<?xml version="1.0" encoding="utf-8" ?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom" xmlns:r="https://r-universe.dev"><channel><title>bioc-release.r-universe.dev</title><link>https://bioc-release.r-universe.dev</link><description>Recent package updates in bioc-release</description><generator>R-universe</generator><image><url>https://github.com/bioc-release.png</url><title>R packages by bioc-release</title><link>https://bioc-release.r-universe.dev</link></image><lastBuildDate>Wed, 10 Jun 2026 07:24:52 GMT</lastBuildDate><item><title>[bioc-release] igblastr 1.2.9</title><author>hpages.on.github@gmail.com (Hervé Pagès)</author><description>The igblastr package provides functions to conveniently
install and use a local IgBLAST installation from within R. The
package also includes a set of built-in IgBLAST-compatible
germline databases from OGRDB, the AIRR Community’s Open
Germline Receptor Database, for various organisms. It provides
functions to create additional IgBLAST-compatible germline
databases using reference sequences retrieved from IMGT/V-QUEST
or local FASTA files supplied by the user. When possible,
annotations for the V and J alleles in a new germline database
are automatically computed and added to the database, so they
can be used as replacements for the internal and auxiliary data
provided by IgBLAST. IgBLAST is described at
&lt;https://pubmed.ncbi.nlm.nih.gov/23671333/&gt;. IgBLAST web
interface: &lt;https://www.ncbi.nlm.nih.gov/igblast/&gt;. OGRDB:
&lt;https://ogrdb.airr-community.org/&gt;. IMGT/V-QUEST download
site: &lt;https://www.imgt.org/download/V-QUEST/&gt;.</description><link>https://github.com/r-universe/bioc-release/actions/runs/27273511231</link><pubDate>Wed, 10 Jun 2026 07:24:52 GMT</pubDate><r:package>igblastr</r:package><r:version>1.2.9</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/igblastr</r:upstream><r:article><r:source>igblastr_overview.Rmd</r:source><r:filename>igblastr_overview.html</r:filename><r:title>igblastr overview</r:title><r:created>2025-03-26 19:33:24</r:created><r:modified>2026-06-10 07:24:07</r:modified></r:article></item><item><title>[bioc-release] rfaRm 1.24.1</title><author>rafael.ayala@oist.jp (Lara Selles Vidal)</author><description>rfaRm provides a client interface to the Rfam database of
RNA families. Data that can be retrieved include RNA families,
secondary structure images, covariance models, sequences within
each family, alignments leading to the identification of a
family and secondary structures in the dot-bracket format.</description><link>https://github.com/r-universe/bioc-release/actions/runs/27259469409</link><pubDate>Wed, 10 Jun 2026 01:05:27 GMT</pubDate><r:package>rfaRm</r:package><r:version>1.24.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/rfaRm</r:upstream><r:article><r:source>rfaRm.Rmd</r:source><r:filename>rfaRm.html</r:filename><r:title>rfaRm</r:title><r:created>2020-04-08 00:33:44</r:created><r:modified>2020-04-08 11:47:47</r:modified></r:article></item><item><title>[bioc-release] Rega 1.0.2</title><author>igor.cervenka@unibas.ch (Igor Cervenka)</author><description>The European Genome-phenome Archive (EGA) provides
long-term storage and controlled sharing of personally
identifiable genetic data. The Rega package offers a
streamlined and extensible R interface to the EGA API,
facilitating the programmatic upload of metadata. GEO-like
Excel submission template is provided as a default method of
organizing submission metadata.</description><link>https://github.com/r-universe/bioc-release/actions/runs/27220796458</link><pubDate>Tue, 09 Jun 2026 14:09:03 GMT</pubDate><r:package>Rega</r:package><r:version>1.0.2</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/Rega</r:upstream><r:article><r:source>Rega.Rmd</r:source><r:filename>Rega.html</r:filename><r:title>The Rega User Guide</r:title><r:created>2023-04-21 14:33:17</r:created><r:modified>2026-02-02 15:03:19</r:modified></r:article></item><item><title>[bioc-release] SPONGE 1.34.1</title><author>markus.list@tum.de (Markus List)</author><description>This package provides methods to efficiently detect
competitive endogeneous RNA interactions between two genes.
Such interactions are mediated by one or several miRNAs such
that both gene and miRNA expression data for a larger number of
samples is needed as input. The SPONGE package now also
includes spongEffects: ceRNA modules offer patient-specific
insights into the miRNA regulatory landscape.</description><link>https://github.com/r-universe/bioc-release/actions/runs/27201542129</link><pubDate>Tue, 09 Jun 2026 09:07:51 GMT</pubDate><r:package>SPONGE</r:package><r:version>1.34.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/SPONGE</r:upstream><r:article><r:source>SPONGE.Rmd</r:source><r:filename>SPONGE.html</r:filename><r:title>SPONGE vignette</r:title><r:created>2017-06-08 09:23:20</r:created><r:modified>2026-06-09 08:43:00</r:modified></r:article><r:article><r:source>spongEffects.Rmd</r:source><r:filename>spongEffects.html</r:filename><r:title>spongEffects vignette</r:title><r:created>2022-02-10 13:48:30</r:created><r:modified>2026-06-09 08:43:00</r:modified></r:article></item><item><title>[bioc-release] Spectra 1.22.2</title><author>maintainer@rformassspectrometry.org (RforMassSpectrometry Package Maintainer)</author><description>The Spectra package defines an efficient infrastructure
for storing and handling mass spectrometry spectra and
functionality to subset, process, visualize and compare spectra
data. It provides different implementations (backends) to store
mass spectrometry data. These comprise backends tuned for fast
data access and processing and backends for very large data
sets ensuring a small memory footprint.</description><link>https://github.com/r-universe/bioc-release/actions/runs/27171162621</link><pubDate>Mon, 08 Jun 2026 13:37:21 GMT</pubDate><r:package>Spectra</r:package><r:version>1.22.2</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/Spectra</r:upstream><r:article><r:source>MsBackend.Rmd</r:source><r:filename>MsBackend.html</r:filename><r:title>Creating new MsBackend classes</r:title><r:created>2023-01-12 06:16:40</r:created><r:modified>2025-10-14 05:35:30</r:modified></r:article><r:article><r:source>Spectra.Rmd</r:source><r:filename>Spectra.html</r:filename><r:title>Description and usage of Spectra objects</r:title><r:created>2019-06-13 05:46:18</r:created><r:modified>2026-06-08 13:37:21</r:modified></r:article><r:article><r:source>Spectra-large-scale.Rmd</r:source><r:filename>Spectra-large-scale.html</r:filename><r:title>Large-scale data handling and processing with Spectra</r:title><r:created>2023-11-30 09:06:55</r:created><r:modified>2026-02-06 07:42:30</r:modified></r:article></item><item><title>[bioc-release] BgeeCall 1.28.2</title><author>julien.wollbrett@unil.ch (Julien Wollbrett)</author><description>BgeeCall allows to generate present/absent gene expression
calls without using an arbitrary cutoff like TPM&lt;1. Calls are
generated based on reference intergenic sequences. These
