutta B, Wallqvist A, and Reifman J. Source Code for Biology and Medicine 2012 Sep 24;7(1):10.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/PathNet.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/clipper.html clipper Gene set analysis exploiting pathway topology</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Paolo Martini &lt;paolo.cavei@gmail.com&gt;, Gabriele Sales &lt;gabriele.sales@unipd.it&gt;, Chiara Romualdi &lt;chiara.romualdi@unipd.it&gt;</author><description disable-output-escaping='yes'>clipper is a package for topological gene set analysis. It implements a two-step empirical approach based on the exploitation of graph decomposition into a junction tree to reconstruct the most relevant signal path. In the first step clipper selects significant pathways according to statistical tests on the means and the concentration matrices of the graphs derived from pathway topologies. Then, it &quot;clips&quot; the whole pathway identifying  the signal paths having the greatest association with a specific phenotype.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/clipper.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/casper.html casper Characterization of Alternative Splicing based on Paired-End Reads</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>David Rossell, Camille Stephan-Otto, Manuel Kroiss</author><description disable-output-escaping='yes'>Infer alternative splicing from paired-end RNA-seq data. The model is based on counting paths across exons, rather than pairwise exon connections, and estimates the fragment size and start distributions non-parametrically, which improves estimation precision.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/casper.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/KEGGREST.html KEGGREST Client-side REST access to KEGG</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Dan Tenenbaum</author><description disable-output-escaping='yes'>A package that provides a client interface to the KEGG REST server. Based on KEGGSOAP by J. Zhang, R. Gentleman, and Marc Carlson, and KEGG (python package) by Aurelien Mazurie.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/KEGGREST.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/QuasR.html QuasR Quantify and Annotate Short Reads in R</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Anita Lerch, Dimos Gaiditzis and Michael Stadler</author><description disable-output-escaping='yes'>This package provides a framework for the quantification and analysis of Short Reads. It covers a complete workflow starting from raw sequence reads, over creation of alignments and quality control plots, to the quantification of genomic regions of interest.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/QuasR.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/Rbowtie.html Rbowtie R bowtie wrapper</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Florian Hahne, Anita Lerch, Michael B Stadler</author><description disable-output-escaping='yes'>This package provides an R wrapper around the popular bowtie short read aligner and around SpliceMap, a de novo splice junction discovery and alignment tool. The package is used by the QuasR bioconductor package. We recommend to use the QuasR package instead of using Rbowtie directly.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/Rbowtie.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/rTANDEM.html rTANDEM Encapsulate X!Tandem in R.</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Frederic Fournier &lt;frederic.fournier@crchuq.ulaval.ca&gt;, Charles Joly Beauparlant &lt;charles.joly-beauparlant@crchul.ulaval.ca&gt;, Rene Paradis &lt;rene.paradis@genome.ulaval.ca&gt;, Arnaud Droit &lt;arnaud.droit@crchuq.ulaval.ca&gt;</author><description disable-output-escaping='yes'>This package encapsulate X!Tandem in R. In its most basic functionality, this package allows to call tandem(input) from R, just as tandem.exe /path/to/input.xml would be used to run X!Tandem from the command line. Classes are also provided for taxonomy and parameters objects and methods are provided to convert xml files to R objects and vice versa. This package is the first step in an attempt to provide a reliable worflow for proteomics analysis in R.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/rTANDEM.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/RSVSim.html RSVSim RSVSim: an R/Bioconductor package for the simulation of structural variations</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Christoph Bartenhagen</author><description disable-output-escaping='yes'>RSVSim is a package for the simulation of deletions, insertions, inversion, tandem-duplications and translocations of various sizes in any genome available as FASTA-file or BSgenome data package. SV breakpoints can be placed uniformly accross the whole genome, with a bias towards repeat regions and regions of high homology (for hg19) or at user-supplied coordinates.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/RSVSim.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/iBMQ.html iBMQ integrated Bayesian Modeling of eQTL data</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Marie-Pier Scott-Boyer and Greg Imholte</author><description disable-output-escaping='yes'>integrated Bayesian Modeling of eQTL data
