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            <description>&lt;p&gt;In this training, we’ll go over how to easily perform DNA-seq analyses (for whole genome, whole exome, panel and similar) easily and effectively using QIAGEN CLC Genomics Workbench.&lt;/p&gt;
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            <media:title> DNA-seq analyses (whole genome, whole exome, panel) using QIAGEN CLC...</media:title>
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• Variant calling (SNPs, mutations, Indels and more)
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            <itunes:subtitle>In this training, we’ll go over how to easily perform DNA-seq analyses (for whole genome, whole exome, panel and similar) easily and effectively using QIAGEN CLC Genomics Workbench.
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            <media:description type="html">&lt;p&gt;In this training, we’ll go over how to easily perform DNA-seq analyses (for whole genome, whole exome, panel and similar) easily and effectively using QIAGEN CLC Genomics Workbench.&lt;/p&gt;
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&lt;p&gt;• Read mapping&lt;br /&gt;
• Variant calling (SNPs, mutations, Indels and more)&lt;br /&gt;
• Annotations and filters&lt;br /&gt;
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            <title> How to perform DNA-seq and resequencing data analyses using QIAGEN CLC...</title>
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            <description>&lt;p&gt;In this webinar, we’ll introduce algorithms required to perform data analysis for resequencing next-generation sequencing data. Together, we’ll explore:&lt;/p&gt;
&lt;p&gt;• Read mapper&lt;br /&gt;
• Variant callers&lt;br /&gt;
• Annotations and filters&lt;br /&gt;
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            <pubDate>Mon, 18 Dec 2023 12:07:03 GMT</pubDate>
            <media:title> How to perform DNA-seq and resequencing data analyses using QIAGEN CLC...</media:title>
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• Variant callers
• Annotations and filters
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• Variant callers
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            <itunes:duration>55:22</itunes:duration>
            <media:description type="html">&lt;p&gt;In this webinar, we’ll introduce algorithms required to perform data analysis for resequencing next-generation sequencing data. Together, we’ll explore:&lt;/p&gt;
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• Variant callers&lt;br /&gt;
• Annotations and filters&lt;br /&gt;
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