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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>Sample to Insight at LightSpeed: A barrier-breaking workflow for inherited...</title>
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            <description>&lt;p&gt;Next-generation sequencing (NGS) has transformed the field of genetic testing, enabling rapid and cost-effective identification of genetic variants associated with inherited diseases. QIAGEN's new groundbreaking Sample to Insight Hereditary solution combines an actionable exome panel built from Human Gene Mutation Database (HGMD) variant information, the fastest and cheapest secondary analysis in the market, and trusted variant interpretation and reporting software powered by augmented molecular intelligence.&lt;p&gt;&lt;/p&gt;
&lt;p&gt;Get a first-hand look at QIAGEN’s new Sample to Insight Hereditary solution. By attending this webinar, you will:&lt;/p&gt;
&lt;p&gt;Learn more about each workflow component.&lt;br&gt;
Hear from experts in the field as they discuss how this technology advances the diagnosis and management of inherited diseases.&lt;/p&gt;
&lt;p&gt;Examine real-world case studies demonstrating the clinical utility and cost-effectiveness of the solution.&lt;br&gt;
If your lab needs a fast, cost-effective, ultra-precise workflow for germline NGS testing, you do not want to miss this webinar.&lt;/p&gt;&lt;/p&gt;&lt;p&gt;&lt;a href="http://tv.qiagenbioinformatics.com/photo/86251572/sample-to-insight-at-lightspeed-a"&gt;&lt;img src="http://tv.qiagenbioinformatics.com/64968556/86251572/48d06de7d70066e8447113e1f8342a80/standard/download-7-thumbnail.jpg" width="75" height=""/&gt;&lt;/a&gt;&lt;/p&gt;</description>
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            <pubDate>Mon, 12 Jun 2023 15:37:35 GMT</pubDate>
            <media:title>Sample to Insight at LightSpeed: A barrier-breaking workflow for inherited...</media:title>
            <itunes:summary>Next-generation sequencing (NGS) has transformed the field of genetic testing, enabling rapid and cost-effective identification of genetic variants associated with inherited diseases. QIAGEN's new groundbreaking Sample to Insight Hereditary solution combines an actionable exome panel built from Human Gene Mutation Database (HGMD) variant information, the fastest and cheapest secondary analysis in the market, and trusted variant interpretation and reporting software powered by augmented molecular intelligence.
Get a first-hand look at QIAGEN’s new Sample to Insight Hereditary solution. By attending this webinar, you will:
Learn more about each workflow component.
Hear from experts in the field as they discuss how this technology advances the diagnosis and management of inherited diseases.
Examine real-world case studies demonstrating the clinical utility and cost-effectiveness of the solution.
If your lab needs a fast, cost-effective, ultra-precise workflow for germline NGS testing, you do not want to miss this webinar.</itunes:summary>
            <itunes:subtitle>Next-generation sequencing (NGS) has transformed the field of genetic testing, enabling rapid and cost-effective identification of genetic variants associated with inherited diseases. QIAGEN's new groundbreaking Sample to Insight Hereditary...</itunes:subtitle>
            <itunes:author>tv.qiagenbioinformatics.com</itunes:author>
            <itunes:duration>49:59</itunes:duration>
            <media:description type="html">&lt;p&gt;Next-generation sequencing (NGS) has transformed the field of genetic testing, enabling rapid and cost-effective identification of genetic variants associated with inherited diseases. QIAGEN's new groundbreaking Sample to Insight Hereditary solution combines an actionable exome panel built from Human Gene Mutation Database (HGMD) variant information, the fastest and cheapest secondary analysis in the market, and trusted variant interpretation and reporting software powered by augmented molecular intelligence.&lt;p&gt;&lt;/p&gt;
&lt;p&gt;Get a first-hand look at QIAGEN’s new Sample to Insight Hereditary solution. By attending this webinar, you will:&lt;/p&gt;
