Next-Generation Sequencing – Multimedia

Unique molecular identifiers (UMIs) now present a solution that can reduce quantitative bias, distinguish between PCR duplicates, and recognize sequencing errors.

The Alissa Clinical Informatics Platform offers integrated sequencing analysis solutions to manage data, helping you to identify, triage and classify variants and generate customizable reports for clinical NGS and CGH.

This eBook has been compiled with this in mind, and has everything you need to know about PCR, including tips on PCT to aid your success, how to set up a PCR lab from scratch plus reducing protocol for PCR.

For this, we need to look at the ultimate output of the genome: the proteome. After many years in the shadow of genomics, proteomics is now ready to step into the spotlight.

Researchers require spatial information and high-plex gene expression data to understand how cells interact with tumors. However, molecular subtyping within a tumor type requires additional stratification at the tissue level to facilitate meaningful subsequent gene expression analysis.

Researchers looking to answer complex biological questions often require increased statistical power, larger studies and deeper sequencing methods.

Explore the psychology of the phenomenon known as cute aggression, which is the urge to squeeze, bite or pinch something cute.

In this infographic, we explore some of the ways that next-generation sequencing (NGS) has changed our understanding of biology and medicine by detailing some of its most important applications.

Genomic DNA (gDNA) is a common input material for next-generation sequencing and gene editing. Therefore, ensuring sample quality prior to analysis is important for generating robust and reliable results.

Scientists are sometimes deemed objective observers of the world in which we live, but that’s not entirely true. They’re still human and can find themselves falling victim to fraudsters just like the lot of us.