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/123905465/long-reads-analysis-using-qiagen-1 <p><p>This webinar will introduce you to the Long Read Support plugin for Oxford Nanopore and PacBio sequencing reads in QIAGEN CLC Genomics Workbench.</p><p>Learn how to:</p><ul><li><p>- Download and install needed plugins</p></li><li><p>- Import data required for the analysis</p></li><li><p>- Perform long read de novo assembly</p></li><li><p>- Map reads to a reference and visualize an assembly</p></li><li><p>- Use BLAST to investigate the contigs</p></li><li><p>- Use additional long read tools: polish with short reads, structural variant calling</p></li><li><p>- Use genome finishing tools: analyze and assemble contigs</p></li><li><p>- Use analytical tools: RNA-seq analysis for long reads, classify long read amplicons for metagenomics</p></li></ul><p><br></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/123905465/long-reads-analysis-using-qiagen-1"><img src="http://tv.qiagenbioinformatics.com/64968579/123905465/0c78a2d5420f4d328276d9d9aaf3bded/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/123905465 Thu, 26 Feb 2026 17:50:30 GMT Long reads analysis using QIAGEN CLC Genomics Workbench This webinar will introduce you to the Long Read Support plugin for Oxford Nanopore and PacBio sequencing reads in QIAGEN CLC Genomics Workbench.Learn how to:- Download and install needed plugins- Import data required for the analysis- Perform long read de novo assembly- Map reads to a reference and visualize an assembly- Use BLAST to investigate the contigs- Use additional long read tools: polish with short reads, structural variant calling- Use genome finishing tools: analyze and assemble contigs- Use analytical tools: RNA-seq analysis for long reads, classify long read amplicons for metagenomics This webinar will introduce you to the Long Read Support plugin for Oxford Nanopore and PacBio sequencing reads in QIAGEN CLC Genomics Workbench.Learn how to:- Download and install needed plugins- Import data required for the analysis- Perform... tv.qiagenbioinformatics.com 01:31:04 <p><p>This webinar will introduce you to the Long Read Support plugin for Oxford Nanopore and PacBio sequencing reads in QIAGEN CLC Genomics Workbench.</p><p>Learn how to:</p><ul><li><p>- Download and install needed plugins</p></li><li><p>- Import data required for the analysis</p></li><li><p>- Perform long read de novo assembly</p></li><li><p>- Map reads to a reference and visualize an assembly</p></li><li><p>- Use BLAST to investigate the contigs</p></li><li><p>- Use additional long read tools: polish with short reads, structural variant calling</p></li><li><p>- Use genome finishing tools: analyze and assemble contigs</p></li><li><p>- Use analytical tools: RNA-seq analysis for long reads, classify long read amplicons for metagenomics</p></li></ul><p><br></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/123905465/long-reads-analysis-using-qiagen-1"><img src="http://tv.qiagenbioinformatics.com/64968579/123905465/0c78a2d5420f4d328276d9d9aaf3bded/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> clc http://tv.qiagenbioinformatics.com/photo/67385051/single-cell-rna-seq-analysis-made <p>Single-cell gene expression analysis starting from either FASTQ or expression data is now supported by QIAGEN CLC Genomics Workbench Premium, the scalable cross-platform desktop software for NGS data analysis. In this webinar, we will re-analyze data from a study on transcriptional profiling of the mouse heart (Skelly et al., 2018), starting from FASTQ and ending with detecting sexually dimorphic genes within different cell types.<p></p> <p>Reference: Skelly, Daniel A., et al. (2018) Single-cell transcriptional profiling reveals cellular diversity and intercommunication in the mouse heart. Cell reports 22.3: 600-610.</p> <p>Topics covered:<br> • Introduction to the QIAGEN CLC Genomics Workbench<br> • Generation of t-SNE and UMAP plots, starting from raw FASTQ read files<br> • Automated annotation of cell types using QIAGEN’s cell type classifier<br> • Detection of differentially expressed genes in different cell types in a case vs. control setting</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/67385051/single-cell-rna-seq-analysis-made"><img src="http://tv.qiagenbioinformatics.com/64968569/67385051/9a9815308a9ac8fce475e79484b3a011/standard/download-4-thumbnail.jpg" width="600" height="338"/></a></p> http://tv.qiagenbioinformatics.com/photo/67385051 Wed, 28 Jan 2026 21:53:39 GMT Single-cell RNA-seq analysis made easy - February 24 Single-cell gene expression analysis starting from either FASTQ or expression data is now supported by QIAGEN CLC Genomics Workbench Premium, the scalable cross-platform desktop software for NGS data analysis. In this webinar, we will re-analyze data from a study on transcriptional profiling of the mouse heart (Skelly et al., 2018), starting from FASTQ and ending with detecting sexually dimorphic genes within different cell types. Reference: Skelly, Daniel A., et al. (2018) Single-cell transcriptional profiling reveals cellular diversity and intercommunication in the mouse heart. Cell reports 22.3: 600-610. Topics covered: • Introduction to the QIAGEN CLC Genomics Workbench • Generation of t-SNE and UMAP plots, starting from raw FASTQ read files • Automated annotation of cell types using QIAGEN’s cell type classifier • Detection of differentially expressed genes in different cell types in a case vs. control setting Single-cell gene expression analysis starting from either FASTQ or expression data is now supported by QIAGEN CLC Genomics Workbench Premium, the scalable cross-platform desktop software for NGS data analysis. In this webinar, we will re-analyze... tv.qiagenbioinformatics.com 40:34 <p>Single-cell gene expression analysis starting from either FASTQ or expression data is now supported by QIAGEN CLC Genomics Workbench Premium, the scalable cross-platform desktop software for NGS data analysis. In this webinar, we will re-analyze data from a study on transcriptional profiling of the mouse heart (Skelly et al., 2018), starting from FASTQ and ending with detecting sexually dimorphic genes within different cell types.<p></p> <p>Reference: Skelly, Daniel A., et al. (2018) Single-cell transcriptional profiling reveals cellular diversity and intercommunication in the mouse heart. Cell reports 22.3: 600-610.</p> <p>Topics covered:<br> • Introduction to the QIAGEN CLC Genomics Workbench<br> • Generation of t-SNE and UMAP plots, starting from raw FASTQ read files<br> • Automated annotation of cell types using QIAGEN’s cell type classifier<br> • Detection of differentially expressed genes in different cell types in a case vs. control setting</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/67385051/single-cell-rna-seq-analysis-made"><img src="http://tv.qiagenbioinformatics.com/64968569/67385051/9a9815308a9ac8fce475e79484b3a011/standard/download-4-thumbnail.jpg" width="600" height="338"/></a></p> clc clc genomics workbench clc webinar http://tv.qiagenbioinformatics.com/photo/122734051/rna-seq-data-analysis-using-qiagen-2 <p><p>For your RNA-seq data, you will learn how to:</p><p>• Import FASTQ files, cell matrix files and metadata</p><p>• Download and/or import reference and annotations files</p><p>• Map reads to a reference genome</p><p>• Generate gene and transcript counts</p><p>• QC reports displaying % mapped reads etc.</p><p>• Generate visualizations of results, such as heatmaps, differential expression tables, PCA/PCOA plots, Venn diagrams, Sankey plot and more</p><p>• Easily customize RNA-seq workflows</p><p>• Export publication-quality graphics, tables and reports</p><p>Per audience request</p><p>• Send differential expression tables to QIAGEN Ingenuity Pathway Analysis directly from QIAGEN CLC Genomics Workbench to analyze and interpret relevant pathways</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/122734051/rna-seq-data-analysis-using-qiagen-2"><img src="http://tv.qiagenbioinformatics.com/64968580/122734051/267ff213640a8dd8138a25507905f03f/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/122734051 Mon, 26 Jan 2026 13:52:53 GMT RNA-seq data analysis using QIAGEN CLC Genomics Workbench For your RNA-seq data, you will learn how to:• Import FASTQ files, cell matrix files and metadata• Download and/or import reference and annotations files• Map reads to a reference genome• Generate gene and transcript counts• QC reports displaying % mapped reads etc.• Generate visualizations of results, such as heatmaps, differential expression tables, PCA/PCOA plots, Venn diagrams, Sankey plot and more• Easily customize RNA-seq workflows• Export publication-quality graphics, tables and reportsPer audience request• Send differential expression tables to QIAGEN Ingenuity Pathway Analysis directly from QIAGEN CLC Genomics Workbench to analyze and interpret relevant pathways For your RNA-seq data, you will learn how to:• Import FASTQ files, cell matrix files and metadata• Download and/or import reference and annotations files• Map reads to a reference genome• Generate gene and transcript counts• QC reports displaying... tv.qiagenbioinformatics.com 01:23:20 <p><p>For your RNA-seq data, you will learn how to:</p><p>• Import FASTQ files, cell matrix files and metadata</p><p>• Download and/or import reference and annotations files</p><p>• Map reads to a reference genome</p><p>• Generate gene and transcript counts</p><p>• QC reports displaying % mapped reads etc.</p><p>• Generate visualizations of results, such as heatmaps, differential expression tables, PCA/PCOA plots, Venn diagrams, Sankey plot and more</p><p>• Easily customize RNA-seq workflows</p><p>• Export publication-quality graphics, tables and reports</p><p>Per audience request</p><p>• Send differential expression tables to QIAGEN Ingenuity Pathway Analysis directly from QIAGEN CLC Genomics Workbench to analyze and interpret relevant pathways</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/122734051/rna-seq-data-analysis-using-qiagen-2"><img src="http://tv.qiagenbioinformatics.com/64968580/122734051/267ff213640a8dd8138a25507905f03f/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> clc workbench http://tv.qiagenbioinformatics.com/photo/122603550/advance-workflow-constructions <p><p>In today’s session, we’ll explore the major enhancements to the workflow system that greatly improve usability, flexibility, and authoring efficiency. We’ll look at new grouping and branching features that simplify complex workflow design, updated editor tools that make navigation and validation easier, and improvements that streamline adding, managing, and reusing workflow components. We’ll also cover the newly workflow-enabled tools and how workflows can now be installed even when some tools are unavailable – making collaboration and sharing smoother than ever.