sequences are generated based on expression of all RNA-Seq
libraries of each species integrated in Bgee
(https://bgee.org).</description><link>https://github.com/r-universe/bioc-release/actions/runs/27171155650</link><pubDate>Mon, 08 Jun 2026 10:28:07 GMT</pubDate><r:package>BgeeCall</r:package><r:version>1.28.2</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/BgeeCall</r:upstream><r:article><r:source>bgeecall-manual.Rmd</r:source><r:filename>bgeecall-manual.html</r:filename><r:title>automatic RNA-Seq present/absent gene expression calls generation</r:title><r:created>2019-02-01 18:57:39</r:created><r:modified>2026-05-26 11:47:45</r:modified></r:article></item><item><title>[bioc-release] profileplyr 1.28.3</title><author>doug.barrows@gmail.com (Doug Barrows)</author><description>Quick and straightforward visualization of read signal
over genomic intervals is key for generating hypotheses from
sequencing data sets (e.g. ChIP-seq, ATAC-seq,
bisulfite/methyl-seq). Many tools both inside and outside of R
and Bioconductor are available to explore these types of data,
and they typically start with a bigWig or BAM file and end with
some representation of the signal (e.g. heatmap). profileplyr
leverages many Bioconductor tools to allow for both flexibility
and additional functionality in workflows that end with
visualization of the read signal.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26980871307</link><pubDate>Thu, 04 Jun 2026 17:51:18 GMT</pubDate><r:package>profileplyr</r:package><r:version>1.28.3</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/profileplyr</r:upstream><r:article><r:source>profileplyr.Rmd</r:source><r:filename>profileplyr.html</r:filename><r:title>Visualization and annotation of read signal over genomic ranges with profileplyr</r:title><r:created>2019-04-10 05:02:34</r:created><r:modified>2022-10-10 19:35:00</r:modified></r:article></item><item><title>[bioc-release] ggtreeExtra 1.22.1</title><author>xshuangbin@163.com (Shuangbin Xu)</author><description>'ggtreeExtra' extends the method for mapping and
visualizing associated data on phylogenetic tree using
'ggtree'. These associated data can be presented on the
external panels to circular layout, fan layout, or other
rectangular layout tree built by 'ggtree' with the grammar of
'ggplot2'.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26947809952</link><pubDate>Thu, 04 Jun 2026 06:23:33 GMT</pubDate><r:package>ggtreeExtra</r:package><r:version>1.22.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/ggtreeExtra</r:upstream><r:article><r:source>ggtreeExtra.Rmd</r:source><r:filename>ggtreeExtra.html</r:filename><r:title>ggtreeExtra</r:title><r:created>2020-07-07 09:04:50</r:created><r:modified>2025-08-11 11:22:50</r:modified></r:article></item><item><title>[bioc-release] rhdf5client 1.34.2</title><author>alsergbox@gmail.com (Alexey Sergushichev)</author><description>This package provides functionality for reading data from
HDF Scalable Data Service from within R.  The HSDSArray
function bridges from HSDS to the user via the DelayedArray
interface.  Bioconductor manages an open HSDS instance
graciously provided by John Readey of the HDF Group.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26787263604</link><pubDate>Mon, 01 Jun 2026 18:46:19 GMT</pubDate><r:package>rhdf5client</r:package><r:version>1.34.2</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/rhdf5client</r:upstream><r:article><r:source>delayed-array.Rmd</r:source><r:filename>delayed-array.html</r:filename><r:title>HSDSArray -- DelayedArray backend for Remote HDF5</r:title><r:created>2018-10-02 15:15:10</r:created><r:modified>2023-07-10 19:15:53</r:modified></r:article></item><item><title>[bioc-release] scDblFinder 1.26.2</title><author>pierre-luc.germain@hest.ethz.ch (Pierre-Luc Germain)</author><description>The scDblFinder package gathers various methods for the
detection and handling of doublets/multiplets in single-cell
sequencing data (i.e. multiple cells captured within the same
droplet or reaction volume). It includes methods formerly found
in the scran package, the new fast and comprehensive
scDblFinder method, and a reimplementation of the Amulet
detection method for single-cell ATAC-seq.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26781749826</link><pubDate>Mon, 01 Jun 2026 18:33:18 GMT</pubDate><r:package>scDblFinder</r:package><r:version>1.26.2</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/scDblFinder</r:upstream><r:article><r:source>introduction.Rmd</r:source><r:filename>introduction.html</r:filename><r:title>Introduction to the scDblFinder package</r:title><r:created>2020-09-07 17:03:25</r:created><r:modified>2026-06-01 18:31:05</r:modified></r:article><r:article><r:source>scDblFinder.Rmd</r:source><r:filename>scDblFinder.html</r:filename><r:title>scDblFinder</r:title><r:created>2019-05-23 16:13:47</r:created><r:modified>2026-02-11 20:35:55</r:modified></r:article><r:article><r:source>findDoubletClusters.Rmd</r:source><r:filename>findDoubletClusters.html</r:filename><r:title>Detecting clusters of doublet cells with DE analyses</r:title><r:created>2020-07-20 09:45:17</r:created><r:modified>2021-04-19 15:59:24</r:modified></r:article><r:article><r:source>computeDoubletDensity.Rmd</r:source><r:filename>computeDoubletDensity.html</r:filename><r:title>Scoring potential doublets from simulated densities</r:title><r:created>2020-08-04 19:48:56</r:created><r:modified>2021-04-19 15:59:24</r:modified></r:article><r:article><r:source>recoverDoublets.Rmd</r:source><r:filename>recoverDoublets.html</r:filename><r:title>Recovering intra-sample doublets</r:title><r:created>2020-09-08 12:59:07</r:created><r:modified>2021-09-10 07:32:19</r:modified></r:article><r:article><r:source>scATAC.Rmd</r:source><r:filename>scATAC.html</r:filename><r:title>Doublet identifiation in single-cell ATAC-seq</r:title><r:created>2022-04-10 08:45:02</r:created><r:modified>2025-07-17 12:56:34</r:modified></r:article></item><item><title>[bioc-release] PhyloProfile 2.4.1</title><author>tran@bio.uni-frankfurt.de (Vinh Tran)</author><description>PhyloProfile is a tool for exploring complex phylogenetic
profiles. Phylogenetic profiles, presence/absence patterns of
genes over a set of species, are commonly used to trace the
functional and evolutionary history of genes across species and
time. With PhyloProfile we can enrich regular phylogenetic
profiles with further data like sequence/structure similarity,
to make phylogenetic profiling more meaningful. Besides the
interactive visualisation powered by R-Shiny, the package
offers a set of further analysis features to gain insights like
the gene age estimation or core gene identification.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26948337480</link><pubDate>Mon, 01 Jun 2026 10:02:57 GMT</pubDate><r:package>PhyloProfile</r:package><r:version>2.4.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/PhyloProfile</r:upstream><r:article><r:source>PhyloProfile-vignette.Rmd</r:source><r:filename>PhyloProfile-vignette.html</r:filename><r:title>PhyloProfile</r:title><r:created>2019-03-07 10:39:56</r:created><r:modified>2025-10-20 18:26:46</r:modified></r:article></item><item><title>[bioc-release] limma 3.68.4</title><author>smyth@wehi.edu.au (Gordon Smyth)</author><description>Data analysis, linear models and differential expression
