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        <title>tv.qiagenbioinformatics.com</title>
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        <itunes:subtitle>CLC bio TV</itunes:subtitle>
        <itunes:summary>Watch tutorials, interviews and much more on our web based TV channel!</itunes:summary>
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            <title>Benefits of integrating targeted next-generation sequencing (NGS) panels into...</title>
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            <description>&lt;p&gt;Variant detection of multiple genes from a single tumor sample requires high-throughput molecular testing. To meet this demand, targeted next-generation sequencing (NGS) panels are useful in clinical settings for accurate tumor profiling and the identification of essential molecular aberrations for personalized therapies. By focusing only on a subset of genes, targeted NGS is not only a cost-effective solution, but can rapidly deliver insights into a tumor molecular profile.&lt;/p&gt;
&lt;p&gt;To address this challenge, a clinical research team led by Dr. Michela Bulfoni at the Istituto di Anatomia Patologica designed custom NGS panels, named “Glioma” and “Routine Diagnostics”, targeting single nucleotide variations, insertions/deletions, fusions, and copy number variations of tumor-associated essential genes.&lt;/p&gt;
&lt;p&gt;In this webinar, attendees will:&lt;br /&gt;
- Understand the clinical utility of custom-designed NGS panels for accurate tumour diagnosis&lt;br /&gt;
- Learn about the design and application of these NGS panels&lt;br /&gt;
- Gain insights into the cost-effectiveness and high sensitivity of NGS panels in improving sample throughput&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Category: QCI Interpret for Oncology, Sample to Insight&lt;/p&gt;&lt;p&gt;&lt;a href="http://tv.qiagenbioinformatics.com/photo/103037588/benefits-of-integrating-targeted"&gt;&lt;img src="http://tv.qiagenbioinformatics.com/64968558/103037588/d8cd6e0b62a97b149226f46fb7bf8873/standard/download-7-thumbnail.jpg" width="75" height=""/&gt;&lt;/a&gt;&lt;/p&gt;</description>
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            <pubDate>Thu, 18 Jul 2024 16:20:54 GMT</pubDate>
            <media:title>Benefits of integrating targeted next-generation sequencing (NGS) panels into...</media:title>
            <itunes:summary>Variant detection of multiple genes from a single tumor sample requires high-throughput molecular testing. To meet this demand, targeted next-generation sequencing (NGS) panels are useful in clinical settings for accurate tumor profiling and the identification of essential molecular aberrations for personalized therapies. By focusing only on a subset of genes, targeted NGS is not only a cost-effective solution, but can rapidly deliver insights into a tumor molecular profile.
To address this challenge, a clinical research team led by Dr. Michela Bulfoni at the Istituto di Anatomia Patologica designed custom NGS panels, named “Glioma” and “Routine Diagnostics”, targeting single nucleotide variations, insertions/deletions, fusions, and copy number variations of tumor-associated essential genes.
In this webinar, attendees will:
- Understand the clinical utility of custom-designed NGS panels for accurate tumour diagnosis
- Learn about the design and application of these NGS panels
- Gain insights into the cost-effectiveness and high sensitivity of NGS panels in improving sample throughput


Category: QCI Interpret for Oncology, Sample to Insight</itunes:summary>
            <itunes:subtitle>Variant detection of multiple genes from a single tumor sample requires high-throughput molecular testing. To meet this demand, targeted next-generation sequencing (NGS) panels are useful in clinical settings for accurate tumor profiling and the...</itunes:subtitle>
            <itunes:author>tv.qiagenbioinformatics.com</itunes:author>
            <itunes:duration>01:01:57</itunes:duration>
            <media:description type="html">&lt;p&gt;Variant detection of multiple genes from a single tumor sample requires high-throughput molecular testing. To meet this demand, targeted next-generation sequencing (NGS) panels are useful in clinical settings for accurate tumor profiling and the identification of essential molecular aberrations for personalized therapies. By focusing only on a subset of genes, targeted NGS is not only a cost-effective solution, but can rapidly deliver insights into a tumor molecular profile.&lt;/p&gt;
&lt;p&gt;To address this challenge, a clinical research team led by Dr. Michela Bulfoni at the Istituto di Anatomia Patologica designed custom NGS panels, named “Glioma” and “Routine Diagnostics”, targeting single nucleotide variations, insertions/deletions, fusions, and copy number variations of tumor-associated essential genes.&lt;/p&gt;
&lt;p&gt;In this webinar, attendees will:&lt;br /&gt;
- Understand the clinical utility of custom-designed NGS panels for accurate tumour diagnosis&lt;br /&gt;