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/iBMQ.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/GraphPAC.html GraphPAC Identification of Mutational Clusters in Proteins via a Graph Theoretical Approach.</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Gregory Ryslik, Hongyu Zhao</author><description disable-output-escaping='yes'>Identifies mutational clusters of amino acids in a protein while utilizing the proteins tertiary structure via a graph theoretical model.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/GraphPAC.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/ensemblVEP.html ensemblVEP R Interface to Ensembl Variant Effect Predictor</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Valerie Obenchain &lt;vobencha@fhcrc.org&gt;,</author><description disable-output-escaping='yes'>Query the Ensembl Variant Effect Predictor via the perl API
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/ensemblVEP.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/wateRmelon.html wateRmelon Illumina 450 methylation array normalization and metrics</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Leonard C Schalkwyk, Ruth Pidsley, Chloe CY Wong, with functions contributed by Nizar Touleimat, Matthieu Defrance, Andrew Teschendorff, Jovana Maksimovic</author><description disable-output-escaping='yes'>15 flavours of betas and three performance metrics, with methods for objects produced by methylumi, minfi and IMA packages.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/wateRmelon.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/bumphunter.html bumphunter Bump Hunter</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Rafael A. Irizarry, Martin Aryee, Hector Corrada Bravo, Kasper D. Hansen, Harris A. Jaffee</author><description disable-output-escaping='yes'>Tools for finding bumps in genomic data
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/bumphunter.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/DriverNet.html DriverNet Drivernet: uncovering somatic driver mutations modulating transcriptional networks in cancer</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Ali Bashashati, Reza Haffari, Jiarui Ding, Gavin Ha, Kenneth Liu, Jamie Rosner and Sohrab Shah</author><description disable-output-escaping='yes'>DriverNet is a package to predict functional important driver genes in cancer by integrating genome data (mutation and copy number variation data) and transcriptome data (gene expression data). The different kinds of data are combined by an influence graph, which is a gene-gene interaction network deduced from pathway data. A greedy algorithm is used to find the possible driver genes, which may mutated in a larger number of patients and these mutations will push the gene expression values of the connected genes to some extreme values.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/DriverNet.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/pRoloc.html pRoloc A unifying bioinformatics framework for spatial proteomics</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Laurent Gatto and Lisa M. Breckels with contributions 	from Thomas Burger and Samuel Wieczorek</author><description disable-output-escaping='yes'>This package implements pattern recognition 	     techniques on quantitiative mass spectrometry data to 	     infer protein sub-cellular localisation.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/pRoloc.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/pvca.html pvca Principal Variance Component Analysis (PVCA)</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Pierre Bushel &lt;bushel@niehs.nih.gov&gt;</author><description disable-output-escaping='yes'>This package contains the function to assess the batch sourcs by fitting all &quot;sources&quot; as random effects including two-way interaction terms in the Mixed Model(depends on lme4 package) to selected principal components, which were obtained from the original data correlation matrix. This package accompanies the book &quot;Batch Effects and Noise in Microarray Experiements, chapter 12.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/pvca.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/BiocParallel.html BiocParallel Bioconductor facilities for parallel evaluation</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Martin Morgan</author><description disable-output-escaping='yes'>This package provides modified versions and novel implementation of functions for parallel evaluation, tailored to use with Bioconductor objects.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/BiocParallel.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/plrs.html plrs Piecewise Linear Regression Splines (PLRS) for the association between DNA copy number and gene expression</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Gwenael G.R. Leday</author><description disable-output-escaping='yes'>The present package implements a flexible framework for modeling the relationship between DNA copy number and gene expression data using Piecewise Linear Regression Splines (PLRS).
