tv.qiagenbioinformatics.com marketingbiox@qiagen.com https://tv.qiagenbioinformatics.com Watch tutorials, interviews and much more on our web based TV channel! en-us Visualplatform http://blogs.law.harvard.edu/tech/rss tv.qiagenbioinformatics.com CLC bio TV Watch tutorials, interviews and much more on our web based TV channel! clc bio tv, bioinformatics, genomics, research episodic no https://tv.qiagenbioinformatics.com/files/rv0.0/sitelogo.gif https://tv.qiagenbioinformatics.com http://tv.qiagenbioinformatics.com/photo/90542138/part-2-ai-powered-hereditary <p>Clinical exome sequencing (CES) is increasingly being adopted by small and mid-sized laboratories to diagnose genetic diseases, aid treatment decisions, and provide prognostic information. However, the exponential increase in genetic data generated from exome and genome panels poses significant workflow challenges. The ability to prioritize potentially pathogenic variants from large datasets and identify the few candidate variants becomes more difficult. This issue is further amplified in cases where labs must use deep phenotyping of patients and compare that to reference genotype-phenotype knowledge associated with each candidate variant. To overcome these challenges, labs are beginning to implement Artificial Intelligence (AI) in their variant analysis, interpretation and reporting workflows.<p></p> <p>Join us for our 2023 Clinical Hereditary Disease Diagnostics Summit, a free-to-attend, two-part event exploring the opportunities and limitations of AI in hereditary disease diagnostics. Designed to help clinical diagnostic labs learn how to safely apply AI to exome and genome sequencing workflows, the content-rich event will feature invited lectures from lab directors and clinical geneticists, thought-provoking discussions on the future of hereditary disease diagnostics, as well as educational presentations on the latest databases and AI-powered software for germline secondary and tertiary analysis.</p> <p>Part II: Roundtable discussion with genomics experts – November 9, 2023</p> <p>A panel discussion featuring experts in the field of clinical genomics that will explore the challenges and opportunities in the future of inherited disease diagnostic testing.</p> <p>For the list of speakers and session information, visit our event page here.</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/90542138/part-2-ai-powered-hereditary"><img src="http://tv.qiagenbioinformatics.com/64968555/90542138/12f4cb5889b569104cf1f1998f89d8a6/standard/download-7-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/90542138 Thu, 30 Nov 2023 12:59:35 GMT Part 2: AI-Powered Hereditary Disease Diagnostics: Closing the Gap in... Clinical exome sequencing (CES) is increasingly being adopted by small and mid-sized laboratories to diagnose genetic diseases, aid treatment decisions, and provide prognostic information. However, the exponential increase in genetic data generated from exome and genome panels poses significant workflow challenges. The ability to prioritize potentially pathogenic variants from large datasets and identify the few candidate variants becomes more difficult. This issue is further amplified in cases where labs must use deep phenotyping of patients and compare that to reference genotype-phenotype knowledge associated with each candidate variant. To overcome these challenges, labs are beginning to implement Artificial Intelligence (AI) in their variant analysis, interpretation and reporting workflows. Join us for our 2023 Clinical Hereditary Disease Diagnostics Summit, a free-to-attend, two-part event exploring the opportunities and limitations of AI in hereditary disease diagnostics. Designed to help clinical diagnostic labs learn how to safely apply AI to exome and genome sequencing workflows, the content-rich event will feature invited lectures from lab directors and clinical geneticists, thought-provoking discussions on the future of hereditary disease diagnostics, as well as educational presentations on the latest databases and AI-powered software for germline secondary and tertiary analysis. Part II: Roundtable discussion with genomics experts – November 9, 2023 A panel discussion featuring experts in the field of clinical genomics that will explore the challenges and opportunities in the future of inherited disease diagnostic testing. For the list of speakers and session information, visit our event page here. Clinical exome sequencing (CES) is increasingly being adopted by small and