- Learn about the design and application of these NGS panels&lt;br /&gt;
- Gain insights into the cost-effectiveness and high sensitivity of NGS panels in improving sample throughput&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
Category: QCI Interpret for Oncology, Sample to Insight&lt;/p&gt;&lt;p&gt;&lt;a href="http://tv.qiagenbioinformatics.com/photo/103037588/benefits-of-integrating-targeted"&gt;&lt;img src="http://tv.qiagenbioinformatics.com/64968558/103037588/d8cd6e0b62a97b149226f46fb7bf8873/standard/download-7-thumbnail.jpg" width="75" height=""/&gt;&lt;/a&gt;&lt;/p&gt;</media:description>
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            <category>qci interpret</category>
            <category>QCI Interpret for Oncology</category>
            <category> Sample to Insight</category>
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            <title>Analyzing QIAseq DNA Panels with QIAGEN CLC Genomics Workbench</title>
            <link>http://tv.qiagenbioinformatics.com/photo/88883036/analyzing-qiaseq-dna-panels-with</link>
            <description>&lt;p&gt;This training will focus on analyzing QIAseq DNA panel datasets with QIAGEN CLC Genomics Workbench and the Biomedical Genomics Analysis plugin, including a live “FASTQ-to-VCF” demo of data import, data analysis and investigation. We will also show how to set up the analysis of a custom QIAseq DNA panel.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
During this training, you’ll learn about:&lt;br /&gt;
• Import of FASTQ files&lt;br /&gt;
• Launching an analysis workflow&lt;br /&gt;
• Inspection of QC reports, genome browser view, detected variants and other workflow outputs&lt;br /&gt;
• Customization of template workflow parameters based on findings in the QC report&lt;br /&gt;
• Import of custom primers and target regions file&lt;br /&gt;
• How to set up an analysis of a custom panel&lt;/p&gt;&lt;p&gt;&lt;a href="http://tv.qiagenbioinformatics.com/photo/88883036/analyzing-qiaseq-dna-panels-with"&gt;&lt;img src="http://tv.qiagenbioinformatics.com/64968555/88883036/a338cd204a76a15ec28fe4ecf5b2197f/standard/download-7-thumbnail.jpg" width="75" height=""/&gt;&lt;/a&gt;&lt;/p&gt;</description>
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            <pubDate>Thu, 21 Sep 2023 15:55:27 GMT</pubDate>
            <media:title>Analyzing QIAseq DNA Panels with QIAGEN CLC Genomics Workbench</media:title>
            <itunes:summary>This training will focus on analyzing QIAseq DNA panel datasets with QIAGEN CLC Genomics Workbench and the Biomedical Genomics Analysis plugin, including a live “FASTQ-to-VCF” demo of data import, data analysis and investigation. We will also show how to set up the analysis of a custom QIAseq DNA panel.


During this training, you’ll learn about:
• Import of FASTQ files
• Launching an analysis workflow
• Inspection of QC reports, genome browser view, detected variants and other workflow outputs
• Customization of template workflow parameters based on findings in the QC report
• Import of custom primers and target regions file
• How to set up an analysis of a custom panel</itunes:summary>
            <itunes:subtitle>This training will focus on analyzing QIAseq DNA panel datasets with QIAGEN CLC Genomics Workbench and the Biomedical Genomics Analysis plugin, including a live “FASTQ-to-VCF” demo of data import, data analysis and investigation. We will also show...</itunes:subtitle>
            <itunes:author>tv.qiagenbioinformatics.com</itunes:author>
            <itunes:duration>51:40</itunes:duration>
            <media:description type="html">&lt;p&gt;This training will focus on analyzing QIAseq DNA panel datasets with QIAGEN CLC Genomics Workbench and the Biomedical Genomics Analysis plugin, including a live “FASTQ-to-VCF” demo of data import, data analysis and investigation. We will also show how to set up the analysis of a custom QIAseq DNA panel.&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
During this training, you’ll learn about:&lt;br /&gt;
• Import of FASTQ files&lt;br /&gt;
• Launching an analysis workflow&lt;br /&gt;
• Inspection of QC reports, genome browser view, detected variants and other workflow outputs&lt;br /&gt;
• Customization of template workflow parameters based on findings in the QC report&lt;br /&gt;
• Import of custom primers and target regions file&lt;br /&gt;
• How to set up an analysis of a custom panel&lt;/p&gt;&lt;p&gt;&lt;a href="http://tv.qiagenbioinformatics.com/photo/88883036/analyzing-qiaseq-dna-panels-with"&gt;&lt;img src="http://tv.qiagenbioinformatics.com/64968555/88883036/a338cd204a76a15ec28fe4ecf5b2197f/standard/download-7-thumbnail.jpg" width="75" height=""/&gt;&lt;/a&gt;&lt;/p&gt;</media:description>
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            <category>clc</category>
            <category>qiaseq</category>
            <category>qiaseq panels</category>
            <category>sample to insight</category>
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