Next-Generation Sequencing – Multimedia

Download this guide to learn how to select the appropriate NGS method and sequencing platform, deal with samples of variable quality, and set up and manage the data analysis pipeline.

Dr. Joseph Regan speaks to Lucy Lawrence and shares information from a recently published protocol for the isolation and functional validation of label-retaining quiescent colorectal cancer stem cells from patient-derived organoids for RNA-seq.

At various points throughout the NGS workflow, QC steps are recommended to avoid time and resource wasting, and to help prevent suboptimal sequencing data.

Download this listicle to explore spatial transcriptomics applications and key technologies including next-generation sequencing based-methods, In situ sequencing-based methods and In situ hybridization-based methods.

In this infographic, we delve into the field of cancer genetics, highlight key milestones and explore how genomic approaches are transforming diagnosis and treatment of the disease in the clinic.

Are you interested in automating your NGS workflows but don't know how to get started? Learn more through Genuity Science's Automation Journey: From laying out all workflow steps and estimating sample throughput, to designing the right deck layout to automate QC, Normalization, Library Prep and Pooling.

In this episode of Opinionated Science, the team reviews two studies that show off the power of genomic technologies, from very different angles. One answers key questions about why some women experience extreme vomiting and sickness during pregnancy, and the other reveals why dog breeds aren’t all they are cracked up to be.

In this episode of Teach Me in 10, Lucy Lawrence is joined by Brian Godwin, director of reagent and assay development at Roche Sequencing to discuss primer extension target enrichment for NGS.

Understanding the integrity and quantity of your nucleic acid samples is critical for next-generation sequencing (NGS) and biobanking workflows.

Researchers have unlocked the final gaps in the human genome, and what they tell us could mean big waves for the future of medicine.