<?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>Virtual Cell on Mike's Blog</title><link>https://mikeogilvy.github.io/tags/virtual-cell/</link><description>Recent content in Virtual Cell on Mike's Blog</description><generator>Hugo</generator><language>zh-cn</language><lastBuildDate>Fri, 05 Jun 2026 07:19:29 +0800</lastBuildDate><atom:link href="https://mikeogilvy.github.io/tags/virtual-cell/index.xml" rel="self" type="application/rss+xml"/><item><title>GEARS Explained: How Graph Neural Networks Predict the Unseen</title><link>https://mikeogilvy.github.io/posts/gears/gears_explained/</link><pubDate>Fri, 05 Jun 2026 07:19:29 +0800</pubDate><guid>https://mikeogilvy.github.io/posts/gears/gears_explained/</guid><description>&lt;p&gt;&lt;em&gt;A deep dive into the model that can forecast what happens when you knock out genes nobody has ever touched.&lt;/em&gt;&lt;/p&gt;
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&lt;h2 id="the-problem"&gt;The Problem&lt;/h2&gt;
&lt;p&gt;You&amp;rsquo;re a biologist. You have a Perturb-seq dataset — 100,000 cells, each with one or two genes CRISPR-knocked out, plus single-cell RNA-seq readouts of the full transcriptome. You&amp;rsquo;ve experimentally perturbed 100 single genes and 130 two-gene combos. But there are 4,950 untested pairwise combinations. Running them all would cost a fortune.&lt;/p&gt;</description></item></channel></rss>