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/plrs.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/UniProt.ws.html UniProt.ws R Interface to UniProt Web Services</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Marc Carlson</author><description disable-output-escaping='yes'>A collection of functions for retrieving, processing and repackaging the Uniprot web services.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/UniProt.ws.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/SNAGEE.html SNAGEE Signal-to-Noise applied to Gene Expression Experiments</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>David Venet &lt;davenet@ulb.ac.be&gt;</author><description disable-output-escaping='yes'>Signal-to-Noise applied to Gene Expression Experiments. Signal-to-noise ratios can be used as a proxy for quality of gene expression studies and samples. The SNRs can be calculated on any gene expression data set as long as gene IDs are available, no access to the raw data files is necessary. This allows to flag problematic studies and samples in any public data set.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/SNAGEE.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/illuminaio.html illuminaio Parsing Illumina microarray output files</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Keith Baggerly, Henrik Bengtsson, Kasper Daniel Hansen, Matt Ritchie</author><description disable-output-escaping='yes'>Tools for parsing Illumina&apos;s microarray output files, including IDAT.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/illuminaio.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/RIPSeeker.html RIPSeeker RIPSeeker: a statistical package for identifying protein-associated transcripts from RIP-seq experiments</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Yue Li</author><description disable-output-escaping='yes'>Infer and discriminate RIP peaks from RIP-seq alignments using two-state HMM with negative binomial emission probability. While RIPSeeker is specifically tailored for RIP-seq data analysis, it also provides a suite of bioinformatics tools integrated within this self-contained software package comprehensively addressing issues ranging from post-alignments processing to visualization and annotation.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/RIPSeeker.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/matchBox.html matchBox Utilities to compute, compare, and plot the agreement between ordered vectors of features (ie. distinct genomic experiments). The package includes Correspondence-At-the-TOP (CAT) analysis.</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Luigi Marchionni &lt;marchion@jhu.edu&gt;, Anuj Gupta &lt;Anuj Gupta &lt;agupta52@jhu.edu&gt;</author><description disable-output-escaping='yes'>The matchBox package enables comparing ranked vectors of features, merging multiple datasets, removing redundant features, using CAT-plots and Venn diagrams, and computing statistical significance.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/matchBox.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/rSFFreader.html rSFFreader rSFFreader reads in sff files generated by Roche 454 and Life Sciences Ion Torrent sequencers</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Matt Settles &lt;msettles@uidaho.edu&gt;, Sam Hunter, Brice Sarver, Ilia Zhbannikov, Kyu-Chul Cho</author><description disable-output-escaping='yes'>rSFFreader reads sequence, qualities and clip point values from sff files generated by Roche 454 and Life Sciences Ion Torrent sequencers. The plan is to also write out sff files and to read in flowgrams with some utils
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/rSFFreader.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/chroGPS.html chroGPS chroGPS: visualizing the epigenome</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Oscar Reina, David Rossell</author><description disable-output-escaping='yes'>We provide intuitive maps to visualize the association between genetic elements, with emphasis on epigenetics. The approach is based on Multi-Dimensional Scaling. We provide several sensible distance metrics, and adjustment procedures to remove systematic biases typically observed when merging data obtained under different technologies or genetic backgrounds.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/chroGPS.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/NOISeq.html NOISeq Exploratory analysis and differential expression for RNA-seq data</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Sonia Tarazona, Pedro Furio-Tari, Alberto Ferrer and Ana Conesa</author><description disable-output-escaping='yes'>Analysis of RNA-seq expression data or other similar kind of data. Exploratory plots to evualuate saturation, count distribution, expression per chromosome, type of detected features, features length, etc. Differential expression between two experimental conditions with no parametric assumptions.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/NOISeq.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/TransView.html TransView Read density map construction and accession. Visualization of ChIPSeq and RNASeq data sets.</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Julius Muller</author><description disable-output-escaping='yes'>This package provides efficient tools to generate, access and  	     display read densities of sequencing based data sets such as from  	     RNA-Seq and ChIP-Seq.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/TransView.