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    <title>Variant-Calling on Pi Stack</title>
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      <title>Self-Hosted Genomic Variant Calling: GATK vs FreeBayes vs BCFtools Compared</title>
      <link>https://www.pistack.xyz/posts/2026-06-10-self-hosted-genomic-variant-calling-gatk-freebayes-bcftools/</link>
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      <description>&lt;h2 id=&#34;introduction&#34;&gt;Introduction&lt;/h2&gt;&#xA;&lt;p&gt;Variant calling — the process of identifying genetic differences between a sequenced genome and a reference genome — is one of the most fundamental workflows in bioinformatics. Whether you&amp;rsquo;re analyzing whole-genome sequencing (WGS), whole-exome sequencing (WES), or targeted gene panels, the choice of variant caller significantly impacts your downstream results.&lt;/p&gt;</description>
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