for omics data.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26711440403</link><pubDate>Sun, 31 May 2026 08:19:44 GMT</pubDate><r:package>limma</r:package><r:version>3.68.4</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/limma</r:upstream><r:article><r:source>intro.Rmd</r:source><r:filename>intro.html</r:filename><r:title>A brief introduction to limma</r:title><r:created>2023-06-10 01:18:21</r:created><r:modified>2026-05-19 12:34:55</r:modified></r:article><r:article><r:source>usersguide.Rnw</r:source><r:filename>usersguide.pdf</r:filename><r:title>limma User's Guide</r:title><r:created>2023-06-18 08:44:54</r:created><r:modified>2023-06-18 08:44:54</r:modified></r:article></item><item><title>[bioc-release] psichomics 1.38.1</title><author>nunodanielagostinho@gmail.com (Nuno Saraiva-Agostinho)</author><description>Interactive R package with an intuitive Shiny-based
graphical interface for alternative splicing quantification and
integrative analyses of alternative splicing and gene
expression based on The Cancer Genome Atlas (TCGA), the
Genotype-Tissue Expression project (GTEx), Sequence Read
Archive (SRA) and user-provided data. The tool interactively
performs survival, dimensionality reduction and median- and
variance-based differential splicing and gene expression
analyses that benefit from the incorporation of clinical and
molecular sample-associated features (such as tumour stage or
survival). Interactive visual access to genomic mapping and
functional annotation of selected alternative splicing events
is also included.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26705920904</link><pubDate>Sat, 30 May 2026 22:21:18 GMT</pubDate><r:package>psichomics</r:package><r:version>1.38.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/psichomics</r:upstream><r:article><r:source>CLI_tutorial.Rmd</r:source><r:filename>CLI_tutorial.html</r:filename><r:title>Case study: command-line interface (CLI) tutorial</r:title><r:created>2016-09-07 15:29:18</r:created><r:modified>2026-01-07 11:09:05</r:modified></r:article><r:article><r:source>GUI_tutorial.Rmd</r:source><r:filename>GUI_tutorial.html</r:filename><r:title>Case study: visual interface tutorial</r:title><r:created>2016-09-07 15:29:18</r:created><r:modified>2026-01-07 11:09:05</r:modified></r:article><r:article><r:source>custom_data.Rmd</r:source><r:filename>custom_data.html</r:filename><r:title>Loading user-provided data</r:title><r:created>2019-03-27 14:21:32</r:created><r:modified>2026-01-07 11:09:05</r:modified></r:article><r:article><r:source>AS_events_preparation.Rmd</r:source><r:filename>AS_events_preparation.html</r:filename><r:title>Preparing an Alternative Splicing Annotation for psichomics</r:title><r:created>2016-10-08 21:55:19</r:created><r:modified>2026-01-07 11:09:05</r:modified></r:article></item><item><title>[bioc-release] SeqArray 1.52.1</title><author>zhengx@u.washington.edu (Xiuwen Zheng)</author><description>Data management of large-scale whole-genome sequencing
variant calls with thousands of individuals: genotypic data
(e.g., SNVs, indels and structural variation calls) and
annotations in SeqArray GDS files are stored in an
array-oriented and compressed manner, with efficient data
access using the R programming language.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26680215571</link><pubDate>Sat, 30 May 2026 05:02:14 GMT</pubDate><r:package>SeqArray</r:package><r:version>1.52.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/SeqArray</r:upstream><r:article><r:source>SeqArray.Rmd</r:source><r:filename>SeqArray.html</r:filename><r:title>Integration with R</r:title><r:created>2019-10-22 02:53:13</r:created><r:modified>2022-07-16 04:35:03</r:modified></r:article><r:article><r:source>SeqArrayTutorial.Rmd</r:source><r:filename>SeqArrayTutorial.html</r:filename><r:title>SeqArray Data Format and Access</r:title><r:created>2015-06-14 01:14:12</r:created><r:modified>2026-04-15 18:54:02</r:modified></r:article><r:article><r:source>OverviewSlides.Rmd</r:source><r:filename>OverviewSlides.html</r:filename><r:title>SeqArray Overview</r:title><r:created>2015-12-02 06:48:45</r:created><r:modified>2022-07-16 04:35:03</r:modified></r:article></item><item><title>[bioc-release] Rarr 2.0.1</title><author>hugo.gruson@embl.de (Hugo Gruson)</author><description>The Zarr specification defines a format for chunked,
compressed, N-dimensional arrays.  It's design allows efficient
access to subsets of the stored array, and supports both local
and cloud storage systems.  Rarr aims to implement this
specification in R with minimal reliance on an external tools
or libraries.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26638382678</link><pubDate>Fri, 29 May 2026 09:25:29 GMT</pubDate><r:package>Rarr</r:package><r:version>2.0.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/Rarr</r:upstream><r:article><r:source>features.Rmd</r:source><r:filename>features.html</r:filename><r:title>Supported Zarr features in Rarr</r:title><r:created>2025-10-31 08:07:06</r:created><r:modified>2026-03-30 14:31:41</r:modified></r:article><r:article><r:source>Rarr.Rmd</r:source><r:filename>Rarr.html</r:filename><r:title>Working with Zarr arrays in R</r:title><r:created>2023-01-23 08:43:30</r:created><r:modified>2026-03-16 17:16:42</r:modified></r:article><r:article><r:source>design.Rmd</r:source><r:filename>design.html</r:filename><r:title>Design principles for the Rarr package</r:title><r:created>2026-03-30 14:31:41</r:created><r:modified>2026-04-18 16:56:34</r:modified></r:article></item><item><title>[bioc-release] BiocBaseUtils 1.14.2</title><author>marcel.ramos@sph.cuny.edu (Marcel Ramos)</author><description>The package coalesces typical helper functions that are
scattered throughout the Bioconductor ecosystem. It aims to
reduce code redundancy by formalizing functions often used by
Bioconductor developers. These functions include operations
such as replacing slots in an object, selecting observations
for show methods, labeling function life cycles, and more.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26496179376</link><pubDate>Tue, 26 May 2026 21:25:06 GMT</pubDate><r:package>BiocBaseUtils</r:package><r:version>1.14.2</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/BiocBaseUtils</r:upstream><r:article><r:source>BiocBaseUtils.Rmd</r:source><r:filename>BiocBaseUtils.html</r:filename><r:title>BiocBaseUtils Quick Start</r:title><r:created>2022-08-18 19:25:58</r:created><r:modified>2026-05-26 21:15:45</r:modified></r:article></item><item><title>[bioc-release] AnVILGCP 1.6.2</title><author>marcel.ramos@sph.cuny.edu (Marcel Ramos)</author><description>The package provides a set of functions to interact with
the Google Cloud Platform (GCP) services on the AnVIL platform.
