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/128385889/franklin-by-qiagen-for-hereditary <p><p>Accurate variant interpretation is critical in hereditary cancer genetics, but it’s often complex due to conflicting data and evolving clinical context. In this webinar, Molecular Geneticist Dr. Ana Krivokuca will lead a live, case-based demonstration using Franklin by QIAGEN, showing how the platform's structured workflows, ACMG criteria and integrated data can support confident, transparent interpretations while addressing uncertainty and real-world clinical decision-making.</p><p>You will learn:</p><p>-&nbsp;How to evaluate complex variants</p><p>&nbsp; &nbsp; &gt; Using real-world cases examples of how Franklin helps users classify variants of unknown significance (VUS) and structural findings</p><p>-&nbsp;How to balance evidence and recognize when a finding is relevant</p><p>&nbsp; &nbsp; &gt; Applying automated ACMG classification, a vast repository of community-shared data and integrated Human Gene Mutation Database (HGMD) content to determine significance and avoid overinterpretation</p><p>-&nbsp;How to develop a practical framework for hereditary cancer variant interpretation</p><p>&nbsp; &nbsp; &gt; Leveraging a platform that acts as a hybrid system that automates technical processes while providing tools for human experts to make final, informed decisions</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/128385889/franklin-by-qiagen-for-hereditary"><img src="http://tv.qiagenbioinformatics.com/64968576/128385889/fb718ad9c4cc26c2c97fa5ed29ffa110/standard/download-9-thumbnail.jpg" width="600" height="338"/></a></p> http://tv.qiagenbioinformatics.com/photo/128385889 Thu, 18 Jun 2026 23:10:30 GMT Franklin by QIAGEN for Hereditary Cancer Variant Interpretation Accurate variant interpretation is critical in hereditary cancer genetics, but it’s often complex due to conflicting data and evolving clinical context. In this webinar, Molecular Geneticist Dr. Ana Krivokuca will lead a live, case-based demonstration using Franklin by QIAGEN, showing how the platform's structured workflows, ACMG criteria and integrated data can support confident, transparent interpretations while addressing uncertainty and real-world clinical decision-making.You will learn:-How to evaluate complex variants Using real-world cases examples of how Franklin helps users classify variants of unknown significance (VUS) and structural findings-How to balance evidence and recognize when a finding is relevant Applying automated ACMG classification, a vast repository of community-shared data and integrated Human Gene Mutation Database (HGMD) content to determine significance and avoid overinterpretation-How to develop a practical framework for hereditary cancer variant interpretation Leveraging a platform that acts as a hybrid system that automates technical processes while providing tools for human experts to make final, informed decisions Accurate variant interpretation is critical in hereditary cancer genetics, but it’s often complex due to conflicting data and evolving clinical context. In this webinar, Molecular Geneticist Dr. Ana Krivokuca will lead a live, case-based... tv.qiagenbioinformatics.com 53:09 <p><p>Accurate variant interpretation is critical in hereditary cancer genetics, but it’s often complex due to conflicting data and evolving clinical context. In this webinar, Molecular Geneticist Dr. Ana Krivokuca will lead a live, case-based demonstration using Franklin by QIAGEN, showing how the platform's structured workflows, ACMG criteria and integrated data can support confident, transparent interpretations while addressing uncertainty and real-world clinical decision-making.</p><p>You will learn:</p><p>-&nbsp;How to evaluate complex variants</p><p>&nbsp; &nbsp; &gt; Using real-world cases examples of how Franklin helps users classify variants of unknown significance (VUS) and structural findings</p><p>-&nbsp;How to balance evidence and recognize when a finding is relevant</p><p>&nbsp; &nbsp; &gt; Applying automated ACMG classification, a vast repository of community-shared data and integrated Human Gene Mutation Database (HGMD) content to determine significance and avoid overinterpretation</p><p>-&nbsp;How to develop a practical framework for hereditary cancer variant interpretation</p><p>&nbsp; &nbsp; &gt; Leveraging a platform that acts as a hybrid system that automates technical processes while providing tools for human experts to make final, informed decisions</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/128385889/franklin-by-qiagen-for-hereditary"><img src="http://tv.qiagenbioinformatics.com/64968576/128385889/fb718ad9c4cc26c2c97fa5ed29ffa110/standard/download-9-thumbnail.jpg" width="600" height="338"/></a></p> http://tv.qiagenbioinformatics.com/photo/128013088/get-hands-on-with-franklin-hgmd-4 <p><p>Welcome to one of our exclusive, hands-on virtual workshops to explore&nbsp;Franklin + HGMD Professional&nbsp;— a powerful variant interpretation and reporting solution combining AI-driven workflows with expertly curated evidence.