</p><p>• Overview of major workflow system enhancements</p><p>• New grouping and branching features for easier design</p><p>• Streamlined workflow editor with improved navigation and validation</p><p>• Faster, more consistent workflow creation and reuse</p><p>• Newly workflow-enabled tools and improved installation flexibility</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/122603550/advance-workflow-constructions"><img src="http://tv.qiagenbioinformatics.com/64968556/122603550/ce5c5296e9858030caa8bfbc562dbfcb/standard/download-11-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/122603550 Thu, 22 Jan 2026 09:56:38 GMT Advance workflow constructions using the CLC Genomics workbench In today’s session, we’ll explore the major enhancements to the workflow system that greatly improve usability, flexibility, and authoring efficiency. We’ll look at new grouping and branching features that simplify complex workflow design, updated editor tools that make navigation and validation easier, and improvements that streamline adding, managing, and reusing workflow components. We’ll also cover the newly workflow-enabled tools and how workflows can now be installed even when some tools are unavailable – making collaboration and sharing smoother than ever.• Overview of major workflow system enhancements• New grouping and branching features for easier design• Streamlined workflow editor with improved navigation and validation• Faster, more consistent workflow creation and reuse• Newly workflow-enabled tools and improved installation flexibility In today’s session, we’ll explore the major enhancements to the workflow system that greatly improve usability, flexibility, and authoring efficiency. We’ll look at new grouping and branching features that simplify complex workflow design, updated... tv.qiagenbioinformatics.com 01:11:16 <p><p>In today’s session, we’ll explore the major enhancements to the workflow system that greatly improve usability, flexibility, and authoring efficiency. We’ll look at new grouping and branching features that simplify complex workflow design, updated editor tools that make navigation and validation easier, and improvements that streamline adding, managing, and reusing workflow components. We’ll also cover the newly workflow-enabled tools and how workflows can now be installed even when some tools are unavailable – making collaboration and sharing smoother than ever.</p><p>• Overview of major workflow system enhancements</p><p>• New grouping and branching features for easier design</p><p>• Streamlined workflow editor with improved navigation and validation</p><p>• Faster, more consistent workflow creation and reuse</p><p>• Newly workflow-enabled tools and improved installation flexibility</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/122603550/advance-workflow-constructions"><img src="http://tv.qiagenbioinformatics.com/64968556/122603550/ce5c5296e9858030caa8bfbc562dbfcb/standard/download-11-thumbnail.jpg" width="75" height=""/></a></p> clc workbench http://tv.qiagenbioinformatics.com/photo/118447890/single-cell-rna-seq-and-spatial <p><p>In this webinar, the speaker will cover how to simplify your single cell RNA-seq analysis with biologist-friendly point and click tools.</p><p>• Generate high-resolution visuals and other files from your analysis for publications and biopharmaceutical discoveries</p><p>• Generate dimension reduction (UMAP, t-SNE) plots to understand differences between cell clusters/experimental conditions</p><p>• Identify and study clusters and cell types specific biomarkers using differential expression tables, gene expression heat maps, dot plots and violin plots</p><p>• Generate desired cell annotations using hashtags</p><p>• Visualize and investigate spatial transcriptomics plot using your Cell Ranger output to better understand cellular organization and generate hypothesis</p><p>• Use preconfigured but customizable pipelines/workflows for single-cell RNA-seq data</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/118447890/single-cell-rna-seq-and-spatial"><img src="http://tv.qiagenbioinformatics.com/64968560/118447890/dfb1c7b72130ead9a62cf283a3ed04f1/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/118447890 Thu, 13 Nov 2025 09:15:18 GMT Single Cell RNA-Seq and Spatial Transcriptomics In this webinar, the speaker will cover how to simplify your single cell RNA-seq analysis with biologist-friendly point and click tools.• Generate high-resolution visuals and other files from your analysis for publications and biopharmaceutical discoveries• Generate dimension reduction (UMAP, t-SNE) plots to understand differences between cell clusters/experimental conditions• Identify and study clusters and cell types specific biomarkers using differential expression tables, gene expression heat maps, dot plots and violin plots• Generate desired cell annotations using hashtags• Visualize and investigate spatial transcriptomics plot using your Cell Ranger output to better understand cellular organization and generate hypothesis• Use preconfigured but customizable pipelines/workflows for single-cell RNA-seq data In this webinar, the speaker will cover how to simplify your single cell RNA-seq analysis with biologist-friendly point and click tools.• Generate high-resolution visuals and other files from your analysis for publications and biopharmaceutical... tv.qiagenbioinformatics.com 46:57 <p><p>In this webinar, the speaker will cover how to simplify your single cell RNA-seq analysis with biologist-friendly point and click tools.</p><p>• Generate high-resolution visuals and other files from your analysis for publications and biopharmaceutical discoveries</p><p>• Generate dimension reduction (UMAP, t-SNE) plots to understand differences between cell clusters/experimental conditions</p><p>• Identify and study clusters and cell types specific biomarkers using differential expression tables, gene expression heat maps, dot plots and violin plots</p><p>• Generate desired cell annotations using hashtags</p><p>• Visualize and investigate spatial transcriptomics plot using your Cell Ranger output to better understand cellular organization and generate hypothesis</p><p>• Use preconfigured but customizable pipelines/workflows for single-cell RNA-seq data</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/118447890/single-cell-rna-seq-and-spatial"><img src="http://tv.qiagenbioinformatics.com/64968560/118447890/dfb1c7b72130ead9a62cf283a3ed04f1/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> clc http://tv.qiagenbioinformatics.com/photo/117724461/single-cell-rna-seq-cell-hashing-4 <p><p>In this training, you will learn how to analyze and interpret your own single cell RNA-seq data using QIAGEN CLC Genomics Workbench starting with either FASTQ or matrix files.</p><p>Using CLC Genomics Workbench, you will learn how to perform secondary analysis on your single cell RNA-seq data. Specifically, you will learn how to:</p><ul><li><p>Import your raw FASTQ or processed cell-matrix files.</p></li><li><p>Use pre-configured but customizable pipelines/workflows for single cell RNA-seq data.</p></li><li><p>Generate high resolution visuals and other files from your analysis for publications and biopharmaceutical discoveries.</p><ul><li><p>Dimension reduction (UMAP, t-SNE) plots</p></li><li><p>Differential expression table for clusters, cell types, or combination of both</p></li><li><p>Heat map</p></li><li><p>Dot plots</p></li><li><p>Violin plots</p></li></ul></li><li><p>Learn how to use “Create Cell Annotations from Hashtags” for cell hashing (i.e., CITE-seq).</p></li><li><p>Dive into spatial transcriptomic analysis, the latest feature in the single cell RNA-seq module.</p></li></ul></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117724461/single-cell-rna-seq-cell-hashing-4"><img src="http://tv.qiagenbioinformatics.com/64968575/117724461/e23896e5dbec242d84758816e39302a0/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/117724461 Fri, 24 Oct 2025 09:52:45 GMT Single-cell RNA-seq, cell hashing and spatial transcriptomics In this training, you will learn how to analyze and interpret your own single cell RNA-seq data using QIAGEN CLC Genomics Workbench starting with either FASTQ or matrix files.Using CLC Genomics Workbench, you will learn how to perform secondary analysis on your single cell RNA-seq data. Specifically, you will learn how to:Import your raw FASTQ or processed cell-matrix files.Use pre-configured but customizable pipelines/workflows for single cell RNA-seq data.Generate high resolution visuals and other files from your analysis for publications and biopharmaceutical discoveries.Dimension reduction (UMAP, t-SNE) plotsDifferential expression table for clusters, cell types, or combination of bothHeat mapDot plotsViolin plotsLearn how to use “Create Cell Annotations from Hashtags” for cell hashing (i.e., CITE-seq).Dive into spatial transcriptomic analysis, the latest feature in the single cell RNA-seq module. In this training, you will learn how to analyze and interpret your own single cell RNA-seq data using QIAGEN CLC Genomics Workbench starting with either FASTQ or matrix files.Using CLC Genomics Workbench, you will learn how to perform secondary... tv.qiagenbioinformatics.com 01:17:34 <p><p>In this training, you will learn how to analyze and interpret your own single cell RNA-seq data using QIAGEN CLC Genomics Workbench starting with either FASTQ or matrix files.</p><p>Using CLC Genomics Workbench, you will learn how to perform secondary analysis on your single cell RNA-seq data. Specifically, you will learn how to:</p><ul><li><p>Import your raw FASTQ or processed cell-matrix files.</p></li><li><p>Use pre-configured but customizable pipelines/workflows for single cell RNA-seq data.</p></li><li><p>Generate high resolution visuals and other files from your analysis for publications and biopharmaceutical discoveries.</p><ul><li><p>Dimension reduction (UMAP, t-SNE) plots</p></li><li><p>Differential expression table for clusters, cell types, or combination of both</p></li><li><p>Heat map</p></li><li><p>Dot plots</p></li><li><p>Violin plots</p></li></ul></li><li><p>Learn how to use “Create Cell Annotations from Hashtags” for cell hashing (i.e., CITE-seq).</p></li><li><p>Dive into spatial transcriptomic analysis, the latest feature in the single cell RNA-seq module.</p></li></ul></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117724461/single-cell-rna-seq-cell-hashing-4"><img src="http://tv.qiagenbioinformatics.com/64968575/117724461/e23896e5dbec242d84758816e39302a0/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> clc genomics http://tv.qiagenbioinformatics.com/photo/117689998/16s18sits-sequencing-analysis-using-1 <p><p>QIAGEN CLC Microbial Genomics Module provides tools and workflows for a broad range of bioinformatics applications, including microbiome analysis, isolate characterization, functional metagenomics and antimicrobial resistance characterization. The module supports the analysis of bacterial, viral and eukaryotic (fungal) genomes and metagenomes.