The package is designed to use the API calls from the AnVIL
package. It coordinates AnVIL workspace functionality with
native GCP tools.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26496177978</link><pubDate>Tue, 26 May 2026 21:04:29 GMT</pubDate><r:package>AnVILGCP</r:package><r:version>1.6.2</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/AnVILGCP</r:upstream><r:article><r:source>AnVILGCPIntroduction.Rmd</r:source><r:filename>AnVILGCPIntroduction.html</r:filename><r:title>Working with AnVIL on GCP</r:title><r:created>2024-03-28 21:34:53</r:created><r:modified>2026-05-26 20:59:00</r:modified></r:article></item><item><title>[bioc-release] GCPtools 1.2.1</title><author>marcel.ramos@sph.cuny.edu (Marcel Ramos)</author><description>Lower-level functionality to interface with Google Cloud
Platform tools. 'gcloud' and 'gsutil' are both supported. The
functionality provided centers around utilities for the AnVIL
platform.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26496180950</link><pubDate>Tue, 26 May 2026 20:50:15 GMT</pubDate><r:package>GCPtools</r:package><r:version>1.2.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/GCPtools</r:upstream><r:article><r:source>GCPtools.Rmd</r:source><r:filename>GCPtools.html</r:filename><r:title>GCPtools</r:title><r:created>2025-05-27 19:26:50</r:created><r:modified>2025-07-17 17:03:53</r:modified></r:article></item><item><title>[bioc-release] DelayedArray 0.38.2</title><author>hpages.on.github@gmail.com (Hervé Pagès)</author><description>Wrapping an array-like object (typically an on-disk
object) in a DelayedArray object allows one to perform common
array operations on it without loading the object in memory. In
order to reduce memory usage and optimize performance,
operations on the object are either delayed or executed using a
block processing mechanism. Note that this also works on
in-memory array-like objects like DataFrame objects (typically
with Rle columns), Matrix objects, ordinary arrays and, data
frames.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26477313525</link><pubDate>Tue, 26 May 2026 17:05:47 GMT</pubDate><r:package>DelayedArray</r:package><r:version>0.38.2</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/DelayedArray</r:upstream><r:article><r:source>A-Working_with_large_arrays.Rnw</r:source><r:filename>A-Working_with_large_arrays.pdf</r:filename><r:title>Working with large arrays in R (slides from July 2017) </r:title><r:created>2024-05-06 23:22:25</r:created><r:modified>2024-05-06 23:22:25</r:modified></r:article><r:article><r:source>B-Implementing_a_backend.Rmd</r:source><r:filename>B-Implementing_a_backend.html</r:filename><r:title>Implementing A DelayedArray Backend</r:title><r:created>2024-05-06 23:22:25</r:created><r:modified>2024-05-06 23:22:25</r:modified></r:article><r:article><r:source>C-DelayedArray_HDF5Array_update.Rnw</r:source><r:filename>C-DelayedArray_HDF5Array_update.pdf</r:filename><r:title>A DelayedArray / HDF5Array update (slides from April 2021) </r:title><r:created>2024-05-06 23:22:25</r:created><r:modified>2024-05-06 23:22:25</r:modified></r:article></item><item><title>[bioc-release] pipeComp 1.22.1</title><author>pierre-luc.germain@hest.ethz.ch (Pierre-Luc Germain)</author><description>A simple framework to facilitate the comparison of
pipelines involving various steps and parameters. The
`pipelineDefinition` class represents pipelines as, minimally,
a set of functions consecutively executed on the output of the
previous one, and optionally accompanied by step-wise
evaluation and aggregation functions. Given such an object, a
set of alternative parameters/methods, and benchmark datasets,
the `runPipeline` function then proceeds through all
combinations arguments, avoiding recomputing the same step
twice and compiling evaluations on the fly to avoid storing
potentially large intermediate data.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26465872677</link><pubDate>Tue, 26 May 2026 07:26:25 GMT</pubDate><r:package>pipeComp</r:package><r:version>1.22.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/pipeComp</r:upstream><r:article><r:source>pipeComp.Rmd</r:source><r:filename>pipeComp.html</r:filename><r:title>The pipeComp framework</r:title><r:created>2020-03-05 10:28:42</r:created><r:modified>2020-09-04 11:42:03</r:modified></r:article><r:article><r:source>pipeComp_dea.Rmd</r:source><r:filename>pipeComp_dea.html</r:filename><r:title>The DEA PipelineDefinition</r:title><r:created>2020-04-20 18:00:22</r:created><r:modified>2020-04-29 15:35:09</r:modified></r:article><r:article><r:source>pipeComp_scRNA.Rmd</r:source><r:filename>pipeComp_scRNA.html</r:filename><r:title>The scRNA PipelineDefinition</r:title><r:created>2020-03-05 10:28:42</r:created><r:modified>2020-07-23 14:12:27</r:modified></r:article></item><item><title>[bioc-release] CellMentor 1.0.1</title><author>petrenko.kate@icloud.com (Ekaterina Petrenko)</author><description>Implements supervised cell type-aware non-negative matrix
factorization (NMF) for dimensional reduction in single-cell
RNA sequencing analysis. The package provides methods for
incorporating cell type information into the dimensionality
reduction process, enabling improved visualization and
downstream analysis of single-cell data while preserving
biological structure. CellMentor employs a unique loss function
that simultaneously minimizes variation within known cell
populations while maximizing distinctions between different
cell types, enabling effective transfer of learned patterns
from labeled reference datasets to new unlabeled data.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26419752035</link><pubDate>Mon, 25 May 2026 16:23:09 GMT</pubDate><r:package>CellMentor</r:package><r:version>1.0.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/CellMentor</r:upstream><r:article><r:source>CellMentor_vignette.Rmd</r:source><r:filename>CellMentor_vignette.html</r:filename><r:title>Introduction to CellMentor</r:title><r:created>2025-10-27 19:17:30</r:created><r:modified>2026-04-02 11:33:07</r:modified></r:article></item><item><title>[bioc-release] ensembldb 2.36.1</title><author>johannes.rainer@eurac.edu (Johannes Rainer)</author><description>The package provides functions to create and use
transcript centric annotation databases/packages. The
annotation for the databases are directly fetched from Ensembl
using their Perl API. The functionality and data is similar to
that of the TxDb packages from the GenomicFeatures package,
but, in addition to retrieve all gene/transcript models and
annotations from the database, ensembldb provides a filter
framework allowing to retrieve annotations for specific entries
like genes encoded on a chromosome region or transcript models
of lincRNA genes. EnsDb databases built with ensembldb contain
also protein annotations and mappings between proteins and
their encoding transcripts. Finally, ensembldb provides
functions to map between genomic, transcript and protein
coordinates.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26398976906</link><pubDate>Mon, 25 May 2026 09:23:58 GMT</pubDate><r:package>ensembldb</r:package><r:version>2.36.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/ensembldb</r:upstream><r:article><r:source>ensembldb.Rmd</r:source><r:filename>ensembldb.html</r:filename><r:title>Generating and using Ensembl based annotation packages</r:title><r:created>2018-02-28 08:01:05</r:created><r:modified>2025-08-18 11:34:41</r:modified></r:article><r:article><r:source>coordinate-mapping.Rmd</r:source><r:filename>coordinate-mapping.html</r:filename><r:title>Mapping between genome, transcript and protein coordinates</r:title><r:created>2018-02-28 08:05:00</r:created><r:modified>2020-01-22 15:14:46</r:modified></r:article><r:article><r:source>proteins.Rmd</r:source><r:filename>proteins.html</r:filename><r:title>Querying protein features</r:title><r:created>2018-02-28 08:02:48</r:created><r:modified>2024-08-21 08:56:10</r:modified></r:article><r:article><r:source>coordinate-mapping-use-cases.Rmd</r:source><r:filename>coordinate-mapping-use-cases.html</r:filename><r:title>Use cases for coordinate mapping with ensembldb</r:title><r:created>2018-11-13 09:30:36</r:created><r:modified>2022-01-31 13:22:32</r:modified></r:article><r:article><r:source>MySQL-backend.Rmd</r:source><r:filename>MySQL-backend.html</r:filename><r:title>Using a MySQL server backend</r:title><r:created>2018-02-28 08:02:48</r:created><r:modified>2024-08-21 08:21:08</r:modified></r:article></item><item><title>[bioc-release] assorthead 1.6.3</title><author>infinite.monkeys.with.keyboards@gmail.com (Aaron Lun)</author><description>Vendors an assortment of useful header-only C++ libraries.