</p><p>During this session, you’ll analyze a&nbsp;real-world case&nbsp;involving a 3-month-old patient with complex neuromuscular phenotypes. Using Franklin + HGMD, you’ll prioritize variants, explore curated evidence (including disease-causing mutations from HGMD), and see how seamlessly the platform integrates clinical data, expert recommendations, and insights from 100+ databases.</p><p>You’ll also discover how Franklin + HGMD:</p><ul><li><p>- Uses advanced AI to prioritize and classify variants efficiently</p></li><li><p>- Automates ACMG classification with integrated HGMD and ClinGen guidance</p></li><li><p>- Enables customizable, AI-assisted reporting for actionable clinical insights</p></li></ul><p></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/128013088/get-hands-on-with-franklin-hgmd-4"><img src="http://tv.qiagenbioinformatics.com/64968561/128013088/d7d68857c3023e2a23942149a08a92c1/standard/download-9-thumbnail.jpg" width="600" height="338"/></a></p> http://tv.qiagenbioinformatics.com/photo/128013088 Wed, 03 Jun 2026 14:56:33 GMT Get Hands-on with Franklin + HGMD – May 28 (Spanish) Welcome to one of our exclusive, hands-on virtual workshops to exploreFranklin + HGMD Professional— a powerful variant interpretation and reporting solution combining AI-driven workflows with expertly curated evidence.During this session, you’ll analyze areal-world caseinvolving a 3-month-old patient with complex neuromuscular phenotypes. Using Franklin + HGMD, you’ll prioritize variants, explore curated evidence (including disease-causing mutations from HGMD), and see how seamlessly the platform integrates clinical data, expert recommendations, and insights from 100+ databases.You’ll also discover how Franklin + HGMD:- Uses advanced AI to prioritize and classify variants efficiently- Automates ACMG classification with integrated HGMD and ClinGen guidance- Enables customizable, AI-assisted reporting for actionable clinical insights Welcome to one of our exclusive, hands-on virtual workshops to exploreFranklin + HGMD Professional— a powerful variant interpretation and reporting solution combining AI-driven workflows with expertly curated evidence.During this session, you’ll... tv.qiagenbioinformatics.com 01:32:57 <p><p>Welcome to one of our exclusive, hands-on virtual workshops to explore&nbsp;Franklin + HGMD Professional&nbsp;— a powerful variant interpretation and reporting solution combining AI-driven workflows with expertly curated evidence.</p><p>During this session, you’ll analyze a&nbsp;real-world case&nbsp;involving a 3-month-old patient with complex neuromuscular phenotypes. Using Franklin + HGMD, you’ll prioritize variants, explore curated evidence (including disease-causing mutations from HGMD), and see how seamlessly the platform integrates clinical data, expert recommendations, and insights from 100+ databases.</p><p>You’ll also discover how Franklin + HGMD:</p><ul><li><p>- Uses advanced AI to prioritize and classify variants efficiently</p></li><li><p>- Automates ACMG classification with integrated HGMD and ClinGen guidance</p></li><li><p>- Enables customizable, AI-assisted reporting for actionable clinical insights</p></li></ul><p></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/128013088/get-hands-on-with-franklin-hgmd-4"><img src="http://tv.qiagenbioinformatics.com/64968561/128013088/d7d68857c3023e2a23942149a08a92c1/standard/download-9-thumbnail.jpg" width="600" height="338"/></a></p> http://tv.qiagenbioinformatics.com/photo/128009177/get-hands-on-with-franklin-hgmd-3 <p><p>Welcome to one of our exclusive, hands-on virtual workshops to explore&nbsp;Franklin + HGMD Professional&nbsp;— a powerful variant interpretation and reporting solution combining AI-driven workflows with expertly curated evidence.</p><p>During this session, you’ll analyze a&nbsp;real-world case&nbsp;involving a 3-month-old patient with complex neuromuscular phenotypes. Using Franklin + HGMD, you’ll prioritize variants, explore curated evidence (including disease-causing mutations from HGMD), and see how seamlessly the platform integrates clinical data, expert recommendations, and insights from 100+ databases.