</p><p>This training will be focused on amplicon-based taxonomic profiling (16S/18S/ITS sequencing OTU clustering). The trainer will cover:</p><ul><li><p>Overview of different tools within QIAGEN CLC Microbial Genomics Module and supported research areas</p></li><li><p>For taxonomic profiling:</p><ul><li><p>Importing data&nbsp;</p></li><li><p>Utilization of metadata&nbsp;</p></li><li><p>Downloading and managing references&nbsp;</p></li><li><p>Walk through of OTU clustering workflow (analytical pipeline)&nbsp;</p></li><li><p>Downstream processing of abundance tables&nbsp;</p></li><li><p>Creating and exporting high-quality graphics</p></li></ul></li></ul></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117689998/16s18sits-sequencing-analysis-using-1"><img src="http://tv.qiagenbioinformatics.com/64968556/117689998/a55e2b8abb882d88d716a26778a5b8dd/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/117689998 Thu, 23 Oct 2025 16:07:15 GMT 16S/18S/ITS sequencing analysis using CLC Genomics Workbench QIAGEN CLC Microbial Genomics Module provides tools and workflows for a broad range of bioinformatics applications, including microbiome analysis, isolate characterization, functional metagenomics and antimicrobial resistance characterization. The module supports the analysis of bacterial, viral and eukaryotic (fungal) genomes and metagenomes.This training will be focused on amplicon-based taxonomic profiling (16S/18S/ITS sequencing OTU clustering). The trainer will cover:Overview of different tools within QIAGEN CLC Microbial Genomics Module and supported research areasFor taxonomic profiling:Importing dataUtilization of metadataDownloading and managing referencesWalk through of OTU clustering workflow (analytical pipeline)Downstream processing of abundance tablesCreating and exporting high-quality graphics QIAGEN CLC Microbial Genomics Module provides tools and workflows for a broad range of bioinformatics applications, including microbiome analysis, isolate characterization, functional metagenomics and antimicrobial resistance characterization. The... tv.qiagenbioinformatics.com 01:27:22 <p><p>QIAGEN CLC Microbial Genomics Module provides tools and workflows for a broad range of bioinformatics applications, including microbiome analysis, isolate characterization, functional metagenomics and antimicrobial resistance characterization. The module supports the analysis of bacterial, viral and eukaryotic (fungal) genomes and metagenomes.</p><p>This training will be focused on amplicon-based taxonomic profiling (16S/18S/ITS sequencing OTU clustering). The trainer will cover:</p><ul><li><p>Overview of different tools within QIAGEN CLC Microbial Genomics Module and supported research areas</p></li><li><p>For taxonomic profiling:</p><ul><li><p>Importing data&nbsp;</p></li><li><p>Utilization of metadata&nbsp;</p></li><li><p>Downloading and managing references&nbsp;</p></li><li><p>Walk through of OTU clustering workflow (analytical pipeline)&nbsp;</p></li><li><p>Downstream processing of abundance tables&nbsp;</p></li><li><p>Creating and exporting high-quality graphics</p></li></ul></li></ul></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117689998/16s18sits-sequencing-analysis-using-1"><img src="http://tv.qiagenbioinformatics.com/64968556/117689998/a55e2b8abb882d88d716a26778a5b8dd/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> clc workbench http://tv.qiagenbioinformatics.com/photo/117114333/somatic-variant-detection-with <p><p>See how highly sensitive somatic detection of classic tumor reference samples is made possible through the Twist Oncology - DNA CGP Panel™ combined with downstream analysis using QIAGEN® CLC Genomics Workbench.</p><p style="text-align: start"></p><p style="text-align: start">What is the Twist Oncology - DNA CGP Panel?</p><p style="text-align: start">It is a panel from Twist Biosciences® that is designed for the comprehensive genomic profiling (CGP) of solid tumors to find pathogenic variants. It also supports the scoring of microsatellite instability (MSI) and tumor mutational burden (TMB).</p><p style="text-align: start">&nbsp;</p><p style="text-align: start">What is QIAGEN CLC Genomics Workbench?</p><p style="text-align: start">A powerful all-in-one analysis and visualization toolkit, it is software filled with various tools and workflows tailored to next-generation sequencing (NGS) data, including data from a wide range of resequencing panel designs.</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117114333/somatic-variant-detection-with"><img src="http://tv.qiagenbioinformatics.com/64968576/117114333/c6173c6be90542424cd3a56502cd5411/standard/download-18-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/117114333 Tue, 07 Oct 2025 12:41:35 GMT Somatic variant detection with Twist Oncology and QIAGEN CLC See how highly sensitive somatic detection of classic tumor reference samples is made possible through the Twist Oncology - DNA CGP Panel™ combined with downstream analysis using QIAGEN® CLC Genomics Workbench.What is the Twist Oncology - DNA CGP Panel?It is a panel from Twist Biosciences® that is designed for the comprehensive genomic profiling (CGP) of solid tumors to find pathogenic variants. It also supports the scoring of microsatellite instability (MSI) and tumor mutational burden (TMB).What is QIAGEN CLC Genomics Workbench?A powerful all-in-one analysis and visualization toolkit, it is software filled with various tools and workflows tailored to next-generation sequencing (NGS) data, including data from a wide range of resequencing panel designs. See how highly sensitive somatic detection of classic tumor reference samples is made possible through the Twist Oncology - DNA CGP Panel™ combined with downstream analysis using QIAGEN® CLC Genomics Workbench.What is the Twist Oncology - DNA CGP... tv.qiagenbioinformatics.com 25:36 <p><p>See how highly sensitive somatic detection of classic tumor reference samples is made possible through the Twist Oncology - DNA CGP Panel™ combined with downstream analysis using QIAGEN® CLC Genomics Workbench.</p><p style="text-align: start"></p><p style="text-align: start">What is the Twist Oncology - DNA CGP Panel?</p><p style="text-align: start">It is a panel from Twist Biosciences® that is designed for the comprehensive genomic profiling (CGP) of solid tumors to find pathogenic variants. It also supports the scoring of microsatellite instability (MSI) and tumor mutational burden (TMB).</p><p style="text-align: start">&nbsp;</p><p style="text-align: start">What is QIAGEN CLC Genomics Workbench?</p><p style="text-align: start">A powerful all-in-one analysis and visualization toolkit, it is software filled with various tools and workflows tailored to next-generation sequencing (NGS) data, including data from a wide range of resequencing panel designs.</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117114333/somatic-variant-detection-with"><img src="http://tv.qiagenbioinformatics.com/64968576/117114333/c6173c6be90542424cd3a56502cd5411/standard/download-18-thumbnail.jpg" width="75" height=""/></a></p> clc genomics http://tv.qiagenbioinformatics.com/photo/117123903/batch-mode-in-clc <p><p>In this video we introduce sample batching using CLC tools. This can be helpful when you need to perform the same analysis on a large number of files. Also see this manual page&nbsp; for more details:</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://resources.qiagenbioinformatics.com/manuals/clcgenomicsworkbench/current/index.php?manual=Batch_processing.html">https://resources.qiagenbioinformatics.com/manuals/clcgenomicsworkbench/current/index.php?manual=Batch_processing.html</a></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117123903/batch-mode-in-clc"><img src="http://tv.qiagenbioinformatics.com/64968558/117123903/05b87d31fce058d5f7a4897c7dcff02d/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/117123903 Mon, 06 Oct 2025 15:16:09 GMT Batch Mode in CLC In this video we introduce sample batching using CLC tools. This can be helpful when you need to perform the same analysis on a large number of files. Also see this manual page for more details:https://resources.qiagenbioinformatics.com/manuals/clcgenomicsworkbench/current/index.php?manual=Batch_processing.html In this video we introduce sample batching using CLC tools. This can be helpful when you need to perform the same analysis on a large number of files. Also see this manual page for more... tv.qiagenbioinformatics.com 03:53 <p><p>In this video we introduce sample batching using CLC tools. This can be helpful when you need to perform the same analysis on a large number of files. Also see this manual page&nbsp; for more details:</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://resources.qiagenbioinformatics.com/manuals/clcgenomicsworkbench/current/index.php?manual=Batch_processing.html">https://resources.qiagenbioinformatics.com/manuals/clcgenomicsworkbench/current/index.php?manual=Batch_processing.html</a></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117123903/batch-mode-in-clc"><img src="http://tv.qiagenbioinformatics.com/64968558/117123903/05b87d31fce058d5f7a4897c7dcff02d/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> clc genomics http://tv.qiagenbioinformatics.com/photo/117123756/analyzing-samples-with-multiple <p><p>This video demonstrates how to analyze multiple input files per sample using batch mode. Please also see this FAQ page for more details:</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://qiagen.my.salesforce-sites.com/KnowledgeBase/KnowledgeNavigatorPage?id=kA41i000000L5tACAS&amp;categoryName=CLC_Software">How can I run a batch job with multiple libraries for each sample?</a>&nbsp; &nbsp;</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117123756/analyzing-samples-with-multiple"><img src="http://tv.qiagenbioinformatics.com/64968579/117123756/f2599aa79eac7a64f18c1381d2ccf904/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/117123756 Mon, 06 Oct 2025 15:14:44 GMT Analyzing Samples with Multiple Inputs in CLC This video demonstrates how to analyze multiple input files per sample using batch mode. Please also see this FAQ page for more details:How can I run a batch job with multiple libraries for each sample? This video demonstrates how to analyze multiple input files per sample using batch mode. Please also see this FAQ page for more details:How can I run a batch job with multiple libraries for each sample? tv.qiagenbioinformatics.com 02:34 <p><p>This video demonstrates how to analyze multiple input files per sample using batch mode. Please also see this FAQ page for more details:</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://qiagen.my.salesforce-sites.com/KnowledgeBase/KnowledgeNavigatorPage?id=kA41i000000L5tACAS&amp;categoryName=CLC_Software">How can I run a batch job with multiple libraries for each sample?</a>&nbsp; &nbsp;</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117123756/analyzing-samples-with-multiple"><img src="http://tv.qiagenbioinformatics.com/64968579/117123756/f2599aa79eac7a64f18c1381d2ccf904/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> clc genomics http://tv.qiagenbioinformatics.com/photo/117123974/comparing-analysis-parameters-using <p><p>The history view keeps track of what tools and parameters were used to generate results in CLC. This video shows how the history view can be used to compare two different analyses when the results are unexpected.</p><p>Details about the history view can be found on this manual page:</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://resources.qiagenbioinformatics.com/manuals/clcgenomicsworkbench/current/index.php?manual=History_Element_Info_views.html">https://resources.qiagenbioinformatics.com/manuals/clcgenomicsworkbench/current/index.php?manual=History_Element_Info_views.html</a></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117123974/comparing-analysis-parameters-using"><img src="http://tv.qiagenbioinformatics.com/64968568/117123974/180d68889c6f05331527767a7f5507aa/standard/download-11-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/117123974 Mon, 06 Oct 2025 15:13:47 GMT Comparing Analysis Parameters using the History View in CLC The history view keeps track of what tools and parameters were used to generate results in CLC. This video shows how the history view can be used to compare two different analyses when the results are unexpected.Details about the history view can be found on this manual page:https://resources.qiagenbioinformatics.com/manuals/clcgenomicsworkbench/current/index.php?manual=History_Element_Info_views.html The history view keeps track of what tools and parameters were used to generate results in CLC. This video shows how the history view can be used to compare two different analyses when the results are unexpected.Details about the history view can... tv.qiagenbioinformatics.com 03:27 <p><p>The history view keeps track of what tools and parameters were used to generate results in CLC. This video shows how the history view can be used to compare two different analyses when the results are unexpected.