Bioconductor packages can use these libraries in their own C++
code by LinkingTo this package without introducing any
additional dependencies. The use of a central repository avoids
duplicate vendoring of libraries across multiple R packages,
and enables better coordination of version updates across
cohorts of interdependent C++ libraries.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26398974963</link><pubDate>Mon, 25 May 2026 07:11:23 GMT</pubDate><r:package>assorthead</r:package><r:version>1.6.3</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/assorthead</r:upstream><r:article><r:source>userguide.Rmd</r:source><r:filename>userguide.html</r:filename><r:title>Assortment of header-only libraries</r:title><r:created>2024-07-18 18:29:28</r:created><r:modified>2024-08-09 17:42:27</r:modified></r:article></item><item><title>[bioc-release] scMitoMut 1.8.0</title><author>sunwjie@gmail.com (Wenjie Sun)</author><description>This package is designed for calling lineage-informative
mitochondrial mutations using single-cell sequencing data, such
as scRNASeq and scATACSeq (preferably the latter due to RNA
editing issues). It includes functions for mutation calling and
visualization. Mutation calling is done using beta-binomial
distribution.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26398979743</link><pubDate>Mon, 25 May 2026 05:23:52 GMT</pubDate><r:package>scMitoMut</r:package><r:version>1.8.0</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/scMitoMut</r:upstream><r:article><r:source>Analysis_colon_cancer_dataset.Rmd</r:source><r:filename>Analysis_colon_cancer_dataset.html</r:filename><r:title>scMitoMut demo: CRC dataset</r:title><r:created>2023-07-27 12:08:18</r:created><r:modified>2026-05-25 05:23:52</r:modified></r:article></item><item><title>[bioc-release] TCGAutils 1.32.1</title><author>marcel.ramos@sph.cuny.edu (Marcel Ramos)</author><description>A suite of helper functions for checking and manipulating
TCGA data including data obtained from the curatedTCGAData
experiment package. These functions aim to simplify and make
working with TCGA data more manageable. Exported functions
include those that import data from flat files into
Bioconductor objects, convert row annotations, and identifier
translation via the GDC API.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26447265151</link><pubDate>Mon, 25 May 2026 02:25:40 GMT</pubDate><r:package>TCGAutils</r:package><r:version>1.32.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/TCGAutils</r:upstream><r:article><r:source>TCGAutils.Rmd</r:source><r:filename>TCGAutils.html</r:filename><r:title>TCGAutils: Helper functions for working with TCGA datasets</r:title><r:created>2017-12-21 01:14:47</r:created><r:modified>2025-07-02 16:09:54</r:modified></r:article></item><item><title>[bioc-release] edgeR 4.10.1</title><author>mark.robinson@imls.uzh.ch (Yunshun Chen)</author><description>Differential expression analysis of sequence count data.
Implements a range of statistical methodology based on the
negative binomial distributions, including empirical Bayes
estimation, exact tests, generalized linear models,
quasi-likelihood, and gene set enrichment. Can perform
differential analyses of any type of omics data that produces
read counts, including RNA-seq, ChIP-seq, ATAC-seq,
Bisulfite-seq, SAGE, CAGE, metabolomics, or proteomics spectral
counts. RNA-seq analyses can be conducted at the gene or
isoform level, and tests can be conducted for differential exon
or transcript usage.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26325852091</link><pubDate>Sat, 23 May 2026 03:30:36 GMT</pubDate><r:package>edgeR</r:package><r:version>4.10.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/edgeR</r:upstream><r:article><r:source>intro.Rmd</r:source><r:filename>intro.html</r:filename><r:title>A brief introduction to edgeR</r:title><r:created>2023-06-21 10:09:59</r:created><r:modified>2025-12-23 06:09:34</r:modified></r:article><r:article><r:source>edgeRUsersGuide.Rnw</r:source><r:filename>edgeRUsersGuide.pdf</r:filename><r:title>edgeR User's Guide</r:title><r:created>2023-06-20 00:55:03</r:created><r:modified>2023-06-20 00:55:03</r:modified></r:article></item><item><title>[bioc-release] GraphExperiment 1.0.1</title><author>fabricio_almeidasilva@hotmail.com (Fabricio Almeida-Silva)</author><description>GraphExperiment provides users and developers with an S4
class that extends `SingleCellExperiment` by offering
infrastructure to store and retrieve networks (`igraph`
objects) representing how assay features and/or observations
are associated with each other. The class was designed to store
networks inferred from high-dimensional quantitative data, with
feature-feature networks including gene coexpression networks
(GCNs), gene regulatory networks (GRNs), and co-abundance
networks (from proteomics and metabolomics), and
observation-observation network including cell-cell distances,
species-species relationships, and sample-sample similarities.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26625036339</link><pubDate>Fri, 22 May 2026 19:37:38 GMT</pubDate><r:package>GraphExperiment</r:package><r:version>1.0.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/GraphExperiment</r:upstream><r:article><r:source>GraphExperiment.Rmd</r:source><r:filename>GraphExperiment.html</r:filename><r:title>Introduction to the GraphExperiment class</r:title><r:created>2026-03-16 09:51:01</r:created><r:modified>2026-05-22 19:37:13</r:modified></r:article></item><item><title>[bioc-release] MsBackendMetaboLights 1.6.1</title><author>johannes.rainer@eurac.edu (Johannes Rainer)</author><description>MetaboLights is one of the main public repositories for
storage of metabolomics experiments, which includes analysis
results as well as raw data. The MsBackendMetaboLights package
provides functionality to retrieve and represent mass
spectrometry (MS) data from MetaboLights. Data files are
downloaded and cached locally avoiding repetitive downloads. MS
data from metabolomics experiments can thus be directly and
seamlessly integrated into R-based analysis workflows with the
Spectra and MsBackendMetaboLights package.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26299368478</link><pubDate>Fri, 22 May 2026 12:31:40 GMT</pubDate><r:package>MsBackendMetaboLights</r:package><r:version>1.6.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/MsBackendMetaboLights</r:upstream><r:article><r:source>MsBackendMetaboLights.Rmd</r:source><r:filename>MsBackendMetaboLights.html</r:filename><r:title>Retrieve and Use Mass Spectrometry Data from MetaboLights</r:title><r:created>2024-09-07 09:49:31</r:created><r:modified>2026-04-13 11:07:16</r:modified></r:article></item><item><title>[bioc-release] Biostrings 2.80.1</title><author>hpages.on.github@gmail.com (Hervé Pagès)</author><description>Memory efficient string containers, string matching
algorithms, and other utilities, for fast manipulation of large
