PODCAST

tv.qiagenbioinformatics.com

Watch tutorials, interviews and much more on our web based TV channel!

science & medicine

All Episodes

55:12

Mining curated knowledge graphs and validating with...

tv.qiagenbioinformatics.com ·

2026/04/13

In an era of near-limitless public experimental data but little standardization, meaningful insights are lost to noise. Large collections of quality experimental data are essential for big-picture discoveries that stand up to scrutiny.In this webinar, you will learn how to feed your drug discovery programs by integrating connections mined from QIAGEN Biomedical Knowledge Base with deeply-curated disease datasets from QIAGEN OmicSoft Lands.Combining unified 'omics datasets with contextual

en-us

56:44

Standardize tumor classification and variant...

tv.qiagenbioinformatics.com ·

2026/04/08

Accurate interpretation of cancer genomics depends on standardized disease classification, tumor characterization and variant annotation. In this joint COSMIC and QIAGEN webinar, we show how these robust frameworks enable reliable cohort building and reproducible research.The webinar covers three themes:Disease classification: COSMIC’s tumor classification and mapping to NCI Thesaurus and EFO.Tumor site and histology subtyping: COSMIC’s highly detailed classification system, conversion of

en-us

01:00:04

Population Genetics in an Era of Genomic Health

tv.qiagenbioinformatics.com ·

2026/03/27

Advances in genomic medicine hold enormous promise, but that promise cannot be fully realized without greater diversity in research and clinical application.In this webinar, Eimear Kenny will discuss how population genetics can drive more accurate, equitable genomic health by expanding representation in genomic studies and databases. Drawing on work from her group at the Icahn School of Medicine at Mount Sinai, she will highlight efforts in expanding the understanding of human genomic diversity by

en-us

01:32:29

Single-cell RNA-seq, cell hashing and spatial...

tv.qiagenbioinformatics.com ·

2026/03/26

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

en-us

29:36

NGS for GMP compliance: New guidelines, new tools

tv.qiagenbioinformatics.com ·

2026/03/23

The updated ICH Q5A(R2) guidelines recommend next-generation sequencing (NGS) as the preferred approach for detecting adventitious agents. From cell line development and viral clearance studies to contamination tracing and product characterization, NGS-based tests outperform older assays in efficacy, sensitivity and reproducibility. This forms the basis for implementation by leading regulatory authorities, including the FDA, EMA, PMDA, and MFDS, signaling a global shift in biosafety testing.Ensure

en-us

01:13:59

From ‘Omics to Insights Part 2: Interpret Your IPA...

tv.qiagenbioinformatics.com ·

2026/03/19

This is the second part of a series on how you can easily turn your ‘omics data into actionable insights using QIAGEN Ingenuity Pathway Analysis (IPA). Here, we’ll introduce you to the QIAGEN Knowledge Base and the different sets of results you can get from an IPA Core Analysis.You will learn:How to predict the activity of enriched pathways, regulators, diseases and moreHow to validate your results by comparing with published datasetsHow to identify key biological themes in your data with the help

en-us

01:23:04

IPA Interpret: A hands-on workshop

tv.qiagenbioinformatics.com ·

2026/03/18

Now, you can access and share the interpretative power of QIAGEN Ingenuity Pathway Analysis (IPA) in an easy-to-consume format – without installing any extra software. IPA Interpret identifies and summarizes the biological themes in your results with the help of AI, creating a shareable, interactive report.You will learn how to:- Create an IPA Interpret report that can be easily shared with others- Gain valuable insight into critical biological pathways, key regulators and more with just a few

en-us

01:23:24

IPA deeper dive miRNA investigation using QIAGEN...

tv.qiagenbioinformatics.com ·

2026/03/16

In this 90-minute training session, you will learn how to identify target mRNAs for your miRNAs of interest and associate them with pathways, diseases, biological functions, tissues and cell types.Topics that will be covered include:How to analyze miRNA-seq datasets alone or both miRNA and corresponding mRNA datasets togetherHow to use QIAGEN IPA without a dataset, using miRNA IDsIntroduction to databases and curated content specific to miRNAHow to effectively apply various filters and

en-us

56:51

From ‘Omics to Insights Part 1: IPA Dataset Prep and...

tv.qiagenbioinformatics.com ·

2026/03/13

This is the first part of a series on how you can easily turn your ‘omics data into actionable insights using QIAGEN Ingenuity Pathway Analysis (IPA). Here, we'll focus on setting up your dataset for IPA upload and analysis.You will learn:The IDs, measurement types and formats that IPA supportsHow IPA uses your data for statistical tests and prediction scoringThe different types and parameters of a Core AnalysisBest practice tips from our expertAbout this seriesFrom ‘Omics to Insights: Data Analysis

en-us

51:43

Hybrid Variant Interpretation: Combining AI + Expert...