</p><p>Details about the history view can be found on this manual page:</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://resources.qiagenbioinformatics.com/manuals/clcgenomicsworkbench/current/index.php?manual=History_Element_Info_views.html">https://resources.qiagenbioinformatics.com/manuals/clcgenomicsworkbench/current/index.php?manual=History_Element_Info_views.html</a></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117123974/comparing-analysis-parameters-using"><img src="http://tv.qiagenbioinformatics.com/64968568/117123974/180d68889c6f05331527767a7f5507aa/standard/download-11-thumbnail.jpg" width="75" height=""/></a></p> clc genomics http://tv.qiagenbioinformatics.com/photo/117124258/myclc-overview <p><p>This video provides a quick introduction to myCLC. If you do not already have access to myCLC Please contact <a target="_blank" rel="noopener noreferrer nofollow" href="mailto:bioinformaticslicense@qiagen.com"><strong>bioinformaticslicense@qiagen.com</strong></a></p><p>Also, check out these FAQ pages:</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://qiagen.my.salesforce-sites.com/KnowledgeBase/KnowledgeNavigatorPage?id=kA41i000000L5oJCAS&amp;categoryName=CLC_Software">What is myCLC?</a> &nbsp;</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://qiagen.my.salesforce-sites.com/KnowledgeBase/KnowledgeNavigatorPage?id=kA41i000000L5o1CAC&amp;categoryName=CLC_Software">How can I get access to myCLC?</a> &nbsp;</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://qiagen.my.salesforce-sites.com/KnowledgeBase/KnowledgeNavigatorPage?id=kA41i000000L64eCAC&amp;categoryName=CLC_Software">How can I find information about my CLC licenses?</a>&nbsp; &nbsp;</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://qiagen.my.salesforce-sites.com/KnowledgeBase/KnowledgeNavigatorPage?id=kA41i000000L5oOCAS&amp;categoryName=CLC_Software">How can I add someone as a technical contact to myCLC?</a> &nbsp;</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://qiagen.my.salesforce-sites.com/KnowledgeBase/KnowledgeNavigatorPage?id=kA41i000000L5o4CAC&amp;categoryName=CLC_Software">How can I view information for another myCLC account?</a></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117124258/myclc-overview"><img src="http://tv.qiagenbioinformatics.com/64968566/117124258/7de71ce06c3eaf891ef14218a8ecab35/standard/download-12-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/117124258 Mon, 06 Oct 2025 15:13:00 GMT MyCLC Overview This video provides a quick introduction to myCLC. If you do not already have access to myCLC Please contact bioinformaticslicense@qiagen.comAlso, check out these FAQ pages:What is myCLC? How can I get access to myCLC? How can I find information about my CLC licenses? How can I add someone as a technical contact to myCLC? How can I view information for another myCLC account? This video provides a quick introduction to myCLC. If you do not already have access to myCLC Please contact bioinformaticslicense@qiagen.comAlso, check out these FAQ pages:What is myCLC? How can I get access to myCLC? How can I find information... tv.qiagenbioinformatics.com 02:42 <p><p>This video provides a quick introduction to myCLC. If you do not already have access to myCLC Please contact <a target="_blank" rel="noopener noreferrer nofollow" href="mailto:bioinformaticslicense@qiagen.com"><strong>bioinformaticslicense@qiagen.com</strong></a></p><p>Also, check out these FAQ pages:</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://qiagen.my.salesforce-sites.com/KnowledgeBase/KnowledgeNavigatorPage?id=kA41i000000L5oJCAS&amp;categoryName=CLC_Software">What is myCLC?</a> &nbsp;</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://qiagen.my.salesforce-sites.com/KnowledgeBase/KnowledgeNavigatorPage?id=kA41i000000L5o1CAC&amp;categoryName=CLC_Software">How can I get access to myCLC?</a> &nbsp;</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://qiagen.my.salesforce-sites.com/KnowledgeBase/KnowledgeNavigatorPage?id=kA41i000000L64eCAC&amp;categoryName=CLC_Software">How can I find information about my CLC licenses?</a>&nbsp; &nbsp;</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://qiagen.my.salesforce-sites.com/KnowledgeBase/KnowledgeNavigatorPage?id=kA41i000000L5oOCAS&amp;categoryName=CLC_Software">How can I add someone as a technical contact to myCLC?</a> &nbsp;</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://qiagen.my.salesforce-sites.com/KnowledgeBase/KnowledgeNavigatorPage?id=kA41i000000L5o4CAC&amp;categoryName=CLC_Software">How can I view information for another myCLC account?</a></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117124258/myclc-overview"><img src="http://tv.qiagenbioinformatics.com/64968566/117124258/7de71ce06c3eaf891ef14218a8ecab35/standard/download-12-thumbnail.jpg" width="75" height=""/></a></p> clc tutorials http://tv.qiagenbioinformatics.com/photo/117124226/how-to-create-a-track-list-in-clc <p><p>In this video you can learn how to import tracks and create a track list in CLC. Track lists enable users to view multiple track elements at once. Track lists also feature an interactive link between the table view and the plot view.</p><p>Use track lists to browse genomic features, zoom into regions of interest, visualize read mappings, inspect variants, and more. Please also see this manual page for more details:</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://resources.qiagenbioinformatics.com/manuals/clcgenomicsworkbench/current/index.php?manual=Track_lists.html">https://resources.qiagenbioinformatics.com/manuals/clcgenomicsworkbench/current/index.php?manual=Track_lists.html</a></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117124226/how-to-create-a-track-list-in-clc"><img src="http://tv.qiagenbioinformatics.com/64968569/117124226/00a9a80bdc8ea998ae469a7c30cd3af8/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/117124226 Mon, 06 Oct 2025 15:12:19 GMT How to Create a Track list in CLC In this video you can learn how to import tracks and create a track list in CLC. Track lists enable users to view multiple track elements at once. Track lists also feature an interactive link between the table view and the plot view.Use track lists to browse genomic features, zoom into regions of interest, visualize read mappings, inspect variants, and more. Please also see this manual page for more details:https://resources.qiagenbioinformatics.com/manuals/clcgenomicsworkbench/current/index.php?manual=Track_lists.html In this video you can learn how to import tracks and create a track list in CLC. Track lists enable users to view multiple track elements at once. Track lists also feature an interactive link between the table view and the plot view.Use track... tv.qiagenbioinformatics.com 06:45 <p><p>In this video you can learn how to import tracks and create a track list in CLC. Track lists enable users to view multiple track elements at once. Track lists also feature an interactive link between the table view and the plot view.</p><p>Use track lists to browse genomic features, zoom into regions of interest, visualize read mappings, inspect variants, and more. Please also see this manual page for more details:</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://resources.qiagenbioinformatics.com/manuals/clcgenomicsworkbench/current/index.php?manual=Track_lists.html">https://resources.qiagenbioinformatics.com/manuals/clcgenomicsworkbench/current/index.php?manual=Track_lists.html</a></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117124226/how-to-create-a-track-list-in-clc"><img src="http://tv.qiagenbioinformatics.com/64968569/117124226/00a9a80bdc8ea998ae469a7c30cd3af8/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> clc genomics http://tv.qiagenbioinformatics.com/photo/117124119/create-publication-ready-volcano <p><p>This video shows how to customize volcano plots in CLC Genomics Workbench. Check out these tutorials for more RNA-seq related topics:</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://digitalinsights.qiagen.com/support/tutorials/#:~:text=Expression%20and%20fusions">https://digitalinsights.qiagen.com/support/tutorials/#:~:text=Expression%20and%20fusions</a></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117124119/create-publication-ready-volcano"><img src="http://tv.qiagenbioinformatics.com/64968555/117124119/f7ee99abcdab1efdf3040a0b65e48d6f/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/117124119 Mon, 06 Oct 2025 15:11:15 GMT Create publication-ready volcano plots for RNA-sq data using CLC genomics... This video shows how to customize volcano plots in CLC Genomics Workbench. Check out these tutorials for more RNA-seq related topics:https://digitalinsights.qiagen.com/support/tutorials/#:~:text=Expression%20and%20fusions This video shows how to customize volcano plots in CLC Genomics Workbench. Check out these tutorials for more RNA-seq related topics:https://digitalinsights.qiagen.com/support/tutorials/#:~:text=Expression%20and%20fusions tv.qiagenbioinformatics.com 04:46 <p><p>This video shows how to customize volcano plots in CLC Genomics Workbench. Check out these tutorials for more RNA-seq related topics:</p><p><a target="_blank" rel="noopener noreferrer nofollow" href="https://digitalinsights.qiagen.com/support/tutorials/#:~:text=Expression%20and%20fusions">https://digitalinsights.qiagen.com/support/tutorials/#:~:text=Expression%20and%20fusions</a></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117124119/create-publication-ready-volcano"><img src="http://tv.qiagenbioinformatics.com/64968555/117124119/f7ee99abcdab1efdf3040a0b65e48d6f/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> clc genomics http://tv.qiagenbioinformatics.com/photo/117057396/scale-up-ngs-bioinformatics-2 <p><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). See how QIAGEN 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 within the CLC Genomics Server software.</p><p style="text-align: start">You will learn to:</p><p style="text-align: start">• Customize template workflows to meet your NGS analysis requirements</p><p style="text-align: start">• Set up a CLC Genomics Cloud environment on AWS</p><p style="text-align: start">• Submit workflows to run on internal servers or AWS and retrieve results from these analyses</p><p style="text-align: start">• Use third-party dockers and automate workflow execution</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117057396/scale-up-ngs-bioinformatics-2"><img src="http://tv.qiagenbioinformatics.com/64968556/117057396/3a3ea5e6882cb2cecda5cf8b09c69c3e/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/117057396 Fri, 03 Oct 2025 12:11:29 GMT Scale up NGS bioinformatics analysis throughput with QIAGEN CLC Genomics... 