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/Rcade.html Rcade R-based analysis of ChIP-seq And Differential Expression - a tool for integrating a count-based ChIP-seq analysis with differential expression summary data.</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Jonathan Cairns</author><description disable-output-escaping='yes'>Rcade (which stands for &quot;R-based analysis of ChIP-seq And  	     Differential Expression&quot;) is a tool for integrating 	     ChIP-seq data with differential expression summary data, 	     through a Bayesian framework. A key application is in 	     identifing the genes targeted by a transcription factor 	     of interest - that is, we collect genes that are 	     associated with a ChIP-seq peak, and differential 	     expression under some perturbation related to that TF.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/Rcade.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/HTSeqGenie.html HTSeqGenie A NGS analysis pipeline.</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Gregoire Pau, Jens Reeder</author><description disable-output-escaping='yes'>Libraries to perform NGS analysis.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/HTSeqGenie.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/HMMcopy.html HMMcopy Copy number prediction with correction for GC and mappability bias for HTS data</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Daniel Lai, Gavin Ha, Sohrab Shah</author><description disable-output-escaping='yes'>Corrects GC and mappability biases for readcounts (i.e. coverage) in non-overlapping windows of fixed length for single whole genome samples, yielding a rough estimate of copy number for furthur analysis.  Designed for rapid correction of high coverage whole genome tumour and normal samples.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/HMMcopy.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/CNORode.html CNORode ODE add-on to CellNOptR</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>David Henriques, Thomas Cokelaer</author><description disable-output-escaping='yes'>ODE add-on to CellNOptR
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/CNORode.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/bigmemoryExtras.html bigmemoryExtras An extension of the bigmemory package with added safety, convenience, and a factor class.</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Peter M. Haverty</author><description disable-output-escaping='yes'>This package defines a &quot;BigMatrix&quot; ReferenceClass which adds safety and convenience features to the filebacked.big.matrix class from the bigmemory package. BigMatrix protects against segfaults by monitoring and gracefully restoring the connection to on-disk data and it also protects against accidental data modification with a filesystem-based permissions system. We provide utilities for using BigMatrix-derived classes as assayData matrices within the Biobase package&apos;s eSet family of classes. BigMatrix provides some optimizations related to attaching to, and indexing into, file-backed matrices with dimnames. Additionally, the package provides a &quot;BigMatrixFactor&quot; class, a file-backed matrix with factor properties.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/bigmemoryExtras.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/CNORdt.html CNORdt Add-on to CellNOptR: Discretized time treatments</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>A. MacNamara</author><description disable-output-escaping='yes'>This add-on to the package CellNOptR handles time-course data, as opposed to steady state data in CellNOptR. It scales the simulation step to allow comparison and model fitting for time-course data. Future versions will optimize delays and strengths for each edge.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/CNORdt.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/agilp.html agilp Agilent expression array processing package</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Benny Chain &lt;b.chain@ucl.ac.uk&gt;</author><description disable-output-escaping='yes'>provides a pipeline for the low-level analysis of gene expression 	microarray data, primarily Agilent data
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/agilp.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/SCAN.UPC.html SCAN.UPC Single-channel array normalization (SCAN) and University Probability of expression Codes (UPC)</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Stephen R. Piccolo and W. Evan Johnson</author><description disable-output-escaping='yes'>SCAN is a microarray normalization method to facilitate personalized-medicine workflows. Rather than processing microarray samples as groups, which can introduce biases and present logistical challenges, SCAN normalizes each sample individually by modeling and removing probe- and array-specific background noise using only data from within each array. SCAN can be applied to one-channel (e.g., Affymetrix) or two-channel (e.g., Agilent) microarrays. The Universal Probability of expression Codes (UPC) method is an extension of SCAN that generates probability-of-expression values. These values can be interpreted as the probability that a given genomic feature (e.g., gene, transcript) is expressed above the background in a given sample. The UPC method can be applied to one-channel or two-channel microarrays as well as to RNA-Seq read counts. Because UPC values are represented on the same scale and have an identical interpretation for each platform, they can be used for cross-platform data integration.)