tv.qiagenbioinformatics.com ·

2026/03/11

As hereditary NGS testing grows more complex, clinical labs must interpret variants with greater speed and accuracy. This webinar introduces Franklin by QIAGEN, now integrated with HGMD Professional, combining AI-powered workflows and automated ACMG annotation with the leading expert-curated germline database. Together, they enable faster, evidence-backed interpretation, reduce manual review, and boost reporting confidence by minimizing missed clinically relevant findings.In this webinar, you’ll see

en-us

08:52

Hybrid Variant Interpretation: Combining AI + Expert...

tv.qiagenbioinformatics.com ·

2026/03/06

en-us

55:50

Is it oncogenic? Comparing guidelines and QCI...

tv.qiagenbioinformatics.com ·

2026/02/27

Accurate clinical interpretation of somatic cancer variants is critical for diagnosis and guidance of precision oncology treatment. Without shared standards, laboratories and clinical decision-support (CDS) systems have implemented independent approaches, leading to significant variability and highlighting a need for standardization.Through a collaborative effort, ClinGen, the Cancer Genomics Consortium (CGC) and the Variant Interpretation for Cancer Consortium (VICC) have developed a framework for

en-us

01:20:30

OmicSoft Explorer Hands-on Workshop: Easily search...

tv.qiagenbioinformatics.com ·

2026/02/27

This hands-on workshop will cover a highly requested use case using OmicSoft Explorer and IPA Interpret, two new features that QIAGEN IPA* and OmicSoft customers can now access.Specifically, the trainer will go over how to:Easily search for deeply curated high-quality 'omics datasets (RNA-seq, scRNA-seq, etc.) based on user-defined criteria (disease name, drug treatment, etc.) curated from sources such as GEO, SRA, TCGA and moreExplore project details to gain a better understanding of the

en-us

01:31:04

Long reads analysis using QIAGEN CLC Genomics Workbench

tv.qiagenbioinformatics.com ·

2026/02/26

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-

en-us

01:31:23

Multi-omics (metabolomics, proteomics,...

tv.qiagenbioinformatics.com ·

2026/02/26

This 90-minute training session will show you how QIAGEN Ingenuity Pathway Analysis (IPA) helps visualize molecular intricacies and variations at multiple levels, such as transcriptome, proteome and metabolome. Through a series of brief technical vignettes, we will demonstrate how to:- Generate associations among molecular signatures obtained via integrating multi-omics data- Extract mechanisms from multi-omics data for precision medicine- Disease stratification based on multi-omics profiles- Map

en-us

59:25

From targets to treatments: Data-driven drug...

tv.qiagenbioinformatics.com ·

2026/02/20

The early stages of drug development are inherently high-risk; molecule screening, target evaluation and lead refinement can take years and cost millions of dollars – often have little to show for the effort. Indication expansion and drug repurposing can open new avenues of possibility, after careful evaluation of the relationships between the drug, its targets and the new disease context. These connections can be uncovered by mining curated, causal knowledge graphs, which inform smarter target

en-us

04:19

Associating metadata with samples in CLC

tv.qiagenbioinformatics.com ·

2026/02/09

In this video, we demonstrate the import and association of metadata with sample files. https://resources.qiagenbioinformatics.com/manuals/clcgenomicsworkbench/current/index.php?manual=Metadata.html

en-us

02:08

How to view overlapping genes in a Venn Diagram using...

tv.qiagenbioinformatics.com ·

2026/02/09

In this video, we demonstrate how to view details of specific data points in plot views using the synchronized table view. See how you can easily access the list of genes that overlap in a Venn diagram for RNA-seq. This functionality is also available for other types of plots like track lists, expression browsers and volcano plots, to name a few.

en-us

02:55

Introduction to Fork Collections

tv.qiagenbioinformatics.com ·

2026/02/09

Starting with CLC version 26, workflow control can be simplified using fork collections.https://resources.qiagenbioinformatics.com/manuals/clcgenomicsworkbench/current/index.php?manual=Fork.html#SECTION001425230000000000000

en-us

01:34:34

Inflammatory Bowel Disease: Drug Target and Biomarker...

tv.qiagenbioinformatics.com ·

2026/01/28

In this 90-minute training using Inflammatory Bowel Disease (IBD) public data from NCBI GEO through Omicsoft DiseaseLand, attendees will learn how to:• Rapidly query and identify public datasets that fit our search criteria • Discover and validate biomarker expression in disease tissue, different treatments, and response groups • Identify a list of biomarkers specific to responders vs non-responders • Confirm condition-specific biomarkers through gene expression heatmaps • Opportunity for live

en-us

401 results

tv.qiagenbioinformatics.com

All Episodes

Similar Podcasts

科学史评话最新专辑

科学史评话

Hablando con Científicos - Cienciaes.com

cienciaes.com

天方烨谈

基因频道

The Permaculture Podcast

Scott Mann

汪诘：科学有故事（主打）

科学有故事