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	<title>reference genome &#8211; BIOENGINEER.ORG</title>
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		<title>A Flawed Genetic Reference Could Trigger False Alarms in Whole-Genome Screening</title>
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		<pubDate>Wed, 07 Oct 2026 18:54:39 +0000</pubDate>
				<category><![CDATA[Biology]]></category>
		<category><![CDATA[Bioinformatics]]></category>
		<category><![CDATA[false positives]]></category>
		<category><![CDATA[Genetic Variants]]></category>
		<category><![CDATA[genomic screening]]></category>
		<category><![CDATA[GeroScience]]></category>
		<category><![CDATA[GRCh38]]></category>
		<category><![CDATA[pan-genome]]></category>
		<category><![CDATA[personalized medicine]]></category>
		<category><![CDATA[preventive medicine]]></category>
		<category><![CDATA[reference genome]]></category>
		<category><![CDATA[Semmelweis University]]></category>
		<category><![CDATA[whole-genome sequencing]]></category>
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					<description><![CDATA[Researchers at Semmelweis University show that the standard human reference genome can cause automated whole-genome analyses to flag healthy individuals with false disease variants, highlighting the need for a graph-based pan-genome reference.]]></description>
		
		
		
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