biological sequences or sets of sequences.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26622187729</link><pubDate>Fri, 22 May 2026 06:02:45 GMT</pubDate><r:package>Biostrings</r:package><r:version>2.80.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/Biostrings</r:upstream><r:article><r:source>Biostrings2Classes.Rnw</r:source><r:filename>Biostrings2Classes.pdf</r:filename><r:title>A short presentation of the basic classes defined in Biostrings 2</r:title><r:created>2013-11-01 19:50:36</r:created><r:modified>2013-11-01 19:50:36</r:modified></r:article><r:article><r:source>BiostringsQuickOverview.Rnw</r:source><r:filename>BiostringsQuickOverview.pdf</r:filename><r:title>Biostrings Quick Overview</r:title><r:created>2013-11-01 19:50:36</r:created><r:modified>2024-04-23 05:10:42</r:modified></r:article><r:article><r:source>matchprobes.Rmd</r:source><r:filename>matchprobes.html</r:filename><r:title>Using oligonucleotide microarray reporter sequence information for preprocessing and quality assessment</r:title><r:created>2023-04-14 03:17:19</r:created><r:modified>2024-02-12 17:48:02</r:modified></r:article><r:article><r:source>MultipleAlignments.Rmd</r:source><r:filename>MultipleAlignments.html</r:filename><r:title>MultipleAlignment Objects</r:title><r:created>2024-06-07 17:02:07</r:created><r:modified>2025-05-09 05:50:52</r:modified></r:article><r:article><r:source>PairwiseAlignments.Rnw</r:source><r:filename>PairwiseAlignments.pdf</r:filename><r:title>Pairwise Sequence Alignments</r:title><r:created>2013-11-01 19:50:36</r:created><r:modified>2024-04-23 05:10:42</r:modified></r:article></item><item><title>[bioc-release] dmGsea 1.2.1</title><author>xuz@niehs.nih.gov (Zongli Xu)</author><description>The R package dmGsea provides efficient gene set
enrichment analysis specifically for DNA methylation data. It
addresses key biases, including probe dependency and varying
probe numbers per gene. The package supports Illumina 450K,
EPIC, and mouse methylation arrays. Users can also apply it to
other omics data by supplying custom probe-to-gene mapping
annotations. dmGsea is flexible, fast, and well-suited for
large-scale epigenomic studies.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26252454838</link><pubDate>Thu, 21 May 2026 16:58:57 GMT</pubDate><r:package>dmGsea</r:package><r:version>1.2.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/dmGsea</r:upstream><r:article><r:source>dmGsea.Rmd</r:source><r:filename>dmGsea.html</r:filename><r:title>dmGsea User's Guide</r:title><r:created>2025-01-19 01:29:41</r:created><r:modified>2026-01-12 19:00:46</r:modified></r:article></item><item><title>[bioc-release] normr 1.38.1</title><author>johannes.helmuth@laborberlin.com (Johannes Helmuth)</author><description>Robust normalization and difference calling procedures for
ChIP-seq and alike data. Read counts are modeled jointly as a
binomial mixture model with a user-specified number of
components. A fitted background estimate accounts for the
effect of enrichment in certain regions and, therefore,
represents an appropriate null hypothesis. This robust
background is used to identify significantly enriched or
depleted regions.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26252458250</link><pubDate>Thu, 21 May 2026 16:33:14 GMT</pubDate><r:package>normr</r:package><r:version>1.38.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/normr</r:upstream><r:article><r:source>normr.Rmd</r:source><r:filename>normr.html</r:filename><r:title>Introduction to the normR package</r:title><r:created>2016-07-12 14:03:46</r:created><r:modified>2020-04-14 15:10:59</r:modified></r:article></item><item><title>[bioc-release] bamsignals 1.44.1</title><author>johannes.helmuth@laborberlin.com (Johannes Helmuth)</author><description>This package allows to efficiently obtain count vectors
from indexed bam files. It counts the number of reads in given
genomic ranges and it computes reads profiles and coverage
profiles. It also handles paired-end data.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26239951552</link><pubDate>Thu, 21 May 2026 15:32:16 GMT</pubDate><r:package>bamsignals</r:package><r:version>1.44.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/bamsignals</r:upstream><r:article><r:source>bamsignals.Rmd</r:source><r:filename>bamsignals.html</r:filename><r:title>Introduction to the bamsignals package</r:title><r:created>2015-02-13 21:00:36</r:created><r:modified>2016-04-11 07:41:32</r:modified></r:article></item><item><title>[bioc-release] MicrobiomeProfiler 1.18.1</title><author>guangchuangyu@gmail.com (Guangchuang Yu)</author><description>This is an R/shiny package to perform functional
enrichment analysis for microbiome data. This package was based
on clusterProfiler. Moreover, MicrobiomeProfiler support KEGG
enrichment analysis, COG enrichment analysis, Microbe-Disease
association enrichment analysis, Metabo-Pathway analysis.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26210335790</link><pubDate>Thu, 21 May 2026 01:10:29 GMT</pubDate><r:package>MicrobiomeProfiler</r:package><r:version>1.18.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/MicrobiomeProfiler</r:upstream><r:article><r:source>MicrobiomeProfiler.Rmd</r:source><r:filename>MicrobiomeProfiler.html</r:filename><r:title>Introduction to MicrobiomeProfiler</r:title><r:created>2021-09-17 08:57:03</r:created><r:modified>2023-04-18 01:40:58</r:modified></r:article></item><item><title>[bioc-release] BiocBuildReporter 1.0.1</title><author>lori.shepherd@roswellpark.org (Lori Shepherd)</author><description>This package reads remote parquet files that have
processed Bioconductor build report logs. Users may query the
tables directly for specific information or use pre-defined
helper functions for common queries. The logs processed are
from https://bioconductor.org/checkResults/. In the future we
will extend this package out to include processing of
r-universe logs.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26177236128</link><pubDate>Wed, 20 May 2026 15:02:30 GMT</pubDate><r:package>BiocBuildReporter</r:package><r:version>1.0.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/BiocBuildReporter</r:upstream><r:article><r:source>BiocBuildReporter.Rmd</r:source><r:filename>BiocBuildReporter.html</r:filename><r:title>BiocBuildReporter Data Use Cases</r:title><r:created>2026-03-06 17:22:27</r:created><r:modified>2026-03-16 17:02:49</r:modified></r:article></item><item><title>[bioc-release] scater 1.40.1</title><author>alan.ocallaghan@outlook.com (Alan OCallaghan)</author><description>A collection of tools for doing various analyses of
single-cell RNA-seq gene expression data, with a focus on
quality control and visualization.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26177244411</link><pubDate>Wed, 20 May 2026 13:26:24 GMT</pubDate><r:package>scater</r:package><r:version>1.40.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/scater</r:upstream><r:article><r:source>overview.Rmd</r:source><r:filename>overview.html</r:filename><r:title>Single-cell analysis toolkit for expression in R</r:title><r:created>2019-07-31 04:35:57</r:created><r:modified>2022-02-21 19:06:35</r:modified></r:article></item><item><title>[bioc-release] COTAN 2.12.1</title><author>silvia.galfre@di.unipi.it (Galfrè Silvia Giulia)</author><description>Statistical and computational method to analyze the
co-expression of gene pairs at single cell level. It provides
the foundation for single-cell gene interactome analysis. The
basic idea is studying the zero UMI counts' distribution
instead of focusing on positive counts; this is done with a
generalized contingency tables framework. COTAN can effectively
assess the correlated or anti-correlated expression of gene
pairs. It provides a numerical index related to the correlation
and an approximate p-value for the associated independence
test. COTAN can also evaluate whether single genes are
differentially expressed, scoring them with a newly defined
global differentiation index. Moreover, this approach provides
ways to plot and cluster genes according to their co-expression
pattern with other genes, effectively helping the study of gene
interactions and becoming a new tool to identify cell-identity
