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	<title>Varyant Önceliklendirme &#8211; BIOENGINEER.ORG</title>
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		<title>Enhancing Rare Disease Diagnostics: Exomiser and Genomiser Insights</title>
		<link>https://bioengineer.org/enhancing-rare-disease-diagnostics-exomiser-and-genomiser-insights/</link>
		
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		<pubDate>Tue, 20 Jan 2026 10:44:54 +0000</pubDate>
				<category><![CDATA[Health]]></category>
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		<category><![CDATA[Genetik Tanı * **Nadir Hastalıklar (Rare Diseases):** Makalenin ana odağı]]></category>
		<category><![CDATA[Genomiser]]></category>
		<category><![CDATA[Nadir Hastalıklar]]></category>
		<category><![CDATA[tanıdaki zorluklar ve iyileştirme çabaları. * **Varyant Önceliklendirme (Variant Prioritization):** Çalışmanın tem]]></category>
		<category><![CDATA[Varyant Önceliklendirme]]></category>
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					<description><![CDATA[In the rapidly evolving field of genomics, the increasing use of next-generation sequencing (NGS) has transformed the approach to disease diagnostics, particularly in the realm of rare diseases. While this technological advancement has equipped researchers and clinicians with incredible tools to decode the human genome, it has simultaneously introduced a myriad of challenges in variant [&#8230;]]]></description>
		
		
		
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