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/101070273/scale-up-ngs-bioinformatics-1 <p>More and more biopharma and academic groups are looking to process a large number of samples simultaneously or for a quicker turnaround time. This webinar will introduce a flexible and powerful setup for running your NGS sequence analyses through servers or Amazon Web Services (AWS), depending on user preference. We will demonstrate how CLC Genomics Workbench can be used to customize workflows and send analyses for batch execution. We will also highlight analysis automation solutions, use of third-party dockers, audit trails and user management – all of which are available with the CLC Genomics Server software.</p> <p>You will learn to:<br /> • Customize template workflows to meet your NGS analysis requirements<br /> • Set up a CLC Genomics Cloud environment on AWS<br /> • Submit workflows to run on internal servers or AWS and retrieve results from these analyses<br /> • Use third-party dockers and automate workflow execution</p><p><a href="http://tv.qiagenbioinformatics.com/photo/101070273/scale-up-ngs-bioinformatics-1"><img src="http://tv.qiagenbioinformatics.com/64968575/101070273/45dee0e037fcd6915ebfdd6056c7d178/standard/download-8-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/101070273 Thu, 23 May 2024 14:00:26 GMT Scale up NGS bioinformatics analysis throughput with CLC Genomics Server and... More and more biopharma and academic groups are looking to process a large number of samples simultaneously or for a quicker turnaround time. This webinar will introduce a flexible and powerful setup for running your NGS sequence analyses through servers or Amazon Web Services (AWS), depending on user preference. We will demonstrate how CLC Genomics Workbench can be used to customize workflows and send analyses for batch execution. We will also highlight analysis automation solutions, use of third-party dockers, audit trails and user management – all of which are available with the CLC Genomics Server software. You will learn to: • Customize template workflows to meet your NGS analysis requirements • Set up a CLC Genomics Cloud environment on AWS • Submit workflows to run on internal servers or AWS and retrieve results from these analyses • Use third-party dockers and automate workflow execution More and more biopharma and academic groups are looking to process a large number of samples simultaneously or for a quicker turnaround time. This webinar will introduce a flexible and powerful setup for running your NGS sequence analyses through... tv.qiagenbioinformatics.com 01:05:43 <p>More and more biopharma and academic groups are looking to process a large number of samples simultaneously or for a quicker turnaround time. This webinar will introduce a flexible and powerful setup for running your NGS sequence analyses through servers or Amazon Web Services (AWS), depending on user preference. We will demonstrate how CLC Genomics Workbench can be used to customize workflows and send analyses for batch execution. We will also highlight analysis automation solutions, use of third-party dockers, audit trails and user management – all of which are available with the CLC Genomics Server software.</p> <p>You will learn to:<br /> • Customize template workflows to meet your NGS analysis requirements<br /> • Set up a CLC Genomics Cloud environment on AWS<br /> • Submit workflows to run on internal servers or AWS and retrieve results from these analyses<br /> • Use third-party dockers and automate workflow execution</p><p><a href="http://tv.qiagenbioinformatics.com/photo/101070273/scale-up-ngs-bioinformatics-1"><img src="http://tv.qiagenbioinformatics.com/64968575/101070273/45dee0e037fcd6915ebfdd6056c7d178/standard/download-8-thumbnail.jpg" width="75" height=""/></a></p> cloud genomics server high-throughput ngs http://tv.qiagenbioinformatics.com/photo/91808655/how-to-perform-dna-seq-and <p>In this webinar, we’ll introduce algorithms required to perform data analysis for resequencing next-generation sequencing data. Together, we’ll explore:</p> <p>• Read mapper<br /> • Variant callers<br /> • Annotations and filters<br /> • Genome Browser</p><p><a href="http://tv.qiagenbioinformatics.com/photo/91808655/how-to-perform-dna-seq-and"><img src="http://tv.qiagenbioinformatics.com/64968561/91808655/c6e71cc45d0445bd19ab6bf7dd6fbc20/standard/download-6-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/91808655 Mon, 18 Dec 2023 12:07:03 GMT How to perform DNA-seq and resequencing data analyses using QIAGEN CLC... In this webinar, we’ll introduce algorithms required to perform data analysis for resequencing next-generation sequencing data. Together, we’ll explore: • Read mapper • Variant callers • Annotations and filters • Genome Browser In this webinar, we’ll introduce algorithms required