marker genes.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26177240645</link><pubDate>Wed, 20 May 2026 13:09:00 GMT</pubDate><r:package>COTAN</r:package><r:version>2.12.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/COTAN</r:upstream><r:article><r:source>Cleaning_GuidedTutorial.Rmd</r:source><r:filename>Cleaning_GuidedTutorial.html</r:filename><r:title>Guided tutorial to datasets cleaning using COTAN</r:title><r:created>2026-03-11 08:24:02</r:created><r:modified>2026-03-19 09:12:28</r:modified></r:article><r:article><r:source>DiffExprAnalysis_GuidedTutorial.Rmd</r:source><r:filename>DiffExprAnalysis_GuidedTutorial.html</r:filename><r:title>Guided tutorial to Differential Expression Analysis using COTAN</r:title><r:created>2026-03-15 10:24:22</r:created><r:modified>2026-03-19 09:12:28</r:modified></r:article><r:article><r:source>GenesClustering_GuidedTutorial.Rmd</r:source><r:filename>GenesClustering_GuidedTutorial.html</r:filename><r:title>Guided tutorial to genes' clustering using COTAN</r:title><r:created>2026-03-11 08:24:02</r:created><r:modified>2026-03-15 11:36:33</r:modified></r:article><r:article><r:source>UniformClustering_GuidedTutorial.Rmd</r:source><r:filename>UniformClustering_GuidedTutorial.html</r:filename><r:title>Guided tutorial to Uniform Transcript cells' clustering using COTAN</r:title><r:created>2026-03-11 08:24:02</r:created><r:modified>2026-03-19 09:12:28</r:modified></r:article></item><item><title>[bioc-release] StatescopeR 1.0.1</title><author>m.f.b.steketee@amsterdamumc.nl (Mischa Steketee)</author><description>StatescopeR is an R wrapper around Statescope, a
computational framework designed to discover cell states from
cell type-specific gene expression profiles inferred from bulk
RNA profiles.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26353575389</link><pubDate>Wed, 20 May 2026 08:46:00 GMT</pubDate><r:package>StatescopeR</r:package><r:version>1.0.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/StatescopeR</r:upstream><r:article><r:source>StatescopeR.Rmd</r:source><r:filename>StatescopeR.html</r:filename><r:title>Introduction to StatescopeR</r:title><r:created>2025-05-07 10:54:54</r:created><r:modified>2026-05-20 08:46:00</r:modified></r:article></item><item><title>[bioc-release] GSVA 2.6.2</title><author>robert.castelo@upf.edu (Robert Castelo)</author><description>Gene Set Variation Analysis (GSVA) is a non-parametric,
unsupervised method for estimating variation of gene set
enrichment through the samples of a expression data set. GSVA
performs a change in coordinate systems, transforming the data
from a gene by sample matrix to a gene-set by sample matrix,
thereby allowing the evaluation of pathway enrichment for each
sample. This new matrix of GSVA enrichment scores facilitates
applying standard analytical methods like functional
enrichment, survival analysis, clustering, CNV-pathway analysis
or cross-tissue pathway analysis, in a pathway-centric manner.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26128573744</link><pubDate>Tue, 19 May 2026 17:26:43 GMT</pubDate><r:package>GSVA</r:package><r:version>2.6.2</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/GSVA</r:upstream><r:article><r:source>GSVA.Rmd</r:source><r:filename>GSVA.html</r:filename><r:title>GSVA: gene set variation analysis</r:title><r:created>2021-02-05 18:07:16</r:created><r:modified>2026-02-19 10:04:05</r:modified></r:article><r:article><r:source>GSVA_proteomics.Rmd</r:source><r:filename>GSVA_proteomics.html</r:filename><r:title>GSVA on proteomics data</r:title><r:created>2026-04-27 18:04:17</r:created><r:modified>2026-05-05 10:36:07</r:modified></r:article><r:article><r:source>GSVA_scRNAseq.Rmd</r:source><r:filename>GSVA_scRNAseq.html</r:filename><r:title>GSVA on single-cell RNA-seq data</r:title><r:created>2025-10-27 18:49:02</r:created><r:modified>2026-04-24 18:44:37</r:modified></r:article></item><item><title>[bioc-release] scrapper 1.6.3</title><author>infinite.monkeys.with.keyboards@gmail.com (Aaron Lun)</author><description>Implements R bindings to C++ code for analyzing
single-cell (expression) data, mostly from various libscran
libraries. Each function performs an individual step in the
single-cell analysis workflow, ranging from quality control to
clustering and marker detection. Additional wrappers are
provided for easy construction of end-to-end workflows
involving Bioconductor objects like SingleCellExperiments.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26092970829</link><pubDate>Tue, 19 May 2026 10:09:14 GMT</pubDate><r:package>scrapper</r:package><r:version>1.6.3</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/scrapper</r:upstream><r:article><r:source>userguide.Rmd</r:source><r:filename>userguide.html</r:filename><r:title>Using scrapper to analyze single-cell data</r:title><r:created>2024-09-08 23:25:44</r:created><r:modified>2025-12-26 02:51:17</r:modified></r:article></item><item><title>[bioc-release] imcRtools 1.18.1</title><author>daniel.schulz@uzh.ch (Daniel Schulz)</author><description>This R package supports the handling and analysis of
imaging mass cytometry and other highly multiplexed imaging
data. The main functionality includes reading in single-cell
data after image segmentation and measurement, data formatting
to perform channel spillover correction and a number of spatial
analysis approaches. First, cell-cell interactions are detected
via spatial graph construction; these graphs can be visualized
with cells representing nodes and interactions representing
edges. Furthermore, per cell, its direct neighbours are
summarized to allow spatial clustering. Per image/grouping
level, interactions between types of cells are counted,
averaged and compared against random permutations. In that way,
types of cells that interact more (attraction) or less
(avoidance) frequently than expected by chance are detected.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26092966968</link><pubDate>Tue, 19 May 2026 07:03:52 GMT</pubDate><r:package>imcRtools</r:package><r:version>1.18.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/imcRtools</r:upstream><r:article><r:source>imcRtools.Rmd</r:source><r:filename>imcRtools.html</r:filename><r:title>Tools for IMC data analysis</r:title><r:created>2020-12-17 16:51:01</r:created><r:modified>2026-03-30 11:32:46</r:modified></r:article></item><item><title>[bioc-release] SEMPLR 1.0.1</title><author>kenney.grace6@gmail.com (Grace Kenney)</author><description>SEMPLR computes transcription factor binding affinity
scores for genomic positions and genetic variants. Scores are
computed from SNP Effect Matrices (SEMs) produced by SEMpl. 223
pre-computed SEMs are included with the package or custom sets
can be provided. Enrichment can be tested among sets of genomic
positions to determine if transcription factor binding events
occur more often than expected. Comparing binding affinity
scores between alleles can reveal differences in transcription
factor binding with genetic variation. This package also
includes several visualization functions to view scores both on
the motif and variant/position level.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26060838870</link><pubDate>Mon, 18 May 2026 19:21:04 GMT</pubDate><r:package>SEMPLR</r:package><r:version>1.0.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/SEMPLR</r:upstream><r:article><r:source>SEMPLR.Rmd</r:source><r:filename>SEMPLR.html</r:filename><r:title>SEMPLR Vignette</r:title><r:created>2026-02-02 23:34:15</r:created><r:modified>2026-05-16 23:53:17</r:modified></r:article></item><item><title>[bioc-release] BatChef 1.0.1</title><author>elena.zuin.3@phd.unipd.it (Elena Zuin)</author><description>This package implements a variety of methods for batch
correction in single-cell RNA sequencing (scRNA-seq) data. It
incorporates quantitative metrics (e.g. Wasserstein distance,
Adjusted Rand Index) to evaluate their performance.