&lt;p&gt;Learn more about each workflow component.&lt;br&gt;
Hear from experts in the field as they discuss how this technology advances the diagnosis and management of inherited diseases.&lt;/p&gt;
&lt;p&gt;Examine real-world case studies demonstrating the clinical utility and cost-effectiveness of the solution.&lt;br&gt;
If your lab needs a fast, cost-effective, ultra-precise workflow for germline NGS testing, you do not want to miss this webinar.&lt;/p&gt;&lt;/p&gt;&lt;p&gt;&lt;a href="http://tv.qiagenbioinformatics.com/photo/86251572/sample-to-insight-at-lightspeed-a"&gt;&lt;img src="http://tv.qiagenbioinformatics.com/64968556/86251572/48d06de7d70066e8447113e1f8342a80/standard/download-7-thumbnail.jpg" width="75" height=""/&gt;&lt;/a&gt;&lt;/p&gt;</media:description>
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            <category>lightspeed</category>
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            <enclosure url="http://tv.qiagenbioinformatics.com/64968556/86003336/7e8f327b11251328979976a47abe8a88/video_medium/beyond-exomes-ultrafast-fastq-to-video.mp4?source=podcast" type="video/mp4" length="238263483"/>
            <title>Beyond exomes: Ultrafast FASTQ to interpretation</title>
            <link>http://tv.qiagenbioinformatics.com/photo/86003336/beyond-exomes-ultrafast-fastq-to</link>
            <description>&lt;p&gt;QIAGEN CLC LightSpeed Module delivers an ultra-fast, end-to-end hereditary NGS FASTQ to VCF pipeline. LightSpeed takes raw FASTQ files generated by paired-end 150 bp sequencing protocols and performs quality trimming, adapter trimming, read mapping, deduplication, local realignment, QC and germline variant calling.&lt;br&gt;
&lt;br&gt;
&lt;br&gt;
QIAGEN CLC Genomics Cloud computing software allows you to launch analyses from CLC Workbenches or CLC Servers for execution on Amazon Web Services (AWS).
&lt;p&gt;For more details, visit https://digitalinsights.qiagen.com/explore/c/qpro-2367_an_clc-lig?x=QbXlDs#page=1 and&lt;br&gt;
&lt;a href="https://digitalinsights.qiagen.com/plugins/clc-cloud-module/"&gt;https://digitalinsights.qiagen.com/plugins/clc-cloud-module/&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;To start a trial of QIAGEN CLC Genomics Workbench Premium, visit:&lt;br&gt;
&lt;a href="https://digitalinsights.qiagen.com/products-overview/discovery-insights-portfolio/analysis-and-visualization/qiagen-clc-workbench-premium/"&gt;https://digitalinsights.qiagen.com/products-overview/discovery-insights-portfolio/analysis-and-visualization/qiagen-clc-workbench-premium/&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;In this training, we’ll explore together:&lt;/p&gt;
&lt;p&gt;• An overview of the QIAGEN CLC Genomics Workbench Premium platform&lt;br&gt;
• An overview of the QIAGEN CLC Genomics Server and Cloud                                                   • Breaking the speed of light&lt;br&gt;
• Why LightSpeed is arguably the fastest and cheapest-to-run hereditary FASTQ-to-VCF WGS pipeline available&lt;br&gt;
• Benchmarks/comparisons&lt;br&gt;
• Demo of lightspeed and cloud module for Fastq to VCF&lt;br&gt;
• Plugin installation&lt;br&gt;
• Download of reference(s)&lt;br&gt;
• Workflow execution and results review&lt;/p&gt;&lt;/p&gt;&lt;p&gt;&lt;a href="http://tv.qiagenbioinformatics.com/photo/86003336/beyond-exomes-ultrafast-fastq-to"&gt;&lt;img src="http://tv.qiagenbioinformatics.com/64968556/86003336/7e8f327b11251328979976a47abe8a88/standard/download-7-thumbnail.jpg" width="75" height=""/&gt;&lt;/a&gt;&lt;/p&gt;</description>
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            <pubDate>Tue, 09 May 2023 20:00:00 GMT</pubDate>
            <media:title>Beyond exomes: Ultrafast FASTQ to interpretation</media:title>
            <itunes:summary>QIAGEN CLC LightSpeed Module delivers an ultra-fast, end-to-end hereditary NGS FASTQ to VCF pipeline. LightSpeed takes raw FASTQ files generated by paired-end 150 bp sequencing protocols and performs quality trimming, adapter trimming, read mapping, deduplication, local realignment, QC and germline variant calling.


