<?xml version="1.0" encoding="utf-8" standalone="yes"?>
<rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom">
  <channel>
    <title>Rnaseq on Pi Stack</title>
    <link>https://www.pistack.xyz/tags/rnaseq/</link>
    <description>Recent content in Rnaseq on Pi Stack</description>
    <generator>Hugo</generator>
    <language>en-us</language>
    <lastBuildDate>Sat, 13 Jun 2026 00:00:00 +0000</lastBuildDate>
    <atom:link href="https://www.pistack.xyz/tags/rnaseq/index.xml" rel="self" type="application/rss+xml" />
    <item>
      <title>Self-Hosted RNA-seq Alignment and Quantification: STAR vs Kallisto vs Salmon vs StringTie</title>
      <link>https://www.pistack.xyz/posts/2026-06-13-self-hosted-rnaseq-alignment-quantification-star-kallisto-salmon-stringtie/</link>
      <pubDate>Sat, 13 Jun 2026 00:00:00 +0000</pubDate>
      <guid>https://www.pistack.xyz/posts/2026-06-13-self-hosted-rnaseq-alignment-quantification-star-kallisto-salmon-stringtie/</guid>
      <description>&lt;h2 id=&#34;introduction&#34;&gt;Introduction&lt;/h2&gt;&#xA;&lt;p&gt;RNA sequencing (RNA-seq) has revolutionized our understanding of gene expression, transcript structure, and RNA biology. But the raw output from a sequencer — millions of short nucleotide reads — is useless without computational processing. Two critical steps transform raw reads into biologically meaningful data: alignment (mapping reads to a reference genome) and quantification (estimating transcript abundance).&lt;/p&gt;</description>
    </item>
  </channel>
</rss>