mid-sized laboratories to diagnose genetic diseases, aid treatment decisions, and provide prognostic information. However, the exponential increase in genetic data... tv.qiagenbioinformatics.com 52:27 <p>Clinical exome sequencing (CES) is increasingly being adopted by small and mid-sized laboratories to diagnose genetic diseases, aid treatment decisions, and provide prognostic information. However, the exponential increase in genetic data generated from exome and genome panels poses significant workflow challenges. The ability to prioritize potentially pathogenic variants from large datasets and identify the few candidate variants becomes more difficult. This issue is further amplified in cases where labs must use deep phenotyping of patients and compare that to reference genotype-phenotype knowledge associated with each candidate variant. To overcome these challenges, labs are beginning to implement Artificial Intelligence (AI) in their variant analysis, interpretation and reporting workflows.<p></p> <p>Join us for our 2023 Clinical Hereditary Disease Diagnostics Summit, a free-to-attend, two-part event exploring the opportunities and limitations of AI in hereditary disease diagnostics. Designed to help clinical diagnostic labs learn how to safely apply AI to exome and genome sequencing workflows, the content-rich event will feature invited lectures from lab directors and clinical geneticists, thought-provoking discussions on the future of hereditary disease diagnostics, as well as educational presentations on the latest databases and AI-powered software for germline secondary and tertiary analysis.</p> <p>Part II: Roundtable discussion with genomics experts – November 9, 2023</p> <p>A panel discussion featuring experts in the field of clinical genomics that will explore the challenges and opportunities in the future of inherited disease diagnostic testing.</p> <p>For the list of speakers and session information, visit our event page here.</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/90542138/part-2-ai-powered-hereditary"><img src="http://tv.qiagenbioinformatics.com/64968555/90542138/12f4cb5889b569104cf1f1998f89d8a6/standard/download-7-thumbnail.jpg" width="75" height=""/></a></p> AI hereditary hereditary ngs summit http://tv.qiagenbioinformatics.com/photo/81422637/emerging-clinical-trends-in-1 <p>Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline Testing <p>Over the past two decades, huge advancements in sequencing technology have transformed our understanding of human genetics, leading to faster diagnoses, earlier prevention, and better treatments. But as more and more people have their genomes sequenced, outpacing our ability to analyze and interpret the generated data, we must embrace new tools, technologies, and strategies to realize the full value of genomic innovation.</p> <p>Advance your lab’s germline testing capabilities by learning how to build a next-gen software workflow, as part of the Hereditary NGS Clinical Summit Series, a two-part, free-to-attend virtual event for variant scientists, bioinformaticians, clinical geneticists, and lab managers.</p> <p>An expert panel of leading medical geneticists, variant scientists and bioinformaticians will discuss emerging scientific and clinical trends in germline NGS testing.</p> <p>Attendees will gain:</p> <p>Insight into how leading laboratories address bottlenecks in their NGS data pipelines<br> Tips on how to solve process inefficiencies of critical workflow components, including variant curation and interpreting rare or novel variants<br> An outlook on how germline NGS analysis and interpretation will change in the next 5 years and how to remain at the forefront of innovation</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/81422637/emerging-clinical-trends-in-1"><img src="http://tv.qiagenbioinformatics.com/64968569/81422637/5bd9dcc53e86885298fe0b0f683b2b65/standard/download-22-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/81422637 Thu, 17 Nov 2022 19:00:47 GMT Emerging clinical trends in germline NGS testing: Expert Panel Discussion in USA Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline Testing Over the past two decades, huge advancements in sequencing technology have transformed our understanding of human genetics, leading to faster diagnoses, earlier prevention, and better treatments. But as more and more people have their genomes sequenced, outpacing our ability to analyze and interpret the generated data, we must embrace new tools, technologies, and