<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Rna-Seq on TouchingFish.top</title><link>https://touchingfish.top/en/tags/rna-seq/</link><description>Recent content in Rna-Seq on TouchingFish.top</description><generator>Hugo</generator><language>en</language><lastBuildDate>Sun, 21 Feb 2021 00:00:00 +0000</lastBuildDate><atom:link href="https://touchingfish.top/en/tags/rna-seq/index.xml" rel="self" type="application/rss+xml"/><item><title>Alternative Splicing Analysis - Algorithm and Workflow</title><link>https://touchingfish.top/en/2021/alternative-splice-algorithm/</link><pubDate>Sun, 21 Feb 2021 00:00:00 +0000</pubDate><guid>https://touchingfish.top/en/2021/alternative-splice-algorithm/</guid><description>&lt;h2 id="1-biological-background"&gt;1. Biological Background&lt;/h2&gt;
&lt;h3 id="11-what-is-alternative-splicing"&gt;1.1 What is Alternative Splicing&lt;/h3&gt;
&lt;p&gt;In eukaryotes, a single gene can produce multiple mRNA isoforms through alternative
splicing (AS) -- the process by which different combinations of exons are joined
during pre-mRNA splicing. This greatly expands proteomic diversity without
increasing gene count.&lt;/p&gt;
&lt;p&gt;A gene with N exons can theoretically produce up to 2^(N-1) splice variants.
In practice, most genes produce 2-10 isoforms, but some (e.g., Drosophila Dscam)
can produce tens of thousands.&lt;/p&gt;</description></item><item><title>Differentially Expressed Gene (DEG) Analysis Across Multiple Tissues of Japanese Eel in Seawater and Freshwater Environments</title><link>https://touchingfish.top/en/2019/anguilla-japonica-deg-analysis/</link><pubDate>Thu, 15 Aug 2019 00:00:00 +0000</pubDate><guid>https://touchingfish.top/en/2019/anguilla-japonica-deg-analysis/</guid><description>&lt;h2 id="abstract"&gt;Abstract&lt;/h2&gt;
&lt;p&gt;This study conducted differentially expressed gene (DEG) analysis on three key tissues (brain, gonad, pectoral fins) of Japanese eel (&lt;em&gt;Anguilla japonica&lt;/em&gt;) under seawater (SEA) and freshwater (TAP) conditions, to elucidate the transcriptomic response mechanisms during salinity adaptation.&lt;/p&gt;
&lt;p&gt;Key findings:&lt;/p&gt;
&lt;ul&gt;
&lt;li&gt;Global analysis (controlling for tissue effects) identified 422 DEGs (303 upregulated, 119 downregulated)&lt;/li&gt;
&lt;li&gt;The brain was the most salinity-sensitive tissue, with 500 DEGs identified&lt;/li&gt;
&lt;li&gt;Eight core response genes were significantly differentially expressed across all three tissues (intersection), all upregulated in the seawater environment&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;Main conclusions:&lt;/p&gt;</description></item></channel></rss>