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). See how QIAGEN 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 within 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 01:25:50 <p><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). See how QIAGEN 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 within the CLC Genomics Server software.</p><p style="text-align: start">You will learn to:</p><p style="text-align: start">• Customize template workflows to meet your NGS analysis requirements</p><p style="text-align: start">• Set up a CLC Genomics Cloud environment on AWS</p><p style="text-align: start">• Submit workflows to run on internal servers or AWS and retrieve results from these analyses</p><p style="text-align: start">• Use third-party dockers and automate workflow execution</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117057396/scale-up-ngs-bioinformatics-2"><img src="http://tv.qiagenbioinformatics.com/64968556/117057396/3a3ea5e6882cb2cecda5cf8b09c69c3e/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> clc genomics http://tv.qiagenbioinformatics.com/photo/117037537/rna-seq-data-analysis-and-4 <p><p>The increasing adoption of next-generation sequencing in many fields has made RNA-seq data analysis and interpretation essential skills for researchers. In this webinar, discover how you can effortlessly process FASTQ files with QIAGEN CLC Genomics Workbench (CLC). Next, you will import differential expression results directly into QIAGEN Ingenuity Pathway Analysis (IPA) for downstream analysis – enabling a smooth path from data to discovery.</p><p>&nbsp;</p><p>You will learn how to:</p><p>• Use CLC to map reads to a reference genome, generate gene/transcript counts and QC reports</p><p>• Use CLC to visualize results, such as heatmaps, differential expression tables, PCA/PCOA plots, Venn diagrams and more</p><p>• Use IPA to identify enriched canonical pathways, diseases and biological functions and predicted upstream regulators</p><p>• Use IPA to compare your analysis results to over 200,000 analyses curated from public ‘omics datasets – including your own projects – to find similarities and differences in pathways, upstream regulators and diseases</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117037537/rna-seq-data-analysis-and-4"><img src="http://tv.qiagenbioinformatics.com/64968579/117037537/06c7bb1606b41859d7500af99f2a282c/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/117037537 Fri, 03 Oct 2025 09:27:56 GMT RNA-Seq Data Analysis and Interpretation using QIAGEN CLC Genomics Workbench... The increasing adoption of next-generation sequencing in many fields has made RNA-seq data analysis and interpretation essential skills for researchers. In this webinar, discover how you can effortlessly process FASTQ files with QIAGEN CLC Genomics Workbench (CLC). Next, you will import differential expression results directly into QIAGEN Ingenuity Pathway Analysis (IPA) for downstream analysis – enabling a smooth path from data to discovery.You will learn how to:• Use CLC to map reads to a reference genome, generate gene/transcript counts and QC reports• Use CLC to visualize results, such as heatmaps, differential expression tables, PCA/PCOA plots, Venn diagrams and more• Use IPA to identify enriched canonical pathways, diseases and biological functions and predicted upstream regulators• Use IPA to compare your analysis results to over 200,000 analyses curated from public ‘omics datasets – including your own projects – to find similarities and differences in pathways, upstream regulators and diseases The increasing adoption of next-generation sequencing in many fields has made RNA-seq data analysis and interpretation essential skills for researchers. In this webinar, discover how you can effortlessly process FASTQ files with QIAGEN CLC... tv.qiagenbioinformatics.com 01:31:54 <p><p>The increasing adoption of next-generation sequencing in many fields has made RNA-seq data analysis and interpretation essential skills for researchers. In this webinar, discover how you can effortlessly process FASTQ files with QIAGEN CLC Genomics Workbench (CLC). Next, you will import differential expression results directly into QIAGEN Ingenuity Pathway Analysis (IPA) for downstream analysis – enabling a smooth path from data to discovery.</p><p>&nbsp;</p><p>You will learn how to:</p><p>• Use CLC to map reads to a reference genome, generate gene/transcript counts and QC reports</p><p>• Use CLC to visualize results, such as heatmaps, differential expression tables, PCA/PCOA plots, Venn diagrams and more</p><p>• Use IPA to identify enriched canonical pathways, diseases and biological functions and predicted upstream regulators</p><p>• Use IPA to compare your analysis results to over 200,000 analyses curated from public ‘omics datasets – including your own projects – to find similarities and differences in pathways, upstream regulators and diseases</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/117037537/rna-seq-data-analysis-and-4"><img src="http://tv.qiagenbioinformatics.com/64968579/117037537/06c7bb1606b41859d7500af99f2a282c/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> clc genomics http://tv.qiagenbioinformatics.com/photo/116903353/discover-microbial-functional <p><p>Join us for an in-depth webinar showcasing the discovery of functional insights in microbial communities using QIAGEN CLC Genomics Workbench tools. Ideal for microbiologists, bioinformaticians and researchers aiming to uncover functional signatures in microbial communities and drive data-driven discoveries, you will learn how to perform a comprehensive whole metagenome functional analysis, from raw NGS data to functional profiling and visualization.</p><p>&nbsp;</p><p>Whether you are working with experimental or clinical samples, this session will equip you with a robust, scalable pipeline for comparative functional metagenomics.</p><p>&nbsp;</p><p>Learn how to:</p><p>• Import and prepare raw NGS data</p><p>• Assemble metagenomes into contigs</p><p>• Map reads and bin pangenomes by sequence</p><p>• Identify genes and coding DNA sequences (CDS)</p><p>• Annotate functional elements using Gene Ontology (GO) and Pfam domains</p><p>• Build functional profiles to explore diversity</p><p>• Visualize and analyze functional differences across sample groups</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/116903353/discover-microbial-functional"><img src="http://tv.qiagenbioinformatics.com/64968569/116903353/6a52640d6029aceaa8619a6666a24def/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/116903353 Thu, 02 Oct 2025 17:04:30 GMT Discover Microbial Functional Insights with QIAGEN CLC Genomics Workbench Join us for an in-depth webinar showcasing the discovery of functional insights in microbial communities using QIAGEN CLC Genomics Workbench tools. Ideal for microbiologists, bioinformaticians and researchers aiming to uncover functional signatures in microbial communities and drive data-driven discoveries, you will learn how to perform a comprehensive whole metagenome functional analysis, from raw NGS data to functional profiling and visualization.Whether you are working with experimental or clinical samples, this session will equip you with a robust, scalable pipeline for comparative functional metagenomics.Learn how to:• Import and prepare raw NGS data• Assemble metagenomes into contigs• Map reads and bin pangenomes by sequence• Identify genes and coding DNA sequences (CDS)• Annotate functional elements using Gene Ontology (GO) and Pfam domains• Build functional profiles to explore diversity• Visualize and analyze functional differences across sample groups Join us for an in-depth webinar showcasing the discovery of functional insights in microbial communities using QIAGEN CLC Genomics Workbench tools. Ideal for microbiologists, bioinformaticians and researchers aiming to uncover functional... tv.qiagenbioinformatics.com 01:13:53 <p><p>Join us for an in-depth webinar showcasing the discovery of functional insights in microbial communities using QIAGEN CLC Genomics Workbench tools. Ideal for microbiologists, bioinformaticians and researchers aiming to uncover functional signatures in microbial communities and drive data-driven discoveries, you will learn how to perform a comprehensive whole metagenome functional analysis, from raw NGS data to functional profiling and visualization.</p><p>&nbsp;</p><p>Whether you are working with experimental or clinical samples, this session will equip you with a robust, scalable pipeline for comparative functional metagenomics.</p><p>&nbsp;</p><p>Learn how to:</p><p>• Import and prepare raw NGS data</p><p>• Assemble metagenomes into contigs</p><p>• Map reads and bin pangenomes by sequence</p><p>• Identify genes and coding DNA sequences (CDS)</p><p>• Annotate functional elements using Gene Ontology (GO) and Pfam domains</p><p>• Build functional profiles to explore diversity</p><p>• Visualize and analyze functional differences across sample groups</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/116903353/discover-microbial-functional"><img src="http://tv.qiagenbioinformatics.com/64968569/116903353/6a52640d6029aceaa8619a6666a24def/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> clc genomics http://tv.qiagenbioinformatics.com/photo/116465220/influenza-virus-typing-and-variant <p><p>Join us for a focused webinar showcasing the Type Influenza Strain workflow within QIAGEN CLC Genomics Workbench. This streamlined, template-based workflow enables efficient typing of targeted Influenza virus sequencing data by integrating consensus sequence refinement, reference-based subtype identification and mixed-infection variant detection.</p><p>&nbsp;</p><p>We’ll show how the workflow:</p><p>&nbsp;</p><ul><li><p>Automatically determines Influenza virus type and subtype</p></li><li><p>Outputs annotated consensus sequences with gene and CDS tracks for intuitive visualization</p></li><li><p>Detects low-frequency variants that may indicate mixed infections</p></li><li><p>Presents results in a consolidated, interactive track list in both nucleotide and amino acid views</p></li></ul><p>&nbsp;</p><p>Whether you’re tracking circulating strains or monitoring for emerging variants, this workflow offers a rapid and insightful approach to Influenza virus analysis.</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/116465220/influenza-virus-typing-and-variant"><img src="http://tv.qiagenbioinformatics.com/64968561/116465220/d890027666527a47113666a745ec7c37/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/116465220 Tue, 16 Sep 2025 16:08:34 GMT Influenza Virus Typing and Variant Detection Using QIAGEN CLC Genomics Workbench Join us for a focused webinar showcasing the Type Influenza Strain workflow within QIAGEN CLC Genomics Workbench. This streamlined, template-based workflow enables efficient typing of targeted Influenza virus sequencing data by integrating consensus sequence refinement, reference-based subtype identification and mixed-infection variant detection.We’ll show how the workflow:Automatically determines Influenza virus type and subtypeOutputs annotated consensus sequences with gene and CDS tracks for intuitive visualizationDetects low-frequency variants that may indicate mixed infectionsPresents results in a consolidated, interactive track list in both nucleotide and amino acid viewsWhether you’re tracking circulating strains or monitoring for emerging variants, this workflow offers a rapid and insightful approach to Influenza virus analysis. Join us for a focused webinar showcasing the Type Influenza Strain workflow within QIAGEN CLC Genomics Workbench. This streamlined, template-based workflow enables efficient typing of targeted Influenza virus sequencing data by integrating... tv.qiagenbioinformatics.com 01:24:40 <p><p>Join us for a focused webinar showcasing the Type Influenza Strain workflow within QIAGEN CLC Genomics Workbench. This streamlined, template-based workflow enables efficient typing of targeted Influenza virus sequencing data by integrating consensus sequence refinement, reference-based subtype identification and mixed-infection variant detection.