to perform data analysis for resequencing next-generation sequencing data. Together, we’ll explore: • Read mapper • Variant callers • Annotations and filters • Genome Browser tv.qiagenbioinformatics.com 55:22 <p>In this webinar, we’ll introduce algorithms required to perform data analysis for resequencing next-generation sequencing data. Together, we’ll explore:</p> <p>• Read mapper<br /> • Variant callers<br /> • Annotations and filters<br /> • Genome Browser</p><p><a href="http://tv.qiagenbioinformatics.com/photo/91808655/how-to-perform-dna-seq-and"><img src="http://tv.qiagenbioinformatics.com/64968561/91808655/c6e71cc45d0445bd19ab6bf7dd6fbc20/standard/download-6-thumbnail.jpg" width="75" height=""/></a></p> dna-seq ngs http://tv.qiagenbioinformatics.com/photo/87882198/immune-repertoire-analysis-using <p>The composition of the immune repertoire, consisting of the T cell and B cell receptors (TCR and BCR), is important for an organism's adaptive immune system and plays a pivotal role in an individual's overall health. Understanding the complex array of TCR and BCR allows for developing precision medicine and immunotherapy. Analyzing next-generation sequencing (NGS) data from RNA-seq experiments to characterize and understand TCR and BCR clonotypes may aid in identifying cases that could benefit from personalized immunotherapy or potentially predict therapeutic outcomes.</p> <p>In this training, we'll use QIAGEN CLC Genomics Workbench to analyze immune repertoire NGS data generated from RNA-seq or single-cell RNA-seq data. Together we'll explore how to import, analyze and interpret your NGS data. Specifically, you'll learn how to:</p> <p>-Import NGS data into QIAGEN CLC Genomics Workbench</p> <p>-Analyze the data using template workflows</p> <p>-Interpret the results using the interactive graphics produced by the workflows</p><p><a href="http://tv.qiagenbioinformatics.com/photo/87882198/immune-repertoire-analysis-using"><img src="http://tv.qiagenbioinformatics.com/64968561/87882198/13c2d9057f9d2c3cf526f657307aaafb/standard/download-8-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/87882198 Mon, 21 Aug 2023 15:57:03 GMT Immune repertoire analysis using QIAGEN CLC Genomics Workbench The composition of the immune repertoire, consisting of the T cell and B cell receptors (TCR and BCR), is important for an organism's adaptive immune system and plays a pivotal role in an individual's overall health. Understanding the complex array of TCR and BCR allows for developing precision medicine and immunotherapy. Analyzing next-generation sequencing (NGS) data from RNA-seq experiments to characterize and understand TCR and BCR clonotypes may aid in identifying cases that could benefit from personalized immunotherapy or potentially predict therapeutic outcomes. In this training, we'll use QIAGEN CLC Genomics Workbench to analyze immune repertoire NGS data generated from RNA-seq or single-cell RNA-seq data. Together we'll explore how to import, analyze and interpret your NGS data. Specifically, you'll learn how to: -Import NGS data into QIAGEN CLC Genomics Workbench -Analyze the data using template workflows -Interpret the results using the interactive graphics produced by the workflows The composition of the immune repertoire, consisting of the T cell and B cell receptors (TCR and BCR), is important for an organism's adaptive immune system and plays a pivotal role in an individual's overall health. Understanding the complex... tv.qiagenbioinformatics.com 01:26:32 <p>The composition of the immune repertoire, consisting of the T cell and B cell receptors (TCR and BCR), is important for an organism's adaptive immune system and plays a pivotal role in an individual's overall health. Understanding the complex array of TCR and BCR allows for developing precision medicine and immunotherapy. Analyzing next-generation sequencing (NGS) data from RNA-seq experiments to characterize and understand TCR and BCR clonotypes may aid in identifying cases that could benefit from personalized immunotherapy or potentially predict therapeutic outcomes.</p> <p>In this training, we'll use QIAGEN CLC Genomics Workbench to analyze immune repertoire NGS data generated from RNA-seq or single-cell RNA-seq data. Together we'll explore how to import, analyze and interpret your NGS data. Specifically, you'll learn how to:</p> <p>-Import NGS data into QIAGEN CLC Genomics Workbench</p> <p>-Analyze the data using template workflows</p> <p>-Interpret the results using the interactive graphics produced by the workflows</p><p><a href="http://tv.qiagenbioinformatics.com/photo/87882198/immune-repertoire-analysis-using"><img src="http://tv.qiagenbioinformatics.com/64968561/87882198/13c2d9057f9d2c3cf526f657307aaafb/standard/download-8-thumbnail.jpg" width="75" height=""/></a></p> clc genomics workbench immunology ngs