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/SCAN.UPC.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/ReportingTools.html ReportingTools Tools for making reports in various formats</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Jason A. Hackney, Melanie Huntley, Jessica L. Larson, Christina Chaivorapol, Gabriel Becker, and Josh Kaminker</author><description disable-output-escaping='yes'>The ReportingTools software package enables users to easily display reports of analysis results generated from sources such as microarray and sequencing data.  The package allows users to create HTML pages that may be viewed on a web browser such as Safari, or in other formats readable by programs such as Excel.  Users can generate tables with sortable and filterable columns, make and display plots, and link table entries to other data sources such as NCBI or larger plots within the HTML page.  Using the package, users can also produce a table of contents page to link various reports together for a particular project that can be viewed in a web browser.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/ReportingTools.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/DeconRNASeq.html DeconRNASeq Deconvolution of Heterogeneous Tissue Samples for mRNA-Seq data</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Ting Gong &lt;tinggong@gmail.com&gt; Joseph D. Szustakowski &lt;joseph.szustakowski@novartis.com&gt;</author><description disable-output-escaping='yes'>DeconSeq is an R package for deconvolution of heterogeneous tissues based on mRNA-Seq data. It modeled expression levels from heterogeneous cell populations in mRNA-Seq as the weighted average of expression from different constituting cell types and predicted cell type proportions of single expression profiles.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/DeconRNASeq.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/motifStack.html motifStack Plot stacked logos for single or multiple DNA, RNA and amino acid sequence</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Jianhong Ou, Michael Brodsky, Scot Wolfe and Lihua Julie Zhu</author><description disable-output-escaping='yes'>The motifStack package is designed for graphic  representation of multiple motifs with different similarity  scores. It works with both DNA/RNA sequence motif and amino  acid sequence motif. In addition, it provides the flexibility  for users to customize the graphic parameters such as the  font type and symbol colors.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/motifStack.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/gCMAP.html gCMAP Tools for Connectivity Map-like analyses</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Thomas Sandmann &lt;sandmann.thomas@gene.com&gt;, Richard Bourgon 	&lt;bourgon.richard@gene.com&gt; and Sarah Kummerfeld 	&lt;kummerfeld.sarah@gene.com&gt;</author><description disable-output-escaping='yes'>The gCMAP package provides a toolkit for comparing differential gene expression profiles through gene set enrichment analysis. Starting from normalized microarray or RNA-seq gene expression values (stored in lists of ExpressionSet and CountDataSet objects) the package performs differential expression analysis using the limma or DESeq packages. Supplying a simple list of gene identifiers, global differential expression profiles or data from complete experiments as input, users can use a unified set of several well-known gene set enrichment analysis methods to retrieve experiments with similar changes in gene expression. To take into account the directionality of gene expression changes, gCMAPQuery introduces the SignedGeneSet class, directly extending GeneSet from the GSEABase package.  To increase performance of large queries, multiple gene sets are stored as sparse incidence matrices within CMAPCollection eSets. gCMAP offers implementations of 1. Fisher&apos;s exact test (Fisher, J R Stat Soc, 1922) 2. The &quot;connectivity map&quot; method (Lamb et al, Science, 2006) 3. Parametric and non-parametric t-statistic summaries (Jiang &amp; Gentleman, Bioinformatics, 2007) and 4. Wilcoxon / Mann-Whitney rank sum statistics (Wilcoxon, Biometrics Bulletin, 1945) as well as wrappers for the 5. camera (Wu &amp; Smyth, Nucleic Acid Res, 2012) 6. mroast and romer (Wu et al, Bioinformatics, 2010) functions from the limma package and 7. wraps the gsea method from the mgsa package  (Bauer et al, NAR, 2010). All methods return CMAPResult objects, an S4 class inheriting from AnnotatedDataFrame, containing enrichment statistics as well as annotation data and providing simple high-level summary plots.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/gCMAP.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/Risa.html Risa Converting experimental metadata from ISA-tab into Bioconductor data structures</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Alejandra Gonzalez-Beltran, Audrey Kauffmann, Steffen Neumann, Gabriella Rustici, ISA Team</author><description disable-output-escaping='yes'>The Investigation / Study / Assay (ISA) tab-delimited  	 format is a general purpose framework with which to collect and communicate  	 complex metadata (i.e. sample characteristics, technologies used, type  	 of measurements made) from experiments employing a combination of  	 technologies, spanning from traditional approaches to high-throughput 	 techniques. Risa allows to access metadata/data in ISA-Tab format and  	 build Bioconductor data structures. Currently, data generated from microarray,  	 flow cytometry and metabolomics-based (i.e. mass spectrometry) assays are supported.  