</p><p>You’ll also discover how Franklin + HGMD:</p><ul><li><p>- Uses advanced AI to prioritize and classify variants efficiently</p></li><li><p>- Automates ACMG classification with integrated HGMD and ClinGen guidance</p></li><li><p>- Enables customizable, AI-assisted reporting for actionable clinical insights</p></li></ul><p></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/128009177/get-hands-on-with-franklin-hgmd-3"><img src="http://tv.qiagenbioinformatics.com/64968569/128009177/f8205308be0b45170d99edcf1bc831a2/standard/download-10-thumbnail.jpg" width="600" height="338"/></a></p> http://tv.qiagenbioinformatics.com/photo/128009177 Wed, 03 Jun 2026 13:17:34 GMT Get Hands-on with Franklin + HGMD – May 27 (Portuguese) Welcome to one of our exclusive, hands-on virtual workshops to exploreFranklin + HGMD Professional— a powerful variant interpretation and reporting solution combining AI-driven workflows with expertly curated evidence.During this session, you’ll analyze areal-world caseinvolving a 3-month-old patient with complex neuromuscular phenotypes. Using Franklin + HGMD, you’ll prioritize variants, explore curated evidence (including disease-causing mutations from HGMD), and see how seamlessly the platform integrates clinical data, expert recommendations, and insights from 100+ databases.You’ll also discover how Franklin + HGMD:- Uses advanced AI to prioritize and classify variants efficiently- Automates ACMG classification with integrated HGMD and ClinGen guidance- Enables customizable, AI-assisted reporting for actionable clinical insights Welcome to one of our exclusive, hands-on virtual workshops to exploreFranklin + HGMD Professional— a powerful variant interpretation and reporting solution combining AI-driven workflows with expertly curated evidence.During this session, you’ll... tv.qiagenbioinformatics.com 01:44:36 <p><p>Welcome to one of our exclusive, hands-on virtual workshops to explore&nbsp;Franklin + HGMD Professional&nbsp;— a powerful variant interpretation and reporting solution combining AI-driven workflows with expertly curated evidence.</p><p>During this session, you’ll analyze a&nbsp;real-world case&nbsp;involving a 3-month-old patient with complex neuromuscular phenotypes. Using Franklin + HGMD, you’ll prioritize variants, explore curated evidence (including disease-causing mutations from HGMD), and see how seamlessly the platform integrates clinical data, expert recommendations, and insights from 100+ databases.</p><p>You’ll also discover how Franklin + HGMD:</p><ul><li><p>- Uses advanced AI to prioritize and classify variants efficiently</p></li><li><p>- Automates ACMG classification with integrated HGMD and ClinGen guidance</p></li><li><p>- Enables customizable, AI-assisted reporting for actionable clinical insights</p></li></ul><p></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/128009177/get-hands-on-with-franklin-hgmd-3"><img src="http://tv.qiagenbioinformatics.com/64968569/128009177/f8205308be0b45170d99edcf1bc831a2/standard/download-10-thumbnail.jpg" width="600" height="338"/></a></p> http://tv.qiagenbioinformatics.com/photo/118478609/accelerating-hereditary-variant <p><p>“Reliable AI”? Sounds like a contradiction, but with HGMD in Franklin, it’s possible.</p><p>&nbsp;</p><p>By combining HGMD Pro’s comprehensive, expert-curated hereditary variant content and Franklin’s AI workflows and user-friendly interface, accelerated hereditary variant interpretation is now within closer reach. Whether you’re in diagnostics, research or bioinformatics, you will gain practical insights into a simplified genomic analysis workflow.</p><p></p><p>You will learn to:</p><ul><li><p>Access HGMD data directly within Franklin by QIAGEN</p></li><li><p>Apply flexible HGMD-based filtering for inherited disease mutations</p></li><li><p>Improve diagnostic efficiency with an AI platform powered by curated, high-quality data and contributions from the medical community</p></li></ul><p></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/118478609/accelerating-hereditary-variant"><img src="http://tv.qiagenbioinformatics.com/64968577/118478609/9f79d795ff6491dafa8ae0d9a2e4412f/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/118478609 Tue, 19 May 2026 11:48:37 GMT Accelerating hereditary variant interpretation: HGMD in Franklin “Reliable AI”? Sounds like a contradiction, but with HGMD in Franklin, it’s possible.By combining HGMD Pro’s comprehensive, expert-curated hereditary variant content and Franklin’s AI workflows and user-friendly interface, accelerated hereditary variant interpretation is now within closer reach. Whether you’re in diagnostics, research or bioinformatics, you will gain practical insights into a simplified genomic analysis workflow.You will learn to:Access HGMD data directly within Franklin by QIAGENApply flexible HGMD-based filtering for inherited disease mutationsImprove diagnostic efficiency with an AI platform powered by curated, high-quality data and contributions from the medical community “Reliable AI”? Sounds like a contradiction, but with HGMD in Franklin, it’s possible.By combining HGMD Pro’s comprehensive, expert-curated hereditary variant content and Franklin’s AI workflows and user-friendly interface, accelerated hereditary... tv.qiagenbioinformatics.com 38:15 <p><p>“Reliable AI”? Sounds like a contradiction, but with HGMD in Franklin, it’s possible.