strategies to realize the full value of genomic innovation. Advance your lab’s germline testing capabilities by learning how to build a next-gen software workflow, as part of the Hereditary NGS Clinical Summit Series, a two-part, free-to-attend virtual event for variant scientists, bioinformaticians, clinical geneticists, and lab managers. An expert panel of leading medical geneticists, variant scientists and bioinformaticians will discuss emerging scientific and clinical trends in germline NGS testing. Attendees will gain: Insight into how leading laboratories address bottlenecks in their NGS data pipelines Tips on how to solve process inefficiencies of critical workflow components, including variant curation and interpreting rare or novel variants An outlook on how germline NGS analysis and interpretation will change in the next 5 years and how to remain at the forefront of innovation Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline Testing Over the past two decades, huge advancements in sequencing technology have transformed our understanding of human genetics, leading to faster diagnoses,... tv.qiagenbioinformatics.com 01:22:05 <p>Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline Testing <p>Over the past two decades, huge advancements in sequencing technology have transformed our understanding of human genetics, leading to faster diagnoses, earlier prevention, and better treatments. But as more and more people have their genomes sequenced, outpacing our ability to analyze and interpret the generated data, we must embrace new tools, technologies, and strategies to realize the full value of genomic innovation.</p> <p>Advance your lab’s germline testing capabilities by learning how to build a next-gen software workflow, as part of the Hereditary NGS Clinical Summit Series, a two-part, free-to-attend virtual event for variant scientists, bioinformaticians, clinical geneticists, and lab managers.</p> <p>An expert panel of leading medical geneticists, variant scientists and bioinformaticians will discuss emerging scientific and clinical trends in germline NGS testing.</p> <p>Attendees will gain:</p> <p>Insight into how leading laboratories address bottlenecks in their NGS data pipelines<br> Tips on how to solve process inefficiencies of critical workflow components, including variant curation and interpreting rare or novel variants<br> An outlook on how germline NGS analysis and interpretation will change in the next 5 years and how to remain at the forefront of innovation</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/81422637/emerging-clinical-trends-in-1"><img src="http://tv.qiagenbioinformatics.com/64968569/81422637/5bd9dcc53e86885298fe0b0f683b2b65/standard/download-22-thumbnail.jpg" width="75" height=""/></a></p> hereditary hereditary ngs summit qci interpret http://tv.qiagenbioinformatics.com/photo/81412632/emerging-clinical-trends-in <p><p><b>Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline Testing</b></p><b> </b><p>Over the past two decades, huge advancements in sequencing technology have transformed our understanding of human genetics, leading to faster diagnoses, earlier prevention, and better treatments. But as more and more people have their genomes sequenced, outpacing our ability to analyze and interpret the generated data, we must embrace new tools, technologies, and strategies to realize the full value of genomic innovation.</p> <p>Advance your lab’s germline testing capabilities by learning how to build a next-gen software workflow, as part of the Hereditary NGS Clinical Summit Series, a two-part, free-to-attend virtual event for variant scientists, bioinformaticians, clinical geneticists, and lab managers.</p> <p>An expert panel of leading medical geneticists, variant scientists and bioinformaticians will discuss emerging scientific and clinical trends in germline NGS testing.</p> <p>Attendees will gain:</p> <ul><li>Insight into how leading laboratories address bottlenecks in their NGS data pipelines</li><li> Tips on how to solve process inefficiencies of critical workflow components, including variant curation and interpreting rare or novel variants</li><li> An outlook on how germline NGS analysis and interpretation will change in the next 5 years and how to remain at the forefront of innovation</li></ul></p><p><a href="http://tv.qiagenbioinformatics.com/photo/81412632/emerging-clinical-trends-in"><img src="http://tv.qiagenbioinformatics.com/64968577/81412632/7f32e5b3f1a7b21070a98391d15d4557/standard/download-13-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/81412632 Thu, 17 Nov 2022 07:03:21 GMT Emerging clinical trends in germline NGS testing: Expert Panel Discussion in... Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline Testing Over the past two decades, huge advancements in sequencing technology have transformed our understanding of human genetics, leading to faster diagnoses, earlier prevention, and better treatments. But as more and more people have their genomes sequenced, outpacing our ability to analyze and interpret the generated data, we must embrace new tools, technologies, and strategies to realize the full value of genomic innovation. Advance your lab’s germline testing capabilities by learning how to build a next-gen software workflow, as part of the Hereditary NGS Clinical Summit Series, a two-part, free-to-attend virtual event for variant scientists, bioinformaticians, clinical geneticists, and lab managers. An expert panel of leading medical geneticists, variant scientists and bioinformaticians will discuss emerging scientific and clinical trends in germline NGS testing. Attendees will gain: Insight into how leading laboratories address bottlenecks in their NGS data pipelines Tips on how to solve process inefficiencies of critical workflow components, including variant curation and interpreting rare or novel variants An outlook on how germline NGS analysis and interpretation will change in the next 5 years and how to remain at the forefront of innovation Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline Testing Over the past two decades, huge advancements in sequencing technology have transformed our understanding of human genetics, leading to faster diagnoses,... tv.qiagenbioinformatics.com 01:10:25 <p><p><b>Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline Testing</b></p><b> </b><p>Over the past two decades, huge advancements in sequencing technology have transformed our understanding of human genetics, leading to faster diagnoses, earlier prevention, and better treatments. But as more and more people have their genomes sequenced, outpacing our ability to analyze and interpret the generated data, we must embrace new tools, technologies, and strategies to realize the full value of genomic innovation.</p> <p>Advance your lab’s germline testing capabilities by learning how to build a next-gen software workflow, as part of the Hereditary NGS Clinical Summit Series, a two-part, free-to-attend virtual event for variant scientists, bioinformaticians, clinical geneticists, and lab managers.</p> <p>An expert panel of leading medical geneticists, variant scientists and bioinformaticians will discuss emerging scientific and clinical trends in germline NGS testing.</p> <p>Attendees will gain:</p> <ul><li>Insight into how leading laboratories address bottlenecks in their NGS data pipelines</li><li> Tips on how to solve process inefficiencies of critical workflow components, including variant curation and interpreting rare or novel variants</li><li> An outlook on how germline NGS analysis and interpretation will change in the next 5 years and how to remain at the forefront of innovation</li></ul></p><p><a href="http://tv.qiagenbioinformatics.com/photo/81412632/emerging-clinical-trends-in"><img src="http://tv.qiagenbioinformatics.com/64968577/81412632/7f32e5b3f1a7b21070a98391d15d4557/standard/download-13-thumbnail.jpg" width="75" height=""/></a></p> hereditary hereditary ngs summit qci interpret http://tv.qiagenbioinformatics.com/photo/79848955/next-gen-software-workflow-for-1 <p><p><b>Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline Testing</b></p><p>Over the past two decades, huge advancements in sequencing technology have transformed our understanding of human genetics, leading to faster diagnoses, earlier prevention, and better treatments. But as more and more people have their genomes sequenced, outpacing our ability to analyze and interpret the generated data, we must embrace new tools, technologies, and strategies to realize the full value of genomic innovation.</p><p>Advance your lab’s germline testing capabilities by learning how to build a next-gen software workflow, as part of the Hereditary NGS Clinical Summit Series, a two-part, free-to-attend virtual event for variant scientists, bioinformaticians, clinical geneticists, and lab managers.</p><p>Part I: Thursday, October 13, 2022&nbsp;</p><p>An informative scientific and clinical segment focusing on how to streamline and scale components of the NGS analytical workflow.