<?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>andrei-stoica26.r-universe.dev</title><link>https://andrei-stoica26.r-universe.dev</link><description>Recent package updates in andrei-stoica26</description><generator>R-universe</generator><image><url>https://github.com/andrei-stoica26.png</url><title>R packages by andrei-stoica26</title><link>https://andrei-stoica26.r-universe.dev</link></image><lastBuildDate>Mon, 25 May 2026 01:46:30 GMT</lastBuildDate><item><title>[andrei-stoica26] LISTO 0.8.0</title><author>andreistoica@foxmail.com (Andrei-Florian Stoica)</author><description>The implementation of a statistical framework for
performing overlap assessments on lists comprising sets of
strings (such as lists of gene sets) described in Stoica (2023)
&lt;https://ora.ox.ac.uk/objects/uuid:b0847284-a02f-47ee-88e3-a3c4e0cdb8b1&gt;.
It can assess overlaps of pairs of sets of strings selected
either from the same universe or from different universes, and
overlaps of triplets of sets of strings selected from the same
universe. Designed for single-cell RNA-sequencing data analysis
applications, but suitable for other purposes as well.</description><link>https://github.com/r-universe/andrei-stoica26/actions/runs/26380921544</link><pubDate>Mon, 25 May 2026 01:46:30 GMT</pubDate><r:package>LISTO</r:package><r:version>0.8.0</r:version><r:status>success</r:status><r:repository>https://andrei-stoica26.r-universe.dev</r:repository><r:upstream>https://github.com/andrei-stoica26/listo</r:upstream></item><item><title>[bioc] scLang 1.1.3</title><author>andreistoica@foxmail.com (Andrei-Florian Stoica)</author><description>scLang is a suite for package development for scRNA-seq
analysis. It offers functions that can operate on both Seurat
and SingleCellExperiment objects. These functions are primarily
aimed to help developers build tools compatible with both types
of input.</description><link>https://github.com/r-universe/bioc/actions/runs/27054519434</link><pubDate>Thu, 07 May 2026 07:22:10 GMT</pubDate><r:package>scLang</r:package><r:version>1.1.3</r:version><r:status>success</r:status><r:repository>https://bioc.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/scLang</r:upstream><r:article><r:source>scLang.Rmd</r:source><r:filename>scLang.html</r:filename><r:title>Introduction to scLang</r:title><r:created>2025-11-07 04:40:57</r:created><r:modified>2026-05-07 07:21:30</r:modified></r:article></item><item><title>[bioc] CSOA 1.3.1</title><author>andreistoica@foxmail.com (Andrei-Florian Stoica)</author><description>Cell Set Overlap Analysis (CSOA) is a tool for calculating
per-cell gene signature scores in an scRNA-seq dataset. CSOA
constructs a set for each gene in the signature, consisting of
the cells that highly express the gene. Next, all overlaps of
pairs of cell sets are computed, ranked, filtered and scored.
The CSOA per-cell score is calculated by summing up all
products of the overlap scores and the min-max-normalized
expression of the two involved genes. CSOA can run on a Seurat
object, a SingleCellExperiment object, a matrix and a
dgCMatrix.</description><link>https://github.com/r-universe/bioc/actions/runs/26999054589</link><pubDate>Wed, 06 May 2026 06:48:28 GMT</pubDate><r:package>CSOA</r:package><r:version>1.3.1</r:version><r:status>success</r:status><r:repository>https://bioc.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/CSOA</r:upstream><r:article><r:source>Advanced-CSOA.Rmd</r:source><r:filename>Advanced-CSOA.html</r:filename><r:title>Advanced CSOA</r:title><r:created>2025-08-13 14:54:36</r:created><r:modified>2026-03-11 06:38:47</r:modified></r:article><r:article><r:source>CSOA.Rmd</r:source><r:filename>CSOA.html</r:filename><r:title>CSOA</r:title><r:created>2025-06-06 15:15:22</r:created><r:modified>2025-10-22 06:13:23</r:modified></r:article><r:article><r:source>The-CSOA-algorithm.Rmd</r:source><r:filename>The-CSOA-algorithm.html</r:filename><r:title>The CSOA algorithm</r:title><r:created>2025-08-13 14:54:36</r:created><r:modified>2026-04-17 08:15:16</r:modified></r:article></item><item><title>[bioc] GSABenchmark 1.1.0</title><author>andreistoica@foxmail.com (Andrei-Florian Stoica)</author><description>GSABenchmark is a package designed for benchmarking
scRNA-seq gene set analysis (scGSA) methods. It provides both
traditional and novel benchmark metrics, as well as
visualization tools. Currently, GSABenchmark supports 17 scGSA
methods.</description><link>https://github.com/r-universe/bioc/actions/runs/26676153437</link><pubDate>Tue, 28 Apr 2026 13:06:52 GMT</pubDate><r:package>GSABenchmark</r:package><r:version>1.1.0</r:version><r:status>success</r:status><r:repository>https://bioc.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/GSABenchmark</r:upstream><r:article><r:source>GSABenchmark.Rmd</r:source><r:filename>GSABenchmark.html</r:filename><r:title>Introduction to GSABenchmark</r:title><r:created>2025-07-27 09:47:38</r:created><r:modified>2026-03-04 07:25:38</r:modified></r:article></item><item><title>[bioc] hammers 1.1.0</title><author>andreistoica@foxmail.com (Andrei-Florian Stoica)</author><description>hammers is a utilities suite for scRNA-seq data analysis
compatible with both Seurat and SingleCellExperiment. It
provides simple tools to address tasks such as retrieving
aggregate gene statistics, finding and removing rare genes,
performing representation analysis, computing the center of
mass for the expression of a gene of interest in
low-dimensional space, and calculating silhouette and
cluster-normalized silhouette.</description><link>https://github.com/r-universe/bioc/actions/runs/26678734934</link><pubDate>Tue, 28 Apr 2026 13:06:50 GMT</pubDate><r:package>hammers</r:package><r:version>1.1.0</r:version><r:status>success</r:status><r:repository>https://bioc.r-universe.dev</r:repository><r:upstream>https://github.com/bioc/hammers</r:upstream><r:article><r:source>hammers.Rmd</r:source><r:filename>hammers.html</r:filename><r:title>Introduction to hammers</r:title><r:created>2025-09-09 01:28:32</r:created><r:modified>2026-03-06 13:03:24</r:modified></r:article></item><item><title>[andrei-stoica26] henna 0.8.4</title><author>andreistoica@foxmail.com (Andrei-Florian Stoica)</author><description>A visualization suite primarily designed for single-cell
RNA-sequencing data analysis applications but well-suited for
other purposes as well. It introduces novel plots to represent
two-variable and frequency data and optimizes some commonly
used plotting options (e.g., correlation, network, density,
alluvial and volcano plots) for ease of usage and flexibility.</description><link>https://github.com/r-universe/andrei-stoica26/actions/runs/26561251294</link><pubDate>Tue, 28 Apr 2026 07:28:28 GMT</pubDate><r:package>henna</r:package><r:version>0.8.4</r:version><r:status>success</r:status><r:repository>https://andrei-stoica26.r-universe.dev</r:repository><r:upstream>https://github.com/andrei-stoica26/henna</r:upstream></item></channel></rss>