</p><p>&nbsp;</p><p>We’ll show how the workflow:</p><p>&nbsp;</p><ul><li><p>Automatically determines Influenza virus type and subtype</p></li><li><p>Outputs annotated consensus sequences with gene and CDS tracks for intuitive visualization</p></li><li><p>Detects low-frequency variants that may indicate mixed infections</p></li><li><p>Presents results in a consolidated, interactive track list in both nucleotide and amino acid views</p></li></ul><p>&nbsp;</p><p>Whether you’re tracking circulating strains or monitoring for emerging variants, this workflow offers a rapid and insightful approach to Influenza virus analysis.</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/116465220/influenza-virus-typing-and-variant"><img src="http://tv.qiagenbioinformatics.com/64968561/116465220/d890027666527a47113666a745ec7c37/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> clc genomics http://tv.qiagenbioinformatics.com/photo/116108098/gene-fusion-detection-using-qiagen <p><p>This webinar will focus on running the fusion detection analysis within QIAGEN CLC Genomics Workbench and annotating the detected fusions using curated clinical knowledge from Human Somatic Mutation Database (HSMD). Finally, the data will be uploaded to QIAGEN Clinical Insight (QCI) applications for further analysis.</p><p>You will learn:</p><p>• How fusion detection algorithms work</p><p>• To run the fusion detection template workflow</p><p>• To interpret the analysis results</p><p>• To annotate fusions with HSMD</p><p>• To upload and analyze the fusions with QCI Interpret</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/116108098/gene-fusion-detection-using-qiagen"><img src="http://tv.qiagenbioinformatics.com/64968568/116108098/ebd9e49765d920d9ca16ab86208d558c/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/116108098 Mon, 15 Sep 2025 09:58:21 GMT Gene Fusion Detection Using QIAGEN CLC Genomics Workbench This webinar will focus on running the fusion detection analysis within QIAGEN CLC Genomics Workbench and annotating the detected fusions using curated clinical knowledge from Human Somatic Mutation Database (HSMD). Finally, the data will be uploaded to QIAGEN Clinical Insight (QCI) applications for further analysis.You will learn:• How fusion detection algorithms work• To run the fusion detection template workflow• To interpret the analysis results• To annotate fusions with HSMD• To upload and analyze the fusions with QCI Interpret This webinar will focus on running the fusion detection analysis within QIAGEN CLC Genomics Workbench and annotating the detected fusions using curated clinical knowledge from Human Somatic Mutation Database (HSMD). Finally, the data will be... tv.qiagenbioinformatics.com 49:47 <p><p>This webinar will focus on running the fusion detection analysis within QIAGEN CLC Genomics Workbench and annotating the detected fusions using curated clinical knowledge from Human Somatic Mutation Database (HSMD). Finally, the data will be uploaded to QIAGEN Clinical Insight (QCI) applications for further analysis.</p><p>You will learn:</p><p>• How fusion detection algorithms work</p><p>• To run the fusion detection template workflow</p><p>• To interpret the analysis results</p><p>• To annotate fusions with HSMD</p><p>• To upload and analyze the fusions with QCI Interpret</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/116108098/gene-fusion-detection-using-qiagen"><img src="http://tv.qiagenbioinformatics.com/64968568/116108098/ebd9e49765d920d9ca16ab86208d558c/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> clc genomics http://tv.qiagenbioinformatics.com/photo/115152885/rna-seq-data-analysis-using-qiagen-1 <p><p>For your RNA-seq data, you will learn how to:</p><p>• Import FASTQ files, cell matrix files and metadata</p><p>• Download and/or import reference and annotations files</p><p>• Map reads to a reference genome</p><p>• Generate gene and transcript counts</p><p>• QC reports displaying % mapped reads etc.</p><p>• Generate visualizations of results, such as heatmaps, differential expression tables, PCA/PCOA plots, Venn diagrams, Sankey plot and more</p><p>• Easily customize RNA-seq workflows</p><p>• Export publication-quality graphics, tables and reports</p><p>Per audience request</p><p>• Send differential expression tables to QIAGEN Ingenuity Pathway Analysis directly from QIAGEN CLC Genomics Workbench to analyze and interpret relevant pathways</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/115152885/rna-seq-data-analysis-using-qiagen-1"><img src="http://tv.qiagenbioinformatics.com/64968566/115152885/19c618ac29c1f5fbc7fd17e2cf95209d/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/115152885 Tue, 12 Aug 2025 16:52:27 GMT RNA-seq data analysis using QIAGEN CLC Genomics Workbench For your RNA-seq data, you will learn how to:• Import FASTQ files, cell matrix files and metadata• Download and/or import reference and annotations files• Map reads to a reference genome• Generate gene and transcript counts• QC reports displaying % mapped reads etc.• Generate visualizations of results, such as heatmaps, differential expression tables, PCA/PCOA plots, Venn diagrams, Sankey plot and more• Easily customize RNA-seq workflows• Export publication-quality graphics, tables and reportsPer audience request• Send differential expression tables to QIAGEN Ingenuity Pathway Analysis directly from QIAGEN CLC Genomics Workbench to analyze and interpret relevant pathways For your RNA-seq data, you will learn how to:• Import FASTQ files, cell matrix files and metadata• Download and/or import reference and annotations files• Map reads to a reference genome• Generate gene and transcript counts• QC reports displaying... tv.qiagenbioinformatics.com 01:32:32 <p><p>For your RNA-seq data, you will learn how to:</p><p>• Import FASTQ files, cell matrix files and metadata</p><p>• Download and/or import reference and annotations files</p><p>• Map reads to a reference genome</p><p>• Generate gene and transcript counts</p><p>• QC reports displaying % mapped reads etc.</p><p>• Generate visualizations of results, such as heatmaps, differential expression tables, PCA/PCOA plots, Venn diagrams, Sankey plot and more</p><p>• Easily customize RNA-seq workflows</p><p>• Export publication-quality graphics, tables and reports</p><p>Per audience request</p><p>• Send differential expression tables to QIAGEN Ingenuity Pathway Analysis directly from QIAGEN CLC Genomics Workbench to analyze and interpret relevant pathways</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/115152885/rna-seq-data-analysis-using-qiagen-1"><img src="http://tv.qiagenbioinformatics.com/64968566/115152885/19c618ac29c1f5fbc7fd17e2cf95209d/standard/download-10-thumbnail.jpg" width="75" height=""/></a></p> clc genomics workbench http://tv.qiagenbioinformatics.com/photo/59979586/qiagen-clc-genomics-workbench-20-2 <p>In this webinar, Leif Schauser, Ph.D., Director Product Management Genome Analysis, will review the latest features in the new QIAGEN CLC Genomics Workbench 20. The following topics will be covered:<br> • One-click solutions and expert tools for NGS data analysis<br> • Working with reads from various platforms (Illumina, IonTorrent, Oxford Nanopore, Pacific Biosciences, BGI/MGI)<br> • Tailored solutions for RNA-seq, DNA-seq and methylation<br> • Efficient algorithms for read trimming, mapping, de novo assembly and variant calling<br> • Effective management of reference data<br> • Scalable processing of many samples, with advanced workflow and reporting capabilities<br> • Easy installation on Windows, Mac and Linux<br><br><p>Interested in learning more?</p><p><b>Click&nbsp;</b><b><u><a href="https://digitalinsights.qiagen.com/products-overview/analysis-and-visualization/qiagen-clc-genomics-workbench?cmpid=BIOX_WEB_BioX_20200128_tv.qiagenbioinformatics_Webinar_BioxBA_Must_Win_1_BIOX">here</a></u></b></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/59979586/qiagen-clc-genomics-workbench-20-2"><img src="http://tv.qiagenbioinformatics.com/49543314/59979586/8b3e66765e2e33a727d4ee57792d20f8/standard/download-3-thumbnail.jpg" width="600" height="375"/></a></p> http://tv.qiagenbioinformatics.com/photo/59979586 Thu, 10 Jul 2025 15:51:32 GMT QIAGEN CLC Genomics Workbench 20 – scalable desktop software for NGS data... In this webinar, Leif Schauser, Ph.D., Director Product Management Genome Analysis, will review the latest features in the new QIAGEN CLC Genomics Workbench 20. The following topics will be covered: • One-click solutions and expert tools for NGS data analysis • Working with reads from various platforms (Illumina, IonTorrent, Oxford Nanopore, Pacific Biosciences, BGI/MGI) • Tailored solutions for RNA-seq, DNA-seq and methylation • Efficient algorithms for read trimming, mapping, de novo assembly and variant calling • Effective management of reference data • Scalable processing of many samples, with advanced workflow and reporting capabilities • Easy installation on Windows, Mac and LinuxInterested in learning more?Clickhere In this webinar, Leif Schauser, Ph.D., Director Product Management Genome Analysis, will review the latest features in the new QIAGEN CLC Genomics Workbench 20. The following topics will be covered: • One-click solutions and expert tools for NGS... tv.qiagenbioinformatics.com 53:47 <p>In this webinar, Leif Schauser, Ph.D., Director Product Management Genome Analysis, will review the latest features in the new QIAGEN CLC Genomics Workbench 20. The following topics will be covered:<br> • One-click solutions and expert tools for NGS data analysis<br> • Working with reads from various platforms (Illumina, IonTorrent, Oxford Nanopore, Pacific Biosciences, BGI/MGI)<br> • Tailored solutions for RNA-seq, DNA-seq and methylation<br> • Efficient algorithms for read trimming, mapping, de novo assembly and variant calling<br> • Effective management of reference data<br> • Scalable processing of many samples, with advanced workflow and reporting capabilities<br> • Easy installation on Windows, Mac and Linux<br><br><p>Interested in learning more?