</p><p>Attendees will learn:</p><ul><li>How to simplify NGS secondary analysis workflows to 5 steps</li><li>How to solve every hereditary disorder case for all types of mutations</li><li>How to address current challenges in germline and exome analytics&nbsp;</li></ul>Click <a href="https://digitalinsights.qiagen.com/products-overview/clinical-insights-portfolio/qiagen-clinical-insight/qci-interpret/">here</a> to learn more.<br></p><p><a href="http://tv.qiagenbioinformatics.com/photo/79848955/next-gen-software-workflow-for-1"><img src="http://tv.qiagenbioinformatics.com/64968561/79848955/7076286132fd906f856326e5d50e4db5/standard/download-20-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/79848955 Tue, 18 Oct 2022 15:18:39 GMT Next-gen software workflow for germline testing: QIAGEN Expert talks in Europe Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline TestingOver the past two decades, huge advancements in sequencing technology have transformed our understanding of human genetics, leading to faster diagnoses, earlier prevention, and better treatments. But as more and more people have their genomes sequenced, outpacing our ability to analyze and interpret the generated data, we must embrace new tools, technologies, and strategies to realize the full value of genomic innovation.Advance your lab’s germline testing capabilities by learning how to build a next-gen software workflow, as part of the Hereditary NGS Clinical Summit Series, a two-part, free-to-attend virtual event for variant scientists, bioinformaticians, clinical geneticists, and lab managers.Part I: Thursday, October 13, 2022An informative scientific and clinical segment focusing on how to streamline and scale components of the NGS analytical workflow.Attendees will learn:How to simplify NGS secondary analysis workflows to 5 stepsHow to solve every hereditary disorder case for all types of mutationsHow to address current challenges in germline and exome analyticsClick here to learn more. Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline TestingOver the past two decades, huge advancements in sequencing technology have transformed our understanding of human genetics, leading to faster diagnoses,... tv.qiagenbioinformatics.com 01:50:33 <p><p><b>Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline Testing</b></p><p>Over the past two decades, huge advancements in sequencing technology have transformed our understanding of human genetics, leading to faster diagnoses, earlier prevention, and better treatments. But as more and more people have their genomes sequenced, outpacing our ability to analyze and interpret the generated data, we must embrace new tools, technologies, and strategies to realize the full value of genomic innovation.</p><p>Advance your lab’s germline testing capabilities by learning how to build a next-gen software workflow, as part of the Hereditary NGS Clinical Summit Series, a two-part, free-to-attend virtual event for variant scientists, bioinformaticians, clinical geneticists, and lab managers.</p><p>Part I: Thursday, October 13, 2022&nbsp;</p><p>An informative scientific and clinical segment focusing on how to streamline and scale components of the NGS analytical workflow.</p><p>Attendees will learn:</p><ul><li>How to simplify NGS secondary analysis workflows to 5 steps</li><li>How to solve every hereditary disorder case for all types of mutations</li><li>How to address current challenges in germline and exome analytics&nbsp;</li></ul>Click <a href="https://digitalinsights.qiagen.com/products-overview/clinical-insights-portfolio/qiagen-clinical-insight/qci-interpret/">here</a> to learn more.<br></p><p><a href="http://tv.qiagenbioinformatics.com/photo/79848955/next-gen-software-workflow-for-1"><img src="http://tv.qiagenbioinformatics.com/64968561/79848955/7076286132fd906f856326e5d50e4db5/standard/download-20-thumbnail.jpg" width="75" height=""/></a></p> hereditary hereditary ngs summit qci interpret http://tv.qiagenbioinformatics.com/photo/79848961/next-gen-software-workflow-for <p><p> <b>Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline Testing</b></p><p>Over the past two decades, huge advancements in sequencing technology have transformed our understanding of human genetics, leading to faster diagnoses, earlier prevention, and better treatments. But as more and more people have their genomes sequenced, outpacing our ability to analyze and interpret the generated data, we must embrace new tools, technologies, and strategies to realize the full value of genomic innovation.