The package is extendable and efforts are undergoing to support metadata associated to proteomics assays.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/Risa.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/hpar.html hpar Human Protein Atlas in R</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Laurent Gatto</author><description disable-output-escaping='yes'>A simple interface to and data from  	     the Human Protein Atlas project.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/hpar.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/hapFabia.html hapFabia hapFabia: Identification of very short segments of identity by descent (IBD) characterized by rare variants in large sequencing data</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Sepp Hochreiter &lt;hochreit@bioinf.jku.at&gt;</author><description disable-output-escaping='yes'>A package to identify very short IBD segments in large sequencing data by FABIA biclustering. Two haplotypes are identical by descent (IBD) if they share a segment that both inherited from a common ancestor. Current IBD methods reliably detect long IBD segments because many minor alleles in the segment are concordant between the two haplotypes. However, many cohort studies contain unrelated individuals which share only short IBD segments. This package provides software to identify short IBD segments in sequencing data. Knowledge of short IBD segments are relevant for phasing of genotyping data, association studies, and for population genetics, where they shed light on the evolutionary history of humans. The package supports VCF formats, is based on sparse matrix operations, and provides visualization of haplotype clusters in different formats.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/hapFabia.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/OrganismDbi.html OrganismDbi Software to enable the smooth interfacing of different database packages.</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Marc Carlson, Herve Pages, Martin Morgan, Valerie Obenchain</author><description disable-output-escaping='yes'>The package enables a simple unified interface to several 	     annotation packages each of which has its own schema by taking 	     advantage of the fact that each of these packages implements a  	     select methods.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/OrganismDbi.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/lmdme.html lmdme Linear Model decomposition for Designed Multivariate Experiments</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Cristobal Fresno and Elmer A. Fernandez</author><description disable-output-escaping='yes'>linear ANOVA decomposition of Multivariate  Designed Experiments implementation based on limma lmFit. Features: i)Flexible formula type interface,  ii) Fast limma based implementation,  iii) p-values for each estimated coefficient levels in each factor, iv) F values for factor effects and  v) plotting functions for PCA and PLS.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/lmdme.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/fmcsR.html fmcsR Flexible Maximum Common Substructure (FMCS) Searching</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Yan Wang, Tyler Backman, Kevin Horan, Thomas Girke</author><description disable-output-escaping='yes'>The fmcsR package introduces an efficient maximum common substructure (MCS) algorithms combined with a novel matching strategy that allows for atom and/or bond mismatches in the substructures shared among two small molecules. The resulting flexible MCSs (FMCSs) are often larger than strict MCSs, resulting in the identification of more common features in their source structures, as well as a higher sensitivity in finding compounds with weak structural similarities. The fmcsR package provides several utilities to use the FMCS algorithm for pairwise compound comparisons, structure similarity searching and clustering.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/fmcsR.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/methyAnalysis.html methyAnalysis DNA methylation data analysis and visualization</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Pan Du, Richard Bourgon</author><description disable-output-escaping='yes'>The methyAnalysis package aims for the DNA methylation data   analysis and visualization. A new class is defined to keep the  chromosome location information together with the data. The current version of the package mainly focus on analyzing the Illumina Infinium  methylation array data, but most methods can be generalized to other  methylation array or sequencing data.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/methyAnalysis.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/CNORfuzzy.html CNORfuzzy Addon to CellNOptR: Fuzzy Logic</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>M. Morris, T. Cokelaer</author><description disable-output-escaping='yes'>This package is an extension to CellNOptR.  It contains additional functionality needed to simulate and train a prior knowledge network to experimental data using constrained fuzzy logic (cFL, rather than Boolean logic as is the case in CellNOptR).  Additionally, this package will contain functions to use for the compilation of multiple optimization results (either Boolean or cFL).