</p><p>&nbsp;</p><p>By combining HGMD Pro’s comprehensive, expert-curated hereditary variant content and Franklin’s AI workflows and user-friendly interface, accelerated hereditary variant interpretation is now within closer reach. Whether you’re in diagnostics, research or bioinformatics, you will gain practical insights into a simplified genomic analysis workflow.</p><p></p><p>You will learn to:</p><ul><li><p>Access HGMD data directly within Franklin by QIAGEN</p></li><li><p>Apply flexible HGMD-based filtering for inherited disease mutations</p></li><li><p>Improve diagnostic efficiency with an AI platform powered by curated, high-quality data and contributions from the medical community</p></li></ul><p></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/118478609/accelerating-hereditary-variant"><img src="http://tv.qiagenbioinformatics.com/64968577/118478609/9f79d795ff6491dafa8ae0d9a2e4412f/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/127293590/get-hands-on-with-franklin-hgmd-1 <p><p>Our exclusive, hands-on virtual workshops will&nbsp; explore&nbsp;Franklin + HGMD Professional:&nbsp;a powerful variant interpretation and reporting solution combining AI-driven workflows with expertly curated evidence.</p><p>During this session, you’ll analyze a&nbsp;real-world case&nbsp;involving a 3-month-old patient with complex neuromuscular phenotypes. Using Franklin + HGMD, you’ll prioritize variants, explore curated evidence (including disease-causing mutations from HGMD), and see how seamlessly the platform integrates clinical data, expert recommendations, and insights from 100+ databases.</p><p><strong>See how Franklin + HGMD:</strong></p><ul><li><p>- Uses advanced AI to prioritize and classify variants efficiently</p></li><li><p>Automates ACMG classification with integrated HGMD and ClinGen guidance</p></li><li><p>- Enables customizable, AI-assisted reporting for actionable clinical insights</p></li><li><p>- Helps labs build a centralized, evolving knowledge base from real-world evidence</p></li></ul><p></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/127293590/get-hands-on-with-franklin-hgmd-1"><img src="http://tv.qiagenbioinformatics.com/64968566/127293590/bd37bfb4f70345c6ead427990b533818/standard/download-13-thumbnail.jpg" width="600" height="338"/></a></p> http://tv.qiagenbioinformatics.com/photo/127293590 Tue, 19 May 2026 07:50:08 GMT Get Hands-on with Franklin + HGMD Our exclusive, hands-on virtual workshops will exploreFranklin + HGMD Professional:a powerful variant interpretation and reporting solution combining AI-driven workflows with expertly curated evidence.During this session, you’ll analyze areal-world caseinvolving a 3-month-old patient with complex neuromuscular phenotypes. Using Franklin + HGMD, you’ll prioritize variants, explore curated evidence (including disease-causing mutations from HGMD), and see how seamlessly the platform integrates clinical data, expert recommendations, and insights from 100+ databases.See how Franklin + HGMD:- Uses advanced AI to prioritize and classify variants efficientlyAutomates ACMG classification with integrated HGMD and ClinGen guidance- Enables customizable, AI-assisted reporting for actionable clinical insights- Helps labs build a centralized, evolving knowledge base from real-world evidence Our exclusive, hands-on virtual workshops will exploreFranklin + HGMD Professional:a powerful variant interpretation and reporting solution combining AI-driven workflows with expertly curated evidence.During this session, you’ll analyze... tv.qiagenbioinformatics.com 01:31:57 <p><p>Our exclusive, hands-on virtual workshops will&nbsp; explore&nbsp;Franklin + HGMD Professional:&nbsp;a powerful variant interpretation and reporting solution combining AI-driven workflows with expertly curated evidence.</p><p>During this session, you’ll analyze a&nbsp;real-world case&nbsp;involving a 3-month-old patient with complex neuromuscular phenotypes. Using Franklin + HGMD, you’ll prioritize variants, explore curated evidence (including disease-causing mutations from HGMD), and see how seamlessly the platform integrates clinical data, expert recommendations, and insights from 100+ databases.</p><p><strong>See how Franklin + HGMD:</strong></p><ul><li><p>- Uses advanced AI to prioritize and classify variants efficiently</p></li><li><p>Automates ACMG classification with integrated HGMD and ClinGen guidance</p></li><li><p>- Enables customizable, AI-assisted reporting for actionable clinical insights</p></li><li><p>- Helps labs build a centralized, evolving knowledge base from real-world evidence</p></li></ul><p></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/127293590/get-hands-on-with-franklin-hgmd-1"><img src="http://tv.qiagenbioinformatics.com/64968566/127293590/bd37bfb4f70345c6ead427990b533818/standard/download-13-thumbnail.jpg" width="600" height="338"/></a></p>