</p><p><b>Click&nbsp;</b><b><u><a href="https://digitalinsights.qiagen.com/products-overview/analysis-and-visualization/qiagen-clc-genomics-workbench?cmpid=BIOX_WEB_BioX_20200128_tv.qiagenbioinformatics_Webinar_BioxBA_Must_Win_1_BIOX">here</a></u></b></p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/59979586/qiagen-clc-genomics-workbench-20-2"><img src="http://tv.qiagenbioinformatics.com/49543314/59979586/8b3e66765e2e33a727d4ee57792d20f8/standard/download-3-thumbnail.jpg" width="600" height="375"/></a></p> clc clc genomics workbench tutorial clc webinar discovery gene regulation genomics workbench webinar http://tv.qiagenbioinformatics.com/photo/113782642/de-novo-assembly-blast-and-genome-2 <p><p>This webinar will introduce users to the tools available for short reads (Illumina) as well as long reads (Oxford Nanopore, Pac Bio) de novo assembly in CLC Genomics Workbench. It will also go over other useful functionalities such as BLAST and genome finishing.</p><p>Participants will learn the following:</p><p>o Download and install needed plugins.</p><p>o Import data required for the analysis.</p><p>o Run the de novo assembly workflow.</p><p>o For long reads, improve a de novo assembly by polishing with short, high-quality reads.</p><p>o Map reads to a reference and visualize an assembly.</p><p>o For long reads, correct raw long reads for further analysis.</p><p>o Use BLAST to investigate the contigs.</p><p>o Analyze and assemble contigs through Genome Finishing tools.</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/113782642/de-novo-assembly-blast-and-genome-2"><img src="http://tv.qiagenbioinformatics.com/64968558/113782642/cf13d497a9767897484ef79a18ab8f51/standard/download-9-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/113782642 Wed, 18 Jun 2025 15:20:48 GMT De novo assembly, BLAST and genome finishing using CLC Genomics Workbench This webinar will introduce users to the tools available for short reads (Illumina) as well as long reads (Oxford Nanopore, Pac Bio) de novo assembly in CLC Genomics Workbench. It will also go over other useful functionalities such as BLAST and genome finishing.Participants will learn the following:o Download and install needed plugins.o Import data required for the analysis.o Run the de novo assembly workflow.o For long reads, improve a de novo assembly by polishing with short, high-quality reads.o Map reads to a reference and visualize an assembly.o For long reads, correct raw long reads for further analysis.o Use BLAST to investigate the contigs.o Analyze and assemble contigs through Genome Finishing tools. This webinar will introduce users to the tools available for short reads (Illumina) as well as long reads (Oxford Nanopore, Pac Bio) de novo assembly in CLC Genomics Workbench. It will also go over other useful functionalities such as BLAST and... tv.qiagenbioinformatics.com 01:27:23 <p><p>This webinar will introduce users to the tools available for short reads (Illumina) as well as long reads (Oxford Nanopore, Pac Bio) de novo assembly in CLC Genomics Workbench. It will also go over other useful functionalities such as BLAST and genome finishing.</p><p>Participants will learn the following:</p><p>o Download and install needed plugins.</p><p>o Import data required for the analysis.</p><p>o Run the de novo assembly workflow.</p><p>o For long reads, improve a de novo assembly by polishing with short, high-quality reads.</p><p>o Map reads to a reference and visualize an assembly.</p><p>o For long reads, correct raw long reads for further analysis.</p><p>o Use BLAST to investigate the contigs.</p><p>o Analyze and assemble contigs through Genome Finishing tools.</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/113782642/de-novo-assembly-blast-and-genome-2"><img src="http://tv.qiagenbioinformatics.com/64968558/113782642/cf13d497a9767897484ef79a18ab8f51/standard/download-9-thumbnail.jpg" width="75" height=""/></a></p> clc clc genomics workbench clc webinar discovery genomics workbench webinar http://tv.qiagenbioinformatics.com/photo/113583070/rna-seq-analysis-for-long-reads <p><p>This training will focus on how a user can analyze their long reads data using QIAGEN CLC Genomics Workbench.</p><p>Specifically, the trainer will cover how to</p><p>• Import the long reads data</p><p>• Download or import reference, metadata and other needed files</p><p>• Process such data and generate downstream RNA-seq outputs</p><p>• Export high resolution graphics and tables</p><p>In addition, per registrant feedback and trainer discretion additional topics such as customizing the workflow, how to send data to Ingenuity Pathway Analysis, Sankey plot and more may be covered.</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/113583070/rna-seq-analysis-for-long-reads"><img src="http://tv.qiagenbioinformatics.com/64968580/113583070/70a7612aac820ed74306a947b2056155/standard/download-9-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/113583070 Tue, 10 Jun 2025 16:43:30 GMT RNA-seq analysis for long reads This training will focus on how a user can analyze their long reads data using QIAGEN CLC Genomics Workbench.Specifically, the trainer will cover how to• Import the long reads data• Download or import reference, metadata and other needed files• Process such data and generate downstream RNA-seq outputs• Export high resolution graphics and tablesIn addition, per registrant feedback and trainer discretion additional topics such as customizing the workflow, how to send data to Ingenuity Pathway Analysis, Sankey plot and more may be covered. This training will focus on how a user can analyze their long reads data using QIAGEN CLC Genomics Workbench.Specifically, the trainer will cover how to• Import the long reads data• Download or import reference, metadata and other needed files•... tv.qiagenbioinformatics.com 01:21:02 <p><p>This training will focus on how a user can analyze their long reads data using QIAGEN CLC Genomics Workbench.</p><p>Specifically, the trainer will cover how to</p><p>• Import the long reads data</p><p>• Download or import reference, metadata and other needed files</p><p>• Process such data and generate downstream RNA-seq outputs</p><p>• Export high resolution graphics and tables</p><p>In addition, per registrant feedback and trainer discretion additional topics such as customizing the workflow, how to send data to Ingenuity Pathway Analysis, Sankey plot and more may be covered.</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/113583070/rna-seq-analysis-for-long-reads"><img src="http://tv.qiagenbioinformatics.com/64968580/113583070/70a7612aac820ed74306a947b2056155/standard/download-9-thumbnail.jpg" width="75" height=""/></a></p> clc clc genomics workbench clc webinar discovery genomics genomics workbench webinar http://tv.qiagenbioinformatics.com/photo/112803888/multimodal-panels-analysis-using <p><p>This training will go over how QIAGEN CLC Genomics Workbench can be used to analyze Multimodal Panels data.</p><p>Trainer will cover</p><p>• How to import your data and metadata and download reference and other needed files</p><p>• How to use workflow and customize it</p><p>• How to visualize and export the results</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/112803888/multimodal-panels-analysis-using"><img src="http://tv.qiagenbioinformatics.com/64968561/112803888/c27582f7d64aa6a49401ba97ab29e544/standard/download-9-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/112803888 Thu, 15 May 2025 10:53:39 GMT Multimodal panels analysis using QIAGEN CLC Genomics Workbench This training will go over how QIAGEN CLC Genomics Workbench can be used to analyze Multimodal Panels data.Trainer will cover• How to import your data and metadata and download reference and other needed files• How to use workflow and customize it• How to visualize and export the results This training will go over how QIAGEN CLC Genomics Workbench can be used to analyze Multimodal Panels data.Trainer will cover• How to import your data and metadata and download reference and other needed files• How to use workflow and customize... tv.qiagenbioinformatics.com 01:24:43 <p><p>This training will go over how QIAGEN CLC Genomics Workbench can be used to analyze Multimodal Panels data.</p><p>Trainer will cover</p><p>• How to import your data and metadata and download reference and other needed files</p><p>• How to use workflow and customize it</p><p>• How to visualize and export the results</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/112803888/multimodal-panels-analysis-using"><img src="http://tv.qiagenbioinformatics.com/64968561/112803888/c27582f7d64aa6a49401ba97ab29e544/standard/download-9-thumbnail.jpg" width="75" height=""/></a></p> clc clc genomics workbench clc webinar discovery genomics genomics workbench webinar http://tv.qiagenbioinformatics.com/photo/112697128/single-cell-rna-seq-cell-hashing-3 <p><p>In this training, you will learn how to analyze and interpret your own single cell RNA-seq data using QIAGEN CLC Genomics Workbench starting with either FASTQ or matrix files.</p><p>&nbsp;</p><p>You will learn how to perform secondary analysis on your single cell RNA-seq data with the Workbench. Specifically, you will learn how to:</p><p>• Import your raw FASTQ or processed cell-matrix files.</p><p>• Use pre-configured but customizable pipelines/workflows for single cell RNA-seq data.</p><p>• Generate high resolution visuals and other files from your analysis for publications and biopharmaceutical discoveries. o Dimension reduction (UMAP, t-SNE) plots o Differential expression table for clusters, cell types, or combination of both o Heat map o Dot plots o Violin plots</p><p>• Learn how to use “Create Cell Annotations from Hashtags” for cell hashing (i.e., CITE-seq).</p><p>• Dive into spatial transcriptomic analysis, the latest feature in the single cell RNA-seq module.</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/112697128/single-cell-rna-seq-cell-hashing-3"><img src="http://tv.qiagenbioinformatics.com/64968579/112697128/df89ae2014770664985e40fd350e7e10/standard/download-11-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/112697128 Mon, 12 May 2025 14:26:40 GMT Single-cell RNA-seq, cell hashing and spatial transcriptomics In this training, you will learn how to analyze and interpret your own single cell RNA-seq data using QIAGEN CLC Genomics Workbench starting with either FASTQ or matrix files.You will learn how to perform secondary analysis on your single cell RNA-seq data with the Workbench. Specifically, you will learn how to:• Import your raw FASTQ or processed cell-matrix files.• Use pre-configured but customizable pipelines/workflows for single cell RNA-seq data.• Generate high resolution visuals and other files from your analysis for publications and biopharmaceutical discoveries. o Dimension reduction (UMAP, t-SNE) plots o Differential expression table for clusters, cell types, or combination of both o Heat map o Dot plots o Violin plots• Learn how to use “Create Cell Annotations from Hashtags” for cell hashing (i.e., CITE-seq).• Dive into spatial transcriptomic analysis, the latest feature in the single cell RNA-seq module. In this training, you will learn how to analyze and interpret your own single cell RNA-seq data using QIAGEN CLC Genomics Workbench starting with either FASTQ or matrix files.You will learn how to perform secondary analysis on your single cell... tv.qiagenbioinformatics.com 01:23:08 <p><p>In this training, you will learn how to analyze and interpret your own single cell RNA-seq data using QIAGEN CLC Genomics Workbench starting with either FASTQ or matrix files.</p><p>&nbsp;</p><p>You will learn how to perform secondary analysis on your single cell RNA-seq data with the Workbench. Specifically, you will learn how to:</p><p>• Import your raw FASTQ or processed cell-matrix files.</p><p>• Use pre-configured but customizable pipelines/workflows for single cell RNA-seq data.