<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>disease-causing non-coding variants &#8211; BIOENGINEER.ORG</title>
	<atom:link href="https://bioengineer.org/tag/disease-causing-non-coding-variants/feed/" rel="self" type="application/rss+xml" />
	<link>https://bioengineer.org</link>
	<description>Bioengineering</description>
	<lastBuildDate>Thu, 17 Apr 2025 15:55:23 +0000</lastBuildDate>
	<language>en-US</language>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	<generator>https://wordpress.org/?v=7.0</generator>

<image>
	<url>https://bioengineer.org/wp-content/uploads/2019/09/cropped-bioengineering-32x32.png</url>
	<title>disease-causing non-coding variants &#8211; BIOENGINEER.ORG</title>
	<link>https://bioengineer.org</link>
	<width>32</width>
	<height>32</height>
</image> 
<site xmlns="com-wordpress:feed-additions:1">72741379</site>	<item>
		<title>Researchers at CHOP and Penn Medicine Employ Deep Learning to Identify Disease-Causing Variants in Non-Coding Human Genome Regions</title>
		<link>https://bioengineer.org/researchers-at-chop-and-penn-medicine-employ-deep-learning-to-identify-disease-causing-variants-in-non-coding-human-genome-regions/</link>
		
		<dc:creator><![CDATA[Bioengineer]]></dc:creator>
		<pubDate>Thu, 17 Apr 2025 15:55:23 +0000</pubDate>
				<category><![CDATA[Health]]></category>
		<category><![CDATA[deep learning in genomics]]></category>
		<category><![CDATA[disease-causing non-coding variants]]></category>
		<category><![CDATA[genomic regulation insights]]></category>
		<category><![CDATA[non-coding genetic variants]]></category>
		<category><![CDATA[transcription factor footprint mapping]]></category>
		<guid isPermaLink="false">https://bioengineer.org/researchers-at-chop-and-penn-medicine-employ-deep-learning-to-identify-disease-causing-variants-in-non-coding-human-genome-regions/</guid>

					<description><![CDATA[In a groundbreaking advancement poised to reshape the landscape of genetic research and precision medicine, scientists at the Children’s Hospital of Philadelphia (CHOP) in collaboration with the Perelman School of Medicine at the University of Pennsylvania have unveiled an innovative approach to decoding the enigmatic noncoding regions of the human genome. These vast stretches of [&#8230;]]]></description>
		
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">241390</post-id>	</item>
	</channel>
</rss>