</p><p>Advance your lab’s germline testing capabilities by learning how to build a next-gen software workflow, as part of the Hereditary NGS Clinical Summit Series, a two-part, free-to-attend virtual event for variant scientists, bioinformaticians, clinical geneticists, and lab managers.&nbsp;&nbsp;</p><p>Part I: Thursday, October 13, 2022&nbsp;</p><p>An informative scientific and clinical segment focusing on how to streamline and scale components of the NGS analytical workflow.</p><p>Attendees will learn:</p><ul><li>How to simplify NGS secondary analysis workflows to 5 steps</li><li>How to solve every hereditary disorder case for all types of mutations</li><li>How to address current challenges in germline and exome analytics&nbsp;</li></ul>Click <a href="https://digitalinsights.qiagen.com/products-overview/clinical-insights-portfolio/qiagen-clinical-insight/qci-interpret/">here</a> to learn more.<br></p><p><a href="http://tv.qiagenbioinformatics.com/photo/79848961/next-gen-software-workflow-for"><img src="http://tv.qiagenbioinformatics.com/64968560/79848961/844065c6f09af7737f2bd428973f3272/standard/download-9-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/79848961 Tue, 18 Oct 2022 15:00:31 GMT Next-gen software workflow for germline testing: QIAGEN Expert talks in USA Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline TestingOver the past two decades, huge advancements in sequencing technology have transformed our understanding of human genetics, leading to faster diagnoses, earlier prevention, and better treatments. But as more and more people have their genomes sequenced, outpacing our ability to analyze and interpret the generated data, we must embrace new tools, technologies, and strategies to realize the full value of genomic innovation.Advance your lab’s germline testing capabilities by learning how to build a next-gen software workflow, as part of the Hereditary NGS Clinical Summit Series, a two-part, free-to-attend virtual event for variant scientists, bioinformaticians, clinical geneticists, and lab managers.Part I: Thursday, October 13, 2022An informative scientific and clinical segment focusing on how to streamline and scale components of the NGS analytical workflow.Attendees will learn:How to simplify NGS secondary analysis workflows to 5 stepsHow to solve every hereditary disorder case for all types of mutationsHow to address current challenges in germline and exome analyticsClick here to learn more. Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline TestingOver the past two decades, huge advancements in sequencing technology have transformed our understanding of human genetics, leading to faster diagnoses,... tv.qiagenbioinformatics.com 02:06:35 <p><p> <b>Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline Testing</b></p><p>Over the past two decades, huge advancements in sequencing technology have transformed our understanding of human genetics, leading to faster diagnoses, earlier prevention, and better treatments. But as more and more people have their genomes sequenced, outpacing our ability to analyze and interpret the generated data, we must embrace new tools, technologies, and strategies to realize the full value of genomic innovation.</p><p>Advance your lab’s germline testing capabilities by learning how to build a next-gen software workflow, as part of the Hereditary NGS Clinical Summit Series, a two-part, free-to-attend virtual event for variant scientists, bioinformaticians, clinical geneticists, and lab managers.&nbsp;&nbsp;</p><p>Part I: Thursday, October 13, 2022&nbsp;</p><p>An informative scientific and clinical segment focusing on how to streamline and scale components of the NGS analytical workflow.</p><p>Attendees will learn:</p><ul><li>How to simplify NGS secondary analysis workflows to 5 steps</li><li>How to solve every hereditary disorder case for all types of mutations</li><li>How to address current challenges in germline and exome analytics&nbsp;</li></ul>Click <a href="https://digitalinsights.qiagen.com/products-overview/clinical-insights-portfolio/qiagen-clinical-insight/qci-interpret/">here</a> to learn more.<br></p><p><a href="http://tv.qiagenbioinformatics.com/photo/79848961/next-gen-software-workflow-for"><img src="http://tv.qiagenbioinformatics.com/64968560/79848961/844065c6f09af7737f2bd428973f3272/standard/download-9-thumbnail.jpg" width="75" height=""/></a></p> hereditary hereditary ngs summit qci interpret