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/CNORfuzzy.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/EasyqpcR.html EasyqpcR EasyqpcR for low-throughput real-time quantitative PCR data analysis</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Le Pape Sylvain</author><description disable-output-escaping='yes'>This package is based on the qBase algorithms published by  Hellemans et al. in 2007. The EasyqpcR package allows you to import easily qPCR data files as described in the vignette. Thereafter, you can calculate  amplification efficiencies, relative quantities and their standard errors,  normalization factors based on the best reference genes choosen (using the  SLqPCR package), and then the normalized relative quantities, the NRQs scaled  to your control and their standard errors. This package has been created for  low-throughput qPCR data analysis.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/EasyqpcR.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/GeneNetworkBuilder.html GeneNetworkBuilder Build Regulatory Network from ChIP-chip/ChIP-seq and Expression Data</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Jianhong Ou and Lihua Julie Zhu</author><description disable-output-escaping='yes'>Appliation for discovering direct or indirect targets of transcription factors  		using ChIP-chip or ChIP-seq, and microarray or RNA-seq gene expression data.  		Inputting a list of genes of potential targets of one TF from ChIP-chip or ChIP-seq,  		and the gene expression results, GeneNetworkBuilder generates a regulatory 		network of the TF.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/GeneNetworkBuilder.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/MotifDb.html MotifDb An Annotated Collection of Protein-DNA Binding Sequence Motifs</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Paul Shannon</author><description disable-output-escaping='yes'>More than 2000 annotated position frequency matrices from five public source, for multiple organisms
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/MotifDb.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/ChIPXpress.html ChIPXpress ChIPXpress: enhanced transcription factor target gene identification from ChIP-seq and ChIP-chip data using publicly available gene expression profiles</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>George Wu</author><description disable-output-escaping='yes'>ChIPXpress takes as input predicted TF bound genes from ChIPx data and uses a corresponding database of gene expression profiles downloaded from NCBI GEO to rank the TF bound targets in order of which gene is most likely to be functional TF target.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/ChIPXpress.html&quot;&gt;link&lt;/a&gt;</description></item><item><title>http://bioconductor.org/packages/2.13/bioc/html/RMassBank.html RMassBank Workflow to process tandem MS files and build MassBank records</title><pubdate>Sat, 1 Jan 2012 00:00:00 GMT</pubdate><author>Michael Stravs, Emma Schymanski</author><description disable-output-escaping='yes'>Workflow to process tandem MS files and build MassBank records. Functions include automated extraction of tandem MS spectra, formula assignment to tandem MS fragments, recalibration of tandem MS spectra with assigned fragments, spectrum cleanup, automated retrieval of compound information from Internet databases, and export to MassBank records.
&lt;br/&gt;&lt;a href=&quot;http://bioconductor.org/packages/2.13/bioc/html/RMassBank.html&quot;&gt;link&lt;/a&gt;</description></item></channel>
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