Furthermore, the package assists users in identifying and
applying the optimal method for specific datasets.</description><link>https://github.com/r-universe/bioc-release/actions/runs/26060831804</link><pubDate>Mon, 18 May 2026 16:26:59 GMT</pubDate><r:package>BatChef</r:package><r:version>1.0.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/BatChef</r:upstream><r:article><r:source>batch_correction.Rmd</r:source><r:filename>batch_correction.html</r:filename><r:title>BatChef package introduction</r:title><r:created>2025-09-04 14:21:58</r:created><r:modified>2026-05-18 16:19:14</r:modified></r:article></item><item><title>[bioc-release] ggsc 1.10.1</title><author>guangchuangyu@gmail.com (Guangchuang Yu)</author><description>Useful functions to visualize single cell and spatial
data. It supports visualizing 'Seurat', 'SingleCellExperiment'
and 'SpatialExperiment' objects through grammar of graphics
syntax implemented in 'ggplot2'.</description><link>https://github.com/r-universe/bioc-release/actions/runs/25994281097</link><pubDate>Sun, 17 May 2026 09:05:54 GMT</pubDate><r:package>ggsc</r:package><r:version>1.10.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/ggsc</r:upstream><r:article><r:source>ggsc.Rmd</r:source><r:filename>ggsc.html</r:filename><r:title>Visualizing single cell data</r:title><r:created>2023-09-08 01:53:45</r:created><r:modified>2023-11-29 07:46:23</r:modified></r:article></item><item><title>[bioc-release] gdsfmt 1.48.1</title><author>zhengx@u.washington.edu (Xiuwen Zheng)</author><description>Provides a high-level R interface to CoreArray Genomic
Data Structure (GDS) data files. GDS is portable across
platforms with hierarchical structure to store multiple
scalable array-oriented data sets with metadata information. It
is suited for large-scale datasets, especially for data which
are much larger than the available random-access memory. The
gdsfmt package offers the efficient operations specifically
designed for integers of less than 8 bits, since a diploid
genotype, like single-nucleotide polymorphism (SNP), usually
occupies fewer bits than a byte. Data compression and
decompression are available with relatively efficient random
access. It is also allowed to read a GDS file in parallel with
multiple R processes supported by the package parallel.</description><link>https://github.com/r-universe/bioc-release/actions/runs/25916401392</link><pubDate>Fri, 15 May 2026 06:29:46 GMT</pubDate><r:package>gdsfmt</r:package><r:version>1.48.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/gdsfmt</r:upstream><r:article><r:source>gdsfmt.Rmd</r:source><r:filename>gdsfmt.html</r:filename><r:title>R Interface to CoreArray Genomic Data Structure (GDS) Files</r:title><r:created>2019-10-14 19:04:19</r:created><r:modified>2022-07-15 22:34:14</r:modified></r:article></item><item><title>[bioc-release] BiocPkgTools 1.30.0</title><author>seandavi@gmail.com (Sean Davis)</author><description>Bioconductor has a rich ecosystem of metadata around
packages, usage, and build status. This package is a simple
collection of functions to access that metadata from R. The
goal is to expose metadata for data mining and value-added
functionality such as package searching, text mining, and
analytics on packages.</description><link>https://github.com/r-universe/bioc-release/actions/runs/25885830231</link><pubDate>Thu, 14 May 2026 20:07:28 GMT</pubDate><r:package>BiocPkgTools</r:package><r:version>1.30.0</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/BiocPkgTools</r:upstream><r:article><r:source>BiocPkgTools.Rmd</r:source><r:filename>BiocPkgTools.html</r:filename><r:title>Overview of BiocPkgTools</r:title><r:created>2017-12-08 16:23:47</r:created><r:modified>2025-07-11 16:14:21</r:modified></r:article></item><item><title>[bioc-release] splicelogic 1.0.1</title><author>beatrizcampillo29@gmail.com (Beatriz Campillo)</author><description>Translate differential transcript usage results into
discrete splice events.</description><link>https://github.com/r-universe/bioc-release/actions/runs/25885832065</link><pubDate>Thu, 14 May 2026 15:31:14 GMT</pubDate><r:package>splicelogic</r:package><r:version>1.0.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/splicelogic</r:upstream><r:article><r:source>splicelogic.Rmd</r:source><r:filename>splicelogic.html</r:filename><r:title>splicelogic: differential transcripts to splice events</r:title><r:created>2026-02-03 19:55:38</r:created><r:modified>2026-05-14 15:31:14</r:modified></r:article></item><item><title>[bioc-release] BiocGenerics 0.58.1</title><author>hpages.on.github@gmail.com (Hervé Pagès)</author><description>The package defines many S4 generic functions used in
Bioconductor.</description><link>https://github.com/r-universe/bioc-release/actions/runs/25854533835</link><pubDate>Thu, 14 May 2026 04:52:20 GMT</pubDate><r:package>BiocGenerics</r:package><r:version>0.58.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/BiocGenerics</r:upstream></item><item><title>[bioc-release] CyTOFpower 1.18.1</title><author>anne-maud.ferreira@epfedu.fr (Anne-Maud Ferreira)</author><description>This package is a tool to predict the power of CyTOF
experiments in the context of differential state analyses. The
package provides a shiny app with two options to predict the
power of an experiment: i. generation of in-sicilico CyTOF
data, using users input ii. browsing in a grid of parameters
for which the power was already precomputed.</description><link>https://github.com/r-universe/bioc-release/actions/runs/25831518997</link><pubDate>Wed, 13 May 2026 19:13:05 GMT</pubDate><r:package>CyTOFpower</r:package><r:version>1.18.1</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/CyTOFpower</r:upstream><r:article><r:source>CyTOFpower.Rmd</r:source><r:filename>CyTOFpower.html</r:filename><r:title>Power analysis for CyTOF experiments</r:title><r:created>2021-09-24 23:25:15</r:created><r:modified>2021-10-18 20:34:24</r:modified></r:article></item><item><title>[bioc-release] spatialHeatmap 2.18.2</title><author>jzhan067@ucr.edu (Jianhai Zhang)</author><description>The spatialHeatmap package offers the primary
functionality for visualizing cell-, tissue- and organ-specific
assay data in spatial anatomical images. Additionally, it
provides extended functionalities for large-scale data mining
routines and co-visualizing bulk and single-cell data. A
description of the project is available here:
https://spatialheatmap.org.</description><link>https://github.com/r-universe/bioc-release/actions/runs/25782349388</link><pubDate>Wed, 13 May 2026 03:58:24 GMT</pubDate><r:package>spatialHeatmap</r:package><r:version>2.18.2</r:version><r:status>failure</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/spatialHeatmap</r:upstream></item><item><title>[bioc-release] epigraHMM 1.20.2</title><author>pedrobaldoni@gmail.com (Pedro Baldoni)</author><description>epigraHMM provides a set of tools for the analysis of
epigenomic data based on hidden Markov Models. It contains two
separate peak callers, one for consensus peaks from biological
or technical replicates, and one for differential peaks from
multi-replicate multi-condition experiments. In differential
peak calling, epigraHMM provides window-specific posterior
probabilities associated with every possible combinatorial
pattern of read enrichment across conditions.</description><link>https://github.com/r-universe/bioc-release/actions/runs/25782335417</link><pubDate>Tue, 12 May 2026 23:41:15 GMT</pubDate><r:package>epigraHMM</r:package><r:version>1.20.2</r:version><r:status>success</r:status><r:repository>https://bioc-release.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/epigraHMM</r:upstream><r:article><r:source>epigraHMM.Rmd</r:source><r:filename>epigraHMM.html</r:filename><r:title>Consensus and differential peak calling with epigraHMM</r:title><r:created>2021-03-01 07:33:54</r:created><r:modified>2026-05-12 23:40:46</r:modified></r:article></item></channel></rss>