</p><p>• Generate high resolution visuals and other files from your analysis for publications and biopharmaceutical discoveries. o Dimension reduction (UMAP, t-SNE) plots o Differential expression table for clusters, cell types, or combination of both o Heat map o Dot plots o Violin plots</p><p>• Learn how to use “Create Cell Annotations from Hashtags” for cell hashing (i.e., CITE-seq).</p><p>• Dive into spatial transcriptomic analysis, the latest feature in the single cell RNA-seq module.</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/112697128/single-cell-rna-seq-cell-hashing-3"><img src="http://tv.qiagenbioinformatics.com/64968579/112697128/df89ae2014770664985e40fd350e7e10/standard/download-11-thumbnail.jpg" width="75" height=""/></a></p> clc genomics http://tv.qiagenbioinformatics.com/photo/105715083/long-reads-analysis-with-qiagen-clc <p><p>This webinar will introduce users to the long read support plugin for Oxford Nanopore and PacBio sequencing reads in QIAGEN CLC Genomics Workbench.</p> <p>&nbsp;</p> <p>Participants will learn how to:</p> <p>&nbsp;</p> <p>• Download and install needed plugins</p> <p>• Import data required for the analysis</p> <p>• Perform long read de novo assembly</p> <p>• Map reads to a reference and visualize an assembly</p> <p>• Use BLAST to investigate the contigs</p> <p>• Use additional long read tools: polish with short reads, structural variant calling</p> <p>• Use genome finishing tools: analyze and assemble contigs</p> <p>• Use analytical tools: RNA-seq analysis for long reads, classify long read amplicons for metagenomics</p> </p><p><a href="http://tv.qiagenbioinformatics.com/photo/105715083/long-reads-analysis-with-qiagen-clc"><img src="http://tv.qiagenbioinformatics.com/64968567/105715083/3ed3b04295a04b99343878e5cb5395db/standard/download-8-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/105715083 Fri, 25 Oct 2024 12:43:16 GMT Long reads analysis with QIAGEN CLC Genomics Workbench This webinar will introduce users to the long read support plugin for Oxford Nanopore and PacBio sequencing reads in QIAGEN CLC Genomics Workbench. Participants will learn how to: • Download and install needed plugins • Import data required for the analysis • Perform long read de novo assembly • Map reads to a reference and visualize an assembly • Use BLAST to investigate the contigs • Use additional long read tools: polish with short reads, structural variant calling • Use genome finishing tools: analyze and assemble contigs • Use analytical tools: RNA-seq analysis for long reads, classify long read amplicons for metagenomics This webinar will introduce users to the long read support plugin for Oxford Nanopore and PacBio sequencing reads in QIAGEN CLC Genomics Workbench. Participants will learn how to: • Download and install needed plugins • Import data required for... tv.qiagenbioinformatics.com 01:27:24 <p><p>This webinar will introduce users to the long read support plugin for Oxford Nanopore and PacBio sequencing reads in QIAGEN CLC Genomics Workbench.</p> <p>&nbsp;</p> <p>Participants will learn how to:</p> <p>&nbsp;</p> <p>• Download and install needed plugins</p> <p>• Import data required for the analysis</p> <p>• Perform long read de novo assembly</p> <p>• Map reads to a reference and visualize an assembly</p> <p>• Use BLAST to investigate the contigs</p> <p>• Use additional long read tools: polish with short reads, structural variant calling</p> <p>• Use genome finishing tools: analyze and assemble contigs</p> <p>• Use analytical tools: RNA-seq analysis for long reads, classify long read amplicons for metagenomics</p> </p><p><a href="http://tv.qiagenbioinformatics.com/photo/105715083/long-reads-analysis-with-qiagen-clc"><img src="http://tv.qiagenbioinformatics.com/64968567/105715083/3ed3b04295a04b99343878e5cb5395db/standard/download-8-thumbnail.jpg" width="75" height=""/></a></p> clc http://tv.qiagenbioinformatics.com/photo/101621396/plugins-installation-for-clc <p>Description: Plugins extend the functionality of CLC Workbenches and CLC Genomics Server. How to install plugins in a CLC Workbench is highlighted in this video. A list of the available plugins is available from the following webpage: <a href="https://digitalinsights.qiagen.com/products-overview/plugins/">https://digitalinsights.qiagen.com/products-overview/plugins/</a></p><p><a href="http://tv.qiagenbioinformatics.com/photo/101621396/plugins-installation-for-clc"><img src="http://tv.qiagenbioinformatics.com/64968567/101621396/174b0572cca7c9672c333cf500e73d3f/standard/download-8-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/101621396 Tue, 04 Jun 2024 13:59:14 GMT Plugins Installation for CLC Workbench Description: Plugins extend the functionality of CLC Workbenches and CLC Genomics Server. How to install plugins in a CLC Workbench is highlighted in this video. A list of the available plugins is available from the following webpage: https://digitalinsights.qiagen.com/products-overview/plugins/ Description: Plugins extend the functionality of CLC Workbenches and CLC Genomics Server. How to install plugins in a CLC Workbench is highlighted in this video. A list of the available plugins is available from the following webpage:... tv.qiagenbioinformatics.com 04:57 <p>Description: Plugins extend the functionality of CLC Workbenches and CLC Genomics Server. How to install plugins in a CLC Workbench is highlighted in this video. A list of the available plugins is available from the following webpage: <a href="https://digitalinsights.qiagen.com/products-overview/plugins/">https://digitalinsights.qiagen.com/products-overview/plugins/</a></p><p><a href="http://tv.qiagenbioinformatics.com/photo/101621396/plugins-installation-for-clc"><img src="http://tv.qiagenbioinformatics.com/64968567/101621396/174b0572cca7c9672c333cf500e73d3f/standard/download-8-thumbnail.jpg" width="75" height=""/></a></p> clc plugin http://tv.qiagenbioinformatics.com/photo/88883036/analyzing-qiaseq-dna-panels-with <p>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.<br /> <br /> <br /> During this training, you’ll learn about:<br /> • Import of FASTQ files<br /> • Launching an analysis workflow<br /> • Inspection of QC reports, genome browser view, detected variants and other workflow outputs<br /> • Customization of template workflow parameters based on findings in the QC report<br /> • Import of custom primers and target regions file<br /> • How to set up an analysis of a custom panel</p><p><a href="http://tv.qiagenbioinformatics.com/photo/88883036/analyzing-qiaseq-dna-panels-with"><img src="http://tv.qiagenbioinformatics.com/64968555/88883036/a338cd204a76a15ec28fe4ecf5b2197f/standard/download-7-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/88883036 Thu, 21 Sep 2023 15:55:27 GMT Analyzing QIAseq DNA Panels with QIAGEN CLC Genomics Workbench 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 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... tv.qiagenbioinformatics.com 51:40 <p>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.<br /> <br /> <br /> During this training, you’ll learn about:<br /> • Import of FASTQ files<br /> • Launching an analysis workflow<br /> • Inspection of QC reports, genome browser view, detected variants and other workflow outputs<br /> • Customization of template workflow parameters based on findings in the QC report<br /> • Import of custom primers and target regions file<br /> • How to set up an analysis of a custom panel</p><p><a href="http://tv.qiagenbioinformatics.com/photo/88883036/analyzing-qiaseq-dna-panels-with"><img src="http://tv.qiagenbioinformatics.com/64968555/88883036/a338cd204a76a15ec28fe4ecf5b2197f/standard/download-7-thumbnail.jpg" width="75" height=""/></a></p> clc qiaseq qiaseq panels sample to insight http://tv.qiagenbioinformatics.com/photo/86003336/beyond-exomes-ultrafast-fastq-to <p>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.<br> <br> <br> QIAGEN CLC Genomics Cloud computing software allows you to launch analyses from CLC Workbenches or CLC Servers for execution on Amazon Web Services (AWS). <p>For more details, visit https://digitalinsights.qiagen.com/explore/c/qpro-2367_an_clc-lig?x=QbXlDs#page=1 and<br> <a href="https://digitalinsights.qiagen.com/plugins/clc-cloud-module/">https://digitalinsights.qiagen.com/plugins/clc-cloud-module/</a></p> <p>To start a trial of QIAGEN CLC Genomics Workbench Premium, visit:<br> <a href="https://digitalinsights.qiagen.com/products-overview/discovery-insights-portfolio/analysis-and-visualization/qiagen-clc-workbench-premium/">https://digitalinsights.qiagen.com/products-overview/discovery-insights-portfolio/analysis-and-visualization/qiagen-clc-workbench-premium/</a></p> <p>In this training, we’ll explore together:</p> <p>• An overview of the QIAGEN CLC Genomics Workbench Premium platform<br> • An overview of the QIAGEN CLC Genomics Server and Cloud • Breaking the speed of light<br> • Why LightSpeed is arguably the fastest and cheapest-to-run hereditary FASTQ-to-VCF WGS pipeline available<br> • Benchmarks/comparisons<br> • Demo of lightspeed and cloud module for Fastq to VCF<br> • Plugin installation<br> • Download of reference(s)<br> • Workflow execution and results review</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/86003336/beyond-exomes-ultrafast-fastq-to"><img src="http://tv.qiagenbioinformatics.com/64968556/86003336/7e8f327b11251328979976a47abe8a88/standard/download-7-thumbnail.jpg" width="75" height=""/></a></p> http://tv.qiagenbioinformatics.com/photo/86003336 Tue, 09 May 2023 20:00:00 GMT Beyond exomes: Ultrafast FASTQ to interpretation 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 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... tv.qiagenbioinformatics.com 01:20:59 <p>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.<br> <br> <br> QIAGEN CLC Genomics Cloud computing software allows you to launch analyses from CLC Workbenches or CLC Servers for execution on Amazon Web Services (AWS). <p>For more details, visit https://digitalinsights.qiagen.com/explore/c/qpro-2367_an_clc-lig?x=QbXlDs#page=1 and<br> <a href="https://digitalinsights.qiagen.com/plugins/clc-cloud-module/">https://digitalinsights.qiagen.com/plugins/clc-cloud-module/</a></p> <p>To start a trial of QIAGEN CLC Genomics Workbench Premium, visit:<br> <a href="https://digitalinsights.qiagen.com/products-overview/discovery-insights-portfolio/analysis-and-visualization/qiagen-clc-workbench-premium/">https://digitalinsights.qiagen.com/products-overview/discovery-insights-portfolio/analysis-and-visualization/qiagen-clc-workbench-premium/</a></p> <p>In this training, we’ll explore together:</p> <p>• An overview of the QIAGEN CLC Genomics Workbench Premium platform<br> • An overview of the QIAGEN CLC Genomics Server and Cloud • Breaking the speed of light<br> • Why LightSpeed is arguably the fastest and cheapest-to-run hereditary FASTQ-to-VCF WGS pipeline available<br> • Benchmarks/comparisons<br> • Demo of lightspeed and cloud module for Fastq to VCF<br> • Plugin installation<br> • Download of reference(s)<br> • Workflow execution and results review</p></p><p><a href="http://tv.qiagenbioinformatics.com/photo/86003336/beyond-exomes-ultrafast-fastq-to"><img src="http://tv.qiagenbioinformatics.com/64968556/86003336/7e8f327b11251328979976a47abe8a88/standard/download-7-thumbnail.jpg" width="75" height=""/></a></p> clc lightspeed