<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom" xmlns:content="http://purl.org/rss/1.0/modules/content/"><channel><title>Transcriptomics on Maragkakis Lab</title><link>http://maragkakislab.com/tags/transcriptomics/</link><description>Recent content in Transcriptomics on Maragkakis Lab</description><generator>Hugo</generator><language>en-us</language><lastBuildDate>Mon, 01 Jun 2026 00:00:00 +0000</lastBuildDate><atom:link href="http://maragkakislab.com/tags/transcriptomics/index.xml" rel="self" type="application/rss+xml"/><item><title>SenCat: Redefining human cell senescence through multiomic profiling of multiple senescent primary cell types</title><link>http://maragkakislab.com/publications/2026-sencat/</link><pubDate>Mon, 01 Jun 2026 00:00:00 +0000</pubDate><guid>http://maragkakislab.com/publications/2026-sencat/</guid><description>&lt;h2 id="summary"&gt;Summary&lt;/h2&gt;
&lt;p&gt;SenCat is a comprehensive multiomic atlas of human cell senescence generated by profiling multiple primary cell types induced to senescence through distinct triggers. Integrated analysis of transcriptome, epigenome, and proteome data across cell types and senescence inducers redefines the core features of the senescent state and identifies cell-type-specific and universal senescence signatures.&lt;/p&gt;</description></item><item><title>Transcript-guided targeted cell enrichment for scalable single-nucleus RNA sequencing</title><link>http://maragkakislab.com/publications/2026-single-nucleus-rna-seq/</link><pubDate>Wed, 11 Mar 2026 00:00:00 +0000</pubDate><guid>http://maragkakislab.com/publications/2026-single-nucleus-rna-seq/</guid><description>&lt;h2 id="summary"&gt;Summary&lt;/h2&gt;
&lt;p&gt;This study introduces a method for transcript-guided targeted enrichment of specific cell populations prior to single-nucleus RNA sequencing. By selecting nuclei based on expression of specific transcripts, the approach achieves deep profiling of rare cell types at scale, enabling discovery of cell-type-specific transcriptional programs that would be missed by unbiased approaches.&lt;/p&gt;</description></item><item><title>TERA-Seq: True end-to-end sequencing of native RNA molecules for transcriptome characterization</title><link>http://maragkakislab.com/publications/2021-tera-seq/</link><pubDate>Tue, 24 Aug 2021 00:00:00 +0000</pubDate><guid>http://maragkakislab.com/publications/2021-tera-seq/</guid><description>&lt;h2 id="summary"&gt;Summary&lt;/h2&gt;
&lt;p&gt;TERA-Seq is a method that combines chemical ligation of adapters to both RNA ends with nanopore direct RNA sequencing to capture complete native RNA molecules from the 5&amp;rsquo; cap to the 3&amp;rsquo; poly(A) tail. This enables simultaneous characterization of RNA modifications, poly(A) tail length, and transcript boundaries at single-molecule resolution.&lt;/p&gt;</description></item><item><title>CLIPSeqTools — a novel bioinformatics CLIP-seq analysis suite</title><link>http://maragkakislab.com/publications/2016-clipseqtools/</link><pubDate>Fri, 01 Jan 2016 00:00:00 +0000</pubDate><guid>http://maragkakislab.com/publications/2016-clipseqtools/</guid><description>&lt;h2 id="summary"&gt;Summary&lt;/h2&gt;
&lt;p&gt;CLIPSeqTools is a modular bioinformatics pipeline for the analysis of CLIP-seq data, providing tools for read processing, peak calling, motif analysis, and visualization. The suite enables comprehensive characterization of RNA-binding protein interaction sites across the transcriptome.&lt;/p&gt;</description></item></channel></rss>