QIAGEN CLC Genomics Cloud computing software allows you to launch analyses from CLC Workbenches or CLC Servers for execution on Amazon Web Services (AWS).
For more details, visit https://digitalinsights.qiagen.com/explore/c/qpro-2367_an_clc-lig?x=QbXlDs#page=1 and
https://digitalinsights.qiagen.com/plugins/clc-cloud-module/
To start a trial of QIAGEN CLC Genomics Workbench Premium, visit:
https://digitalinsights.qiagen.com/products-overview/discovery-insights-portfolio/analysis-and-visualization/qiagen-clc-workbench-premium/
In this training, we’ll explore together:
• An overview of the QIAGEN CLC Genomics Workbench Premium platform
• An overview of the QIAGEN CLC Genomics Server and Cloud                                                   • Breaking the speed of light
• Why LightSpeed is arguably the fastest and cheapest-to-run hereditary FASTQ-to-VCF WGS pipeline available
• Benchmarks/comparisons
• Demo of lightspeed and cloud module for Fastq to VCF
• Plugin installation
• Download of reference(s)
• Workflow execution and results review</itunes:summary>
            <itunes:subtitle>QIAGEN CLC LightSpeed Module delivers an ultra-fast, end-to-end hereditary NGS FASTQ to VCF pipeline. LightSpeed takes raw FASTQ files generated by paired-end 150 bp sequencing protocols and performs quality trimming, adapter trimming, read...</itunes:subtitle>
            <itunes:author>tv.qiagenbioinformatics.com</itunes:author>
            <itunes:duration>01:20:59</itunes:duration>
            <media:description type="html">&lt;p&gt;QIAGEN CLC LightSpeed Module delivers an ultra-fast, end-to-end hereditary NGS FASTQ to VCF pipeline. LightSpeed takes raw FASTQ files generated by paired-end 150 bp sequencing protocols and performs quality trimming, adapter trimming, read mapping, deduplication, local realignment, QC and germline variant calling.&lt;br&gt;
&lt;br&gt;
&lt;br&gt;
QIAGEN CLC Genomics Cloud computing software allows you to launch analyses from CLC Workbenches or CLC Servers for execution on Amazon Web Services (AWS).
&lt;p&gt;For more details, visit https://digitalinsights.qiagen.com/explore/c/qpro-2367_an_clc-lig?x=QbXlDs#page=1 and&lt;br&gt;
&lt;a href="https://digitalinsights.qiagen.com/plugins/clc-cloud-module/"&gt;https://digitalinsights.qiagen.com/plugins/clc-cloud-module/&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;To start a trial of QIAGEN CLC Genomics Workbench Premium, visit:&lt;br&gt;
&lt;a href="https://digitalinsights.qiagen.com/products-overview/discovery-insights-portfolio/analysis-and-visualization/qiagen-clc-workbench-premium/"&gt;https://digitalinsights.qiagen.com/products-overview/discovery-insights-portfolio/analysis-and-visualization/qiagen-clc-workbench-premium/&lt;/a&gt;&lt;/p&gt;
&lt;p&gt;In this training, we’ll explore together:&lt;/p&gt;
&lt;p&gt;• An overview of the QIAGEN CLC Genomics Workbench Premium platform&lt;br&gt;
• An overview of the QIAGEN CLC Genomics Server and Cloud                                                   • Breaking the speed of light&lt;br&gt;
• Why LightSpeed is arguably the fastest and cheapest-to-run hereditary FASTQ-to-VCF WGS pipeline available&lt;br&gt;
• Benchmarks/comparisons&lt;br&gt;
• Demo of lightspeed and cloud module for Fastq to VCF&lt;br&gt;
• Plugin installation&lt;br&gt;
• Download of reference(s)&lt;br&gt;
• Workflow execution and results review&lt;/p&gt;&lt;/p&gt;&lt;p&gt;&lt;a href="http://tv.qiagenbioinformatics.com/photo/86003336/beyond-exomes-ultrafast-fastq-to"&gt;&lt;img src="http://tv.qiagenbioinformatics.com/64968556/86003336/7e8f327b11251328979976a47abe8a88/standard/download-7-thumbnail.jpg" width="75" height=""/&gt;&lt;/a&gt;&lt;/p&gt;</media:description>
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